82 results on '"Miller, Walter L"'
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2. Cortisol Response to Operative Stress With Anesthesia in Healthy Children
3. Varied Clinical Presentations of Seven Patients With Mutations in CYP11A1 Encoding the Cholesterol Side-Chain Cleavage Enzyme, P450scc
4. Congenital Adrenal Hyperplasia—More Dogma Bites the Dust
5. The Syndrome of 17,20 Lyase Deficiency
6. Naturally-Occurring Mutation in the Calcium-Sensing Receptor Reveals the Significance of Extracellular Domain Loop III Region for Class C G-Protein-Coupled Receptor Function
7. Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline
8. Clinical, Genetic, and Functional Characterization of Four Patients Carrying Partial Loss-of-Function Mutations in the Steroidogenic Acute Regulatory Protein (StAR)
9. Clinical, Genetic, and Enzymatic Characterization of P450 Oxidoreductase Deficiency in Four Patients
10. Novel P450c17 Mutation H373D Causing Combined 17α-Hydroxylase/17,20-Lyase Deficiency
11. Extraadrenal 21-Hydroxylation by CYP2C19 and CYP3A4: Effect on 21-Hydroxylase Deficiency
12. Homozygous Mutation G539R in the Gene for P450 Oxidoreductase in a Family Previously Diagnosed as Having 17,20-Lyase Deficiency
13. The Common P450 Oxidoreductase Variant A503V Is Not a Modifier Gene for 21-Hydroxylase Deficiency
14. Severe Combined Adrenal and Gonadal Deficiency Caused by Novel Mutations in the Cholesterol Side Chain Cleavage Enzyme, P450scc
15. Vitamin D 1α-Hydroxylase Gene Mutations in Patients with 1α-Hydroxylase Deficiency
16. Apparent Manifesting Heterozygosity in P450 Oxidoreductase Deficiency and Its Effect on Coexisting 21-Hydroxylase Deficiency
17. Nonclassic Congenital Lipoid Adrenal Hyperplasia: A New Disorder of the Steroidogenic Acute Regulatory Protein with Very Late Presentation and Normal Male Genitalia
18. A Genetic Isolate of Congenital Lipoid Adrenal Hyperplasia with Atypical Clinical Findings
19. Lack of Defects in Androgen Production in Children with Hypospadias
20. Editorial: Steroid 17α-Hydroxylase Deficiency—Not Rare Everywhere
21. The 17, 20-Lyase Activity of Cytochrome P450c17 from Human Fetal Testis Favors the Δ5 Steroidogenic Pathway
22. Authors’ Response: Regarding the Consensus Statement on 21-Hydroxylase Deficiency from the Lawson Wilkins Pediatric Endocrine Society and The European Society for Paediatric Endocrinology
23. Clinical, Genetic, and Functional Characterization of Adrenocorticotropin Receptor Mutations Using a Novel Receptor Assay
24. Novel Gene Mutations in Patients with 1α-Hydroxylase Deficiency That Confer Partial Enzyme Activity in Vitro
25. Heterozygous Mutation in the Cholesterol Side Chain Cleavage Enzyme (P450scc) Gene in a Patient with 46,XY Sex Reversal and Adrenal Insufficiency
26. Enzymatic Activities of P450c17 Stably Expressed in Fibroblasts from Patients with the Polycystic Ovary Syndrome*
27. Mutations in the Steroidogenic Acute Regulatory Protein (StAR) in Six Patients with Congenital Lipoid Adrenal Hyperplasia*
28. Role of Cytochrome b5 in the 17,20-Lyase Activity of P450c17
29. Medroxyprogesterone Acetate and Dexamethasone Are Competitive Inhibitors of Different Human Steroidogenic Enzymes*
30. Response to Letter to the Editor: “Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline”
31. Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society* Clinical Practice Guideline
32. In Memoriam: Melvin M. Grumbach (1925–2016)
33. Varied Clinical Presentations of Seven Patients With Mutations inCYP11A1Encoding the Cholesterol Side-Chain Cleavage Enzyme, P450scc
34. Partial Defect in the Cholesterol Side-Chain Cleavage Enzyme P450scc (CYP11A1) Resembling Nonclassic Congenital Lipoid Adrenal Hyperplasia
35. Clinical, Biochemical, and Molecular Characterization of Macronodular Adrenocortical Hyperplasia of the Zona Reticularis: A New Syndrome
36. Steroid 17α-Hydroxylase Deficiency—Not Rare Everywhere
37. The 17, 20-Lyase Activity of Cytochrome P450c17 from Human Fetal Testis Favors the Δ5Steroidogenic Pathway
38. Novel Gene Mutations in Patients with 1α-Hydroxylase Deficiency That Confer Partial Enzyme Activityin Vitro
39. Role of Cytochrome b5in the 17,20-Lyase Activity of P450c17
40. Why Nobody Has P450scc (20,22 Desmoslase) Deficiencyg
41. Long-Term Outcome in Children and Adolescents after Transsphenoidal Surgery for Cushing’s Disease1
42. Spontaneous Feminization in a 46,XX Female Patient with Congenital Lipoid Adrenal Hyperplasia Due to a Homozygous Frameshift Mutation in the Steroidogenic Acute Regulatory Protein*
43. Transcription of the Human Genes for Cytochrome P450scc and P450c17 Is Regulated Differently in Human Adrenal NCI-H295 Cells Than in Mouse Adrenal Y1 Cells1
44. Human Proopiomelanocortin-(79–96), a Proposed Androgen Stimulatory Hormone, Does not Affect Steroidogenesis in Cultured Human Fetal Adrenal Cells*
45. Developmental Expression of Genes for the Stereoidogenic Enzymes P450scc (20,22-Desmolase), P450cl7 (17αHydroxylase/17,20-Lyase), and P450c21 (21-Hydroxylase) in the Human Fetus*
46. Hormonal and Developmental Regulation of Adrenodoxin Messenger Ribonucleic Acid in Steroidogenic Tissues*
47. Hormonal Regulation of P450scc (20,22-desmolase) and P450cl7 (17α-hydroxylase/17,20-lyase) in Cultured Human Granulosa Cells*
48. Endocrine, Histological, and Biochemical Studies of Adrenocorticotropin-Producing Islet Cell Carcinoma of the Pancreas in Childhood with Characterization of Proopiomelanocortin*
49. Synthesis and Glycosylation of Proopiomelanocortin by a Cushing Tumor*
50. Hormonal Regulation of Messenger Ribonucleic Acids for P450scc (Cholesterol Side-Chain Cleavage Enzyme) and P450cl7 (17α-Hydroxylase/17,20-lyase) in Cultured Human Fetal Adrenal Cells*
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