MSH3

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MutS homolog 3 (E. coli)
Identifiers
Symbols MSH3 ; MRP1; DUP; MGC163306; MGC163308
External IDs Template:OMIM5 Template:MGI HomoloGene1829
RNA expression pattern
File:PBB GE MSH3 210947 s at tn.png
File:PBB GE MSH3 205887 x at tn.png
More reference expression data
Orthologs
Template:GNF Ortholog box
Species Human Mouse
Entrez n/a n/a
Ensembl n/a n/a
UniProt n/a n/a
RefSeq (mRNA) n/a n/a
RefSeq (protein) n/a n/a
Location (UCSC) n/a n/a
PubMed search n/a n/a

MutS homolog 3 (E. coli), also known as MSH3, is a human gene.[1]


References

  1. "Entrez Gene: MSH3 mutS homolog 3 (E. coli)".

Further reading

  • Marti TM, Kunz C, Fleck O (2002). "DNA mismatch repair and mutation avoidance pathways". J. Cell. Physiol. 191 (1): 28–41. doi:10.1002/jcp.10077. PMID 11920679.
  • Fujii H, Shimada T (1989). "Isolation and characterization of cDNA clones derived from the divergently transcribed gene in the region upstream from the human dihydrofolate reductase gene". J. Biol. Chem. 264 (17): 10057–64. PMID 2722860.
  • Chen MJ, Shimada T, Moulton AD; et al. (1984). "The functional human dihydrofolate reductase gene". J. Biol. Chem. 259 (6): 3933–43. PMID 6323448.
  • Shinya E, Shimada T (1994). "Identification of two initiator elements in the bidirectional promoter of the human dihydrofolate reductase and mismatch repair protein 1 genes". Nucleic Acids Res. 22 (11): 2143–9. PMID 8029024.
  • Risinger JI, Umar A, Boyd J; et al. (1996). "Mutation of MSH3 in endometrial cancer and evidence for its functional role in heteroduplex repair". Nat. Genet. 14 (1): 102–5. doi:10.1038/ng0996-102. PMID 8782829.
  • Watanabe A, Ikejima M, Suzuki N, Shimada T (1997). "Genomic organization and expression of the human MSH3 gene". Genomics. 31 (3): 311–8. doi:10.1006/geno.1996.0053. PMID 8838312.
  • Nakajima E, Orimo H, Ikejima M, Shimada T (1996). "Nine-bp repeat polymorphism in exon 1 of the hMSH3 gene". Jpn. J. Hum. Genet. 40 (4): 343–5. PMID 8851770.
  • Acharya S, Wilson T, Gradia S; et al. (1997). "hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6". Proc. Natl. Acad. Sci. U.S.A. 93 (24): 13629–34. PMID 8942985.
  • Guerrette S, Wilson T, Gradia S, Fishel R (1998). "Interactions of human hMSH2 with hMSH3 and hMSH2 with hMSH6: examination of mutations found in hereditary nonpolyposis colorectal cancer". Mol. Cell. Biol. 18 (11): 6616–23. PMID 9774676.
  • Ceccotti S, Ciotta C, Fronza G; et al. (2000). "Multiple mutations and frameshifts are the hallmark of defective hPMS2 in pZ189-transfected human tumor cells". Nucleic Acids Res. 28 (13): 2577–84. PMID 10871409.
  • Orimo H, Nakajima E, Yamamoto M; et al. (2000). "Association between single nucleotide polymorphisms in the hMSH3 gene and sporadic colon cancer with microsatellite instability". J. Hum. Genet. 45 (4): 228–30. PMID 10944853.
  • Clark AB, Valle F, Drotschmann K; et al. (2001). "Functional interaction of proliferating cell nuclear antigen with MSH2-MSH6 and MSH2-MSH3 complexes". J. Biol. Chem. 275 (47): 36498–501. doi:10.1074/jbc.C000513200. PMID 11005803.
  • Kleczkowska HE, Marra G, Lettieri T, Jiricny J (2001). "hMSH3 and hMSH6 interact with PCNA and colocalize with it to replication foci". Genes Dev. 15 (6): 724–36. doi:10.1101/gad.191201. PMID 11274057.
  • Schmutte C, Sadoff MM, Shim KS; et al. (2001). "The interaction of DNA mismatch repair proteins with human exonuclease I.". J. Biol. Chem. 276 (35): 33011–8. doi:10.1074/jbc.M102670200. PMID 11427529.
  • Wang Q, Zhang H, Guerrette S; et al. (2001). "Adenosine nucleotide modulates the physical interaction between hMSH2 and BRCA1". Oncogene. 20 (34): 4640–9. doi:10.1038/sj.onc.1204625. PMID 11498787.
  • Mazurek A, Berardini M, Fishel R (2002). "Activation of human MutS homologs by 8-oxo-guanine DNA damage". J. Biol. Chem. 277 (10): 8260–6. doi:10.1074/jbc.M111269200. PMID 11756455.
  • Plotz G, Raedle J, Brieger A; et al. (2002). "hMutSalpha forms an ATP-dependent complex with hMutLalpha and hMutLbeta on DNA". Nucleic Acids Res. 30 (3): 711–8. PMID 11809883.
  • Arzimanoglou II, Hansen LL, Chong D; et al. (2002). "Frequent LOH at hMLH1, a highly variable SNP in hMSH3, and negligible coding instability in ovarian cancer". Anticancer Res. 22 (2A): 969–75. PMID 12014680.
  • Ohta S, Shiomi Y, Sugimoto K; et al. (2002). "A proteomics approach to identify proliferating cell nuclear antigen (PCNA)-binding proteins in human cell lysates. Identification of the human CHL12/RFCs2-5 complex as a novel PCNA-binding protein". J. Biol. Chem. 277 (43): 40362–7. doi:10.1074/jbc.M206194200. PMID 12171929.

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