Mapping of steroid 21-hydroxylase genes adjacent to complement component C4 genes in HLA, the major histocompatibility complex in man.
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The G9a gene in the human major histocompatibility complex encodes a novel protein containing ankyrin-like repeatsEvidence that gene G7a in the human major histocompatibility complex encodes valyl-tRNA synthetaseIdentification of multiple HTF-island associated genes in the human major histocompatibility complex class III regionHuman major histocompatibility complex contains a new cluster of genes between the HLA-D and complement C4 lociThe molecular biology, biochemistry, and physiology of human steroidogenesis and its disordersHuman major histocompatibility complex contains genes for the major heat shock protein HSP70Human cholesterol side-chain cleavage enzyme, P450scc: cDNA cloning, assignment of the gene to chromosome 15, and expression in the placentaComplete nucleotide sequence of two steroid 21-hydroxylase genes tandemly arranged in human chromosome: a pseudogene and a genuine geneMolecular characterization of the HLA-linked steroid 21-hydroxylase B gene from an individual with congenital adrenal hyperplasiaStructure of human steroid 21-hydroxylase genesMutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency.Pulsed 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.Characterization of frequent deletions causing steroid 21-hydroxylase deficiency.21-hydroxylase deficiency families with HLA identical affected and unaffected sibs.Highly polymorphic XbaI RFLPs of the human 21-hydroxylase genes among Chinese.Variations in the 3'UTR of the CYP21A2 Gene in Heterozygous Females with Hyperandrogenaemia.Aberrant splicing and missense mutations cause steroid 21-hydroxylase [P-450(C21)] deficiency in humans: possible gene conversion products.C4 null phenotypes among lupus erythematosus patients are predominantly the result of deletions covering C4 and closely linked 21-hydroxylase A genes.Direct molecular diagnosis of CYP21 mutations in congenital adrenal hyperplasiaThe swine steroid 21-hydroxylase gene (CYP21): cloning and mapping within the swine leucocyte antigen complex.Dating the primigenial C4-CYP21 duplication in primates.Uniparental isodisomy 6 associated with deficiency of the fourth component of complement.P450XXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasia.Molecular mapping of the human major histocompatibility complex by pulsed-field gel electrophoresisGene conversion-like events cause steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia.Linkage map of the human major histocompatibility complex including the tumor necrosis factor genes.Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants.Extended major histocompatibility complex haplotypes in patients with gluten-sensitive enteropathy.Nonsense mutation causing steroid 21-hydroxylase deficiency.Rearrangements and point mutations of P450c21 genes are distinguished by five restriction endonuclease haplotypes identified by a new probing strategy in 57 families with congenital adrenal hyperplasia.Congenital adrenal hyperplasia and P450 oxidoreductase deficiency.Lethal deletion of the complement component C4 and steroid 21-hydroxylase genes in the mouse H-2 class III region, caused by meiotic recombination.Evolutionary origin of mutations in the primate cytochrome P450c21 geneDistribution of deletions and seven point mutations on CYP21B genes in three clinical forms of steroid 21-hydroxylase deficiencyGene conversion in steroid 21-hydroxylase genes.The immunological detection of a 21-OH deficiency mutation HLA supratype.Evidence for frequent gene conversion in the steroid 21-hydroxylase P-450(C21) gene: implications for steroid 21-hydroxylase deficiencyGene conversions, deletions, and polymorphisms in congenital adrenal hyperplasia.Mutation screening in British 21-hydroxylase deficiency families and development of novel microsatellite based approaches to prenatal diagnosis.Defective antigen presentation and novel structural properties of DR1 from an HLA haplotype associated with 21-hydroxylase deficiency
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P2860
Mapping of steroid 21-hydroxylase genes adjacent to complement component C4 genes in HLA, the major histocompatibility complex in man.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on January 1985
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Mapping of steroid 21-hydroxyl ...... ocompatibility complex in man.
@en
Mapping of steroid 21-hydroxyl ...... ocompatibility complex in man.
@nl
type
label
Mapping of steroid 21-hydroxyl ...... ocompatibility complex in man.
@en
Mapping of steroid 21-hydroxyl ...... ocompatibility complex in man.
@nl
prefLabel
Mapping of steroid 21-hydroxyl ...... ocompatibility complex in man.
@en
Mapping of steroid 21-hydroxyl ...... ocompatibility complex in man.
@nl
P2093
P2860
P356
P1476
Mapping of steroid 21-hydroxyl ...... ocompatibility complex in man.
@en
P2093
M C Carroll
R D Campbell
R R Porter
P2860
P304
P356
10.1073/PNAS.82.2.521
P407
P577
1985-01-01T00:00:00Z