Nicolaides NC, Papadopoulos N, Liu B, Wei YF, Carter KC, Ruben SM, Rosen CA, Haseltine WA, Fleischmann RD, Fraser CM (Sep 1994). "Mutations of two PMS homologues in hereditary nonpolyposis colon cancer". Nature371 (6492): 75–80. PMID8072530. doi:10.1038/371075a0.
Nicolaides NC, Carter KC, Shell BK, Papadopoulos N, Vogelstein B, Kinzler KW (November 1995). "Genomic organization of the human PMS2 gene family". Genomics30 (2): 195–206. PMID8586419. doi:10.1006/geno.1995.9885.
Mac Partlin M, Homer E, Robinson H, McCormick CJ, Crouch DH, Durant ST, Matheson EC, Hall AG, Gillespie DA, Brown R (February 2003). "Interactions of the DNA mismatch repair proteins MLH1 and MSH2 with c-MYC and MAX". Oncogene22 (6): 819–25. PMID12584560. doi:10.1038/sj.onc.1206252.
Guerrette S, Acharya S, Fishel R (March 1999). "The interaction of the human MutL homologues in hereditary nonpolyposis colon cancer". J. Biol. Chem.274 (10): 6336–41. PMID10037723. doi:10.1074/jbc.274.10.6336.
Cannavo E, Gerrits B, Marra G, Schlapbach R, Jiricny J (February 2007). "Characterization of the interactome of the human MutL homologues MLH1, PMS1, and PMS2". J. Biol. Chem.282 (5): 2976–86. PMID17148452. doi:10.1074/jbc.M609989200.
Johannesma PC, van der Klift HM, van Grieken NC, Troost D, Te Riele H, Jacobs MA, Postma TJ, Heideman DA, Tops CM, Wijnen JT, Menko FH (September 2011). "Childhood brain tumours due to germline bi-allelic mismatch repair gene mutations". Clin. Genet.80 (3): 243–55. PMID21261604. doi:10.1111/j.1399-0004.2011.01635.x.
De Rosa M, Fasano C, Panariello L, Scarano MI, Belli G, Iannelli A, Ciciliano F, Izzo P (March 2000). "Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene". Oncogene19 (13): 1719–23. PMID10763829. doi:10.1038/sj.onc.1203447.
Herkert JC, Niessen RC, Olderode-Berends MJ, Veenstra-Knol HE, Vos YJ, van der Klift HM, Scheenstra R, Tops CM, Karrenbeld A, Peters FT, Hofstra RM, Kleibeuker JH, Sijmons RH (May 2011). "Paediatric intestinal cancer and polyposis due to bi-allelic PMS2 mutations: case series, review and follow-up guidelines". Eur. J. Cancer47 (7): 965–82. PMID21376568. doi:10.1016/j.ejca.2011.01.013.
Gibson SL, Narayanan L, Hegan DC, Buermeyer AB, Liskay RM, Glazer PM (December 2006). "Overexpression of the DNA mismatch repair factor, PMS2, confers hypermutability and DNA damage tolerance". Cancer Lett.244 (2): 195–202. PMID16426742. doi:10.1016/j.canlet.2005.12.009.
Chang DK, Ricciardiello L, Goel A, Chang CL, Boland CR (2000). "Steady-state regulation of the human DNA mismatch repair system". J. Biol. Chem.275 (24): 18424–31. PMID10747992. doi:10.1074/jbc.M001140200.
"PMS2 Gene". The GeneCards Human Gene Database. Weizmann Institute of Science.
nih.gov
ncbi.nlm.nih.gov
Nicolaides NC, Papadopoulos N, Liu B, Wei YF, Carter KC, Ruben SM, Rosen CA, Haseltine WA, Fleischmann RD, Fraser CM (Sep 1994). "Mutations of two PMS homologues in hereditary nonpolyposis colon cancer". Nature371 (6492): 75–80. PMID8072530. doi:10.1038/371075a0.
Nicolaides NC, Carter KC, Shell BK, Papadopoulos N, Vogelstein B, Kinzler KW (November 1995). "Genomic organization of the human PMS2 gene family". Genomics30 (2): 195–206. PMID8586419. doi:10.1006/geno.1995.9885.
Mac Partlin M, Homer E, Robinson H, McCormick CJ, Crouch DH, Durant ST, Matheson EC, Hall AG, Gillespie DA, Brown R (February 2003). "Interactions of the DNA mismatch repair proteins MLH1 and MSH2 with c-MYC and MAX". Oncogene22 (6): 819–25. PMID12584560. doi:10.1038/sj.onc.1206252.
Guerrette S, Acharya S, Fishel R (March 1999). "The interaction of the human MutL homologues in hereditary nonpolyposis colon cancer". J. Biol. Chem.274 (10): 6336–41. PMID10037723. doi:10.1074/jbc.274.10.6336.
Cannavo E, Gerrits B, Marra G, Schlapbach R, Jiricny J (February 2007). "Characterization of the interactome of the human MutL homologues MLH1, PMS1, and PMS2". J. Biol. Chem.282 (5): 2976–86. PMID17148452. doi:10.1074/jbc.M609989200.
Meyers M, Theodosiou M, Acharya S, Odegaard E, Wilson T, Lewis JE, Davis TW, Wilson-Van Patten C, Fishel R, Boothman DA (January 1997). "Cell cycle regulation of the human DNA mismatch repair genes hMSH2, hMLH1, and hPMS2". Cancer Res.57 (2): 206–8. PMID9000555.
Johannesma PC, van der Klift HM, van Grieken NC, Troost D, Te Riele H, Jacobs MA, Postma TJ, Heideman DA, Tops CM, Wijnen JT, Menko FH (September 2011). "Childhood brain tumours due to germline bi-allelic mismatch repair gene mutations". Clin. Genet.80 (3): 243–55. PMID21261604. doi:10.1111/j.1399-0004.2011.01635.x.
De Rosa M, Fasano C, Panariello L, Scarano MI, Belli G, Iannelli A, Ciciliano F, Izzo P (March 2000). "Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene". Oncogene19 (13): 1719–23. PMID10763829. doi:10.1038/sj.onc.1203447.
Herkert JC, Niessen RC, Olderode-Berends MJ, Veenstra-Knol HE, Vos YJ, van der Klift HM, Scheenstra R, Tops CM, Karrenbeld A, Peters FT, Hofstra RM, Kleibeuker JH, Sijmons RH (May 2011). "Paediatric intestinal cancer and polyposis due to bi-allelic PMS2 mutations: case series, review and follow-up guidelines". Eur. J. Cancer47 (7): 965–82. PMID21376568. doi:10.1016/j.ejca.2011.01.013.
Gibson SL, Narayanan L, Hegan DC, Buermeyer AB, Liskay RM, Glazer PM (December 2006). "Overexpression of the DNA mismatch repair factor, PMS2, confers hypermutability and DNA damage tolerance". Cancer Lett.244 (2): 195–202. PMID16426742. doi:10.1016/j.canlet.2005.12.009.
Chang DK, Ricciardiello L, Goel A, Chang CL, Boland CR (2000). "Steady-state regulation of the human DNA mismatch repair system". J. Biol. Chem.275 (24): 18424–31. PMID10747992. doi:10.1074/jbc.M001140200.
Nara K, Nagashima F, Yasui A (2001). "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. PMID11196196.