MSH2 (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "MSH2" in Japanese language version.

refsWebsite

Global rank Japanese rank

4^th place

24^th place

2^nd place

6^th place

18^th place

107^th place

1,626^th place

2,625^th place

low place

low place

621^st place

4,635^th place

low place

low place

doi.org (Global: 2^nd place; Japanese: 6^th place)

“Transcription-coupled repair deficiency and mutations in human mismatch repair genes”. Science 272 (5261): 557–60. (April 1996). Bibcode: 1996Sci...272..557M. doi:10.1126/science.272.5261.557. PMID 8614807. https://zenodo.org/record/1231074.
“Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer”. Cell 82 (2): 321–30. (July 1995). doi:10.1016/0092-8674(95)90319-4. PMID 7628020.
“Reduced host cell reactivation of oxidative DNA damage in human cells deficient in the mismatch repair gene hMSH2”. Mutagenesis 22 (3): 235–43. (May 2007). doi:10.1093/mutage/gem008. PMID 17351251.
“Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases”. Scientific Reports 9 (1): 18577. (December 2019). Bibcode: 2019NatSR...918577S. doi:10.1038/s41598-019-54976-4. PMC 6901466. PMID 31819097.
“Mismatch repair and the hereditary non-polyposis colorectal cancer syndrome (HNPCC)”. Cancer Invest. 20 (1): 102–9. (2002). doi:10.1081/cnv-120000371. PMID 11852992.
“Structure of the human MutSalpha DNA lesion recognition complex”. Mol. Cell 26 (4): 579–92. (May 2007). doi:10.1016/j.molcel.2007.04.018. PMID 17531815.
“Era of universal testing of microsatellite instability in colorectal cancer”. World J Gastrointest Oncol 5 (2): 12–9. (February 2013). doi:10.4251/wjgo.v5.i2.12. PMC 3613766. PMID 23556052.
“Interaction between the Msh2 and Msh6 nucleotide-binding sites in the Saccharomyces cerevisiae Msh2-Msh6 complex”. J. Biol. Chem. 285 (12): 9301–10. (March 2010). doi:10.1074/jbc.M109.096388. PMC 2838348. PMID 20089866.
“Isolation of an hMSH2-p160 heterodimer that restores DNA mismatch repair to tumor cells”. Science 268 (5219): 1909–12. (June 1995). Bibcode: 1995Sci...268.1909D. doi:10.1126/science.7604264. PMID 7604264.
“Nuclear translocation of mismatch repair proteins MSH2 and MSH6 as a response of cells to alkylating agents”. J. Biol. Chem. 275 (46): 36256–62. (November 2000). doi:10.1074/jbc.M005377200. PMID 10954713.
“Structural, molecular and cellular functions of MSH2 and MSH6 during DNA mismatch repair, damage signaling and other noncanonical activities”. Mutat. Res. 743–744: 53–66. (February 2013). doi:10.1016/j.mrfmmm.2012.12.008. PMC 3659183. PMID 23391514.
“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. (November 1998). doi:10.1128/mcb.18.11.6616. PMC 109246. PMID 9774676.
“Large conformational changes in MutS during DNA scanning, mismatch recognition and repair signalling”. EMBO J. 31 (11): 2528–40. (May 2012). doi:10.1038/emboj.2012.95. PMC 3365432. PMID 22505031.
“Functional studies and homology modeling of Msh2-Msh3 predict that mispair recognition involves DNA bending and strand separation”. Mol. Cell. Biol. 30 (13): 3321–8. (July 2010). doi:10.1128/MCB.01558-09. PMC 2897569. PMID 20421420.
“Mechanism of mismatch recognition revealed by human MutSβ bound to unpaired DNA loops”. Nat. Struct. Mol. Biol. 19 (1): 72–8. (January 2012). doi:10.1038/nsmb.2175. PMC 3252464. PMID 22179786.
“MSH2 and ATR form a signaling module and regulate two branches of the damage response to DNA methylation”. Proc. Natl. Acad. Sci. U.S.A. 100 (26): 15387–92. (December 2003). Bibcode: 2003PNAS..10015387W. doi:10.1073/pnas.2536810100. PMC 307577. PMID 14657349.
“Adenosine nucleotide modulates the physical interaction between hMSH2 and BRCA1”. Oncogene 20 (34): 4640–9. (August 2001). doi:10.1038/sj.onc.1204625. PMID 11498787.
“BASC, a super complex of BRCA1-associated proteins involved in the recognition and repair of aberrant DNA structures”. Genes Dev. 14 (8): 927–39. (April 2000). doi:10.1101/gad.14.8.927. PMC 316544. PMID 10783165.
“Methylator-induced, mismatch repair-dependent G2 arrest is activated through Chk1 and Chk2”. Mol. Biol. Cell 16 (3): 1513–26. (March 2005). doi:10.1091/mbc.E04-02-0089. PMC 551512. PMID 15647386.
“The mismatch repair system is required for S-phase checkpoint activation”. Nat. Genet. 33 (1): 80–4. (January 2003). doi:10.1038/ng1052. PMID 12447371.
“Identification of factors interacting with hMSH2 in the fetal liver utilizing the yeast two-hybrid system. In vivo interaction through the C-terminal domains of hEXO1 and hMSH2 and comparative expression analysis”. Mutat. Res. 460 (1): 41–52. (June 2000). doi:10.1016/S0921-8777(00)00012-4. PMID 10856833.
“The interaction of DNA mismatch repair proteins with human exonuclease I”. J. Biol. Chem. 276 (35): 33011–8. (August 2001). doi:10.1074/jbc.M102670200. PMID 11427529.
“Interactions of the DNA mismatch repair proteins MLH1 and MSH2 with c-MYC and MAX”. Oncogene 22 (6): 819–25. (February 2003). doi:10.1038/sj.onc.1206252. PMID 12584560.
“hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6”. Proc. Natl. Acad. Sci. U.S.A. 93 (24): 13629–34. (November 1996). Bibcode: 1996PNAS...9313629A. doi:10.1073/pnas.93.24.13629. PMC 19374. PMID 8942985.
“Specific in vitro binding of p53 to the promoter region of the human mismatch repair gene hMSH2”. Biochem. Biophys. Res. Commun. 221 (3): 722–8. (April 1996). doi:10.1006/bbrc.1996.0663. PMID 8630028.
“DNA damage responses: mechanisms and roles in human disease: 2007 G.H.A. Clowes Memorial Award Lecture”. Molecular Cancer Research 6 (4): 517–24. (April 2008). doi:10.1158/1541-7786.MCR-08-0020. PMID 18403632.
“The DNA damage response: ten years after”. Molecular Cell 28 (5): 739–45. (December 2007). doi:10.1016/j.molcel.2007.11.015. PMID 18082599.
“Molecular pathways: exploiting tumor-specific molecular defects in DNA repair pathways for precision cancer therapy”. Clinical Cancer Research 20 (23): 5882–7. (December 2014). doi:10.1158/1078-0432.CCR-14-1165. PMID 25451105.
“Double strand breaks can initiate gene silencing and SIRT1-dependent onset of DNA methylation in an exogenous promoter CpG island”. PLOS Genetics 4 (8): e1000155. (2008). doi:10.1371/journal.pgen.1000155. PMC 2491723. PMID 18704159.
“DNA damage, homology-directed repair, and DNA methylation”. PLOS Genetics 3 (7): e110. (July 2007). doi:10.1371/journal.pgen.0030110. PMC 1913100. PMID 17616978.
“Inactivation of hMLH1 and hMSH2 by promoter methylation in primary non-small cell lung tumors and matched sputum samples”. J. Clin. Invest. 111 (6): 887–95. (2003). doi:10.1172/JCI15475. PMC 153761. PMID 12639995.
“Somatic deletions of genes regulating MSH2 protein stability cause DNA mismatch repair deficiency and drug resistance in human leukemia cells”. Nat. Med. 17 (10): 1298–303. (2011). doi:10.1038/nm.2430. PMC 3192247. PMID 21946537.
“Aberrant DNA methylation and epigenetic inactivation of hMSH2 decrease overall survival of acute lymphoblastic leukemia patients via modulating cell cycle and apoptosis”. Asian Pac. J. Cancer Prev. 15 (1): 355–62. (2014). doi:10.7314/apjcp.2014.15.1.355. PMID 24528056.
“Aberrant methylation of different DNA repair genes demonstrates distinct prognostic value for esophageal cancer”. Dig. Dis. Sci. 56 (10): 2992–3004. (2011). doi:10.1007/s10620-011-1774-z. PMID 21674174.
“Promoter hypermethylation is the predominant mechanism in hMLH1 and hMSH2 deregulation and is a poor prognostic factor in nonsmoking lung cancer”. Clin. Cancer Res. 11 (15): 5410–6. (2005). doi:10.1158/1078-0432.CCR-05-0601. PMID 16061855.
“Promoter methylation status of hMLH1, hMSH2, and MGMT genes in colorectal cancer associated with adenoma-carcinoma sequence”. Langenbecks Arch Surg 396 (7): 1017–26. (2011). doi:10.1007/s00423-011-0812-9. PMID 21706233.
“Repair of double-strand breaks by homologous recombination in mismatch repair-defective mammalian cells”. Mol. Cell. Biol. 21 (8): 2671–82. (2001). doi:10.1128/MCB.21.8.2671-2682.2001. PMC 86898. PMID 11283247.
“Mismatch repair proteins hMLH1 and hMSH2 are differently expressed in the three main subtypes of sporadic renal cell carcinoma”. Pathobiology 79 (3): 162–8. (2012). doi:10.1159/000335642. PMID 22378480.
“Deficiency of MSH2 expression is associated with clear cell renal cell carcinoma”. Oncol Lett 8 (5): 2135–2139. (2014). doi:10.3892/ol.2014.2482. PMC 4186615. PMID 25295100.
“MSH2 promoter hypermethylation in circulating tumor DNA is a valuable predictor of disease-free survival for patients with esophageal squamous cell carcinoma”. Eur J Surg Oncol 38 (4): 326–32. (2012). doi:10.1016/j.ejso.2012.01.008. PMID 22265839.
“Inactivation of human mutL homolog 1 and mutS homolog 2 genes in head and neck squamous cell carcinoma tumors and leukoplakia samples by promoter hypermethylation and its relation with microsatellite instability phenotype”. Cancer 109 (4): 703–12. (2007). doi:10.1002/cncr.22430. PMID 17219447.
“Microsatellite instability and methylation of the DNA mismatch repair genes in head and neck cancer”. Ann. Oncol. 17 (6): 995–9. (2006). doi:10.1093/annonc/mdl048. PMID 16569647.
“Promoter hypermethylation of mismatch repair genes, hMLH1 and hMSH2 in oral squamous cell carcinoma”. Oral Dis 15 (3): 206–13. (2009). doi:10.1111/j.1601-0825.2008.01510.x. PMID 19207881.
“Promoter methylation of MLH1, PMS2, MSH2 and p16 is a phenomenon of advanced-stage HCCs”. PLOS ONE 9 (1): e84453. (2014). Bibcode: 2014PLoSO...984453H. doi:10.1371/journal.pone.0084453. PMC 3882222. PMID 24400091.
“Promoter methylation and immunohistochemical expression of hMLH1 and hMSH2 in sporadic colorectal cancer: a study from India”. Tumour Biol. 35 (4): 3679–87. (2014). doi:10.1007/s13277-013-1487-3. PMID 24317816.
“Alterations of copy number of methylation pattern in mismatch repair genes by methylation specific-multiplex ligation-dependent probe amplification in cases of colon cancer”. Balkan J. Med. Genet. 14 (2): 25–34. (2011). doi:10.2478/v10034-011-0044-x. PMC 3776700. PMID 24052709.
“DNA hypermethylation status of multiple genes in soft tissue sarcomas”. Mod. Pathol. 19 (1): 106–14. (2006). doi:10.1038/modpathol.3800502. PMID 16258501.

ensembl.org (Global: 1,626^th place; Japanese: 2,625^th place)

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000095002 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000024151 - Ensembl, May 2017

harvard.edu (Global: 18^th place; Japanese: 107^th place)

ui.adsabs.harvard.edu

“Transcription-coupled repair deficiency and mutations in human mismatch repair genes”. Science 272 (5261): 557–60. (April 1996). Bibcode: 1996Sci...272..557M. doi:10.1126/science.272.5261.557. PMID 8614807. https://zenodo.org/record/1231074.
“Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases”. Scientific Reports 9 (1): 18577. (December 2019). Bibcode: 2019NatSR...918577S. doi:10.1038/s41598-019-54976-4. PMC 6901466. PMID 31819097.
“Isolation of an hMSH2-p160 heterodimer that restores DNA mismatch repair to tumor cells”. Science 268 (5219): 1909–12. (June 1995). Bibcode: 1995Sci...268.1909D. doi:10.1126/science.7604264. PMID 7604264.
“MSH2 and ATR form a signaling module and regulate two branches of the damage response to DNA methylation”. Proc. Natl. Acad. Sci. U.S.A. 100 (26): 15387–92. (December 2003). Bibcode: 2003PNAS..10015387W. doi:10.1073/pnas.2536810100. PMC 307577. PMID 14657349.
“hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6”. Proc. Natl. Acad. Sci. U.S.A. 93 (24): 13629–34. (November 1996). Bibcode: 1996PNAS...9313629A. doi:10.1073/pnas.93.24.13629. PMC 19374. PMID 8942985.
“Promoter methylation of MLH1, PMS2, MSH2 and p16 is a phenomenon of advanced-stage HCCs”. PLOS ONE 9 (1): e84453. (2014). Bibcode: 2014PLoSO...984453H. doi:10.1371/journal.pone.0084453. PMC 3882222. PMID 24400091.

kobv.de (Global: low place; Japanese: low place)

opus4.kobv.de

“Mismatch repair proteins hMLH1 and hMSH2 are differently expressed in the three main subtypes of sporadic renal cell carcinoma”. Pathobiology 79 (3): 162–8. (2012). doi:10.1159/000335642. PMID 22378480.

nih.gov (Global: 4^th place; Japanese: 24^th place)

pubmed.ncbi.nlm.nih.gov

“Transcription-coupled repair deficiency and mutations in human mismatch repair genes”. Science 272 (5261): 557–60. (April 1996). Bibcode: 1996Sci...272..557M. doi:10.1126/science.272.5261.557. PMID 8614807. https://zenodo.org/record/1231074.
“Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer”. Cell 82 (2): 321–30. (July 1995). doi:10.1016/0092-8674(95)90319-4. PMID 7628020.
“Reduced host cell reactivation of oxidative DNA damage in human cells deficient in the mismatch repair gene hMSH2”. Mutagenesis 22 (3): 235–43. (May 2007). doi:10.1093/mutage/gem008. PMID 17351251.
“Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases”. Scientific Reports 9 (1): 18577. (December 2019). Bibcode: 2019NatSR...918577S. doi:10.1038/s41598-019-54976-4. PMC 6901466. PMID 31819097.
“Mismatch repair and the hereditary non-polyposis colorectal cancer syndrome (HNPCC)”. Cancer Invest. 20 (1): 102–9. (2002). doi:10.1081/cnv-120000371. PMID 11852992.
“Structure of the human MutSalpha DNA lesion recognition complex”. Mol. Cell 26 (4): 579–92. (May 2007). doi:10.1016/j.molcel.2007.04.018. PMID 17531815.
“Hereditary nonpolyposis colorectal cancer: diagnostic strategies and their implications”. Evid Rep Technol Assess (Full Rep) (150): 1–180. (May 2007). PMC 4781224. PMID 17764220.
“Era of universal testing of microsatellite instability in colorectal cancer”. World J Gastrointest Oncol 5 (2): 12–9. (February 2013). doi:10.4251/wjgo.v5.i2.12. PMC 3613766. PMID 23556052.
“Interaction between the Msh2 and Msh6 nucleotide-binding sites in the Saccharomyces cerevisiae Msh2-Msh6 complex”. J. Biol. Chem. 285 (12): 9301–10. (March 2010). doi:10.1074/jbc.M109.096388. PMC 2838348. PMID 20089866.
“Isolation of an hMSH2-p160 heterodimer that restores DNA mismatch repair to tumor cells”. Science 268 (5219): 1909–12. (June 1995). Bibcode: 1995Sci...268.1909D. doi:10.1126/science.7604264. PMID 7604264.
“Nuclear translocation of mismatch repair proteins MSH2 and MSH6 as a response of cells to alkylating agents”. J. Biol. Chem. 275 (46): 36256–62. (November 2000). doi:10.1074/jbc.M005377200. PMID 10954713.
“Structural, molecular and cellular functions of MSH2 and MSH6 during DNA mismatch repair, damage signaling and other noncanonical activities”. Mutat. Res. 743–744: 53–66. (February 2013). doi:10.1016/j.mrfmmm.2012.12.008. PMC 3659183. PMID 23391514.
“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. (November 1998). doi:10.1128/mcb.18.11.6616. PMC 109246. PMID 9774676.
“Large conformational changes in MutS during DNA scanning, mismatch recognition and repair signalling”. EMBO J. 31 (11): 2528–40. (May 2012). doi:10.1038/emboj.2012.95. PMC 3365432. PMID 22505031.
“Functional studies and homology modeling of Msh2-Msh3 predict that mispair recognition involves DNA bending and strand separation”. Mol. Cell. Biol. 30 (13): 3321–8. (July 2010). doi:10.1128/MCB.01558-09. PMC 2897569. PMID 20421420.
“Mechanism of mismatch recognition revealed by human MutSβ bound to unpaired DNA loops”. Nat. Struct. Mol. Biol. 19 (1): 72–8. (January 2012). doi:10.1038/nsmb.2175. PMC 3252464. PMID 22179786.
“MSH2 and ATR form a signaling module and regulate two branches of the damage response to DNA methylation”. Proc. Natl. Acad. Sci. U.S.A. 100 (26): 15387–92. (December 2003). Bibcode: 2003PNAS..10015387W. doi:10.1073/pnas.2536810100. PMC 307577. PMID 14657349.
“Adenosine nucleotide modulates the physical interaction between hMSH2 and BRCA1”. Oncogene 20 (34): 4640–9. (August 2001). doi:10.1038/sj.onc.1204625. PMID 11498787.
“BASC, a super complex of BRCA1-associated proteins involved in the recognition and repair of aberrant DNA structures”. Genes Dev. 14 (8): 927–39. (April 2000). doi:10.1101/gad.14.8.927. PMC 316544. PMID 10783165.
“Methylator-induced, mismatch repair-dependent G2 arrest is activated through Chk1 and Chk2”. Mol. Biol. Cell 16 (3): 1513–26. (March 2005). doi:10.1091/mbc.E04-02-0089. PMC 551512. PMID 15647386.
“The mismatch repair system is required for S-phase checkpoint activation”. Nat. Genet. 33 (1): 80–4. (January 2003). doi:10.1038/ng1052. PMID 12447371.
“Identification of factors interacting with hMSH2 in the fetal liver utilizing the yeast two-hybrid system. In vivo interaction through the C-terminal domains of hEXO1 and hMSH2 and comparative expression analysis”. Mutat. Res. 460 (1): 41–52. (June 2000). doi:10.1016/S0921-8777(00)00012-4. PMID 10856833.
“Human exonuclease I interacts with the mismatch repair protein hMSH2”. Cancer Res. 58 (20): 4537–42. (October 1998). PMID 9788596.
“The interaction of DNA mismatch repair proteins with human exonuclease I”. J. Biol. Chem. 276 (35): 33011–8. (August 2001). doi:10.1074/jbc.M102670200. PMID 11427529.
“Interactions of the DNA mismatch repair proteins MLH1 and MSH2 with c-MYC and MAX”. Oncogene 22 (6): 819–25. (February 2003). doi:10.1038/sj.onc.1206252. PMID 12584560.
“hMSH5: a human MutS homologue that forms a novel heterodimer with hMSH4 and is expressed during spermatogenesis”. Cancer Res. 59 (4): 816–22. (February 1999). PMID 10029069.
“hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6”. Proc. Natl. Acad. Sci. U.S.A. 93 (24): 13629–34. (November 1996). Bibcode: 1996PNAS...9313629A. doi:10.1073/pnas.93.24.13629. PMC 19374. PMID 8942985.
“Specific in vitro binding of p53 to the promoter region of the human mismatch repair gene hMSH2”. Biochem. Biophys. Res. Commun. 221 (3): 722–8. (April 1996). doi:10.1006/bbrc.1996.0663. PMID 8630028.
“DNA damage responses: mechanisms and roles in human disease: 2007 G.H.A. Clowes Memorial Award Lecture”. Molecular Cancer Research 6 (4): 517–24. (April 2008). doi:10.1158/1541-7786.MCR-08-0020. PMID 18403632.
“The DNA damage response: ten years after”. Molecular Cell 28 (5): 739–45. (December 2007). doi:10.1016/j.molcel.2007.11.015. PMID 18082599.
“Molecular pathways: exploiting tumor-specific molecular defects in DNA repair pathways for precision cancer therapy”. Clinical Cancer Research 20 (23): 5882–7. (December 2014). doi:10.1158/1078-0432.CCR-14-1165. PMID 25451105.
“Double strand breaks can initiate gene silencing and SIRT1-dependent onset of DNA methylation in an exogenous promoter CpG island”. PLOS Genetics 4 (8): e1000155. (2008). doi:10.1371/journal.pgen.1000155. PMC 2491723. PMID 18704159.
“DNA damage, homology-directed repair, and DNA methylation”. PLOS Genetics 3 (7): e110. (July 2007). doi:10.1371/journal.pgen.0030110. PMC 1913100. PMID 17616978.
“Inactivation of hMLH1 and hMSH2 by promoter methylation in primary non-small cell lung tumors and matched sputum samples”. J. Clin. Invest. 111 (6): 887–95. (2003). doi:10.1172/JCI15475. PMC 153761. PMID 12639995.
“Somatic deletions of genes regulating MSH2 protein stability cause DNA mismatch repair deficiency and drug resistance in human leukemia cells”. Nat. Med. 17 (10): 1298–303. (2011). doi:10.1038/nm.2430. PMC 3192247. PMID 21946537.
“Aberrant DNA methylation and epigenetic inactivation of hMSH2 decrease overall survival of acute lymphoblastic leukemia patients via modulating cell cycle and apoptosis”. Asian Pac. J. Cancer Prev. 15 (1): 355–62. (2014). doi:10.7314/apjcp.2014.15.1.355. PMID 24528056.
“Aberrant methylation of different DNA repair genes demonstrates distinct prognostic value for esophageal cancer”. Dig. Dis. Sci. 56 (10): 2992–3004. (2011). doi:10.1007/s10620-011-1774-z. PMID 21674174.
“Promoter hypermethylation is the predominant mechanism in hMLH1 and hMSH2 deregulation and is a poor prognostic factor in nonsmoking lung cancer”. Clin. Cancer Res. 11 (15): 5410–6. (2005). doi:10.1158/1078-0432.CCR-05-0601. PMID 16061855.
“Promoter methylation status of hMLH1, hMSH2, and MGMT genes in colorectal cancer associated with adenoma-carcinoma sequence”. Langenbecks Arch Surg 396 (7): 1017–26. (2011). doi:10.1007/s00423-011-0812-9. PMID 21706233.
“MSH2-deficient human cells exhibit a defect in the accurate termination of homology-directed repair of DNA double-strand breaks”. Cancer Res. 63 (12): 3334–9. (2003). PMID 12810667.
“Repair of double-strand breaks by homologous recombination in mismatch repair-defective mammalian cells”. Mol. Cell. Biol. 21 (8): 2671–82. (2001). doi:10.1128/MCB.21.8.2671-2682.2001. PMC 86898. PMID 11283247.
“Mismatch repair proteins hMLH1 and hMSH2 are differently expressed in the three main subtypes of sporadic renal cell carcinoma”. Pathobiology 79 (3): 162–8. (2012). doi:10.1159/000335642. PMID 22378480.
“Deficiency of MSH2 expression is associated with clear cell renal cell carcinoma”. Oncol Lett 8 (5): 2135–2139. (2014). doi:10.3892/ol.2014.2482. PMC 4186615. PMID 25295100.
“MSH2 promoter hypermethylation in circulating tumor DNA is a valuable predictor of disease-free survival for patients with esophageal squamous cell carcinoma”. Eur J Surg Oncol 38 (4): 326–32. (2012). doi:10.1016/j.ejso.2012.01.008. PMID 22265839.
“Inactivation of human mutL homolog 1 and mutS homolog 2 genes in head and neck squamous cell carcinoma tumors and leukoplakia samples by promoter hypermethylation and its relation with microsatellite instability phenotype”. Cancer 109 (4): 703–12. (2007). doi:10.1002/cncr.22430. PMID 17219447.
“Microsatellite instability and methylation of the DNA mismatch repair genes in head and neck cancer”. Ann. Oncol. 17 (6): 995–9. (2006). doi:10.1093/annonc/mdl048. PMID 16569647.
“Promoter hypermethylation of mismatch repair genes, hMLH1 and hMSH2 in oral squamous cell carcinoma”. Oral Dis 15 (3): 206–13. (2009). doi:10.1111/j.1601-0825.2008.01510.x. PMID 19207881.
“Promoter methylation of MLH1, PMS2, MSH2 and p16 is a phenomenon of advanced-stage HCCs”. PLOS ONE 9 (1): e84453. (2014). Bibcode: 2014PLoSO...984453H. doi:10.1371/journal.pone.0084453. PMC 3882222. PMID 24400091.
“Microsatellite instability and promoter hypermethylation of MLH1 and MSH2 in patients with sporadic colorectal cancer”. J BUON 16 (2): 265–73. (2011). PMID 21766496.
“Promoter methylation and immunohistochemical expression of hMLH1 and hMSH2 in sporadic colorectal cancer: a study from India”. Tumour Biol. 35 (4): 3679–87. (2014). doi:10.1007/s13277-013-1487-3. PMID 24317816.
“Alterations of copy number of methylation pattern in mismatch repair genes by methylation specific-multiplex ligation-dependent probe amplification in cases of colon cancer”. Balkan J. Med. Genet. 14 (2): 25–34. (2011). doi:10.2478/v10034-011-0044-x. PMC 3776700. PMID 24052709.
“DNA hypermethylation status of multiple genes in soft tissue sarcomas”. Mod. Pathol. 19 (1): 106–14. (2006). doi:10.1038/modpathol.3800502. PMID 16258501.

pmc.ncbi.nlm.nih.gov

ncbi.nlm.nih.gov

wikipedia.org (Global: low place; Japanese: low place)

en.wikipedia.org

GRCh38: Ensembl release 89: ENSG00000095002 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000024151 - Ensembl, May 2017

zenodo.org (Global: 621^st place; Japanese: 4,635^th place)

“Transcription-coupled repair deficiency and mutations in human mismatch repair genes”. Science 272 (5261): 557–60. (April 1996). Bibcode: 1996Sci...272..557M. doi:10.1126/science.272.5261.557. PMID 8614807. https://zenodo.org/record/1231074.