MLH1 (Galician Wikipedia)

Analysis of information sources in references of the Wikipedia article "MLH1" in Galician language version.

refsWebsite

Global rank Galician rank

39nih.gov

4^th place

6^th place

37doi.org

2^nd place

7^th place

7archive.org

6^th place

8^th place

archive.org (Global: 6^th place; Galician: 8^th place)

Truninger K, Menigatti M, Luz J, Russell A, Haider R, Gebbers JO, Bannwart F, Yurtsever H, Neuweiler J, Riehle HM, Cattaruzza MS, Heinimann K, Schär P, Jiricny J, Marra G (2005). "Immunohistochemical analysis reveals high frequency of PMS2 defects in colorectal cancer". Gastroenterology 128 (5): 1160–71. PMID 15887099. doi:10.1053/j.gastro.2005.01.056.
Zuo C, Zhang H, Spencer HJ, Vural E, Suen JY, Schichman SA, Smoller BR, Kokoska MS, Fan CY (2009). "Increased microsatellite instability and epigenetic inactivation of the hMLH1 gene in head and neck squamous cell carcinoma". Otolaryngol Head Neck Surg 141 (4): 484–90. PMID 19786217. doi:10.1016/j.otohns.2009.07.007.
Jiang Z, Hu J, Li X, Jiang Y, Zhou W, Lu D (2006). "Expression analyses of 27 DNA repair genes in astrocytoma by TaqMan low-density array". Neurosci. Lett. 409 (2): 112–7. PMID 17034947. doi:10.1016/j.neulet.2006.09.038.
Langland G, Kordich J, Creaney J, Goss KH, Lillard-Wetherell K, Bebenek K, Kunkel TA, Groden J (August 2001). "The Bloom's syndrome protein (BLM) interacts with MLH1 but is not required for DNA mismatch repair". J. Biol. Chem. 276 (32): 30031–5. PMID 11325959. doi:10.1074/jbc.M009664200.
Schmutte C, Sadoff MM, Shim KS, Acharya S, Fishel R (August 2001). "The interaction of DNA mismatch repair proteins with human exonuclease I". J. Biol. Chem. 276 (35): 33011–8. PMID 11427529. doi:10.1074/jbc.M102670200.
Santucci-Darmanin S, Walpita D, Lespinasse F, Desnuelle C, Ashley T, Paquis-Flucklinger V (August 2000). "MSH4 acts in conjunction with MLH1 during mammalian meiosis". FASEB J. 14 (11): 1539–47. PMID 10928988. doi:10.1096/fj.14.11.1539.
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. PMID 10037723. doi:10.1074/jbc.274.10.6336.

doi.org (Global: 2^nd place; Galician: 7^th place)

dx.doi.org

Pal T, Permuth-Wey J, Sellers TA (2008). "A review of the clinical relevance of mismatch-repair deficiency in ovarian cancer". Cancer 113 (4): 733–42. PMC 2644411. PMID 18543306. doi:10.1002/cncr.23601.
Truninger K, Menigatti M, Luz J, Russell A, Haider R, Gebbers JO, Bannwart F, Yurtsever H, Neuweiler J, Riehle HM, Cattaruzza MS, Heinimann K, Schär P, Jiricny J, Marra G (2005). "Immunohistochemical analysis reveals high frequency of PMS2 defects in colorectal cancer". Gastroenterology 128 (5): 1160–71. PMID 15887099. doi:10.1053/j.gastro.2005.01.056.
Goellner EM, Putnam CD, Kolodner RD (2015). "Exonuclease 1-dependent and independent mismatch repair". DNA Repair (Amst.) 32: 24–32. PMID 25956862. doi:10.1016/j.dnarep.2015.04.010.
Li GM (2008). "Mechanisms and functions of DNA mismatch repair". Cell Res. 18 (1): 85–98. PMID 18157157. doi:10.1038/cr.2007.115.
Li GM (2014). "New insights and challenges in mismatch repair: getting over the chromatin hurdle". DNA Repair (Amst.) 19: 48–54. PMC 4127414. PMID 24767944. doi:10.1016/j.dnarep.2014.03.027.
Waki T, Tamura G, Tsuchiya T, Sato K, Nishizuka S, Motoyama T (2002). "Promoter methylation status of E-cadherin, hMLH1, and p16 genes in nonneoplastic gastric epithelia". Am. J. Pathol. 161 (2): 399–403. PMC 1850716. PMID 12163364. doi:10.1016/S0002-9440(10)64195-8.
Endoh Y, Tamura G, Ajioka Y, Watanabe H, Motoyama T (2000). "Frequent hypermethylation of the hMLH1 gene promoter in differentiated-type tumors of the stomach with the gastric foveolar phenotype". Am. J. Pathol. 157 (3): 717–22. PMC 1949419. PMID 10980110. doi:10.1016/S0002-9440(10)64584-1.
Wani M, Afroze D, Makhdoomi M, Hamid I, Wani B, Bhat G, Wani R, Wani K (2012). "Promoter methylation status of DNA repair gene (hMLH1) in gastric carcinoma patients of the Kashmir valley". Asian Pac. J. Cancer Prev. 13 (8): 4177–81. PMID 23098428. doi:10.7314/apjcp.2012.13.8.4177.
Chang Z, Zhang W, Chang Z, Song M, Qin Y, Chang F, Guo H, Wei Q (2015). "Expression characteristics of FHIT, p53, BRCA2 and MLH1 in families with a history of oesophageal cancer in a region with a high incidence of oesophageal cancer". Oncol Lett 9 (1): 430–436. PMC 4246613. PMID 25436004. doi:10.3892/ol.2014.2682.
Tawfik HM, El-Maqsoud NM, Hak BH, El-Sherbiny YM (2011). "Head and neck squamous cell carcinoma: mismatch repair immunohistochemistry and promoter hypermethylation of hMLH1 gene". Am J Otolaryngol 32 (6): 528–36. PMID 21353335. doi:10.1016/j.amjoto.2010.11.005.
Zuo C, Zhang H, Spencer HJ, Vural E, Suen JY, Schichman SA, Smoller BR, Kokoska MS, Fan CY (2009). "Increased microsatellite instability and epigenetic inactivation of the hMLH1 gene in head and neck squamous cell carcinoma". Otolaryngol Head Neck Surg 141 (4): 484–90. PMID 19786217. doi:10.1016/j.otohns.2009.07.007.
Safar AM, Spencer H, Su X, Coffey M, Cooney CA, Ratnasinghe LD, Hutchins LF, Fan CY (2005). "Methylation profiling of archived non-small cell lung cancer: a promising prognostic system". Clin. Cancer Res. 11 (12): 4400–5. PMID 15958624. doi:10.1158/1078-0432.CCR-04-2378.
Bernstein C, Bernstein H (2015). "Epigenetic reduction of DNA repair in progression to gastrointestinal cancer". World J Gastrointest Oncol 7 (5): 30–46. PMC 4434036. PMID 25987950. doi:10.4251/wjgo.v7.i5.30.
Valeri N, Gasparini P, Fabbri M, Braconi C, Veronese A, Lovat F, Adair B, Vannini I, Fanini F, Bottoni A, Costinean S, Sandhu SK, Nuovo GJ, Alder H, Gafa R, Calore F, Ferracin M, Lanza G, Volinia S, Negrini M, McIlhatton MA, Amadori D, Fishel R, Croce CM (2010). "Modulation of mismatch repair and genomic stability by miR-155". Proc. Natl. Acad. Sci. U.S.A. 107 (15): 6982–7. PMC 2872463. PMID 20351277. doi:10.1073/pnas.1002472107.
Rubin H (March 2011). "Fields and field cancerization: the preneoplastic origins of cancer: asymptomatic hyperplastic fields are precursors of neoplasia, and their progression to tumors can be tracked by saturation density in culture". BioEssays 33 (3): 224–31. PMID 21254148. doi:10.1002/bies.201000067.
Tsao JL, Yatabe Y, Salovaara R, Järvinen HJ, Mecklin JP, Aaltonen LA, Tavaré S, Shibata D (February 2000). "Genetic reconstruction of individual colorectal tumor histories". Proc. Natl. Acad. Sci. U.S.A. 97 (3): 1236–41. PMC 15581. PMID 10655514. doi:10.1073/pnas.97.3.1236.
Vogelstein B, Papadopoulos N, Velculescu VE, Zhou S, Diaz LA, Kinzler KW (March 2013). "Cancer genome landscapes". Science 339 (6127): 1546–58. PMC 3749880. PMID 23539594. doi:10.1126/science.1235122.
Jiang Z, Hu J, Li X, Jiang Y, Zhou W, Lu D (2006). "Expression analyses of 27 DNA repair genes in astrocytoma by TaqMan low-density array". Neurosci. Lett. 409 (2): 112–7. PMID 17034947. doi:10.1016/j.neulet.2006.09.038.
Kitajima Y, Miyazaki K, Matsukura S, Tanaka M, Sekiguchi M (2003). "Loss of expression of DNA repair enzymes MGMT, hMLH1, and hMSH2 during tumor progression in gastric cancer". Gastric Cancer 6 (2): 86–95. PMID 12861399. doi:10.1007/s10120-003-0213-z.
Baker SM, Plug AW, Prolla TA, Bronner CE, Harris AC, Yao X, Christie DM, Monell C, Arnheim N, Bradley A, Ashley T, Liskay RM (1996). "Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over". Nat. Genet. 13 (3): 336–42. PMID 8673133. doi:10.1038/ng0796-336.
Kan R, Sun X, Kolas NK, Avdievich E, Kneitz B, Edelmann W, Cohen PE (2008). "Comparative analysis of meiotic progression in female mice bearing mutations in genes of the DNA mismatch repair pathway". Biol. Reprod. 78 (3): 462–71. PMID 18057311. doi:10.1095/biolreprod.107.065771.
Wei K, Kucherlapati R, Edelmann W (2002). "Mouse models for human DNA mismatch-repair gene defects". Trends Mol Med 8 (7): 346–53. PMID 12114115. doi:10.1016/s1471-4914(02)02359-6.
Ji G, Long Y, Zhou Y, Huang C, Gu A, Wang X (2012). "Common variants in mismatch repair genes associated with increased risk of sperm DNA damage and male infertility". BMC Med 10: 49. PMC 3378460. PMID 22594646. doi:10.1186/1741-7015-10-49.
Ranjha L, Anand R, Cejka P (2014). "The Saccharomyces cerevisiae Mlh1-Mlh3 heterodimer is an endonuclease that preferentially binds to Holliday junctions". J. Biol. Chem. 289 (9): 5674–86. PMC 3937642. PMID 24443562. doi:10.1074/jbc.M113.533810.
Rogacheva MV, Manhart CM, Chen C, Guarne A, Surtees J, Alani E (2014). "Mlh1-Mlh3, a meiotic crossover and DNA mismatch repair factor, is a Msh2-Msh3-stimulated endonuclease". J. Biol. Chem. 289 (9): 5664–73. PMC 3937641. PMID 24403070. doi:10.1074/jbc.M113.534644.
Zakharyevich K, Tang S, Ma Y, Hunter N (2012). "Delineation of joint molecule resolution pathways in meiosis identifies a crossover-specific resolvase". Cell 149 (2): 334–47. PMC 3377385. PMID 22500800. doi:10.1016/j.cell.2012.03.023.
Lebrun C, Olschwang S, Jeannin S, Vandenbos F, Sobol H, Frenay M (2007). "Turcot syndrome confirmed with molecular analysis". Eur. J. Neurol. 14 (4): 470–2. PMID 17389002. doi:10.1111/j.1468-1331.2006.01669.x.
Wang Y, Cortez D, Yazdi P, Neff N, Elledge SJ, Qin J (April 2000). "BASC, a super complex of BRCA1-associated proteins involved in the recognition and repair of aberrant DNA structures". Genes Dev. 14 (8): 927–39. PMC 316544. PMID 10783165. doi:10.1101/gad.14.8.927.
Langland G, Kordich J, Creaney J, Goss KH, Lillard-Wetherell K, Bebenek K, Kunkel TA, Groden J (August 2001). "The Bloom's syndrome protein (BLM) interacts with MLH1 but is not required for DNA mismatch repair". J. Biol. Chem. 276 (32): 30031–5. PMID 11325959. doi:10.1074/jbc.M009664200.
Freire R, d'Adda Di Fagagna F, Wu L, Pedrazzi G, Stagljar I, Hickson ID, Jackson SP (August 2001). "Cleavage of the Bloom's syndrome gene product during apoptosis by caspase-3 results in an impaired interaction with topoisomerase IIIalpha". Nucleic Acids Res. 29 (15): 3172–80. PMC 55826. PMID 11470874. doi:10.1093/nar/29.15.3172.
Pedrazzi G, Perrera C, Blaser H, Kuster P, Marra G, Davies SL, Ryu GH, Freire R, Hickson ID, Jiricny J, Stagljar I (November 2001). "Direct association of Bloom's syndrome gene product with the human mismatch repair protein MLH1". Nucleic Acids Res. 29 (21): 4378–86. PMC 60193. PMID 11691925. doi:10.1093/nar/29.21.4378.
Schmutte C, Sadoff MM, Shim KS, Acharya S, Fishel R (August 2001). "The interaction of DNA mismatch repair proteins with human exonuclease I". J. Biol. Chem. 276 (35): 33011–8. PMID 11427529. doi:10.1074/jbc.M102670200.
Bellacosa A, Cicchillitti L, Schepis F, Riccio A, Yeung AT, Matsumoto Y, Golemis EA, Genuardi M, Neri G (March 1999). "MED1, a novel human methyl-CpG-binding endonuclease, interacts with DNA mismatch repair protein MLH1". Proc. Natl. Acad. Sci. U.S.A. 96 (7): 3969–74. PMC 22404. PMID 10097147. doi:10.1073/pnas.96.7.3969.
Santucci-Darmanin S, Walpita D, Lespinasse F, Desnuelle C, Ashley T, Paquis-Flucklinger V (August 2000). "MSH4 acts in conjunction with MLH1 during mammalian meiosis". FASEB J. 14 (11): 1539–47. PMID 10928988. doi:10.1096/fj.14.11.1539.
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". Oncogene 22 (6): 819–25. PMID 12584560. doi:10.1038/sj.onc.1206252.
Kondo E, Horii A, Fukushige S (April 2001). "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. PMC 31313. PMID 11292842. doi:10.1093/nar/29.8.1695.
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. PMID 10037723. doi:10.1074/jbc.274.10.6336.

nih.gov (Global: 4^th place; Galician: 6^th place)

ncbi.nlm.nih.gov

"Entrez Gene: MLH1 mutL homolog 1, colon cancer, nonpolyposis type 2 (E. coli)".
Pal T, Permuth-Wey J, Sellers TA (2008). "A review of the clinical relevance of mismatch-repair deficiency in ovarian cancer". Cancer 113 (4): 733–42. PMC 2644411. PMID 18543306. doi:10.1002/cncr.23601.
Truninger K, Menigatti M, Luz J, Russell A, Haider R, Gebbers JO, Bannwart F, Yurtsever H, Neuweiler J, Riehle HM, Cattaruzza MS, Heinimann K, Schär P, Jiricny J, Marra G (2005). "Immunohistochemical analysis reveals high frequency of PMS2 defects in colorectal cancer". Gastroenterology 128 (5): 1160–71. PMID 15887099. doi:10.1053/j.gastro.2005.01.056.
Goellner EM, Putnam CD, Kolodner RD (2015). "Exonuclease 1-dependent and independent mismatch repair". DNA Repair (Amst.) 32: 24–32. PMID 25956862. doi:10.1016/j.dnarep.2015.04.010.
Li GM (2008). "Mechanisms and functions of DNA mismatch repair". Cell Res. 18 (1): 85–98. PMID 18157157. doi:10.1038/cr.2007.115.
Li GM (2014). "New insights and challenges in mismatch repair: getting over the chromatin hurdle". DNA Repair (Amst.) 19: 48–54. PMC 4127414. PMID 24767944. doi:10.1016/j.dnarep.2014.03.027.
Kupčinskaitė-Noreikienė R, Skiecevičienė J, Jonaitis L, Ugenskienė R, Kupčinskas J, Markelis R, Baltrėnas V, Sakavičius L, Semakina I, Grižas S, Juozaitytė E (2013). "CpG island methylation of the MLH1, MGMT, DAPK, and CASP8 genes in cancerous and adjacent noncancerous stomach tissues". Medicina (Kaunas) 49 (8): 361–6. PMID 24509146.
Waki T, Tamura G, Tsuchiya T, Sato K, Nishizuka S, Motoyama T (2002). "Promoter methylation status of E-cadherin, hMLH1, and p16 genes in nonneoplastic gastric epithelia". Am. J. Pathol. 161 (2): 399–403. PMC 1850716. PMID 12163364. doi:10.1016/S0002-9440(10)64195-8.
Endoh Y, Tamura G, Ajioka Y, Watanabe H, Motoyama T (2000). "Frequent hypermethylation of the hMLH1 gene promoter in differentiated-type tumors of the stomach with the gastric foveolar phenotype". Am. J. Pathol. 157 (3): 717–22. PMC 1949419. PMID 10980110. doi:10.1016/S0002-9440(10)64584-1.
Wani M, Afroze D, Makhdoomi M, Hamid I, Wani B, Bhat G, Wani R, Wani K (2012). "Promoter methylation status of DNA repair gene (hMLH1) in gastric carcinoma patients of the Kashmir valley". Asian Pac. J. Cancer Prev. 13 (8): 4177–81. PMID 23098428. doi:10.7314/apjcp.2012.13.8.4177.
Chang Z, Zhang W, Chang Z, Song M, Qin Y, Chang F, Guo H, Wei Q (2015). "Expression characteristics of FHIT, p53, BRCA2 and MLH1 in families with a history of oesophageal cancer in a region with a high incidence of oesophageal cancer". Oncol Lett 9 (1): 430–436. PMC 4246613. PMID 25436004. doi:10.3892/ol.2014.2682.
Tawfik HM, El-Maqsoud NM, Hak BH, El-Sherbiny YM (2011). "Head and neck squamous cell carcinoma: mismatch repair immunohistochemistry and promoter hypermethylation of hMLH1 gene". Am J Otolaryngol 32 (6): 528–36. PMID 21353335. doi:10.1016/j.amjoto.2010.11.005.
Zuo C, Zhang H, Spencer HJ, Vural E, Suen JY, Schichman SA, Smoller BR, Kokoska MS, Fan CY (2009). "Increased microsatellite instability and epigenetic inactivation of the hMLH1 gene in head and neck squamous cell carcinoma". Otolaryngol Head Neck Surg 141 (4): 484–90. PMID 19786217. doi:10.1016/j.otohns.2009.07.007.
Safar AM, Spencer H, Su X, Coffey M, Cooney CA, Ratnasinghe LD, Hutchins LF, Fan CY (2005). "Methylation profiling of archived non-small cell lung cancer: a promising prognostic system". Clin. Cancer Res. 11 (12): 4400–5. PMID 15958624. doi:10.1158/1078-0432.CCR-04-2378.
Bernstein C, Bernstein H (2015). "Epigenetic reduction of DNA repair in progression to gastrointestinal cancer". World J Gastrointest Oncol 7 (5): 30–46. PMC 4434036. PMID 25987950. doi:10.4251/wjgo.v7.i5.30.
Valeri N, Gasparini P, Fabbri M, Braconi C, Veronese A, Lovat F, Adair B, Vannini I, Fanini F, Bottoni A, Costinean S, Sandhu SK, Nuovo GJ, Alder H, Gafa R, Calore F, Ferracin M, Lanza G, Volinia S, Negrini M, McIlhatton MA, Amadori D, Fishel R, Croce CM (2010). "Modulation of mismatch repair and genomic stability by miR-155". Proc. Natl. Acad. Sci. U.S.A. 107 (15): 6982–7. PMC 2872463. PMID 20351277. doi:10.1073/pnas.1002472107.
Rubin H (March 2011). "Fields and field cancerization: the preneoplastic origins of cancer: asymptomatic hyperplastic fields are precursors of neoplasia, and their progression to tumors can be tracked by saturation density in culture". BioEssays 33 (3): 224–31. PMID 21254148. doi:10.1002/bies.201000067.
Tsao JL, Yatabe Y, Salovaara R, Järvinen HJ, Mecklin JP, Aaltonen LA, Tavaré S, Shibata D (February 2000). "Genetic reconstruction of individual colorectal tumor histories". Proc. Natl. Acad. Sci. U.S.A. 97 (3): 1236–41. PMC 15581. PMID 10655514. doi:10.1073/pnas.97.3.1236.
Vogelstein B, Papadopoulos N, Velculescu VE, Zhou S, Diaz LA, Kinzler KW (March 2013). "Cancer genome landscapes". Science 339 (6127): 1546–58. PMC 3749880. PMID 23539594. doi:10.1126/science.1235122.
Jiang Z, Hu J, Li X, Jiang Y, Zhou W, Lu D (2006). "Expression analyses of 27 DNA repair genes in astrocytoma by TaqMan low-density array". Neurosci. Lett. 409 (2): 112–7. PMID 17034947. doi:10.1016/j.neulet.2006.09.038.
Kitajima Y, Miyazaki K, Matsukura S, Tanaka M, Sekiguchi M (2003). "Loss of expression of DNA repair enzymes MGMT, hMLH1, and hMSH2 during tumor progression in gastric cancer". Gastric Cancer 6 (2): 86–95. PMID 12861399. doi:10.1007/s10120-003-0213-z.
Baker SM, Plug AW, Prolla TA, Bronner CE, Harris AC, Yao X, Christie DM, Monell C, Arnheim N, Bradley A, Ashley T, Liskay RM (1996). "Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over". Nat. Genet. 13 (3): 336–42. PMID 8673133. doi:10.1038/ng0796-336.
Kan R, Sun X, Kolas NK, Avdievich E, Kneitz B, Edelmann W, Cohen PE (2008). "Comparative analysis of meiotic progression in female mice bearing mutations in genes of the DNA mismatch repair pathway". Biol. Reprod. 78 (3): 462–71. PMID 18057311. doi:10.1095/biolreprod.107.065771.
Wei K, Kucherlapati R, Edelmann W (2002). "Mouse models for human DNA mismatch-repair gene defects". Trends Mol Med 8 (7): 346–53. PMID 12114115. doi:10.1016/s1471-4914(02)02359-6.
Ji G, Long Y, Zhou Y, Huang C, Gu A, Wang X (2012). "Common variants in mismatch repair genes associated with increased risk of sperm DNA damage and male infertility". BMC Med 10: 49. PMC 3378460. PMID 22594646. doi:10.1186/1741-7015-10-49.
Ranjha L, Anand R, Cejka P (2014). "The Saccharomyces cerevisiae Mlh1-Mlh3 heterodimer is an endonuclease that preferentially binds to Holliday junctions". J. Biol. Chem. 289 (9): 5674–86. PMC 3937642. PMID 24443562. doi:10.1074/jbc.M113.533810.
Rogacheva MV, Manhart CM, Chen C, Guarne A, Surtees J, Alani E (2014). "Mlh1-Mlh3, a meiotic crossover and DNA mismatch repair factor, is a Msh2-Msh3-stimulated endonuclease". J. Biol. Chem. 289 (9): 5664–73. PMC 3937641. PMID 24403070. doi:10.1074/jbc.M113.534644.
Zakharyevich K, Tang S, Ma Y, Hunter N (2012). "Delineation of joint molecule resolution pathways in meiosis identifies a crossover-specific resolvase". Cell 149 (2): 334–47. PMC 3377385. PMID 22500800. doi:10.1016/j.cell.2012.03.023.
Lebrun C, Olschwang S, Jeannin S, Vandenbos F, Sobol H, Frenay M (2007). "Turcot syndrome confirmed with molecular analysis". Eur. J. Neurol. 14 (4): 470–2. PMID 17389002. doi:10.1111/j.1468-1331.2006.01669.x.
Wang Y, Cortez D, Yazdi P, Neff N, Elledge SJ, Qin J (April 2000). "BASC, a super complex of BRCA1-associated proteins involved in the recognition and repair of aberrant DNA structures". Genes Dev. 14 (8): 927–39. PMC 316544. PMID 10783165. doi:10.1101/gad.14.8.927.
Langland G, Kordich J, Creaney J, Goss KH, Lillard-Wetherell K, Bebenek K, Kunkel TA, Groden J (August 2001). "The Bloom's syndrome protein (BLM) interacts with MLH1 but is not required for DNA mismatch repair". J. Biol. Chem. 276 (32): 30031–5. PMID 11325959. doi:10.1074/jbc.M009664200.
Freire R, d'Adda Di Fagagna F, Wu L, Pedrazzi G, Stagljar I, Hickson ID, Jackson SP (August 2001). "Cleavage of the Bloom's syndrome gene product during apoptosis by caspase-3 results in an impaired interaction with topoisomerase IIIalpha". Nucleic Acids Res. 29 (15): 3172–80. PMC 55826. PMID 11470874. doi:10.1093/nar/29.15.3172.
Pedrazzi G, Perrera C, Blaser H, Kuster P, Marra G, Davies SL, Ryu GH, Freire R, Hickson ID, Jiricny J, Stagljar I (November 2001). "Direct association of Bloom's syndrome gene product with the human mismatch repair protein MLH1". Nucleic Acids Res. 29 (21): 4378–86. PMC 60193. PMID 11691925. doi:10.1093/nar/29.21.4378.
Schmutte C, Sadoff MM, Shim KS, Acharya S, Fishel R (August 2001). "The interaction of DNA mismatch repair proteins with human exonuclease I". J. Biol. Chem. 276 (35): 33011–8. PMID 11427529. doi:10.1074/jbc.M102670200.
Bellacosa A, Cicchillitti L, Schepis F, Riccio A, Yeung AT, Matsumoto Y, Golemis EA, Genuardi M, Neri G (March 1999). "MED1, a novel human methyl-CpG-binding endonuclease, interacts with DNA mismatch repair protein MLH1". Proc. Natl. Acad. Sci. U.S.A. 96 (7): 3969–74. PMC 22404. PMID 10097147. doi:10.1073/pnas.96.7.3969.
Santucci-Darmanin S, Walpita D, Lespinasse F, Desnuelle C, Ashley T, Paquis-Flucklinger V (August 2000). "MSH4 acts in conjunction with MLH1 during mammalian meiosis". FASEB J. 14 (11): 1539–47. PMID 10928988. doi:10.1096/fj.14.11.1539.
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". Oncogene 22 (6): 819–25. PMID 12584560. doi:10.1038/sj.onc.1206252.
Kondo E, Horii A, Fukushige S (April 2001). "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. PMC 31313. PMID 11292842. doi:10.1093/nar/29.8.1695.
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. PMID 10037723. doi:10.1074/jbc.274.10.6336.

MLH1 (Galician Wikipedia)

archive.org (Global: 6th place; Galician: 8th place)

doi.org (Global: 2nd place; Galician: 7th place)

dx.doi.org

nih.gov (Global: 4th place; Galician: 6th place)

ncbi.nlm.nih.gov

archive.org (Global: 6^th place; Galician: 8^th place)

doi.org (Global: 2^nd place; Galician: 7^th place)

nih.gov (Global: 4^th place; Galician: 6^th place)