about
Cloning of cDNA and genomic DNA for human cytochrome P-45011 betaPulsed field gel electrophoresis identifies a high degree of variability in the number of tandem 21-hydroxylase and complement C4 gene repeats in 21-hydroxylase deficiency haplotypes.The physiological and pharmacological roles of cytochrome P450 isoenzymes.Aberrant splicing and missense mutations cause steroid 21-hydroxylase [P-450(C21)] deficiency in humans: possible gene conversion products.Congenital adrenal hyperplasia: molecular genetics and alternative approaches to treatment.Dating the primigenial C4-CYP21 duplication in primates.Recent advances in the molecular genetics of congenital and acquired primary adrenocortical failure.CYP21 mutations and congenital adrenal hyperplasia.Management of congenital adrenal hyperplasia.Endocrine disrupting contaminants--beyond the dogmaThe next 150 years of congenital adrenal hyperplasia.Steroid disorders in children: congenital adrenal hyperplasia and apparent mineralocorticoid excessTestis-/embryo-expressed genes are clustered in the mouse H-2K regionThe major histocompatibility complex: the value of extended haplotypes in the analysis of associated immune diseases and disordersDirect Molecular Diagnosis of CYP21A2 Point Mutations in Macedonian and Serbian Patients with 21-Hydroxylase Deficiency.Differential diagnosis of hyperkalemia: an update to a complex problem.Steroid 21-hydroxylase deficiency: three additional mutated alleles and establishment of phenotype-genotype relationships of common mutationsAdrenal changes associated with adrenarcheVariation in clitoral length in rhesus macaques (Macaca mulatta)Haplotypes of the steroid 21-hydroxylase gene region encoding mild steroid 21-hydroxylase deficiency.In Vitro Enzyme Assay of CYP21A2 Mutation (R483Q) by A Novel Method Using Liquid Chromatography-Electrospray Ionization Tandem Mass Spectrometry (LC-ESI-MS/MS).Hirsutism: pilosebaceous unit dysregulation. Role of peripheral and glandular factors.Identifiable hypertension: a new spectrum.Salt-inducible kinase represses cAMP-dependent protein kinase-mediated activation of human cholesterol side chain cleavage cytochrome P450 promoter through the CREB basic leucine zipper domain.Hormonal profiles in Italian late-onset adrenal hyperplasia correlate with HLA class III polymorphisms.Adrenal-specific transgene expression and derivation of conditionally immortal rat adrenocortical cell lines.Congenital adrenal hyperplasia due to combined 21- and 11 beta-hydroxylase deficiency.Regulation of 21-hydroxylase gene expression.[Genetic aspects of fertility disorders].17-alpha-hydroxylase deficiency in three siblings: short- and long-term studies.Hydrocortisone treatment in girls with congenital adrenal hyperplasia inhibits serum dehydroepiandrosterone sulfate and affects the GH-IGF-I system.Clinical and genetic characterization of nonclassic 21-hydroxylase deficiency.Mothers' reactions to prenatal diagnostic procedures and dexamethasone treatment of congenital adrenal hyperplasia.Hirsutism. A practical approach to improving physical and mental well-being.Polymorphism of C4 and CYP21 genes in various primate species.Increased prevalence of heterozygous 21-OH germline mutations in patients with adrenal incidentalomas.Adrenocortical-specific transgene expression directed by steroid hydroxylase gene promoters.Early Androgens Are Related to Childhood Sex-Typed Toy PreferencesDifferential Expression of a Stress-modulating Gene, BRE, in the Adrenal Gland, in Adrenal Neoplasia, and in Abnormal Adrenal Tissues
P2860
Q28298066-0EDD166B-D754-49B4-A189-5DE270D68953Q33564724-CCCC0299-CF77-475B-B4C4-7ABFF1D1A759Q33597477-115C2DCB-729E-4D91-8A53-0F7F9A8B2E6DQ33654059-09D6674C-C2AB-4FD0-B0FF-403EFF55EF71Q33732658-89614287-18BD-45B8-AF97-BF05619146F0Q33960897-9A76F613-E8C8-4958-8B5C-67AC8BB77D53Q34049839-23EFB7A8-3517-4F2A-AD1E-4FF8728AC55AQ34255314-ECD02990-1FBF-45B2-943B-BD0BE47EFF15Q35605081-4D955341-556F-4A98-B673-AEEE5E27448AQ35803357-438C9E70-D5B3-4BA8-BFB9-F6B31098FF36Q36055119-96408CDC-87C6-4896-BFC2-3FB54314F7ADQ36556877-7FAEA60E-943C-4725-A20D-264CBC701750Q36799283-E0B18474-BDFB-4930-8033-91CDBFA9FE7BQ36988175-BA7943A8-073B-4968-BF22-0DA6D1368B22Q37041272-BC356AE9-973D-4E2D-BEED-41E11BC5EA09Q37082990-D446F611-3547-4118-AC5F-806451A2E78DQ37141446-FFD26BAF-8274-4DA5-987A-B10B955F8BFEQ37280754-1AEE3B4F-73D6-436F-BB6D-BAC7983867B9Q37370065-FEFD853A-8516-4340-856C-BF5CA39674A5Q37596669-B087288D-EBC1-4095-A325-49D7BA97E0D1Q37732879-1EDDFADB-B3F7-4AEA-8A3E-5BA617751883Q37771103-452621B0-ED37-45AD-BFA8-DCD584BBD3FCQ38148619-129D255C-D8E4-40DF-8FB2-EF348AA821DFQ38291680-31DE1FB1-79E0-4F14-9BEC-53274FDE81B0Q41090299-2B130D81-4FEB-445F-AA1B-7F4F15E5A48CQ41377387-3A5E13EE-A33E-4383-B64A-A282795C7683Q42193749-F6288787-A848-444C-BC43-6C04CCF10E65Q42493411-B04147D0-3C2F-42ED-8496-BB8BBD4D3003Q43783524-12F97A43-BE28-4D83-A74F-E999046BC357Q44610199-7F7560CB-53A1-434B-BD09-B2DAF747892BQ45984692-A5FA7F6D-ECDC-45B8-B0EB-8DFA3EDF2C82Q46594050-FB35E128-7407-4901-8CB1-9EFFCEC239E5Q51111211-6875BFA2-29A5-4E94-ACBE-B9B820032357Q52057575-15CCB56A-6ED9-427E-99ED-8AC5CA5CDCD3Q52847812-AC64D07A-82AE-4FC3-AF1A-02EAE5999356Q53677744-C7A0F420-48F2-40AA-BEC9-1606B8F20053Q54577701-67A7FFF6-85ED-446A-800F-9A1AD33229F0Q56485283-55CEBE2D-97F9-44C9-893D-951BEC9692CFQ56593639-F6ACBFF9-55D8-408F-AE23-19490C0885D1
P2860
description
1987 nî lūn-bûn
@nan
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
1987年论文
@zh
1987年论文
@zh-cn
name
Congenital adrenal hyperplasia. (1).
@en
Congenital adrenal hyperplasia.
@nl
type
label
Congenital adrenal hyperplasia. (1).
@en
Congenital adrenal hyperplasia.
@nl
prefLabel
Congenital adrenal hyperplasia. (1).
@en
Congenital adrenal hyperplasia.
@nl
P2093
P1476
Congenital adrenal hyperplasia. (1).
@en
P2093
P304
P356
10.1056/NEJM198706113162406
P407
P577
1987-06-01T00:00:00Z