Molecular basis of genetic instability of triplet repeats
about
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophyHuman amiloride-sensitive epithelial Na+ channel gamma subunit promoter: functional analysis and identification of a polypurine-polypyrimidine tract with the potential for triplex DNA formationReplication slippage involves DNA polymerase pausing and dissociation.The fragile X gene and its functionRecombination-dependent deletion formation in mammalian cells deficient in the nucleotide excision repair gene ERCC1Analysis of strand slippage in DNA polymerase expansions of CAG/CTG triplet repeats associated with neurodegenerative diseaseGenome instability: a mechanistic view of its causes and consequencesInstability of CTG repeats is governed by the position of a DNA base lesion through base excision repairRepeat polymorphisms within gene regions: phenotypic and evolutionary implicationsDNA secondary structure: a common and causative factor for expansion in human disease.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 structuresModulation of trinucleotide repeat instability by DNA polymerase β polymorphic variant R137Q.Trinucleotide insertions, deletions, and point mutations in glucose transporters confer K+ uptake in Saccharomyces cerevisiaeNew structural and functional contexts of the Dx[DN]xDG linear motif: insights into evolution of calcium-binding proteinsConformational energetics of stable and metastable states formed by DNA triplet repeat oligonucleotides: implications for triplet expansion diseasesZ-DNA-forming sequences generate large-scale deletions in mammalian cells.Factors affecting inverted repeat stimulation of recombination and deletion in Saccharomyces cerevisiaeLong inverted repeats are an at-risk motif for recombination in mammalian cells.Transcription increases the deletion frequency of long CTG.CAG triplet repeats from plasmids in Escherichia coli.Myotonic dystrophy: molecular windows on a complex etiology.Fluorescent dyes specific for quadruplex DNAA 5', 8-cyclo-2'-deoxypurine lesion induces trinucleotide repeat deletion via a unique lesion bypass by DNA polymerase βTriplet repeats form secondary structures that escape DNA repair in yeast.Mutation patterns of amino acid tandem repeats in the human proteomeUnusual DNA duplex and hairpin motifs.The preference for GT-rich DNA by the yeast Rad51 protein defines a set of universal pairing sequencesIncrease 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?Single-stranded DNA-binding protein enhances the stability of CTG triplet repeats in Escherichia coliAP endonuclease 1 prevents trinucleotide repeat expansion via a novel mechanism during base excision repair.Non-B DNA conformations, genomic rearrangements, and human disease.DNA base excision repair: a mechanism of trinucleotide repeat expansion.Perspective on mutagenesis and repair: the standard model and alternate modes of mutagenesis.Msh2-Msh3 interferes with Okazaki fragment processing to promote trinucleotide repeat expansions.Orientation-dependent and sequence-specific expansions of CTG/CAG trinucleotide repeats in Saccharomyces cerevisiae.Fine-resolution analysis of products of intrachromosomal homeologous recombination in mammalian cells.Trinucleotide repeat deletion via a unique hairpin bypass by DNA polymerase β and alternate flap cleavage by flap endonuclease 1.Misregulation of alternative splicing causes pathogenesis in myotonic dystrophy.Replication fork stalling at natural impediments.Transglutaminase-catalyzed inactivation of glyceraldehyde 3-phosphate dehydrogenase and alpha-ketoglutarate dehydrogenase complex by polyglutamine domains of pathological lengthProbing DNA bulges with designed helical spirocyclic molecules.
P2860
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P2860
Molecular basis of genetic instability of triplet repeats
description
1996 nî lūn-bûn
@nan
1996 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
Molecular basis of genetic instability of triplet repeats
@ast
Molecular basis of genetic instability of triplet repeats
@en
Molecular basis of genetic instability of triplet repeats
@nl
type
label
Molecular basis of genetic instability of triplet repeats
@ast
Molecular basis of genetic instability of triplet repeats
@en
Molecular basis of genetic instability of triplet repeats
@nl
prefLabel
Molecular basis of genetic instability of triplet repeats
@ast
Molecular basis of genetic instability of triplet repeats
@en
Molecular basis of genetic instability of triplet repeats
@nl
P2860
P356
P1476
Molecular basis of genetic instability of triplet repeats
@en
P2093
P2860
P304
P356
10.1074/JBC.271.6.2875
P407
P577
1996-02-09T00:00:00Z