Characterization of the full fragile X syndrome mutation in fetal gametes.
about
Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiaeFragile X syndrome: the FMR1 CGG repeat distribution among world populationsComparative genomics and molecular dynamics of DNA repeats in eukaryotesFragile X syndromeThe role of AGG interruptions in fragile X repeat expansions: a twenty-year perspectiveRepeat-mediated genetic and epigenetic changes at the FMR1 locus in the Fragile X-related disordersThe unstable repeats--three evolving faces of neurological diseaseMolecular genetics and genetic testing in myotonic dystrophy type 1.A chromatin-dependent role of the fragile X mental retardation protein FMRP in the DNA damage responseThe fragile X gene and its functionRNA and microRNAs in fragile X mental retardationDNA secondary structure: a common and causative factor for expansion in human disease.CGG allele size somatic mosaicism and methylation in FMR1 premutation alleles.Interruption of the fragile X syndrome expanded sequence d(CGG)(n) by interspersed d(AGG) trinucleotides diminishes the formation and stability of d(CGG)(n) tetrahelical structuresEvidence for RNA-mediated toxicity in the fragile X-associated tremor/ataxia syndrome.Increased instability of human CTG repeat tracts on yeast artificial chromosomes during gametogenesis.Unusual mutations in high functioning fragile X males: apparent instability of expanded unmethylated CGG repeats.Stability of the human fragile X (CGG)(n) triplet repeat array in Saccharomyces cerevisiae deficient in aspects of DNA metabolism.Advances in research on the fragile X syndrome.Expansions and contractions in a tandem repeat induced by double-strand break repair.Demethylation, reactivation, and destabilization of human fragile X full-mutation alleles in mouse embryocarcinoma cells.FMR1 gene and fragile X syndrome.Imprinting effect in premature ovarian failure confined to paternally inherited fragile X premutationsClinical and molecular implications of mosaicism in FMR1 full mutations.FMR1 and the fragile X syndrome: human genome epidemiology reviewReduced FMR1 mRNA translation efficiency in fragile X patients with premutations.Fragile sites-cytogenetic similarity with molecular diversity.FMR1 CGG-repeat instability in single sperm and lymphocytes of fragile-X premutation males.Expansions and contractions in 36-bp minisatellites by gene conversion in yeast.Cloned human FMR1 trinucleotide repeats exhibit a length- and orientation-dependent instability suggestive of in vivo lagging strand secondary structure.CTG repeat instability and size variation timing in DNA repair-deficient mice.Meiotic instability of CAG repeat tracts occurs by double-strand break repair in yeast.The FMR1 gene and fragile X-associated tremor/ataxia syndrome.Microsatellite repeat instability and neurological disease.The fragile x mental retardation syndrome 20 years after the FMR1 gene discovery: an expanding universe of knowledge.Mechanisms of trinucleotide repeat instability during human developmentDeletion of all CGG repeats plus flanking sequences in FMR1 does not abolish gene expressionFragile X premutations are not a major cause of early menopause.Increase of FMRP expression, raised levels of FMR1 mRNA, and clonal selection in proliferating cells with unmethylated fragile X repeat expansions: a clue to the sex bias in the transmission of full mutations?
P2860
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P2860
Characterization of the full fragile X syndrome mutation in fetal gametes.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年学术文章
@wuu
1997年学术文章
@zh
1997年学术文章
@zh-cn
1997年学术文章
@zh-hans
1997年学术文章
@zh-my
1997年学术文章
@zh-sg
1997年學術文章
@yue
1997年學術文章
@zh-hant
name
Characterization of the full fragile X syndrome mutation in fetal gametes.
@en
Characterization of the full fragile X syndrome mutation in fetal gametes.
@nl
type
label
Characterization of the full fragile X syndrome mutation in fetal gametes.
@en
Characterization of the full fragile X syndrome mutation in fetal gametes.
@nl
prefLabel
Characterization of the full fragile X syndrome mutation in fetal gametes.
@en
Characterization of the full fragile X syndrome mutation in fetal gametes.
@nl
P2093
P2860
P356
P1433
P1476
Characterization of the full fragile X syndrome mutation in fetal gametes.
@en
P2093
Tarleton JC
Willemsen R
de Graaff E
P2860
P2888
P304
P356
10.1038/NG0297-165
P407
P577
1997-02-01T00:00:00Z