PMS2 (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "PMS2" in Japanese language version.

refsWebsite

Global rank Japanese rank

4^th place

24^th place

2^nd place

6^th place

1,626^th place

2,625^th place

low place

low place

1web.archive.org

1^st place

1^st place

3,633^rd place

low place

low place

low place

2,779^th place

8,003^rd place

doi.org

“Mutations of two PMS homologues in hereditary nonpolyposis colon cancer”. Nature 371 (6492): 75–80. (Sep 1994). doi:10.1038/371075a0. PMID 8072530.
“Genomic organization of the human PMS2 gene family”. Genomics 30 (2): 195–206. (November 1995). doi:10.1006/geno.1995.9885. PMID 8586419.
“PMS2 endonuclease activity has distinct biological functions and is essential for genome maintenance”. Proc. Natl. Acad. Sci. U.S.A. 107 (30): 13384–9. (12 July 2010). doi:10.1073/pnas.1008589107. PMC 2922181. PMID 20624957.
“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.
“The interacting domains of three MutL heterodimers in man: hMLH1 interacts with 36 homologous amino acid residues within hMLH3, hPMS1 and hPMS2”. Nucleic Acids Res. 29 (8): 1695–702. (April 2001). doi:10.1093/nar/29.8.1695. PMC 31313. PMID 11292842.
“The interaction of the human MutL homologues in hereditary nonpolyposis colon cancer”. J. Biol. Chem. 274 (10): 6336–41. (March 1999). doi:10.1074/jbc.274.10.6336. PMID 10037723.
“Identification of the mismatch repair genes PMS2 and MLH1 as p53 target genes by using serial analysis of binding elements”. Proc. Natl. Acad. Sci. U.S.A. 102 (13): 4813–8. (March 2005). doi:10.1073/pnas.0407069102. PMC 555698. PMID 15781865.
“Interaction of mismatch repair protein PMS2 and the p53-related transcription factor p73 in apoptosis response to cisplatin”. Proc. Natl. Acad. Sci. U.S.A. 100 (5): 2420–5. (March 2003). doi:10.1073/pnas.0438031100. PMC 151356. PMID 12601175.
“Characterization of the interactome of the human MutL homologues MLH1, PMS1, and PMS2”. J. Biol. Chem. 282 (5): 2976–86. (February 2007). doi:10.1074/jbc.M609989200. PMID 17148452. オリジナルの2018-07-19時点におけるアーカイブ。 2019年9月17日閲覧。.
“Increased sensitivity of p53-deficient cells to anticancer agents due to loss of Pms2”. Br. J. Cancer 87 (9): 1027–33. (October 2002). doi:10.1038/sj.bjc.6600599. PMC 2364320. PMID 12434296.
“Mismatch repair gene PMS2: disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation”. Cancer Res. 64 (14): 4721–7. (July 2004). doi:10.1158/0008-5472.CAN-03-2879. PMID 15256438.
“Polymorphisms in a pseudogene highly homologous to PMS2”. Hum. Mutat. 16 (6): 530. (December 2000). doi:10.1002/1098-1004(200012)16:6<530::AID-HUMU15>3.0.CO;2-6. PMID 11102987.
“Analysis of 100,000 human cancer genomes reveals the landscape of tumor mutational burden”. Genome Med. 9 (34): epub. (April 2017). doi:10.1186/s13073-017-0424-2. PMC 5395719. PMID 28420421. >
“Tumor Mutational Burden as an Independent Predictor of Response to Immunotherapy in Diverse Cancers”. Mol. Cancer Ther. 16 (11): 2598–2608. (November 2017). doi:10.1158/1535-7163.MCT-17-0386. PMC 5670009. PMID 28835386. >
“The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations”. Gastroenterology 135 (2): 419–28. (August 2008). doi:10.1053/j.gastro.2008.04.026. PMC 2759321. PMID 18602922.
“Childhood brain tumours due to germline bi-allelic mismatch repair gene mutations”. Clin. Genet. 80 (3): 243–55. (September 2011). doi:10.1111/j.1399-0004.2011.01635.x. PMID 21261604.
“Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene”. Oncogene 19 (13): 1719–1723. (March 2000). doi:10.1038/sj.onc.1203447. PMID 10763829.
“Paediatric intestinal cancer and polyposis due to bi-allelic PMS2 mutations: case series, review and follow-up guidelines”. Eur. J. Cancer 47 (7): 965–82. (May 2011). doi:10.1016/j.ejca.2011.01.013. PMID 21376568.
“Overexpression of the DNA mismatch repair factor, PMS2, confers hypermutability and DNA damage tolerance”. Cancer Lett. 244 (2): 195–202. (December 2006). doi:10.1016/j.canlet.2005.12.009. PMID 16426742.
“Deficient expression of DNA repair enzymes in early progression to sporadic colon cancer”. Genome Integr 3 (1): 3. (2012). doi:10.1186/2041-9414-3-3. PMC 3351028. PMID 22494821.
“Quantification of crypt and stem cell evolution in the normal and neoplastic human colon”. Cell Rep 8 (4): 940–7. (2014). doi:10.1016/j.celrep.2014.07.019. PMC 4471679. PMID 25127143.
“Age-associated mitochondrial DNA mutations lead to small but significant changes in cell proliferation and apoptosis in human colonic crypts”. Aging Cell 9 (1): 96–9. (2010). doi:10.1111/j.1474-9726.2009.00531.x. PMC 2816353. PMID 19878146.
“Immunohistochemical analysis reveals high frequency of PMS2 defects in colorectal cancer”. Gastroenterology 128 (5): 1160–71. (2005). doi:10.1053/j.gastro.2005.01.056. PMID 15887099.
“Steady-state regulation of the human DNA mismatch repair system”. J. Biol. Chem. 275 (24): 18424–31. (2000). doi:10.1074/jbc.M001140200. PMID 10747992.
“DNA damage-induced apoptosis”. Oncogene 23 (16): 2797–808. (2004). doi:10.1038/sj.onc.1207532. PMID 15077143.
“Functional role of DNA mismatch repair gene PMS2 in prostate cancer cells”. Oncotarget 6 (18): 16341–51. (2015). doi:10.18632/oncotarget.3854. PMC 4599273. PMID 26036629.
“Apoptotic function of human PMS2 compromised by the nonsynonymous single-nucleotide polymorphic variant R20Q”. Proc. Natl. Acad. Sci. U.S.A. 105 (37): 13993–8. (2008). doi:10.1073/pnas.0806435105. PMC 2528866. PMID 18768816.
“Human cancers express mutator phenotypes: origin, consequences and targeting”. Nat. Rev. Cancer 11 (6): 450–7. (2011). doi:10.1038/nrc3063. PMC 4007007. PMID 21593786.
“The DNA damage response: ten years after”. Mol. Cell 28 (5): 739–45. (2007). doi:10.1016/j.molcel.2007.11.015. PMID 18082599.

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000122512 - Ensembl, May 2017

genecards.org

“PMS2 Gene”. The GeneCards Human Gene Database. Weizmann Institute of Science. 2022年12月11日閲覧。

nih.gov

pubmed.ncbi.nlm.nih.gov

“Mutations of two PMS homologues in hereditary nonpolyposis colon cancer”. Nature 371 (6492): 75–80. (Sep 1994). doi:10.1038/371075a0. PMID 8072530.
“Genomic organization of the human PMS2 gene family”. Genomics 30 (2): 195–206. (November 1995). doi:10.1006/geno.1995.9885. PMID 8586419.
“PMS2 endonuclease activity has distinct biological functions and is essential for genome maintenance”. Proc. Natl. Acad. Sci. U.S.A. 107 (30): 13384–9. (12 July 2010). doi:10.1073/pnas.1008589107. PMC 2922181. PMID 20624957.
“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.
“The interacting domains of three MutL heterodimers in man: hMLH1 interacts with 36 homologous amino acid residues within hMLH3, hPMS1 and hPMS2”. Nucleic Acids Res. 29 (8): 1695–702. (April 2001). doi:10.1093/nar/29.8.1695. PMC 31313. PMID 11292842.
“The interaction of the human MutL homologues in hereditary nonpolyposis colon cancer”. J. Biol. Chem. 274 (10): 6336–41. (March 1999). doi:10.1074/jbc.274.10.6336. PMID 10037723.
“Identification of the mismatch repair genes PMS2 and MLH1 as p53 target genes by using serial analysis of binding elements”. Proc. Natl. Acad. Sci. U.S.A. 102 (13): 4813–8. (March 2005). doi:10.1073/pnas.0407069102. PMC 555698. PMID 15781865.
“Interaction of mismatch repair protein PMS2 and the p53-related transcription factor p73 in apoptosis response to cisplatin”. Proc. Natl. Acad. Sci. U.S.A. 100 (5): 2420–5. (March 2003). doi:10.1073/pnas.0438031100. PMC 151356. PMID 12601175.
“Characterization of the interactome of the human MutL homologues MLH1, PMS1, and PMS2”. J. Biol. Chem. 282 (5): 2976–86. (February 2007). doi:10.1074/jbc.M609989200. PMID 17148452. オリジナルの2018-07-19時点におけるアーカイブ。 2019年9月17日閲覧。.
“Cell cycle regulation of the human DNA mismatch repair genes hMSH2, hMLH1, and hPMS2”. Cancer Res. 57 (2): 206–8. (January 1997). PMID 9000555.
“Increased sensitivity of p53-deficient cells to anticancer agents due to loss of Pms2”. Br. J. Cancer 87 (9): 1027–33. (October 2002). doi:10.1038/sj.bjc.6600599. PMC 2364320. PMID 12434296.
“Mismatch repair gene PMS2: disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation”. Cancer Res. 64 (14): 4721–7. (July 2004). doi:10.1158/0008-5472.CAN-03-2879. PMID 15256438.
“Polymorphisms in a pseudogene highly homologous to PMS2”. Hum. Mutat. 16 (6): 530. (December 2000). doi:10.1002/1098-1004(200012)16:6<530::AID-HUMU15>3.0.CO;2-6. PMID 11102987.
“Analysis of 100,000 human cancer genomes reveals the landscape of tumor mutational burden”. Genome Med. 9 (34): epub. (April 2017). doi:10.1186/s13073-017-0424-2. PMC 5395719. PMID 28420421. >
“Tumor Mutational Burden as an Independent Predictor of Response to Immunotherapy in Diverse Cancers”. Mol. Cancer Ther. 16 (11): 2598–2608. (November 2017). doi:10.1158/1535-7163.MCT-17-0386. PMC 5670009. PMID 28835386. >
“The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations”. Gastroenterology 135 (2): 419–28. (August 2008). doi:10.1053/j.gastro.2008.04.026. PMC 2759321. PMID 18602922.
“Childhood brain tumours due to germline bi-allelic mismatch repair gene mutations”. Clin. Genet. 80 (3): 243–55. (September 2011). doi:10.1111/j.1399-0004.2011.01635.x. PMID 21261604.
“Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene”. Oncogene 19 (13): 1719–1723. (March 2000). doi:10.1038/sj.onc.1203447. PMID 10763829.
“Paediatric intestinal cancer and polyposis due to bi-allelic PMS2 mutations: case series, review and follow-up guidelines”. Eur. J. Cancer 47 (7): 965–82. (May 2011). doi:10.1016/j.ejca.2011.01.013. PMID 21376568.
“Overexpression of the DNA mismatch repair factor, PMS2, confers hypermutability and DNA damage tolerance”. Cancer Lett. 244 (2): 195–202. (December 2006). doi:10.1016/j.canlet.2005.12.009. PMID 16426742.
“Deficient expression of DNA repair enzymes in early progression to sporadic colon cancer”. Genome Integr 3 (1): 3. (2012). doi:10.1186/2041-9414-3-3. PMC 3351028. PMID 22494821.
“Quantification of crypt and stem cell evolution in the normal and neoplastic human colon”. Cell Rep 8 (4): 940–7. (2014). doi:10.1016/j.celrep.2014.07.019. PMC 4471679. PMID 25127143.
“Age-associated mitochondrial DNA mutations lead to small but significant changes in cell proliferation and apoptosis in human colonic crypts”. Aging Cell 9 (1): 96–9. (2010). doi:10.1111/j.1474-9726.2009.00531.x. PMC 2816353. PMID 19878146.
“Immunohistochemical analysis reveals high frequency of PMS2 defects in colorectal cancer”. Gastroenterology 128 (5): 1160–71. (2005). doi:10.1053/j.gastro.2005.01.056. PMID 15887099.
“Steady-state regulation of the human DNA mismatch repair system”. J. Biol. Chem. 275 (24): 18424–31. (2000). doi:10.1074/jbc.M001140200. PMID 10747992.
“DNA damage-induced apoptosis”. Oncogene 23 (16): 2797–808. (2004). doi:10.1038/sj.onc.1207532. PMID 15077143.
“Functional role of DNA mismatch repair gene PMS2 in prostate cancer cells”. Oncotarget 6 (18): 16341–51. (2015). doi:10.18632/oncotarget.3854. PMC 4599273. PMID 26036629.
“Apoptotic function of human PMS2 compromised by the nonsynonymous single-nucleotide polymorphic variant R20Q”. Proc. Natl. Acad. Sci. U.S.A. 105 (37): 13993–8. (2008). doi:10.1073/pnas.0806435105. PMC 2528866. PMID 18768816.
“Highly elevated ultraviolet-induced mutation frequency in isolated Chinese hamster cell lines defective in nucleotide excision repair and mismatch repair proteins”. Cancer Res. 61 (1): 50–2. (2001). PMID 11196196.
“Human cancers express mutator phenotypes: origin, consequences and targeting”. Nat. Rev. Cancer 11 (6): 450–7. (2011). doi:10.1038/nrc3063. PMC 4007007. PMID 21593786.
“The DNA damage response: ten years after”. Mol. Cell 28 (5): 739–45. (2007). doi:10.1016/j.molcel.2007.11.015. PMID 18082599.

ncbi.nlm.nih.gov

pmc.ncbi.nlm.nih.gov

ghr.nlm.nih.gov

“PMS2 - PMS2 postmeiotic segregation increased 2 (S. cerevisiae)”. Genetics Home Reference. U.S. National Library of Medicine. 2022年12月20日閲覧。

rug.nl

research.rug.nl

“Paediatric intestinal cancer and polyposis due to bi-allelic PMS2 mutations: case series, review and follow-up guidelines”. Eur. J. Cancer 47 (7): 965–82. (May 2011). doi:10.1016/j.ejca.2011.01.013. PMID 21376568.

uzh.ch

zora.uzh.ch

“Characterization of the interactome of the human MutL homologues MLH1, PMS1, and PMS2”. J. Biol. Chem. 282 (5): 2976–86. (February 2007). doi:10.1074/jbc.M609989200. PMID 17148452. オリジナルの2018-07-19時点におけるアーカイブ。 2019年9月17日閲覧。.

web.archive.org

“Characterization of the interactome of the human MutL homologues MLH1, PMS1, and PMS2”. J. Biol. Chem. 282 (5): 2976–86. (February 2007). doi:10.1074/jbc.M609989200. PMID 17148452. オリジナルの2018-07-19時点におけるアーカイブ。 2019年9月17日閲覧。.

wikipedia.org

en.wikipedia.org

GRCh38: Ensembl release 89: ENSG00000122512 - Ensembl, May 2017