A human sex-chromosomal gene family expressed in male germ cells and encoding variably charged proteins
about
The DNA sequence of the human X chromosomeA member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardationExpression and localization of VCX/Y proteins and their possible involvement in regulation of ribosome assembly during spermatogenesisStrict evolutionary conservation followed rapid gene loss on human and rhesus Y chromosomesMale infertility and the involvement of the X chromosomeA novel gene family NBPF: intricate structure generated by gene duplications during primate evolutionMutations in apoptosis-inducing factor cause X-linked recessive auditory neuropathy spectrum disorderFrequent gene conversion events between the X and Y homologous chromosomal regions in primates.The role of human and mouse Y chromosome genes in male infertility.The human Y chromosome, in the light of evolution.Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis.Sequencing the mouse Y chromosome reveals convergent gene acquisition and amplification on both sex chromosomes.A Turner syndrome neurocognitive phenotype maps to Xp22.3.A search for novel cancer/testis antigens in lung cancer identifies VCX/Y genes, expanding the repertoire of potential immunotherapeutic targets.X-linked ichthyosis and Crigler-Najjar syndrome I: Coexistence in a male patient with two copy number variable regions of 2q37.1 and Xp22.3.Adaptive evolution of young gene duplicates in mammals.Analysis of X chromosome genomic DNA sequence copy number variation associated with premature ovarian failure (POF).Modulation of neuritogenesis by a protein implicated in X-linked mental retardation.Copy number gain of VCX, X-linked multi-copy gene, leads to cell proliferation and apoptosis during spermatogenesis.Identification of an mRNA-decapping regulator implicated in X-linked mental retardation.The origin and evolution of human ampliconic gene families and ampliconic structure.A map of human PRDM9 binding provides evidence for novel behaviors of PRDM9 and other zinc-finger proteins in meiosis.Characterization of novel genes in AZF regions.Deletions of VCX-A and NLGN4: a variable phenotype including normal intellect.Genetic Villains: Killer Meiotic Drivers.Common structural features characterize interstitial intrachromosomal Xp and 18q triplications.
P2860
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P2860
A human sex-chromosomal gene family expressed in male germ cells and encoding variably charged proteins
description
2000 nî lūn-bûn
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2000 թուականի Յունուարին հրատարակուած գիտական յօդուած
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2000 թվականի հունվարին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年论文
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name
A human sex-chromosomal gene f ...... ding variably charged proteins
@ast
A human sex-chromosomal gene f ...... ding variably charged proteins
@en
A human sex-chromosomal gene f ...... ding variably charged proteins
@en-gb
A human sex-chromosomal gene f ...... ding variably charged proteins
@nl
type
label
A human sex-chromosomal gene f ...... ding variably charged proteins
@ast
A human sex-chromosomal gene f ...... ding variably charged proteins
@en
A human sex-chromosomal gene f ...... ding variably charged proteins
@en-gb
A human sex-chromosomal gene f ...... ding variably charged proteins
@nl
prefLabel
A human sex-chromosomal gene f ...... ding variably charged proteins
@ast
A human sex-chromosomal gene f ...... ding variably charged proteins
@en
A human sex-chromosomal gene f ...... ding variably charged proteins
@en-gb
A human sex-chromosomal gene f ...... ding variably charged proteins
@nl
P356
P1476
A human sex-chromosomal gene f ...... ding variably charged proteins
@en
P2093
P356
10.1093/HMG/9.2.311
P407
P577
2000-01-22T00:00:00Z