Advances in mechanisms of genetic instability related to hereditary neurological diseases. - Test2 - elhamkhani - TriplyDB

Advances in mechanisms of genetic instability related to hereditary neurological diseases.

Advances in mechanisms of genetic instability related to hereditary neurological diseases.

http://www.wikidata.org/entity/Q24816457

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New insights into repeat instability: role of RNA•DNA hybrids DNA slip-outs cause RNA polymerase II arrest in vitro: potential implications for genetic instability Comparative genomics and molecular dynamics of DNA repeats in eukaryotes Zinc-finger directed double-strand breaks within CAG repeat tracts promote repeat instability in human cells Mechanistic features of CAG*CTG repeat contractions in cultured cells revealed by a novel genetic assay Microsatellites in Pursuit of Microbial Genome Evolution Structural studies of CNG repeats DNA triplet repeat expansion and mismatch repair The role of variable DNA tandem repeats in bacterial adaptation The balancing act of DNA repeat expansions The hidden side of unstable DNA repeats: Mutagenesis at a distance Self-association of short DNA loops through minor groove C:G:G:C tetrads Structural basis for the identification of an i-motif tetraplex core with a parallel-duplex junction as a structural motif in CCG triplet repeats Polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome: rs17884724:A>C is associated with 7-alanine expansion Instability of CTG repeats is governed by the position of a DNA base lesion through base excision repair Whole-genome sequencing in outbreak analysis A Multilocus Sequence Typing System (MLST) reveals a high level of diversity and a genetic component to Entamoeba histolytica virulence.Gene conversion causing human inherited disease: evidence for involvement of non-B-DNA-forming sequences and recombination-promoting motifs in DNA breakage and repair.Somatic CTG*CAG repeat instability in a mouse model for myotonic dystrophy type 1 is associated with changes in cell nuclearity and DNA ploidy.PeakSeeker: a program for interpreting genotypes of mononucleotide repeats Ancestral origin of the ATTCT repeat expansion in spinocerebellar ataxia type 10 (SCA10)Diverse effects of individual mismatch repair components on transcription-induced CAG repeat instability in human cells.Coexistence of an ILPR i-motif and a partially folded structure with comparable mechanical stability revealed at the single-molecule level.R loops stimulate genetic instability of CTG.CAG repeats.Mechanistic studies of hairpin to duplex conversion for trinucleotide repeat sequences.Xpa deficiency reduces CAG trinucleotide repeat instability in neuronal tissues in a mouse model of SCA1.Analysis of microsatellite variation in Drosophila melanogaster with population-scale genome sequencing Tandem repeats discovery service (TReaDS) applied to finding novel cis-acting factors in repeat expansion diseases.Mitochondrial DNA deletions are associated with non-B DNA conformations Nucleotide excision repair, mismatch repair, and R-loops modulate convergent transcription-induced cell death and repeat instability Lentivector integration sites in ependymal cells from a model of metachromatic leukodystrophy: non-B DNA as a new factor influencing integration.Non-B DNA structure-induced genetic instability and evolution.Z-DNA-forming sequences generate large-scale deletions in mammalian cells.DNA and RNA quadruplex-binding proteins.Direct and inverted repeats elicit genetic instability by both exploiting and eluding DNA double-strand break repair systems in mycobacteria.Long homopurine*homopyrimidine sequences are characteristic of genes expressed in brain and the pseudoautosomal region.Non-B DNA-forming sequences and WRN deficiency independently increase the frequency of base substitution in human cells.A 5', 8-cyclo-2'-deoxypurine lesion induces trinucleotide repeat deletion via a unique lesion bypass by DNA polymerase β Sporadic breast cancer patients' germline DNA exhibit an AT-rich microsatellite signature.STaRRRT: a table of short tandem repeats in regulatory regions of the human genome.

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Advances in mechanisms of genetic instability related to hereditary neurological diseases.

http://www.wikidata.org/entity/Q24816457

description

2005 nî lūn-bûn

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2005 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2005年の論文

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2005年論文

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Advances in mechanisms of genetic instability related to hereditary neurological diseases

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Advances in mechanisms of gene ...... editary neurological diseases.

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Advances in mechanisms of gene ...... editary neurological diseases.

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Advances in mechanisms of genetic instability related to hereditary neurological diseases

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Advances in mechanisms of gene ...... editary neurological diseases.

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Advances in mechanisms of genetic instability related to hereditary neurological diseases

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Advances in mechanisms of gene ...... editary neurological diseases.

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Nucleic Acids Research

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Advances in mechanisms of gene ...... editary neurological diseases.

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Leslie S Son

http://www.w3.org/2001/XMLSchema#string

Marek Napierala

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Micheal L Hebert

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Robert D Wells

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Ruhee Dere

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P2860

Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10

Replication slippage involves DNA polymerase pausing and dissociation.

The GAA triplet-repeat expansion in Friedreich ataxia interferes with transcription and may be associated with an unusual DNA structure

Structural roles of CTG repeats in slippage expansion during DNA replication

The DNA replication fork in eukaryotic cells.

CGG/CCG repeats exhibit orientation-dependent instability and orientation-independent fragility in Saccharomyces cerevisiae

Inhibition of FEN-1 processing by DNA secondary structure at trinucleotide repeats

Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9

Reconstitution of complete SV40 DNA replication with purified replication factors

Trinucleotide repeats that expand in human disease form hairpin structures in vitro

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10.1093/NAR/GKI697

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12

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33

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7737189

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16006624

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neurological disorder

genetic variation

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1174910

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