scholarly article | Q13442814 |
P50 | author | Andrés Aguilera | Q37382275 |
María L García-Rubio | Q43158419 | ||
P2093 | author name string | Karlene A Cimprich | |
Caroline Townsend Stork | |||
Julie Sollier | |||
Renee D Paulsen | |||
P2860 | cites work | Instability and decay of the primary structure of DNA | Q22122361 |
Cockayne syndrome A and B proteins differentially regulate recruitment of chromatin remodeling and repair factors to stalled RNA polymerase II in vivo | Q24300037 | ||
Human senataxin resolves RNA/DNA hybrids formed at transcriptional pause sites to promote Xrn2-dependent termination | Q24307617 | ||
Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair | Q24312736 | ||
DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4) | Q24533845 | ||
SF1 and SF2 helicases: family matters | Q24596016 | ||
Ataxia telangiectasia mutated activation by transcription- and topoisomerase I-induced DNA double-strand breaks | Q24651854 | ||
A protein complex containing Tho2, Hpr1, Mft1 and a novel protein, Thp2, connects transcription elongation with mitotic recombination in Saccharomyces cerevisiae | Q27929512 | ||
Senataxin associates with replication forks to protect fork integrity across RNA-polymerase-II-transcribed genes | Q27935087 | ||
Transcription-associated R-loop formation across the human FMR1 CGG-repeat region | Q28537978 | ||
Growth retardation, early death, and DNA repair defects in mice deficient for the nucleotide excision repair enzyme XPF | Q28592372 | ||
Class switch recombination and hypermutation require activation-induced cytidine deaminase (AID), a potential RNA editing enzyme | Q29547201 | ||
Loss of Topoisomerase I leads to R-loop-mediated transcriptional blocks during ribosomal RNA synthesis | Q30435228 | ||
Senataxin, defective in the neurodegenerative disorder ataxia with oculomotor apraxia 2, lies at the interface of transcription and the DNA damage response | Q30532840 | ||
A genome-wide siRNA screen reveals diverse cellular processes and pathways that mediate genome stability | Q33489221 | ||
C9orf72 nucleotide repeat structures initiate molecular cascades of disease. | Q33715387 | ||
A double-edged sword: R loops as threats to genome integrity and powerful regulators of gene expression | Q33850539 | ||
Topoisomerase I suppresses genomic instability by preventing interference between replication and transcription | Q34031653 | ||
Yeast Sen1 helicase protects the genome from transcription-associated instability. | Q34157855 | ||
R-loops at immunoglobulin class switch regions in the chromosomes of stimulated B cells | Q34188845 | ||
Collisions between replication and transcription complexes cause common fragile site instability at the longest human genes | Q34242723 | ||
RNase H and multiple RNA biogenesis factors cooperate to prevent RNA:DNA hybrids from generating genome instability | Q34242729 | ||
R-loop formation is a distinctive characteristic of unmethylated human CpG island promoters | Q34258378 | ||
Cotranscriptionally Formed DNA:RNA Hybrids Mediate Transcription Elongation Impairment and Transcription-Associated Recombination | Q34267573 | ||
R loops: from transcription byproducts to threats to genome stability | Q34271508 | ||
Deficiency in the nuclease activity of xeroderma pigmentosum G in mice leads to hypersensitivity to UV irradiation | Q34302249 | ||
GC skew at the 5' and 3' ends of human genes links R-loop formation to epigenetic regulation and transcription termination | Q34358463 | ||
Characterization of monoclonal antibody to DNA.RNA and its application to immunodetection of hybrids | Q34384604 | ||
Promoter-bound trinucleotide repeat mRNA drives epigenetic silencing in fragile X syndrome | Q34407383 | ||
Genome-wide profiling of yeast DNA:RNA hybrid prone sites with DRIP-chip | Q34415765 | ||
Inactivation of the SR protein splicing factor ASF/SF2 results in genomic instability | Q34442378 | ||
Mechanisms of transcription-coupled DNA repair | Q34514438 | ||
R-loops associated with triplet repeat expansions promote gene silencing in Friedreich ataxia and fragile X syndrome. | Q35160930 | ||
R-loop-mediated genomic instability is caused by impairment of replication fork progression | Q35393287 | ||
R-loop-mediated genome instability in mRNA cleavage and polyadenylation mutants | Q35740611 | ||
The RNA binding protein RNPS1 alleviates ASF/SF2 depletion-induced genomic instability | Q36148332 | ||
Regulation of endonuclease activity in human nucleotide excision repair | Q37877050 | ||
The contribution of co-transcriptional RNA:DNA hybrid structures to DNA damage and genome instability | Q38205642 | ||
Replication fork progression is impaired by transcription in hyperrecombinant yeast cells lacking a functional THO complex | Q42941871 | ||
Role of reciprocal exchange, one-ended invasion crossover and single-strand annealing on inverted and direct repeat recombination in yeast: different requirements for the RAD1, RAD10, and RAD52 genes | Q42965264 | ||
NER factors are recruited to active promoters and facilitate chromatin modification for transcription in the absence of exogenous genotoxic attack. | Q45079199 | ||
AID binds to transcription-induced structures in c-MYC that map to regions associated with translocation and hypermutation | Q46531711 | ||
Interdependence between Transcription and mRNP Processing and Export, and Its Impact on Genetic Stability | Q61827948 | ||
Transcription-induced cleavage of immunoglobulin switch regions by nucleotide excision repair nucleases in vitro | Q73794379 | ||
A spliceosomal intron binding protein, IBP160, links position-dependent assembly of intron-encoded box C/D snoRNP to pre-mRNA splicing | Q80204773 | ||
P433 | issue | 6 | |
P921 | main subject | genome stability | Q98655700 |
P304 | page(s) | 777-785 | |
P577 | publication date | 2014-11-26 | |
P1433 | published in | Molecular Cell | Q3319468 |
P1476 | title | Transcription-coupled nucleotide excision repair factors promote R-loop-induced genome instability | |
P478 | volume | 56 |
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