Sex difference in methylation of single-copy genes in human meiotic germ cells: implications for X chromosome inactivation, parental imprinting, and origin of CpG mutations.
about
A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical regionDNA methylation is the primary silencing mechanism for a set of germ line- and tumor-specific genes with a CpG-rich promoterRett syndrome and MeCP2: linking epigenetics and neuronal functionA maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndromeA novel chromatin protein, distantly related to histone H2A, is largely excluded from the inactive X chromosomeXIST RNA paints the inactive X chromosome at interphase: evidence for a novel RNA involved in nuclear/chromosome structureGene structure, DNA methylation, and imprinted expression of the human SNRPN geneSex chromosomal transposable element accumulation and male-driven substitutional evolution in humans.Histone variant macroH2A contains two distinct macrochromatin domains capable of directing macroH2A to the inactive X chromosome.Differential X reactivation in human placental cells: implications for reversal of X inactivation.The ontogeny of allele-specific methylation associated with imprinted genes in the mouse.Cytosine methylation and the unequal developmental potentials of the oocyte and sperm genomesMethylation levels at selected CpG sites in the factor VIII and FGFR3 genes, in mature female and male germ cells: implications for male-driven evolutionProteolipoprotein gene analysis in 82 patients with sporadic Pelizaeus-Merzbacher Disease: duplications, the major cause of the disease, originate more frequently in male germ cells, but point mutations do not. The Clinical European Network on BrainImpact of cadmium exposure during pregnancy on hepatic glucocorticoid receptor methylation and expression in rat fetus.Germ-line origins of mutation in families with hemophilia B: the sex ratio varies with the type of mutationDirect and indirect estimation of the sex ratio of mutation frequencies in hemophilia AGenomic imprinting: mechanism and role in human pathology.Characterization of the factor VIII defect in 147 patients with sporadic hemophilia A: family studies indicate a mutation type-dependent sex ratio of mutation frequencies.Epigenetic changes in response to tai chi practice: a pilot investigation of DNA methylation marks.Phenotypic variation in a genetically identical population of mice.Developmental differences in methylation of human Alu repeatsProgrammed genetic instability: a tumor-permissive mechanism for maintaining the evolvability of higher species through methylation-dependent mutation of DNA repair genes in the male germ line.Analysis of CpG suppression in methylated and nonmethylated species.A potentially critical Hpa II site of the X chromosome-linked PGK1 gene is unmethylated prior to the onset of meiosis of human oogenic cellsDNA methylation and gene expression.Inactive X chromosome-specific reduction in placental DNA methylation.Methylation patterns of testis-specific genes.Dynamic histone modifications mark sex chromosome inactivation and reactivation during mammalian spermatogenesisWhat does the nature of the MECP2 mutation tell us about parental origin and recurrence risk in Rett syndrome?The factor IX gene as a model for analysis of human germline mutations: an update.Myopia, intelligence, and the expanding human neocortex: behavioral influences and evolutionary implications.Characteristics, causes and evolutionary consequences of male-biased mutation.Differences between human sperm and somatic cell DNA in CpG methylation within the HLA class I chromosomal region.How important is DNA replication for mutagenesis?The importance of advanced parental age in the origin of neurofibromatosis type 1.Monozygotic twins discordant for neurofibromatosis 1.
P2860
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P2860
Sex difference in methylation of single-copy genes in human meiotic germ cells: implications for X chromosome inactivation, parental imprinting, and origin of CpG mutations.
description
1990 nî lūn-bûn
@nan
1990年の論文
@ja
1990年学术文章
@wuu
1990年学术文章
@zh
1990年学术文章
@zh-cn
1990年学术文章
@zh-hans
1990年学术文章
@zh-my
1990年学术文章
@zh-sg
1990年學術文章
@yue
1990年學術文章
@zh-hant
name
Sex difference in methylation ...... , and origin of CpG mutations.
@en
Sex difference in methylation ...... , and origin of CpG mutations.
@nl
type
label
Sex difference in methylation ...... , and origin of CpG mutations.
@en
Sex difference in methylation ...... , and origin of CpG mutations.
@nl
prefLabel
Sex difference in methylation ...... , and origin of CpG mutations.
@en
Sex difference in methylation ...... , and origin of CpG mutations.
@nl
P356
P1476
Sex difference in methylation ...... , and origin of CpG mutations.
@en
P2093
Driscoll DJ
P304
P356
10.1007/BF01233363
P577
1990-05-01T00:00:00Z