Identification of regulatory factor X as a novel mismatch repair stimulatory factor

scientific article published on 4 March 2008

Identification of regulatory factor X as a novel mismatch repair stimulatory factor is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1074/JBC.M800460200
P932PMC publication ID2442326
P698PubMed publication ID18319249

P50authorYanbin ZhangQ44027005
Guo-Min LiQ50637024
P2093author name stringFenghua Yuan
Liya Gu
Daojing Wang
P2860cites workHuman exonuclease I interacts with the mismatch repair protein hMSH2Q22004013
RFX-B is the gene responsible for the most common cause of the bare lymphocyte syndrome, an MHC class II immunodeficiencyQ22009001
Human exonuclease I is required for 5' and 3' mismatch repairQ24292224
A defined human system that supports bidirectional mismatch-provoked excisionQ24298110
The bare lymphocyte syndrome: molecular clues to the transcriptional regulation of major histocompatibility complex class II genesQ24540091
exo1-Dependent mutator mutations: model system for studying functional interactions in mismatch repairQ27935389
Eukaryotic DNA mismatch repairQ27939116
Inactivation of Exonuclease 1 in mice results in DNA mismatch repair defects, increased cancer susceptibility, and male and female sterilityQ28182219
The bare lymphocyte syndrome and the regulation of MHC expressionQ28204378
DNA mismatch repairQ28256190
Mechanisms and functions of DNA mismatch repairQ28262719
Identification of a human gene encoding a homologue of Saccharomyces cerevisiae EXO1, an exonuclease implicated in mismatch repair and recombinationQ28289308
Mismatch repair in replication fidelity, genetic recombination, and cancer biologyQ29616483
Reconstitution of 5'-directed human mismatch repair in a purified systemQ33222844
Human mismatch repair: reconstitution of a nick-directed bidirectional reactionQ33224078
Strand-specific mismatch correction in nuclear extracts of human and Drosophila melanogaster cell linesQ33720790
Deficiency of a novel mismatch repair activity in a bladder tumor cell lineQ33888905
Multiple interactions between BRG1 and MHC class II promoter binding proteins.Q34405074
DNA mismatch correction in a defined systemQ34674714
Chromatin remodeling and extragenic transcription at the MHC class II locus control region.Q40678210
Major histocompatibility complex class II deficiency: a clinical reviewQ41333663
Hypermutability and mismatch repair deficiency in RER+ tumor cellsQ41508298
Germline transmission of RNAi in miceQ44283786
Differential requirement for proliferating cell nuclear antigen in 5' and 3' nick-directed excision in human mismatch repairQ44761854
Proteomic profiling of bone marrow mesenchymal stem cells upon transforming growth factor beta1 stimulationQ46455111
Endonucleolytic function of MutLalpha in human mismatch repairQ50335575
Characterization of the RFX complex and the RFX5(L66A) mutant: implications for the regulation of MHC class II gene expressionQ79722457
P433issue19
P407language of work or nameEnglishQ1860
P921main subjectDNA mismatch repairQ2984243
coagulation factor x humanQ28859740
P304page(s)12730-12735
P577publication date2008-03-04
P1433published inJournal of Biological ChemistryQ867727
P1476titleIdentification of regulatory factor X as a novel mismatch repair stimulatory factor
P478volume283

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cites work (P2860)
Q36540457A personal historical view of DNA mismatch repair with an emphasis on eukaryotic DNA mismatch repair
Q37446019Evidence that nucleosomes inhibit mismatch repair in eukaryotic cells
Q27011117New insights and challenges in mismatch repair: getting over the chromatin hurdle
Q57009219Nucleosomes around a mismatched base pair are excluded via an Msh2-dependent reaction with the aid of SNF2 family ATPase Smarcad1
Q27321262RFX transcription factors are essential for hearing in mice.
Q36972154Rad9 plays an important role in DNA mismatch repair through physical interaction with MLH1
Q36540486Regulation of mismatch repair by histone code and posttranslational modifications in eukaryotic cells
Q35212382iRegulon: from a gene list to a gene regulatory network using large motif and track collections

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