scholarly article | Q13442814 |
P50 | author | Yanbin Zhang | Q44027005 |
Guo-Min Li | Q50637024 | ||
P2093 | author name string | Fenghua Yuan | |
Liya Gu | |||
Daojing Wang | |||
P2860 | cites work | Human exonuclease I interacts with the mismatch repair protein hMSH2 | Q22004013 |
RFX-B is the gene responsible for the most common cause of the bare lymphocyte syndrome, an MHC class II immunodeficiency | Q22009001 | ||
Human exonuclease I is required for 5' and 3' mismatch repair | Q24292224 | ||
A defined human system that supports bidirectional mismatch-provoked excision | Q24298110 | ||
The bare lymphocyte syndrome: molecular clues to the transcriptional regulation of major histocompatibility complex class II genes | Q24540091 | ||
exo1-Dependent mutator mutations: model system for studying functional interactions in mismatch repair | Q27935389 | ||
Eukaryotic DNA mismatch repair | Q27939116 | ||
Inactivation of Exonuclease 1 in mice results in DNA mismatch repair defects, increased cancer susceptibility, and male and female sterility | Q28182219 | ||
The bare lymphocyte syndrome and the regulation of MHC expression | Q28204378 | ||
DNA mismatch repair | Q28256190 | ||
Mechanisms and functions of DNA mismatch repair | Q28262719 | ||
Identification of a human gene encoding a homologue of Saccharomyces cerevisiae EXO1, an exonuclease implicated in mismatch repair and recombination | Q28289308 | ||
Mismatch repair in replication fidelity, genetic recombination, and cancer biology | Q29616483 | ||
Reconstitution of 5'-directed human mismatch repair in a purified system | Q33222844 | ||
Human mismatch repair: reconstitution of a nick-directed bidirectional reaction | Q33224078 | ||
Strand-specific mismatch correction in nuclear extracts of human and Drosophila melanogaster cell lines | Q33720790 | ||
Deficiency of a novel mismatch repair activity in a bladder tumor cell line | Q33888905 | ||
Multiple interactions between BRG1 and MHC class II promoter binding proteins. | Q34405074 | ||
DNA mismatch correction in a defined system | Q34674714 | ||
Chromatin remodeling and extragenic transcription at the MHC class II locus control region. | Q40678210 | ||
Major histocompatibility complex class II deficiency: a clinical review | Q41333663 | ||
Hypermutability and mismatch repair deficiency in RER+ tumor cells | Q41508298 | ||
Germline transmission of RNAi in mice | Q44283786 | ||
Differential requirement for proliferating cell nuclear antigen in 5' and 3' nick-directed excision in human mismatch repair | Q44761854 | ||
Proteomic profiling of bone marrow mesenchymal stem cells upon transforming growth factor beta1 stimulation | Q46455111 | ||
Endonucleolytic function of MutLalpha in human mismatch repair | Q50335575 | ||
Characterization of the RFX complex and the RFX5(L66A) mutant: implications for the regulation of MHC class II gene expression | Q79722457 | ||
P433 | issue | 19 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | DNA mismatch repair | Q2984243 |
coagulation factor x human | Q28859740 | ||
P304 | page(s) | 12730-12735 | |
P577 | publication date | 2008-03-04 | |
P1433 | published in | Journal of Biological Chemistry | Q867727 |
P1476 | title | Identification of regulatory factor X as a novel mismatch repair stimulatory factor | |
P478 | volume | 283 |
Q36540457 | A personal historical view of DNA mismatch repair with an emphasis on eukaryotic DNA mismatch repair |
Q37446019 | Evidence that nucleosomes inhibit mismatch repair in eukaryotic cells |
Q27011117 | New insights and challenges in mismatch repair: getting over the chromatin hurdle |
Q57009219 | Nucleosomes around a mismatched base pair are excluded via an Msh2-dependent reaction with the aid of SNF2 family ATPase Smarcad1 |
Q27321262 | RFX transcription factors are essential for hearing in mice. |
Q36972154 | Rad9 plays an important role in DNA mismatch repair through physical interaction with MLH1 |
Q36540486 | Regulation of mismatch repair by histone code and posttranslational modifications in eukaryotic cells |
Q35212382 | iRegulon: from a gene list to a gene regulatory network using large motif and track collections |
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