Unstable spinocerebellar ataxia type 10 (ATTCT*(AGAAT) repeats are associated with aberrant replication at the ATX10 locus and replication origin-dependent expansion at an ectopic site in human cells.
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Inheritance patterns of ATCCT repeat interruptions in spinocerebellar ataxia type 10 (SCA10) expansionsThe DNA unwinding element binding protein DUE-B interacts with Cdc45 in preinitiation complex formation.Brain pathology of spinocerebellar ataxias.Replication fork stalling and checkpoint activation by a PKD1 locus mirror repeat polypurine-polypyrimidine (Pu-Py) tract.Direct and inverted repeats elicit genetic instability by both exploiting and eluding DNA double-strand break repair systems in mycobacteria.Expansions, contractions, and fragility of the spinocerebellar ataxia type 10 pentanucleotide repeat in yeast.Protein phosphatase 2A and Cdc7 kinase regulate the DNA unwinding element-binding protein in replication initiationInstability of (CTG)n•(CAG)n trinucleotide repeats and DNA synthesisAltered replication in human cells promotes DMPK (CTG)(n) · (CAG)(n) repeat instabilityOligodeoxynucleotide binding to (CTG) · (CAG) microsatellite repeats inhibits replication fork stalling, hairpin formation, and genome instability.Activation of a human chromosomal replication origin by protein tethering.A Z-DNA sequence reduces slipped-strand structure formation in the myotonic dystrophy type 2 (CCTG) x (CAGG) repeatThe biological effects of simple tandem repeats: lessons from the repeat expansion diseases.FANCJ is essential to maintain microsatellite structure genome-wide during replication stress.Transgenic models of spinocerebellar ataxia type 10: modeling a repeat expansion disorder.Replication stalling and DNA microsatellite instability.Paradoxical effects of repeat interruptions on spinocerebellar ataxia type 10 expansions and repeat instability.Replication-dependent instability at (CTG) x (CAG) repeat hairpins in human cells.One-way PCR-based mapping of a replication initiation point (RIP).Homologous recombination occurs frequently at innate GT microsatellites in normal somatic and germ cells in vivo.
P2860
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P2860
Unstable spinocerebellar ataxia type 10 (ATTCT*(AGAAT) repeats are associated with aberrant replication at the ATX10 locus and replication origin-dependent expansion at an ectopic site in human cells.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Unstable spinocerebellar ataxi ...... n ectopic site in human cells.
@en
Unstable spinocerebellar ataxia type 10
@nl
type
label
Unstable spinocerebellar ataxi ...... n ectopic site in human cells.
@en
Unstable spinocerebellar ataxia type 10
@nl
prefLabel
Unstable spinocerebellar ataxi ...... n ectopic site in human cells.
@en
Unstable spinocerebellar ataxia type 10
@nl
P2093
P2860
P356
P1476
Unstable spinocerebellar ataxi ...... an ectopic site in human cells
@en
P2093
Michael Leffak
Richard R Sinden
P2860
P304
P356
10.1128/MCB.01276-07
P407
P577
2007-09-10T00:00:00Z