DNA methylation of the fragile X locus in somatic and germ cells during fetal development: relevance to the fragile X syndrome and X inactivation.

scientific article published in July 1993

DNA methylation of the fragile X locus in somatic and germ cells during fetal development: relevance to the fragile X syndrome and X inactivation. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1007/BF01232750
P698PubMed publication ID8211380

P2093author name stringLuo S
Reiss AL
Migeon BR
Robinson JC
P433issue4
P921main subjectfragile X syndromeQ221472
DNA methylationQ874745
P304page(s)393-404
P577publication date1993-07-01
P1433published inSomatic Cell and Molecular GeneticsQ7559232
P1476titleDNA methylation of the fragile X locus in somatic and germ cells during fetal development: relevance to the fragile X syndrome and X inactivation.
P478volume19

Reverse relations

cites work (P2860)
Q36140127A variable domain of delayed replication in FRAXA fragile X chromosomes: X inactivation-like spread of late replication
Q35049830AGG/CCT interruptions affect nucleosome formation and positioning of healthy-length CGG/CCG triplet repeats
Q41185035An assay for X inactivation based on differential methylation at the fragile X locus, FMR1.
Q48964703Characterization of the full fragile X syndrome mutation in fetal gametes
Q35889273DNA replication analysis of FMR1, XIST, and factor 8C loci by FISH shows nontranscribed X-linked genes replicate late
Q34021115Differential X reactivation in human placental cells: implications for reversal of X inactivation
Q28566079Downregulation of DNA (cytosine-5-)methyltransferase is a late event in NGF-induced PC12 cell differentiation
Q26770705Epigenetics and Triplet-Repeat Neurological Diseases
Q40855229Genomic structure of the human DNA methyltransferase gene
Q34145956Hypomethylation of an expanded FMR1 allele is not associated with a global DNA methylation defect
Q40868842In vitro reactivation of the FMR1 gene involved in fragile X syndrome
Q37342948Inactive X chromosome-specific reduction in placental DNA methylation
Q40397023Reactivation of inactive X-linked genes
Q41579814Screening for fragile X syndrome: information needs for health planners
Q38318863Synergistic effect of histone hyperacetylation and DNA demethylation in the reactivation of the FMR1 gene.
Q73357821Tetrahelical forms of the fragile X syndrome expanded sequence d(CGG)(n) are destabilized by two heterogeneous nuclear ribonucleoprotein-related telomeric DNA-binding proteins
Q33682895X inactivation of the FMR1 fragile X mental retardation gene
Q73046585X-chromosome inactivation (XCI) patterns in placental tissues of a paternally derived bal t(X;20) case
Q73013123X-linked mental retardation
Q43105065XIST expression and X-chromosome inactivation in human preimplantation embryos
Q49074365XIST expression is repressed when X inactivation is reversed in human placental cells: A model for study ofXIST regulation

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