- Society for Pediatric Research (1987)
- The Endocrine Society (1989)
- American Society for Clinical Investigation (1990)
- American Pediatric Society (2006)
Perrin White, M.D.
Chief, Division of Pediatric Endocrinology
- Audre Newman Rapoport Distinguished Chair in Pediatric Endocrinology
- Pediatrics - Endocrinology
Biography
Dr. White is the first holder of the Audre Newman Rapoport Distinguished Chair in Pediatric Endocrinology. Recruited to UT Southwestern in 1994 from Cornell University Medical College in New York City, he is a Professor of Pediatrics and directs the pediatric endocrinology program at UT Southwestern.
Dr. White holds undergraduate and medical degrees from Harvard University. He was a resident in pediatrics at Johns Hopkins Hospital and a research fellow in molecular biology at Rockefeller University. He was on the faculty at Cornell for 13 years and reached the rank of Professor of Pediatrics. His laboratory has studied the molecular basis of several genetic diseases of steroid hormone synthesis and metabolism. Some of these diseases affect growth, sexual differentiation or the ability to conserve salt in the blood, whereas others cause high blood pressure. Most recently, he has branched into study of a very large cell-surface molecule that his laboratory discovered by accident. It is important for development of the nervous system; mutations in this protein cause seizures, deafness and progressive blindness.
Dr. White has received a number of awards and honors. Most recently, he was included in D Magazine's Best Pediatric Specialists list for 2020 and 2021. He also received the Ernst Oppenheimer Award of the Endocrine Society in 1991 and the Mead-Johnson Award of the Society for Pediatric Research in 1996. He has served on several advisory committees for the National Institutes of Health and several editorial boards.
Education & Training
- Fellowship - Rockefeller University Hospital (1978-1980), Molecular Biology
- Residency - Johns Hopkins School of Medicine (1976-1978), Pediatrics
- Medical School - Harvard Medical School (1972-1976)
Professional Associations & Affiliations
Honors & Awards
- D Magazine Best Doctor 2022
- D Magazine Best Pediatric Specialist 2020-2021
- Judson J. Van Wyk Prize 2019, Pediatric Endocrine Society
- Mead Johnson Award 1996, Society for Pediatric Research
- MERIT Award 1994, National Institutes of Health
- The Audre Newman Rapoport Distinguished Chair 1994, Pediatric Endocrinology
- Ernst Oppenheimer Award 1991, The Endocrine Society
- Young Investigator Award 1984, American Society for Histocompatibility and Immunogenetics
Books & Publications
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Books
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Disorders of the Adrenal Gland in Nelson Textbook of Pediatrics, 19th edition, Kliegman RM, Stanton B, Geme JS, Schor NF, Behrman RE, eds.
White PC (2011), Elsevier Saunders -
Genes and Hormones in Textbook of Endocrine Physiology, 6th edition, Kovacs WJ, Ojeda SR, eds.
White PC (2011), Oxford University Press -
Steroid 11ß-Hydroxylase Isozymes in Genetics of Steroid Biosynthesis and Function, 1st edition, Mason JI, ed.
White PC, Rainey WE (2002), London, Taylor & Francis -
The Syndrome of Apparent Mineralocorticoid Excess in Genetic Diseases of the Kidney, 1st edition, Lifton RP, Somlo S, Giebisch GH, Seldin DW, eds.
White PC (2009), Elsevier -
Steroid 11ß-Hydroxylase Deficiency and Related Disorders in Genetic Steroid Disorders, 1st edition, New MI, Lekarev O, Parsa A, Yuen TT, O'Malley B, Hammer GD, eds.
White PC (2013), Elsevier -
Primary Adrenal Insufficiency in Pediatric Endocrinology and Inborn Errors of Metabolism, 2nd Edition.
White PC, Sarafoglou K. (2017), McGraw Hill -
Synthesis and Metabolism of Corticosteroids; Corticosteroid Action in Principles and Practice of Endocrinology and Metabolism, 3rd edition, Becker KL, Rebar RW, eds.
White PC (2001), Lippincott Williams & Wilkins -
Disorders of sexual development in Goldman-Cecil Medicine, 25th edition, Goldman L, Schafer AI, eds.
White PC (2015), Elsevier Saunders -
Endocrine Hypertension in Pediatric Hypertension, 3rd edition, Flynn JT, Ingelfinger JR, Portman RJ, eds.
White PC (2013), New York, Springer
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Disorders of the Adrenal Gland in Nelson Textbook of Pediatrics, 19th edition, Kliegman RM, Stanton B, Geme JS, Schor NF, Behrman RE, eds.
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Publications
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INHALE-1: A Multicenter Randomized Trial of Inhaled Technosphere Insulin in Children With Type 1 Diabetes
Author Collaboration IS, Haller MJ, Kanapka L, Monzavi R, Mouse TJ, Prakasam G, Dewan AK, Dimeglio LA, Laffel LM, Willi SM, Tansey MJ, Nelson BA, Kashmiri H, Wood JR, Latif K, White P, Kipnes M, Rodriguez H, Smith J, Sparling DP, Malik FS, Cymbaluk A, Bhargava A, Ekhlaspour L, Beasley S, Cossen K, Wintergerst KA, Fiallo-Scharer R, Maahs DM, Bethin KE, Wood MA, Hanley PC, Mulukutla SN, Name MV, Blackman SM, Gallagher MP, Clements MA, Sheanon N, Reddy K, Reiner BJ, Gal R, Beck RW Diabetes Care 2026 Jan 49 179-187 -
Disparities in diabetes technology utilization in youth with diabetes
Singh P, Garcia A, Grishman EK, Naranjo D, Hynan LS, Lau M, White P, Gupta OT BMJ Open Diabetes Research and Care 2025 Nov 13 -
A Nested Case-Control Study of Adverse Outcomes in Children With Diabetic Ketoacidosis
Yousif MF, Dolak KD, Adhikari S, White PC Journal of Clinical Endocrinology and Metabolism 2025 Aug 110 e2517-e2522 -
Diabetic Ketoacidosis in a Pediatric Patient with Cystic Fibrosis-related Diabetes
Harinarayanan S, Merritt T, White PC JCEM Case Reports 2025 Jul 3 -
Type 2 Diabetes in a Patient With IMAGe Syndrome Secondary to Polymerase Epsilon Pathogenic Variants
Horvit A, Mulpuri N, Mirfakhraee S, White PC, Abramowitz J JCEM Case Reports 2025 Jul 3 -
Risk Factors for Adverse Outcomes in Children with Diabetic Ketoacidosis
Yousif MF, Dolak KD, Adhikari S, White PC Journal of Clinical Endocrinology and Metabolism 2025 May 110 e1609-e1618 -
Genetics and Pathophysiology of Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Yang M, White PC Journal of Clinical Endocrinology and Metabolism 2025 Feb 110 S1-S12 -
Continuous Glucose Monitor Accuracy for Diabetes Management in Hospitalized Children
Garg N, Lewis K, White PC, Adhikari S Diabetes Care 2025 Feb 48 259-264 -
Maria Iandolo New (1928-2024): Pioneering pediatric endocrinologist
White PC, Miller WL Proceedings of the National Academy of Sciences of the United States of America 2025 Feb 122 e2424275122 -
Adrenocortical Carcinoma
White PC 2024 Jan 3472-3474.e1 -
Adrenal Medulla
White PC 2024 Jan 3444-3449.e2 -
Lipoid Adrenal Hyperplasia
White PC, Yang M 2024 Jan 3462-3471.e1 -
Primary Adrenal Insufficiency
White PC 2024 Jan 3450-3462.e1 -
Pheochromocytoma
White PC 2024 Jan 3479-3481 -
Adrenal Incidentaloma
White PC 2024 Jan 3472-3474.e1 -
Regulation of the Adrenal Cortex
White PC 2024 Jan 3444-3449.e2 -
Virilizing and Feminizing Adrenal Tumors
White PC 2024 Jan 3475-3475.e1 -
Altered End-Organ Sensitivity to Corticosteroids
White PC 2024 Jan 3450-3462.e1 -
Glucocorticoid-Remediable Aldosteronism
White PC, Yang M 2024 Jan 3462-3471.e1 -
Adrenal Insufficiency in the Critical Care Setting
White PC 2024 Jan 3450-3462.e1 -
Primary Aldosteronism
White PC 2024 Jan 3478-3479.e1 -
Deficiency of P450 Oxidoreductase (Antley-Bixler Syndrome)
White PC, Yang M 2024 Jan 3462-3471.e1 -
Aldosterone Synthase Deficiency
White PC, Yang M 2024 Jan 3462-3471.e1 -
Adrenal Steroid Biosynthesis
White PC 2024 Jan 3444-3449.e2 -
Congenital Adrenal Hyperplasia Caused by 21-Hydroxylase Deficiency
White PC, Yang M 2024 Jan 3462-3471.e1 -
Cushing Syndrome
White PC 2024 Jan 3475-3478.e1 -
Adrenal Calcification
White PC 2024 Jan 3472-3474.e1 -
Histology and Embryology
White PC 2024 Jan 3444-3449.e2 -
Secondary and Tertiary Adrenal Insufficiency
White PC 2024 Jan 3450-3462.e1 -
Hydroxychloroquine in Stage 1 Type 1 Diabetes
Author Collaboration ft, Libman I, Bingley PJ, Becker D, Buckner JH, Dimeglio LA, Gitelman SE, Greenbaum C, Haller MJ, Ismail HM, Krischer J, Moore WV, Moran A, Muir AB, Raman V, Steck AK, Toledo FG, Wentworth J, Wherrett D, White P, You L, Herold KC Diabetes Care 2023 Nov 46 2035-2043 -
History of Adrenal Research: From Ancient Anatomy to Contemporary Molecular Biology
Miller WL, White PC Endocrine reviews 2023 Feb 44 70-116 -
Endocrine Hypertension
White PC 2023 Jan 549-571 -
Implementation of After-Hours Nurse Line in an Academic Pediatric Endocrinology Practice
Choudhary A, Adhikari S, White PC Pediatric Diabetes 2023 2023 -
Sexual Development
White PC 2023 Jan 2 1569-1576.e1 -
Steroid 11β-hydroxylase deficiency and related disorders
White PC 2023 Jan 63-79 -
Impact of the COVID-19 pandemic on management of children and adolescents with Type 1 diabetes
Choudhary A, Adhikari S, White PC BMC Pediatrics 2022 Dec 22 -
A Brief History of Congenital Adrenal Hyperplasia
Miller WL, White PC Hormone Research in Paediatrics 2022 Nov 95 529-545 -
Precocious Puberty in a Boy with Bilateral Leydig Cell Tumors due to a Somatic Gain-of-Function LHCGR Variant
Flippo C, Kolli V, Andrew M, Berger S, Bhatti T, Boyce AM, Casella D, Collins MT, Délot E, Devaney J, Hewitt SM, Kolon T, Mallappa A, White PC, Merke DP, Dauber A Journal of the Endocrine Society 2022 Oct 6 -
Positive Impact of the Bionic Pancreas on Diabetes Control in Youth 6-17 Years Old with Type 1 Diabetes: A Multicenter Randomized Trial
Messer LH, Buckingham BA, Cogen F, Daniels M, Forlenza G, Jafri RZ, Mauras N, Muir A, Wadwa RP, White PC, Russell SJ, Damiano ER, El-Khatib FH, Ruedy KJ, Balliro CA, Li Z, Marak MC, Calhoun P, Beck RW Diabetes Technology and Therapeutics 2022 Oct 24 712-725 -
Multicenter, Randomized Trial of a Bionic Pancreas in Type 1 Diabetes
Author Collaboration BP, Russell SJ, Beck RW, Damiano ER, El-Khatib FH, Ruedy KJ, Balliro CA, Li Z, Calhoun P, Wadwa RP, Buckingham B, Zhou K, Daniels M, Raskin P, White PC, Lynch J, Pettus J, Hirsch IB, Goland R, Buse JB, Kruger D, Mauras N, Muir A, McGill JB, Cogen F, Weissberg-Benchell J, Sherwood JS, Castellanos LE, Hillard MA, Tuffaha M, Putman MS, Sands MY, Forlenza G, Slover R, Messer LH, Cobry E, Shah VN, Polsky S, Lal R, Ekhlaspour L, Hughes MS, Basina M, Hatipoglu B, Olansky L, Bhangoo A, Forghani N, Kashmiri H, Sutton F, Choudhary A, Penn J, Jafri R New England Journal of Medicine 2022 Sep 387 1161-1172 -
Emerging treatment for congenital adrenal hyperplasia
White PC Current Opinion in Endocrinology, Diabetes and Obesity 2022 Jun 29 271-276 -
Congenital Adrenal Hyperplasia—Current Insights in Pathophysiology, Diagnostics, and Management
van der Grinten HL, Speiser PW, Faisal Ahmed S, Arlt W, Auchus RJ, Falhammar H, Flück CE, Guasti L, Huebner A, Kortmann BB, Krone N, Merke DP, Miller WL, Nordenström A, Reisch N, Sandberg DE, Stikkelbroeck NM, Touraine P, Utari A, Wudy SA, White PC Endocrine reviews 2022 43 91-159 -
Erratum: Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: An endocrine society clinical practice guideline (The Journal of Clinical Endocrinology and Metabolism (2018) 103:11 (4043-4088) DOI: 10.1210/jc.2018-01865)
Speiser PW, Arlt W, Auchus RJ, Baskin LS, Conway GS, Merke DP, Meyer-Bahlburg HF, Miller WL, Murad MH, Oberfield SE, White PC Journal of Clinical Endocrinology and Metabolism 2021 Jul 106 E2853 -
Effectiveness of Puberty Suppression with Gonadotropin-Releasing Hormone Agonists in Transgender Youth
Mejia-Otero JD, White P, Lopez X Transgender Health 2021 Feb 6 31-35 -
Risk factors for hospitalization in youth with type 1 diabetes: Development and validation of a multivariable prediction model
Mejia-Otero JD, Adhikari S, White PC Pediatric Diabetes 2020 Nov 21 1268-1276 -
Impact of insulin reduction on glycemic control in children attending a residential diabetes camp
Lo HL, Adhikari S, White PC, Grishman EK, Gupta OT Pediatric Diabetes 2019 Dec 20 1094-1099 -
Referrals for Elevated Thyroid Stimulating Hormone to Pediatric Endocrinologists
Gammons S, Presley BK, White PC Journal of the Endocrine Society 2019 Nov 3 2032-2040 -
Letter to the Editor: "Genetic Link between Gender Dysphoria and Sex Hormone Signaling"
White PC Journal of Clinical Endocrinology and Metabolism 2019 Oct 104 4418-4419 -
Case 3: Hypoglycemia in an Infant with Cholestasis
Patni N, Collins K, White P Pediatrics in review 2019 Sep 40 488-490 -
Parental Involvement and Executive Function in Emerging Adults with Type 1 Diabetes
Berg CA, Wiebe DJ, Lee Tracy E, Kelly CS, Mello D, Turner SL, Butner JE, Munion AK, Mansfield JH, White PC, Murray M, Suchy Y Journal of pediatric psychology 2019 Sep 44 970-979 -
Response to letter to the editor: “Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: An endocrine society clinical practice guideline”
Speiser PW, Auchus RJ, Merke DP, Miller WL, White PC Journal of Clinical Endocrinology and Metabolism 2019 Jun 104 1928 -
DNA Polymerase Epsilon Deficiency Causes IMAGe Syndrome with Variable Immunodeficiency
Author Collaboration SC, Logan CV, Murray JE, Parry DA, Robertson A, Bellelli R, Tarnauskaitė Ž, Challis R, Cleal L, Borel V, Fluteau A, Santoyo-Lopez J, Aitman TJ, Biankin AV, Cooke SL, Humphrey WI, Martin S, Mennie L, Meynert A, Miedzybrodzka Z, Murphy F, Nourse C, Semple CA, Williams N, Aitman T, Barroso I, Basel D, Bicknell LS, Goel H, Hu H, Huff C, Hutchison M, Joyce C, Knox R, Lacroix AE, Langlois S, McCandless S, McCarrier J, Metcalfe KA, Morrissey R, Murphy N, Netchine I, O'Connell SM, Olney AH, Paria N, Rosenfeld JA, Sherlock M, Syverson E, White PC, Wise C, Rios JJ American Journal of Human Genetics 2018 Dec 103 1038-1044 -
Executive function predicting longitudinal change in type 1 diabetes management during the transition to emerging adulthood
Berg CA, Wiebe DJ, Suchy Y, Turner SL, Butner J, Munion A, Lansing AH, White PC, Murray M Diabetes Care 2018 Nov 41 2281-2288 -
Fluid Infusion Rates for Pediatric Diabetic Ketoacidosis
White PC The New England journal of medicine 2018 Sep 379 1182-1183 -
Alterations of Cortisol Metabolism in Human Disorders
White PC Hormone Research in Paediatrics 2018 Jul 89 320-330 -
A phase I study of anti-inflammatory therapy with rilonacept in adolescents and adults with type 1 diabetes mellitus
White PC, Adhikari S, Grishman EK, Sumpter KM Pediatric Diabetes 2018 Jun 19 788-793 -
Update on diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
White PC Current Opinion in Endocrinology, Diabetes and Obesity 2018 Jun 25 178-184 -
Camp-based multi-component intervention for families of young children with type 1 diabetes: A pilot and feasibility study
Gupta OT, Mackenzie M, Burris A, Jenkins BB, Collins N, Shade M, Santa-Sosa E, Stewart SM, White PC Pediatric Diabetes 2018 Jun 19 761-768 -
Effects of residential summer camp on body mass index and body composition in type 1 diabetes
Oden JD, Franklin B, Fernandez E, Adhikari S, White PC Pediatric Diabetes 2018 Jun 19 782-787 -
Adolescent Information Management and Parental Knowledge in Non-Latino White and Latino Youth Managing Type 1 Diabetes
Tucker C, Wiebe DJ, Main A, Lee AG, White PC Journal of pediatric psychology 2018 Mar 43 207-217 -
Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: An endocrine society* clinical practice guideline
Speiser PW, Arlt W, Auchus RJ, Baskin LS, Conway GS, Merke DP, Meyer-Bahlburg HF, Miller WL, Murad MH, Oberfield SE, White PC Journal of Clinical Endocrinology and Metabolism 2018 103 4043-4088 -
11-Ketotestosterone Is the Dominant Circulating Bioactive Androgen during Normal and Premature Adrenarche
Rege J, Turcu AF, Kasa-Vubu JZ, Lerario AM, Auchus GC, Auchus RJ, Smith JM, White PC, Rainey WE Journal of Clinical Endocrinology and Metabolism 2018 103 4589-4598 -
Weight gain after treatment of Graves’ disease in children
Alonso GT, Rabon S, White PC Clinical Endocrinology 2018 Jan 88 66-70 -
Endocrine hypertension
White PC 2018 Jan 517-537 -
Risk factors for hospitalization of children with congenital adrenal hyperplasia
Yang M, White PC Clinical Endocrinology 2017 May 86 669-673 -
Iowa Gambling Task Performance Prospectively Predicts Changes in Glycemic Control among Adolescents with Type 1 Diabetes
Suchy Y, Queen TL, Huntbach B, Wiebe DJ, Turner SL, Butner J, Kelly CS, White PC, Murray M, Swinyard M, Berg CA Journal of the International Neuropsychological Society 2017 Mar 23 204-213 -
Age-dependent increases in adrenal cytochrome b5 and serum 5-androstenediol-3-sulfate
Rege J, Karashima S, Lerario AM, Smith JM, Auchus RJ, Kasa-Vubu JZ, Sasano H, Nakamura Y, White PC, Rainey WE Journal of Clinical Endocrinology and Metabolism 2016 Dec 101 4585-4593 -
Graves' disease in children: long-term outcomes of medical therapy
Rabon S, Burton AM, White PC Clinical Endocrinology 2016 Oct 85 632-635 -
The relation of questionnaire and performance-based measures of executive functioning with type 1 diabetes outcomes among late adolescents
Suchy Y, Turner SL, Queen TL, Durracio K, Wiebe DJ, Butner J, Franchow EI, White PC, Murray MA, Swinyard M, Berg CA Health Psychology 2016 Jul 35 661-669 -
Aldosterone Synthase Promoter Polymorphism and Cardiovascular Phenotypes in a Large, Multiethnic Population-Based Study
Byrd JB, Auchus RJ, White PC Journal of Investigative Medicine 2015 Oct 63 862-866 -
Optimizing fluid management of diabetic ketoacidosis
White PC Pediatric Diabetes 2015 Aug 16 317-319 -
Prostacyclin Regulates Bone Growth via the Epac/Rap1 Pathway
Hutchison MR, White PC Endocrinology 2015 Feb 156 499-510 -
Menor morbilidad y mortalidad en niños con cetoacidosis diabética tratados con soluciones isotónicas
White PC, Dickson BA Archivos Argentinos de Pediatria 2014 Dec 112 582 -
Associations of parent-adolescent relationship quality with type 1 diabetes management and depressive symptoms in Latino and Caucasian youth
Main A, Wiebe DJ, Croom AR, Sardone K, Godbey E, Tucker C, White PC Journal of pediatric psychology 2014 Nov 39 1104-1114 -
Individual differences and day-to-day fluctuations in perceived self-regulation associated with daily adherence in late adolescents with type 1 diabetes
Berg CA, Wiebe DJ, Suchy Y, Hughes AE, Anderson JH, Godbey EI, Butner J, Tucker C, Franchow EI, Pihlaskari AK, King PS, Murray MA, White PC Journal of pediatric psychology 2014 Oct 39 1038-1048 -
Fertility in patients with congenital adrenal hyperplasia
Reichman DE, White PC, New MI, Rosenwaks Z Fertility and sterility 2014 Feb 101 301-309 -
Steroid 11β-Hydroxylase Deficiency and Related Disorders
White PC 2013 Sep 71-85 -
Maternal depressive symptoms predict adolescent healthcare utilization and charges in youth with type 1 diabetes (T1D)
Clayton KM, Stewart SM, Wiebe DJ, McConnel CE, Hughes CW, White PC Health Psychology 2013 Sep 32 1013-1022 -
Low morbidity and mortality in children with diabetic ketoacidosis treated with isotonic fluids
White PC, Dickson BA Journal of Pediatrics 2013 Sep 163 761-766 -
HSD11B2 CA-repeat and sodium balance
Mune T, Morita H, Takada N, Yamamoto Y, Isomura Y, Suwa T, Takeda J, White PC, Kaku K Hypertension Research 2013 Jul 36 614-619 -
Longer HSD11B2 CA-repeat in impaired glucose tolerance and type 2 diabetes
Mune T, Suwa T, Morita H, Isomura Y, Takada N, Yamamoto Y, Hayashi M, Yamakita N, Sasaki A, Takeda N, Takeda J, White PC, Kaku K Endocrine Journal 2013 60 671-678 -
P53 and cellular glucose uptake
De La Torre AJ, Rogoff D, White PC Endocrine Research 2013 38 32-39 -
Optimizing newborn screening for congenital adrenal hyperplasia
White PC Journal of Pediatrics 2013 163 10-12 -
Endocrine hypertension
White PC 2013 Jan 379-394 -
Time to failure of oral therapy in children with type 2 diabetes: A single center retrospective chart review
Barnes NS, White PC, Hutchison MR Pediatric Diabetes 2012 Nov 13 578-582 -
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency: From birth to adulthood
White P, Bachega TS Seminars in reproductive medicine 2012 Oct 30 400-409 -
Transient neonatal hypocalcemia: Presentation and outcomes
Thomas TC, Smith JM, White PC, Adhikari S Pediatrics 2012 Jun 129 e1461-e1467 -
Toll-like receptors, the NLRP3 inflammasome, and interleukin-1Β in the development and progression of type 1 diabetes
Grishman EK, White PC, Savani RC Pediatric Research 2012 Jun 71 626-632 -
Vitamin D deficiency in obese children and its relationship to glucose homeostasis
Olson ML, Maalouf NM, Oden JD, White PC, Hutchison MR Journal of Clinical Endocrinology and Metabolism 2012 Jan 97 279-285 -
Preliminary studies related to anti-interleukin-1β therapy in children with newly diagnosed type 1 diabetes
Sumpter KM, Adhikari S, Grishman EK, White PC Pediatric Diabetes 2011 Nov 12 656-667 -
Developmental trajectories of metabolic control among white, black, and Hispanic youth with type 1 diabetes
Wang JT, Wiebe DJ, White PC Journal of Pediatrics 2011 Oct 159 571-576 -
Disorders of Sexual Development
White PC 2011 Jul 2 1511-1519 -
Presentation of primary adrenal insufficiency in childhood
Hsieh S, White PC Journal of Clinical Endocrinology and Metabolism 2011 Jun 96 E925-E928 -
Somatic items in the assessment of depressive symptoms in pediatric patients with diabetes
Stewart SM, Simmons A, White PC Journal of Behavioral Medicine 2011 Apr 34 112-119 -
Congenital adrenal hyperplasia owing to 11β-hydroxylase deficiency
White PC 2011 7-8 -
Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: An endocrine society clinical practice guideline (The Journal of Clinical Endocrinology & Metabolism (2010) 95 (4133-4160))
Speiser PW, Azziz R, Baskin LS, Ghizzoni L, Hensle TW, Merke DP, Meyer-Bahlburg HF, Miller WL, Montori VM, Oberfield SE, Ritzen M, White PC Journal of Clinical Endocrinology and Metabolism 2010 Nov 95 5137 -
Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: An Endocrine Society clinical practice guideline
Speiser PW, Azziz R, Baskin LS, Ghizzoni L, Hensle TW, Merke DP, Meyer-Bahlburg HF, Miller WL, Montori VM, Oberfield SE, Ritzen M, White PC Journal of Clinical Endocrinology and Metabolism 2010 Sep 95 4133-4160 -
A randomized controlled trial comparing motivational interviewing in education to structured diabetes education in teens with type 1 diabetes
Wang YC, Stewart SM, Mackenzie M, Nakonezny PA, Edwards D, White PC Diabetes Care 2010 Aug 33 1741-1743 -
Minireview: Steroidogenic factor 1: Its roles in differentiation, development, and disease
Schimmer BP, White PC Molecular Endocrinology 2010 Jul 24 1322-1337 -
Sitagliptin treatment of patients with type 2 diabetes does not affect CD4+ T-cell activation
White PC, Chamberlain-Shea H, de la Morena MT Journal of Diabetes and its Complications 2010 May 24 209-213 -
Contribution of hexose-6-phosphate dehydrogenase to NADPH content and redox environment in the endoplasmic reticulum
Rogoff D, Black K, Mcmillan DR, White PC Redox Report 2010 Apr 15 64-70 -
Stimulated growth hormone concentrations in obese pediatric patients with mild and severe insulin resistance: A pilot study
Radack JA, White PC, Adams-Huet B, Oden JD Journal of Pediatric Endocrinology and Metabolism 2010 Apr 23 355-361 -
Autosomal recessive familial neurohypophyseal diabetes insipidus: Onset in early infancy
Libdeh AA, Levy-Khademi F, Abdulhadi-Atwan M, Bosin E, Korner M, White PC, Zangen DH European Journal of Endocrinology 2010 Feb 162 221-226 -
SCF, BDNF, and Gas6 are regulators of growth plate chondrocyte proliferation and differentiation
Hutchison MR, Bassett MH, White PC Molecular Endocrinology 2010 Jan 24 193-203 -
Studies on the very large G protein-coupled receptor: From initial discovery to determining its role in sensorineural deafness in higher animals
McMillan DR, White PC 2010 76-86 -
Neonatal screening for congenital adrenal hyperplasia
White PC Nature Reviews Endocrinology 2009 Sep 5 490-498 -
Screening for type 2 diabetes in obese youth
Shah S, Kublaoui BM, Oden JD, White PC Pediatrics 2009 Aug 124 573-579 -
Patient- versus parent-reported psychological symptoms as predictors of type 1 diabetes management in adolescents
Stewart SM, Wang JT, Wang YC, White PC children's Health Care 2009 Jul 38 200-212 -
Institution of basal-bolus therapy at diagnosis for children with type 1 diabetes mellitus
Adhikari S, Adams-Huet B, Wang YC, Marks JF, White PC Pediatrics 2009 Apr 123 e673-e678 -
Adrenarche
Oberfield SE, White PC Reviews in Endocrine and Metabolic Disorders 2009 Mar 10 1-2 -
The Syndrome of Apparent Mineralocorticoid Excess
White PC 2009 291-300 -
Physiological roles of 11β-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase
White PC, Rogoff D, McMillan DR Current opinion in pediatrics 2008 Aug 20 453-457 -
A Modular Analysis Framework for Blood Genomics Studies: Application to Systemic Lupus Erythematosus
Chaussabel D, Quinn C, Shen J, Patel P, Glaser C, Baldwin N, Stichweh D, Blankenship D, Li L, Munagala I, Bennett L, Allantaz F, Mejias A, Ardura M, Kaizer E, Monnet L, Allman W, Randall H, Johnson D, Lanier A, Punaro M, Wittkowski KM, White P, Fay J, Klintmalm G, Ramilo O, Palucka AK, Banchereau J, Pascual V Immunity 2008 Jul 29 150-164 -
Predictors of first-year growth response to a fixed-dose growth hormone treatment in children born small for gestational age: Results of an open-label, multicenter trial in the United States
Rapaport R, Saenger P, Wajnrajch MP, Boston B, Carakushansky M, Chernausek S, Clark P, Cohen J, Counts D, Donohoue P, Fuqua J, Geffner M, Harbison M, Hardin D, White P, Kemp S, Lee P, Mauras N, Neufeld N, Oberfield S, Plotnick L, Reiter E, Richards G, Richton S, Schultz R, Silverman L, Tollefsen S, Wright N, Yu M, Zipf W Journal of Pediatric Endocrinology and Metabolism 2008 May 21 411-422 -
Deletion of hexose-6-phosphate dehydrogenase activates the unfolded protein response pathway and induces skeletal myopathy
Lavery GG, Walker EA, Turan N, Rogoff D, Ryder JW, Shelton JM, Richardson JA, Falciani F, White PC, Stewart PM, Parker KL, McMillan DR Journal of Biological Chemistry 2008 Mar 283 8453-8461 -
Improved glycemic control in adolescents with type 1 diabetes mellitus who attend diabetes camp
Wang YC, Stewart S, Tuli E, White P Pediatric Diabetes 2008 Feb 9 29-34 -
Abnormalities of glucose homeostasis and the hypothalamic-pituitary-adrenal axis in mice lacking hexose-6-phosphate dehydrogenase
Rogoff D, Ryder JW, Black K, Yan Z, Burgess SC, McMillan DR, White PC Endocrinology 2007 Oct 148 5072-5080 -
Gene expression in peripheral blood mononuclear cells from children with diabetes
Kaizer EC, Glaser CL, Chaussabel D, Banchereau J, Pascual V, White PC Journal of Clinical Endocrinology and Metabolism 2007 Sep 92 3705-3711 -
Impaired overnight counterregulatory hormone responses to spontaneous hypoglycemia in children with type 1 diabetes
Mauras N, Chase PH, Fiallo-Scharer R, Fisher JH, Tallant B, Tsalikian E, Tansey MJ, Larson LF, Coffey J, Wysocki T, Mauras N, Fox LA, Bird K, Lofton KL, Buckingham BA, Wilson DM, Block JM, Clinton P, Weinzimer SA, Tamborlane WV, Doyle EA, Sikes K, Beck RW, Ruedy KJ, Kollman C, Xing D, Kalajian A, Stockdale CR, Steffes MW, Bucksa JM, Nowicki ML, Van Hale CA, Makky V, Singh R, Grave GD, Linder B, Winer KK, Becker DM, Cox C, Ryan CM, White NH, White PC Pediatric Diabetes 2007 Aug 8 199-205 -
Insulin-like growth factor-I and fibroblast growth factor, but not growth hormone, affect growth plate chondrocyte proliferation
Hutchison MR, Bassett MH, White PC Endocrinology 2007 Jul 148 3122-3130 -
Hexose 6-phosphate dehydrogenase (H6PD) and corticosteroid metabolism
White PC, Rogoff D, McMillan DR, Lavery GG Molecular and Cellular Endocrinology 2007 Feb 265-266 89-92 -
The accuracy of the FreeStyle Navigator continuous glucose monitoring system in children with type 1 diabetes
Wilson DM, Beck RW, Tamborlane WV, Dontchev MJ, Kollman C, Chase P, Fox LA, Ruedy KJ, Tsalikian E, Weinzimer SA, Fiallo-Scharer R, Messer L, Tallant B, Tansey MJ, Larson LF, Coffey J, Cabbage J, Wysocki T, Mauras N, Bird K, Englert K, Buckingham BA, Block JM, Clinton P, Caswell K, Doyle EA, Mokotoff H, Steffen A, Xing D, Stockdale CR, Jackson J, Steffes MW, Bucksa JM, Nowicki ML, Van Hale CA, Makky V, Grave GD, Horlick M, Teff K, Winer KK, Becker DM, Cleary P, Ryan CM, White NH, White PC Diabetes Care 2007 Jan 30 59-64 -
Prevention of hypoglycemia during exercise in children with type 1 diabetes by suspending basal insulin
Tsalikian E, Fox L, Janz KF, Wilson D, Chase HP, Fiallo-Scharer R, Messer L, Tallant B, Tansey MJ, Larson LF, Coffey J, Wysocki T, Mauras N, Fox LA, Bird K, Englert K, Buckingham BA, Wilson DM, Block JM, Clinton P, Weinzimer SA, Tamborlane WV, Doyle EA, Sikes K, Beck RW, Ruedy KJ, Kollman C, Xing D, Stockdale CR, Steffes MW, Bucksa JM, Nowicki ML, Van Hale CA, Makky V, Grave GD, Teff K, Winer KK, Becker DM, Cleary P, Ryan CM, White NH, White PC Diabetes Care 2006 Oct 29 2200-2204 -
The 2006 Annual Meeting of the Lawson Wilkins Pediatric Endocrine Society (LWPES), April 29 - May 2, San Francisco
Geffner ME, Clarke WL, Fuqua J, Gordon CM, Kasa-Vubu JZ, Lee MM, Levitsky LL, Lustig RH, Menon RK, Rogol AD, Saenger P, Silverman L, Silverstein JH, White PC Pediatric Endocrinology Reviews 2006 Jun 3 403-410 -
Ontogeny of adrenal steroid biosynthesis: Why girls will be girls
White PC Journal of Clinical Investigation 2006 Apr 116 872-874 -
Elevated expression of luteinizing hormone receptor in aldosterone- producing adenomas
Saner-Amigh K, Mayhew BA, Mantero F, Schiavi F, White PC, Rao CV, Rainey WE Journal of Clinical Endocrinology and Metabolism 2006 Mar 91 1136-1142 -
Hexose-6-phosphate dehydrogenase knock-out mice lack 11β- hydroxysteroid dehydrogenase type 1-mediated glucocorticoid generation
Lavery GG, Walker EA, Draper N, Jeyasuria P, Marcos J, Shackleton CH, Parker KL, White PC, Stewart PM Journal of Biological Chemistry 2006 Mar 281 6546-6551 -
The very large G-protein-coupled receptor VLGR1: A component of the ankle link complex required for the normal development of auditory hair bundles
McGee J, Goodyear RJ, McMillan DR, Stauffer EA, Holt JR, Locke KG, Birch DG, Legan PK, White PC, Walsh EJ, Richardson GP Journal of Neuroscience 2006 26 6543-6553 -
Genetic interaction among three genomic regions creates distinct contributions to early-and late-onset type 1 diabetes mellitus
Felner EI, Klitz W, Ham M, Lazaro AM, Stastny P, Dupont B, White PC Pediatric Diabetes 2005 Dec 6 213-220 -
Association of Lys173Arg polymorphism with CYP11B2 expression in normal adrenal glands and aldosterone-producing adenomas
Tanahashi H, Mune T, Takahashi Y, Isaji M, Suwa T, Morita H, Yamakita N, Yasuda K, Deguchi T, White PC, Takeda J Journal of Clinical Endocrinology and Metabolism 2005 Nov 90 6226-6231 -
Genotypes at 11β-hydroxysteroid dehydrogenase type 11B1 and hexose-6-phosphate dehydrogenase loci are not risk factors for apparent cortisone reductase deficiency in a large population-based sample
White PC Journal of Clinical Endocrinology and Metabolism 2005 Oct 90 5880-5883 -
Depression and diabetes in children and adolescents
Stewart SM, Rao U, White P Current opinion in pediatrics 2005 Oct 17 626-631 -
Expression profiles for steroidogenic enzymes in adrenocortical disease
Bassett MH, Mayhew B, Rehman K, White PC, Mantero F, Arnaldi G, Stewart PM, Bujalska I, Rainey WE Journal of Clinical Endocrinology and Metabolism 2005 Sep 90 5446-5455 -
Analysis of the very large G-protein coupled receptor gene (Vlgr1/Mass1/USH2C) in zebrafish
Gibert Y, McMillan DR, Kayes-Wandover K, Meyer A, Begemann G, White PC Gene 2005 Jul 353 200-206 -
Correlation between left ventricular mass and urinary sodium excretion in specific genotypes of CYP11B2
Isaji M, Mune T, Takada N, Yamamoto Y, Suwa T, Morita H, Takeda J, White PC Journal of hypertension 2005 Jun 23 1149-1157 -
Self-care and glycemic control in adolescents with type I diabetes
Stewart SM, Emslie GJ, Klein D, Haus S, White P children's Health Care 2005 Jun 34 235-244 -
Hexose-6-phosphate dehydrogenase confers oxo-reductase activity upon 11β-hydroxysteroid dehydrogenase type 1
Bujalska IJ, Draper N, Michailidou Z, Tomlinson JW, White PC, Chapman KE, Walker EA, Stewart PM Journal of molecular endocrinology 2005 Jun 34 675-684 -
Depressive symptoms predict hospitalization for adolescents with type 1 diabetes mellitus
Stewart SM, Rao U, Emslie GJ, Klein D, White PC Pediatrics 2005 May 115 1315-1319 -
Comparison of fingerstick hemoglobin A1c levels assayed by DCA 2000 with the DCCT/EDIC central laboratory assay: Results of a Diabetes Research in Children Network (DirecNet) Study
Chase HP, Fiallo-Scharer R, Fisher JH, Tallant B, Tsalikian E, Tansey MJ, Larson LF, Coffey J, Wysocki T, Mauras N, Fox LA, Bird K, Lofton KL, Buckingham BA, Wilson DM, Block JM, Clinton P, Weinzimer SA, Tamborlane WV, Doyle EA, Sikes K, Beck RW, Ruedy KJ, Kollman C, Xing D, Silvester CR, Becker DM, Cox C, Ryan CM, White NH, White PC, Steffes MW, Bucksa JM, Nowicki ML, Van Hale CA, Grave GD, Linder B, Winer KK Pediatric Diabetes 2005 Mar 6 13-16 -
Editorial: Polymorphisms in CYP11B genes and 11-hydroxylase activity
White PC, Rainey WE Journal of Clinical Endocrinology and Metabolism 2005 Feb 90 1252-1255 -
Loss of the transmembrane and cytoplasmic domains of the very large G-protein-coupled receptor-1 (VLGR1 or Mass1) causes audiogenic seizures in mice
McMillan DR, White PC Molecular and Cellular Neuroscience 2004 Jun 26 322-329 -
Aldosterone synthase deficiency and related disorders
White PC Molecular and Cellular Endocrinology 2004 Mar 217 81-87 -
The regulation of aldosterone synthase expression
Bassett MH, White PC, Rainey WE Molecular and Cellular Endocrinology 2004 Mar 217 67-74 -
Bedside ketone determination in diabetic children with hyperglycemia and ketosis in the acute care setting
Ham MR, Okada P, White PC Pediatric Diabetes 2004 Mar 5 39-43 -
The Orphan Nuclear Receptors NURR1 and NGFIB Regulate Adrenal Aldosterone Production
Bassett MH, Suzuki T, Sasano H, White PC, Rainey WE Molecular Endocrinology 2004 Feb 18 279-290 -
Hypothyroidism in siblings due to a homozygous mutation of the TSH-β subunit gene
Felner EI, Dickson BA, White PC Journal of Pediatric Endocrinology and Metabolism 2004 17 669-672 -
A role for the NGFI-B family in adrenal zonation and adrenocortical disease
Bassett MH, White PC, Rainey WE Endocrine Research 2004 30 567-574 -
Mutations in the genes encoding 11β-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase interact to cause cortisone reductase deficiency
Draper N, Walker EA, Bujalska IJ, Tomlinson JW, Chalder SM, Arlt W, Lavery GG, Bedendo O, Ray DW, Laing I, Malunowicz E, White PC, Hewison M, Mason PJ, Connell JM, Shackleton CH, Stewart PM Nature genetics 2003 Aug 34 434-439 -
Congenital adrenal hyperplasia
Speiser PW, White PC New England Journal of Medicine 2003 Aug 349 776-788 -
Aldosterone: Direct effects on and production by the heart
White PC Journal of Clinical Endocrinology and Metabolism 2003 Jun 88 2376-2383 -
Role of local 11β-hydroxysteroid dehydrogenase type 2 expression in determining the phenotype of adrenal adenomas
Mune T, Morita H, Suzuki T, Takahashi Y, Isomura Y, Tanahashi T, Daido H, Yamakita N, Deguchi T, Sasano H, White PC, Yasuda K Journal of Clinical Endocrinology and Metabolism 2003 Feb 88 864-870 -
Differential regulation of aldosterone synthase and 11β-hydroxylase transcription by steroidogenic factor-1
Bassett MH, Zhang Y, Clyne C, White PC, Rainey WE Journal of molecular endocrinology 2002 28 125-135 -
The endocrinologist's approach to the intersex patient
White PC Advances in experimental medicine and biology 2002 511 107-120 -
Role of local 11β-hydroxysteroid dehydrogenase type 2 (HSD11B2) expression in determining the phenotype of adrenal adenomas
Mune T, Morita H, Suzuki T, Takahashi Y, Isomura Y, Tanahashi T, Daido H, Yamakita N, Deguchi T, Sasano H, Yasuda K, White PC Endocrine Research 2002 28 751-752 -
Very large G protein-coupled receptor-1, the largest known cell surface protein, is highly expressed in the developing central nervous system
Randy McMillan D, Kayes-Wandover KM, Richardson JA, White PC Journal of Biological Chemistry 2002 Jan 277 785-792 -
Long-term consequences of childhood-onset congenital adrenal hyperplasia
White PC, Speiser PW Best Practice and Research: Clinical Endocrinology and Metabolism 2002 Jan 16 273-288 -
Clinical case seminar: Type 1 aldosterone synthase deficiency presenting in a middle-aged man
Kayes-Wandover KM, Lee Schindler RE, Taylor HC, White PC Journal of Clinical Endocrinology and Metabolism 2001 Apr 86 1008-1012 -
Congenital hyperreninemic hypoaldosteronism unlinked to the aldosterone synthase (CYP11B2) gene
Kayes-Wandover KM, Tannin GM, Shulman D, Peled D, Jones KL, Karaviti L, White PC Journal of Clinical Endocrinology and Metabolism 2001 86 5379-5382 -
Steroid 11β-hydroxylase deficiency and related steroid
White PC Endocrinology and Metabolism Clinics of North America 2001 30 61-79 -
Possible association but no linkage of the HSD11B2 gene encoding the kidney isozyme of 11β-hydroxysteroid dehydrogenase to hypertension in Black people
White PC, Agarwal AK, Li A, Howard Pratt HN, Caulfield M, Clark A, McTernan C, Stewart PM Clinical Endocrinology 2001 55 249-252 -
Improving management of diabetic ketoacidosis in children
Felner EI, White PC Pediatrics 2001 108 735-740 -
11Β-hydroxysteroid dehydrogenase and its role in the syndrome of apparent mineralocorticoid excess
White PC American Journal of the Medical Sciences 2001 322 308-315 -
Congenital adrenal hyperplasias
White PC Best Practice and Research: Clinical Endocrinology and Metabolism 2001 15 17-41 -
Structure of the VPATPD gene encoding subunit D of the human vacuolar proton ATPase
Agarwal AK, White PC Biochemical and Biophysical Research Communications 2000 Dec 279 543-547 -
Time course of recovery of adrenal function in children treated for leukemia
Felner EI, Thompson MT, Ratliff AF, White PC, Dickson BA Journal of Pediatrics 2000 Jul 137 21-24 -
Prepubertal gynecomastia: indirect exposure to estrogen cream.
Felner EI, White PC Pediatrics 2000 Apr 105 E55 -
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
White PC, Speiser PW Endocrine reviews 2000 21 245-291 -
Steroidogenic enzyme gene expression in the human heart
Kayes-Wandover KM, White PC Journal of Clinical Endocrinology and Metabolism 2000 85 2519-2525 -
Regulation of human CYP11B2 and CYP11B1: Comparing the role of the common CRE/Ad1 element
Bassett MH, Zhang Y, White PC, Rainey WE Endocrine Research 2000 26 941-951 -
CA-repeat polymorphism in intron 1 of HSD11B2: Effects on gene expression and salt sensitivity
Agarwal AK, Giacchetti G, Lavery G, Nikkila H, Palermo M, Ricketts M, McTernan C, Bianchi G, Manunta P, Strazzullo P, Mantero F, White PC, Stewart PM Hypertension 2000 36 187-194 -
Erratum: Congenital adrenal hyperplasia due to 21-hydroxylase deficiency (Endocrine Reviews (2000) 21 (245-291))
White PC, Speiser PW Endocrine reviews 2000 21 550 -
Transcriptional regulation of human 11β-hydroxylase (hCYP11B1)
Wang XL, Bassett M, Zhang Y, Su Y, Clyne C, White PC, Rainey WE Endocrinology 2000 141 3587-3594 -
Genotype-phenotype correlations of mutations and polymorphisms in HSD11B2, the gene encoding the kidney isozyme of 11β-hydroxysteroid dehydrogenase
White PC, Agarwal AK, Nunez BS, Giacchetti G, Mantero F, Stewart PM Endocrine Research 2000 26 771-780 -
Sequence similarities between a novel putative G protein-coupled receptor and Na+/Ca2+ exchangers define a cation binding domain
Nikkila H, McMillan DR, Nunez BS, Pascoe L, Curnow KM, White PC Molecular Endocrinology 2000 14 1351-1364 -
Baroreflex sensitivity and variants of the renin angiotensin system genes
Ylitalo A, Juhani Airaksinen KE, Hautanen A, Kupari M, Carson M, Virolainen J, Savolainen M, Kauma H, Antero Kesäniemi Y, White PC, Huikuri HV Journal of the American College of Cardiology 2000 Jan 35 194-200 -
Joint effects of an aldosterone synthase (CYP11B2) gene polymorphism and classic risk factors on risk of myocardial infarction
Hautanen A, Toivanen P, Mänttäri M, Tenkanen L, Kupari M, Manninen V, Kayes KM, Rosenfeld S, White PC Circulation 1999 Nov 100 2213-2218 -
Mutants of 11-hydroxysteroid dehydrogenase (11-hsd2) with partial activity: Improved correlations between genotype and biochemical phenotype in apparent mineralocorticoid excess
Nunez BS, Rogerson FM, Mune T, Igarashi Y, Nakagawa Y, Phillipov G, Moudgil A, Travis LB, Palermo M, Shackleton C, White PC Hypertension 1999 Oct 34 638-642 -
Functional analysis of four CYP21 mutations from Spanish patients with congenital adrenal hyperplasia
Nunez BS, Lobato MN, White PC, Meseguer A Biochemical and Biophysical Research Communications 1999 Sep 262 635-637 -
Aldosterone synthase (CYP11B2) polymorphisms and cardiovascular function
White PC, Hautanen A, Kupari M Journal of Steroid Biochemistry and Molecular Biology 1999 Apr 69 409-412 -
Expression of human kidney 11β-hydroxysteroid dehydrogenase (11-HSD2) in bacteria
Nunez BS, Mune T, White PC Biochemical and Biophysical Research Communications 1999 Feb 255 652-656 -
Apparent cortisone reductase deficiency: A functional defect in 11β-hydroxysteroid dehydrogenase type 1
Jamieson A, Wallace AM, Andrew R, Nunez BS, Walker BR, Fraser R, White PC, Connell JM Journal of Clinical Endocrinology and Metabolism 1999 84 3570-3574 -
Pseudoaldosteronism and the epithelial sodium channel
Nunez BS, White PC Current Opinion in Endocrinology and Diabetes 1999 6 238-244 -
Autosomal recessive familial neurohypophyseal diabetes insipidus with continued secretion of mutant weakly active vasopressin
Willcutts MD, Felner E, White PC Human molecular genetics 1999 8 1303-1307 -
Prominent sex steroid metabolism in human lymphocytes
Zhou Z, Shackleton CH, Pahwa S, White PC, Speiser PW Molecular and Cellular Endocrinology 1998 Mar 138 61-69 -
Associations between human aldosterone synthase (CYP11B2) gene polymorphisms and left ventricular size, mass, and function
Kupari M, Hautanen A, Lankinen L, Koskinen P, Virolainen J, Nikkila H, White PC Circulation 1998 Feb 97 569-575 -
Functional adrenal zonation and regulation of aldosterone biosynthesis
Rainey WE, White P Current Opinion in Endocrinology and Diabetes 1998 Jan 5 175-182 -
Associations between aldosterone synthase gene polymorphism and the adrenocortical function in males
Hautanena A, Lankinen L, Kupari M, Jänne OA, Adlercreutz H, Nikkilä H, White PC Journal of Internal Medicine 1998 244 11-18 -
Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency
Speiser PW, White PC Clinical Endocrinology 1998 49 411-417 -
Aldosterone synthase (CYP11B2) polymorphisms and cardiovascular function
White PC, Hautanen A, Kupari M Endocrine Research 1998 24 797-804 -
CYP11B1 mutations causing non-classic adrenal hyperplasia due to 11β- hydroxylase deficiency
Joehrer K, Geley S, Strasser-Wozak EM, Azziz R, Wollmann HA, Schmitt K, Kofler R, White PC Human molecular genetics 1997 Oct 6 1829-1834 -
Variation in placental type 2 11β-hydroxysteroid dehydrogenase activity is not related to birth weight or placental weight
Rogerson FM, Kayes KM, White PC Molecular and Cellular Endocrinology 1997 Apr 128 103-109 -
Steroid 21-hydroxylase expression and activity in human lymphocytes
Zhou Z, Agarwal VR, Dixit N, White P, Speiser PW Molecular and Cellular Endocrinology 1997 Mar 127 11-18 -
11β-Hydroxysteroid dehydrogenase and the syndrome of apparent mineralocorticoid excess
White PC, Mune T, Agarwal AK Endocrine reviews 1997 18 135-156 -
11β-Hydroxysteroid dehydrogenase and its role in the syndrome of apparent mineralocorticoid excess
White PC, Mune T, Rogerson FM, Kayes KM, Agarwal AK Pediatric Research 1997 Jan 41 25-29 -
Molecular analysis of 11β-hydroxysteroid dehydrogenase and its role in the syndrome of apparent mineralocorticoid excess
White PC, Mune T, Rogerson FM, Kayes KM, Agarwal AK Steroids 1997 Jan 62 83-88 -
Abnormalities of aldosterone synthesis and action in children
White PC Current opinion in pediatrics 1997 Jan 9 424-430 -
Corrigendum: Analysis of the promoter of the NAD + dependent 11β-hydroxysteroid dehydrogenase (HSD11K) gene in JEG3 human choricarcinoma cells (Molecular and Cellular Endocrinology (1996) 121 (93-99) PII: S0303720796038555)
Agarwal AK, White PC Molecular and Cellular Endocrinology 1997 Jan 129 241-242 -
Angiotensin II and potassium regulate human CYP11B2 transcription through common cis-elements
Clyne CD, Zhang Y, Slutsker L, Mathis JM, White PC, Rainey WE Molecular Endocrinology 1997 11 638-649 -
Identification of non-amplifying CYP21 genes when using PCR-based diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH) affected pedigrees
Day DJ, Speiser PW, Schulze E, Bettendorf M, Fitness J, Barany F, White PC Human molecular genetics 1996 Dec 5 2039-2048 -
Inherited forms of mineralocorticoid hypertension
White PC Hypertension 1996 Dec 28 927-936 -
Analysis of the promoter of the NAD + dependent 11β-hydroxysteroid dehydrogenase (HSD11K) gene in JEG-3 human choriocarcinoma cells
Agarwal AK, White PC Molecular and Cellular Endocrinology 1996 Jul 121 93-99 -
Apparent mineralocorticoid excess: Genotype is correlated with biochemical phenotype
Mune T, White PC Hypertension 1996 27 1193-1199 -
CYP11B1 mutations causing congenital adrenal hyperplasia due to 11β- hydroxylase deficiency
Geley S, Kapelari K, Jöhrer K, Peter M, Glatzl J, Vierhapper H, Schwarz S, Helmberg A, Sippell WG, White PC, Kofler R Journal of Clinical Endocrinology and Metabolism 1996 81 2896-2901 -
Calcium regulates human CYP11B2 transcription
Clyne CD, White PC, Rainey WE Endocrine Research 1996 22 485-492 -
Genetic disorders affecting aldosterone synthesis and action
White PC Current Opinion in Endocrinology and Diabetes 1996 Jan 3 220-226 -
Analysis of the human gene encoding the kidney isozyme of 11β-hydroxysteroid dehydrogenase
Agarwal AK, Rogerson FM, Mune T, White PC Journal of Steroid Biochemistry and Molecular Biology 1995 Dec 55 473-479 -
Gene conversions and unequal crossovers between CYP21 (steroid 21-hydroxylase gene) and CYP21P involve different mechanisms
Tusié-Luna MT, White PC Proceedings of the National Academy of Sciences of the United States of America 1995 Nov 92 10796-10800 -
Alternatively spliced human type 1 angiotensin II receptor mRNAs are translated at different efficiencies and encode two receptor isoforms
Curnow KM, Pascoe L, Davies E, White PC, Corvol P, Clauser E Molecular Endocrinology 1995 Sep 9 1250-1262 -
Detection of steroid 21-hydroxylase alleles using gene-specific PCR and a multiplexed ligation detection reaction
Day DJ, Speiser PW, White PC, Barany F Genomics 1995 Sep 29 152-162 -
Gene structure and chromosomal localization of the human HSD11K gene encoding the kidney (Type 2) isozyme of 11β-hydroxysteroid dehydrogenase
Agarwal AK, Rogerson FM, Mune T, White PC Genomics 1995 Sep 29 195-199 -
Human hypertension caused by mutations in the kidney isozyme of 11β–hydroxysteroid dehydrogenase
Mune T, Rogerson FM, Nikkilä H, Agarwal AK, White PC Nature genetics 1995 Aug 10 394-399 -
Genetic disorders of steroid hormone synthesis and metabolism
New MI, White PC Bailliere's Clinical Endocrinology and Metabolism 1995 Jul 9 525-554 -
Mutations in putative glycosylation sites of rat 11β-hydroxysteroid dehydrogenase affect enzymatic activity
Agarwal AK, Mune T, Monder C, White PC Biochimica et Biophysica Acta - Protein Structure and Molecular Enzymology 1995 Apr 1248 70-74 -
Clinical, biochemical and genetic features of five extended kindred's with glucocorticoid-suppressible hyperaldosteronism
Jamieson A, Slutsker L, Inglis G, Campbell M, Fraser R, White P, Connell J Endocrine Research 1995 21 463-469 -
Haplotype analysis of CYP11b2
White PC, Slutsker L Endocrine Research 1995 21 437-442 -
Functional studies of 11β-hydroxysteroid dehydrogenase
White PC, Mune T, Agarwal AK Steroids 1995 Jan 60 65-68 -
Four is not more than two
Russell DW, White PC American Journal of Human Genetics 1995 57 1002-1005 -
Cloning of cDNA encoding an NAD+-dependent isoform of 11βhydroxysteroid dehydrogenase in sheep kidney
Agarwal AK, Mune T, Monder C, White PC Endocrine Research 1995 21 389-397 -
Glucocorticoid-suppressible hyperaldosteronism: Effects of crossover site and parental origin of chimaeric gene on phenotypic expression
Jamieson A, Slutsker L, Inglis GC, Fraser R, White PC, Connell JM Clinical Science 1995 88 563-570 -
NAD+-dependent Isoform of 11β-Hydroxysteroid Dehydrogenase: Cloning and Characterization of cDNA from Sheep Kidney
Agarwal AK, Mune T, Monder C, White PC Journal of Biological Chemistry 1994 Oct 269 25959-25962 -
Disorders of steroid 11β-hydroxylase isozymes
White PC, Curnow KM, Pascoe L Endocrine reviews 1994 Aug 15 421-438 -
Disorders of aldosterone biosynthesis and action
White PC New England Journal of Medicine 1994 Jul 331 250-258 -
Defects in the HSD11 gene encoding 11β-hydroxysteroid dehydrogenase are not found in patients with apparent mineralocorticoid excess or 11-oxoreductase deficiency
Nikkilä H, Tannin GM, New MI, Taylor NF, Kalaitzoglou G, Monder C, White PC Pediatric Nephrology 1994 Jun 8 -
Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization and Southern blot
Speiser PW, White PC, Dupont J, Zhu D, Mercado AB, New MI Human genetics 1994 Apr 93 424-428 -
Genetic analysis of 11β-hydroxysteroid dehydrogenase
White PC, Obeid J, Agarwal AK, Tannin GM, Nikkila H Steroids 1994 Feb 59 111-115 -
Steroid 11β-hydroxylase deficiency and related disorders
White PC, Speiser PW Endocrinology and Metabolism Clinics of North America 1994 23 325-339 -
Molecular genetic prenatal diagnosis of congenital adrenalhyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization
Speiser PW, White PC, Dupont J, Zhu D, Mercado A, New MI Recent progress in hormone research 1994 49 367-371 -
Genetic diseases of steroid metabolism.
White PC Vitamins and Hormones 1994 49 131-195 -
Mutations in Steroid 21‐Hydroxylase (CYP21)
White PC, Tusie-Luna MT, New MI, Speiser PW Human mutation 1994 3 373-378 -
Defects in the HSD11 gene encoding 11β-hydroxysteroid dehydrogenase are not found in patients with apparent mineralocorticoid excess or 11-oxoreductase deficiency
Nikkilä H, Tannin GM, New MI, Taylor NF, Kalaitzoglou G, Monder C, White PC Journal of Clinical Endocrinology and Metabolism 1993 Sep 77 687-691 -
Genomic organization of the mouse B-lymphocyte activation antigen B7
Selvakumar A, White PC, Dupont B Immunogenetics 1993 Jun 38 292-295 -
Mutations in the CYP11B1 gene causing congenital adrenal hyperplasia and hypertension cluster in exons 6, 7, and 8
Curnow KM, Slutsker L, Vitek J, Cole T, Speiser PW, New MI, White PC, Pascoe L Proceedings of the National Academy of Sciences of the United States of America 1993 May 90 4552-4556 -
Mutations in human 11β-hydroxylase genes: 11β-hydroxylase deficiency in Jews of Morocco and corticosterone methyl-oxidase II deficiency in Jews of Iran
Rösler A, White PC Journal of Steroid Biochemistry and Molecular Biology 1993 Apr 45 99-106 -
Transcripts originating in intron 1 of the HSD11 (11β-Hydroxysteroid dehydrogenase) gene encode a truncated polypeptide that is enzymatically inactive
Obeid J, Curnow KM, Aisenberg J, White PC Molecular Endocrinology 1993 Feb 7 154-160 -
11β-Hydroxysteroid Dehydrogenase
Monder C, White PC Vitamins and Hormones 1993 Jan 47 187-271 -
Molecular biology of 11β-hydroxylase and 11β-hydroxysteroid dehydrogenase enzymes
White PC, Pascoe L, Curnow KM, Tannin G, Rösler A Journal of Steroid Biochemistry and Molecular Biology 1992 Dec 43 827-835 -
Tyr-179 and Lys-183 are essential for enzymatic activity of 11β-hydroxysteroid dehydrogenase
Obeid J, White PC Biochemical and Biophysical Research Communications 1992 Oct 188 222-227 -
A novel gene constitutively expressed in human lymphoid cells is inducible with interferon-γ in myeloid cells
Trapani JA, Browne KA, Dawson MJ, Ramsay RG, Eddy RL, Shows TB, White PC, Dupont B Immunogenetics 1992 Sep 36 369-376 -
Disorders of steroid 11β-hydroxylase isozymes
White PC, Pascoe L Trends in Endocrinology and Metabolism 1992 Aug 3 229-234 -
R339H and P453S: CYP21 mutations associated with nonclassic steroid 21-hydroxylase deficiency that are not apparent gene conversions
Helmberg A, Tusie-Luna MT, Tabarelli M, Kofler R, White PC Molecular Endocrinology 1992 Aug 6 1318-1322 -
Genetic analysis of the human type-1 angiotensin II receptor
Curnow KM, Pascoe L, White PC Molecular Endocrinology 1992 Jul 6 1113-1118 -
Genomic organization and chromosomal location of the human gene encoding the B-lymphocyte activation antigen B7
Selvakumar A, Mohanraj BK, Eddy RL, Shows TB, White PC, Dupont B Immunogenetics 1992 May 36 175-181 -
Polymorphism in the RD (D6S45) gene
White PC, Vitek J, Lahita RG, Speiser PW Human genetics 1992 May 89 243-244 -
Genotype of Yupik Eskimos with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Speisere PW, New MI, Tannin GM, Pickering D, Yang SY, White PC Human genetics 1992 Mar 88 647-648 -
Prenatal diagnosis/treatment in families at risk for infants with steroid 21-hydroxylase deficiency (congenital adrenal hyperplasia)
Karaviti LP, Mercado AB, Mercado MB, Speiser PW, Buegeleisen M, Crawford C, Antonian L, White PC, New MI Journal of Steroid Biochemistry and Molecular Biology 1992 Mar 41 445-451 -
Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Speiser PW, Dupont J, Zhu D, Serrat J, Buegeleisen M, Tusie-Luna MT, Lesser M, New MI, White PC Journal of Clinical Investigation 1992 90 584-595 -
Glucocorticoid-suppressible hyperaldosteronism results from hybrid genes created by unequal crossovers between CYP11B1 and CYP11B2
Pascoe L, Curnow KM, Slutsker L, Connell JM, Speiser PW, New MI, White PC Proceedings of the National Academy of Sciences of the United States of America 1992 89 8327-8331 -
Genetic basis of endocrine disease 2: Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
White PC, New MI Journal of Clinical Endocrinology and Metabolism 1992 Jan 74 6-11 -
Mutations in the human CYP11B2 (aldosterone synthase) gene causing corticosterone methyloxidase II deficiency
Pascoe L, Curnow KM, Slutsker L, Rösler A, White PC Proceedings of the National Academy of Sciences of the United States of America 1992 89 4996-5000 -
Molecular cloning and expression of rat liver 3α-hydroxysteroid dehydrogenase
Cheng KC, White PC, Qin KN Molecular Endocrinology 1991 Jun 5 823-828 -
A mutation in CYP11B1 (Arg-448 → His) associated with steroid 11β-hydroxylase deficiency in jews of Moroccan origin
White PC, Dupont J, New MI, Leiberman E, Hochberg Z, Rösler A Journal of Clinical Investigation 1991 May 87 1664-1667 -
A mutation (Pro-30 to Leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency allele
Tusie-Luna MT, Speiser PW, Dumic M, New MI, White PC Molecular Endocrinology 1991 May 5 685-692 -
The human gene for 11β-hydroxysteroid dehydrogenase: Structure, tissue distribution, and chromosomal localization
Tannin GM, Agarwal AK, Monder C, New MI, White PC Journal of Biological Chemistry 1991 266 16653-16658 -
Defects in cortisol metabolism causing low-renin hypertension
White PC Endocrine Research 1991 17 85-107 -
The product of the CYP11B2 gene is required for aldosterone biosynthesis in the human adrenal cortex
Curnow KM, Tusie-Luna MT, Pascoe L, Natarajan R, Gu JL, Nadler JL, White PC Molecular Endocrinology 1991 5 1513-1522 -
Distribution of deletions and seven point mutations on CYP21B genes in three clinical forms of steroid 21-hydroxylase deficiency
Mornet E, Crété P, Kuttenn F, Raux-Demay MC, Boué J, White PC, Boué A American Journal of Human Genetics 1991 Jan 48 79-88 -
Aldosterone Synthesis in Salt-Wasting Congenital Adrenal Hyperplasia with Complete Absence of Adrenal 21-Hydroxylase
Speiser PW, Agdere L, Ueshiba H, White PC, New MI New England Journal of Medicine 1991 Jan 324 145-149 -
Molecular pathology of steroid 21-hydroxylase deficiency
Strachan T, White PC Journal of Steroid Biochemistry and Molecular Biology 1991 40 537-543 -
11Beta‐Hydroxysteroid Dehydrogenase Messenger Ribonucleic Acid Expression, Bioactivity and Immunoreactivity in Rat Cerebellum
Moisan MP, Seckl JR, Brett LP, Monder C, Agarwal AK, White PC, Edwards CR Journal of Neuroendocrinology 1990 Dec 2 853-858 -
Determination of functional effects of mutations in the steroid 21-hydroxylase gene (CYP21) using recombinant vaccinia virus
Tusie-Luna MT, Traktman P, White PC Journal of Biological Chemistry 1990 Dec 265 20916-20922 -
Characterization of 11 β-hydroxysteroid dehydrogenase gene expression: Identification of multiple unique forms of messenger ribonucleic acid in the rat kidney
Krozowski Z, Stuchbery S, White P, Monder C, Funder JW Endocrinology 1990 Dec 127 3009-3013 -
First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency)
Speiser PW, Laforgia N, Kato K, Pareira J, Khan R, Yang SY, Whorwood C, White PC, Elias S, Schriock E, Schriock E, Simpson JL, Taslimi M, Najjar J, May S, Mills G, Crawford C, New MI Obstetrical and Gynecological Survey 1990 Oct 45 707-709 -
First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency)
Speiser PW, Laforgia N, Kato K, Pareira J, Khan R, Yang SY, Whorwood C, White PC, Elias S, Schriock E, Schriock E, Simpson JL, Taslimi M, Najjar J, May S, Mills G, Crawford C, New MI Journal of Clinical Endocrinology and Metabolism 1990 Apr 70 838-848 -
Expression of 11β-hydroxysteroid dehydrogenase using recombinant vaccinia virus
Agarwal AK, Tusie-Luna MT, Monder C, White PC Molecular Endocrinology 1990 4 1827-1832 -
Structure of the Human RD Gene: A Highly Conserved Gene in the Class III Region of the Major Histocompatibility Complex
Speiser PW, White PC DNA 1989 Dec 8 745-751 -
Clinical and genetic characterization of nonclassic 21-hydroxylase deficiency
Speiser PW, New MI, White PC Endocrine Research 1989 Jan 15 257-276 -
Characterization of two genes encoding human steroid 11β-hydroxylase (P-450(11β))
Mornet E, Dupont J, Vitek A, White PC Journal of Biological Chemistry 1989 264 20961-20967 -
Analysis of mutations causing steroid 21-hydroxylase deficiency
White PC Endocrine Research 1989 15 239-256 -
Structural and functional analysis of the promoter region of the gene encoding mouse steroid 11β-hydroxylase
Mouw AR, Rice DA, Meade JC, Chua SC, White PC, Schimmer BP, Parker KL Journal of Biological Chemistry 1989 264 1305-1309 -
Steroid 21-hydroxylase deficiency
White PC, Crawford C, New MI Current opinion in pediatrics 1989 1 436-440 -
Cloning and expression of rat cDNA encoding corticosteroid 11β-dehydrogenase
Agarwal AK, Monder C, Eckstein B, White PC Journal of Biological Chemistry 1989 264 18939-18943 -
λPMV: A Bacteriophage Vector Allowing Single-Step Retrieval of cDNAs Following Expression in Mammalian Cells
DiSanto JP, Small TN, Flomenberg N, White PC DNA 1988 Dec 7 735-741 -
An Inherited Defect in Aldosterone Biosynthesis Caused by a Mutation in or near the Gene for Steroid 11-Hydroxylase
Globerman H, Rosler A, Theodor R, New MI, White PC New England Journal of Medicine 1988 Nov 319 1193-1197 -
6 Molecular genetics of congenital adrenal hyperplasia
White PC, New MI Bailliere's Clinical Endocrinology and Metabolism 1988 Nov 2 941-965 -
Molecular genetic analysis of nonclassic steroid 21 hydroxylase deficiency associated with hla b14 dri
Speiser PW, New MI, White PC Obstetrical and Gynecological Survey 1988 Nov 43 693-694 -
Molecular Genetic Analysis of Nonclassic Steroid 21-Hydroxylase Deficiency Associated with HLA-B14,DR1
Speiser PW, New MI, White PC New England Journal of Medicine 1988 Jul 319 19-23 -
Prenatal diagnosis of 21-hydroxylase deficiency by the complementary deoxyribonucleic acid probe for cytochrome P-450C-21OH
Reindollar RH, Lewis JB, White PC, Fernhoff PM, McDonough PG, Whitney JB American journal of obstetrics and gynecology 1988 Mar 158 545-547 -
Immunohistochemical localization of cytochrome P-450C21 in human adrenal cortex and its relation to endocrine function
Sasano H, White PC, New MI, Sasano N Human Pathology 1988 Feb 19 181-185 -
Molecular cloning of an inducible serine esterase gene from human cytotoxic lymphocytes
Trapani JA, Klein JL, White PC, Dupont B Proceedings of the National Academy of Sciences of the United States of America 1988 85 6924-6928 -
Nonsense mutation causing steroid 21-hydroxylase deficiency
Globerman H, Amor M, Parker KL, New MI, White PC Journal of Clinical Investigation 1988 82 139-144 -
Immunohistochemistry of cytochrome P-450 21-hydroxylase: Microscopic examination of the enzyme in the bovine adrenal cortex and kidney
Sasano H, White PC, New MI, Sasano N Endocrinology 1988 Jan 122 291-295 -
Mutation in the CYP21B gene (Ile-172→Asn) causes steroid 21-hydroxylase deficiency
Amor M, Parker KL, Globerman H, New MI, White PC Proceedings of the National Academy of Sciences of the United States of America 1988 85 1600-1604 -
Characterization of frequent deletions causing steroid 21-hydroxylase deficiency
White PC, Vitek A, Dupont B, New MI Proceedings of the National Academy of Sciences of the United States of America 1988 85 4436-4440 -
Congenital Adrenal Hyperplasia
Miller WL, White PC, New M, Dupont b New England Journal of Medicine 1987 Nov 317 1413-1415 -
Cloning of cDNA encoding steroid 11 beta-hydroxylase (P450c11).
Chua SC, Szabo P, Vitek A, Grzeschik KH, John M, White PC Proceedings of the National Academy of Sciences of the United States of America 1987 Oct 84 7193-7197 -
Frequent deletion and duplication of the steroid 21-hydroxylase genes
Werkmeister JW, New MI, Dupont BO, White PC Obstetrical and Gynecological Survey 1987 Sep 42 572-573 -
Congenital Adrenal Hyperplasia
White PC, New MI, Dupont B New England Journal of Medicine 1987 Jun 316 1519-1524 -
Congenital Adrenal Hyperplasia
White PC, New MI, Dupont B New England Journal of Medicine 1987 Jun 316 1580-1586 -
UNTERSUCHUNGEN ZUR MOLEKULAREN BIOLOGIE DES ADRENOGENITALEN SYNDROMS. NEUE MOGLICHKEITEN DES HETERO-ZYGOTEN-SCREENING
Bohm BO, Rosak C, Bohm TL, White PC, Schöffling K Deutsche Medizinische Wochenschrift 1987 112 87-89 -
Genetics of steroid 21-hydroxylase deficiency.
White PC Recent progress in hormone research 1987 43 305-336 -
Analysis of Steroid 21-Hydroxylase Gene in Five Unrelated Japanese Patients with 21-Hydroxylase Deficiency
Nakura J, Miki T, Fukuchi KI, Shimizu K, Nose O, Takai S, White PC, Honjo T, Kumahara Y Endocrinologia Japonica 1987 34 373-379 -
Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiency
Mornet E, Couillin P, Kutten F, Raux MC, White PC, Cohen D, Boué A, Dausset J Human genetics 1986 Dec 74 402-408 -
Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein
Donohoue PA, van Dop C, McLean RH, White PC, Jospe N, Migeon CJ Journal of Clinical Endocrinology and Metabolism 1986 May 62 995-1002 -
Bovine Steroid 21-Hydroxylase: Regulation of Biosynthesis
John ME, Okamura T, Dee A, Adler B, John MC, White PC, Simpson ER, Waterman MR Biochemistry 1986 May 25 2846-2853 -
Restriction maps and restriction fragment length polymorphisms of the human 21-hydroxylase genes
Donohoue PA, Jospe N, Migeon CJ, McLean RH, Bias WB, White PC, Van Dop C Biochemical and Biophysical Research Communications 1986 Apr 136 722-729 -
Steroid 21-hydroxylase deficiency and the major histocompatibility complex
White PC, Werkmeister J, New MI, Dupont B Human Immunology 1986 Apr 15 404-415 -
Rearrangement of 21-hydroxylase genes in disease-associated MHC supratypes
Garlepp MJ, Wilton AN, Dawkins RL, White PC Immunogenetics 1986 Feb 23 100-105 -
Frequency deletion and duplication of the steroid 21-hydroxylase genes
Werkmeister JW, New MI, Dupont B, White PC American Journal of Human Genetics 1986 39 461-469 -
Nucleotide sequence analysis of murine 21-hydroxylase genes: Mutations affecting gene expression
Chaplin DD, Galbraith LJ, Seidman JG, White PC, Parker KL Proceedings of the National Academy of Sciences of the United States of America 1986 83 9601-9605 -
Structure of human steroid 21-hydroxylase genes
White PC, New MI, Dupont B Proceedings of the National Academy of Sciences of the United States of America 1986 83 5111-5115 -
Classical and late-onset forms of congenital adrenal hyperplasia caused by 21-OH deficiency reveal different alterations in the C4/21-OH gene region
Boehm BO, Rosak C, Boehm TL, Kuehnl P, White PC, Schöffling K Molecular Biology and Medicine 1986 3 437-448 -
Molecular Cloning of Steroid 21‐Hydroxylase
White PC, New MI, Dupont B Annals of the New York Academy of Sciences 1985 Nov 458 277-287 -
Adrenal 21‐Hydroxylase Cytochrome P‐450 Genes within the MHC Class III Region
White PC, New MI, Dupont B Immunological Reviews 1985 Oct 87 123-150 -
Molecular linkage of the genes encoding adrenal steroid 21-hydroxylase to the S region of the murine major histocompatibility complex (MHC)
Chaplin D, Parker K, White P, Seidman J Federation Proceedings 1985 44 No. 2175 -
Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man
White PC, Grossberger D, Onufer BJ, Chaplin DD, New MI, Dupont B, Strominger JL Proceedings of the National Academy of Sciences of the United States of America 1985 82 1089-1093 -
Cloning and Expression of cDNA Encoding a Bovine Adrenal Cytochrome P‐450 Specific for Steroid 21‐Hydroxylation (P‐450C21)
White PC, New MI, Dupont B Annals of the New York Academy of Sciences 1984 Dec 435 229-230 -
Cloning and expression of cDNA encoding a bovine adrenal cytochrome P-450 specific for steroid 21-hydroxylation
White PC, New MI, Dupont B Proceedings of the National Academy of Sciences of the United States of America 1984 81 1986-1990 -
Two steroid 21-hydroxylase genes are located in the murine S region
White PC, Chaplin DD, Weis JH, Dupont B, New MI, Seidman JG Nature 1984 312 465-467 -
HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation
White PC, New MI, Dupont B Proceedings of the National Academy of Sciences of the United States of America 1984 81 7505-7509 -
Molecular cloning of steroid 21-hydroxylase
White PC, Dupont B, New MI Endocrine Research 1984 10 335-345 -
Nonelectrolyte diffusion across lipid bilayer systems
Poznansky M, Tong S, White PC, Milgram JM, Solomon AK Journal of General Physiology 1976 Jan 67 45-66
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INHALE-1: A Multicenter Randomized Trial of Inhaled Technosphere Insulin in Children With Type 1 Diabetes
Research
- Type 2 diabetes
- Type 1 diabetes
- Genetic diseases of steroid hormone biosynthesis and metabolism
Children's Medical Center of Dallas
1935 Medical District DriveDallas, Texas 75235 214-730-5437 Directions to Children's Medical Center of Dallas at Children's Medical Center of Dallas, Dallas