MSH6 (Catalan Wikipedia)

Analysis of information sources in references of the Wikipedia article "MSH6" in Catalan language version.

refsWebsite

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9doi.org

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5elsevier.com

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4nih.gov

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4worldcat.org

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1ensembl.org

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1rupress.org

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1cshlp.org

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1uniprot.org

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1jamanetwork.com

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1lww.com

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cshlp.org

genesdev.cshlp.org

Marsischky, G T; Filosi, N; Kane, M F; Kolodner, R «Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair.» (en anglès). Genes & Development, 10, 4, 15-02-1996, pàg. 407–420. DOI: 10.1101/gad.10.4.407. ISSN: 0890-9369.

doi.org

dx.doi.org

Edelmann, Winfried; Yang, Kan; Umar, Asad; Heyer, Joerg; Lau, Kirkland «Mutation in the Mismatch Repair Gene Msh6 Causes Cancer Susceptibility» (en anglès). Cell, 91, 4, 1997-11, pàg. 467–477. DOI: 10.1016/S0092-8674(00)80433-X.
DuPrie, Matthew L.; Palacio, Tatiana; Calil, Felipe A.; Kolodner, Richard D.; Putnam, Christopher D. «Mlh1 interacts with both Msh2 and Msh6 for recruitment during mismatch repair» (en anglès). DNA Repair, 119, 2022-11, pàg. 103405. DOI: 10.1016/j.dnarep.2022.103405.
Edelbrock, Michael A.; Kaliyaperumal, Saravanan; Williams, Kandace J. «Structural, molecular and cellular functions of MSH2 and MSH6 during DNA mismatch repair, damage signaling and other noncanonical activities» (en anglès). Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 743-744, 2013-03, pàg. 53–66. DOI: 10.1016/j.mrfmmm.2012.12.008. PMC: PMC3659183. PMID: 23391514.
Wiesendanger, Margrit; Kneitz, Burkhard; Edelmann, Winfried; Scharff, Matthew D. «Somatic Hypermutation in Muts Homologue (Msh)3-, Msh6-, and Msh3/Msh6-Deficient Mice Reveals a Role for the Msh2–Msh6 Heterodimer in Modulating the Base Substitution Pattern» (en anglès). Journal of Experimental Medicine, 191, 3, 07-02-2000, pàg. 579–584. DOI: 10.1084/jem.191.3.579. ISSN: 0022-1007. PMC: PMC2195810. PMID: 10662804.
Tajima, Akihiro; Hess, Martin T.; Cabrera, Betty L.; Kolodner, Richard D.; Carethers, John M. «The mismatch repair complex hMutSα recognizes 5-fluorouracil-modified DNA: Implications for chemosensitivity and resistance» (en anglès). Gastroenterology, 127, 6, 2004-12, pàg. 1678–1684. DOI: 10.1053/j.gastro.2004.10.001.
Marsischky, G T; Filosi, N; Kane, M F; Kolodner, R «Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair.» (en anglès). Genes & Development, 10, 4, 15-02-1996, pàg. 407–420. DOI: 10.1101/gad.10.4.407. ISSN: 0890-9369.
Rey, Jean-Marc; Noruzinia, Mehrdad; Brouillet, Jean-Paul; Sarda, Pierre; Maudelonde, Thierry «Six novel heterozygous MLH1, MSH2, and MSH6 and one homozygous MLH1 germline mutations in hereditary nonpolyposis colorectal cancer» (en anglès). Cancer Genetics and Cytogenetics, 155, 2, 2004-12, pàg. 149–151. DOI: 10.1016/j.cancergencyto.2004.03.012.
Bonadona, Valérie «Cancer Risks Associated With Germline Mutations in MLH1, MSH2, and MSH6 Genes in Lynch Syndrome» (en anglès). JAMA, 305, 22, 08-06-2011, pàg. 2304. DOI: 10.1001/jama.2011.743. ISSN: 0098-7484.
Mahalingam, Meera «MSH6, Past and Present and Muir–Torre Syndrome—Connecting the Dots» (en anglès). The American Journal of Dermatopathology, 39, 4, 2017-04, pàg. 239–249. DOI: 10.1097/DAD.0000000000000633. ISSN: 0193-1091.

elsevier.com

linkinghub.elsevier.com

Edelmann, Winfried; Yang, Kan; Umar, Asad; Heyer, Joerg; Lau, Kirkland «Mutation in the Mismatch Repair Gene Msh6 Causes Cancer Susceptibility» (en anglès). Cell, 91, 4, 1997-11, pàg. 467–477. DOI: 10.1016/S0092-8674(00)80433-X.
DuPrie, Matthew L.; Palacio, Tatiana; Calil, Felipe A.; Kolodner, Richard D.; Putnam, Christopher D. «Mlh1 interacts with both Msh2 and Msh6 for recruitment during mismatch repair» (en anglès). DNA Repair, 119, 2022-11, pàg. 103405. DOI: 10.1016/j.dnarep.2022.103405.
Edelbrock, Michael A.; Kaliyaperumal, Saravanan; Williams, Kandace J. «Structural, molecular and cellular functions of MSH2 and MSH6 during DNA mismatch repair, damage signaling and other noncanonical activities» (en anglès). Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 743-744, 2013-03, pàg. 53–66. DOI: 10.1016/j.mrfmmm.2012.12.008. PMC: PMC3659183. PMID: 23391514.
Tajima, Akihiro; Hess, Martin T.; Cabrera, Betty L.; Kolodner, Richard D.; Carethers, John M. «The mismatch repair complex hMutSα recognizes 5-fluorouracil-modified DNA: Implications for chemosensitivity and resistance» (en anglès). Gastroenterology, 127, 6, 2004-12, pàg. 1678–1684. DOI: 10.1053/j.gastro.2004.10.001.
Rey, Jean-Marc; Noruzinia, Mehrdad; Brouillet, Jean-Paul; Sarda, Pierre; Maudelonde, Thierry «Six novel heterozygous MLH1, MSH2, and MSH6 and one homozygous MLH1 germline mutations in hereditary nonpolyposis colorectal cancer» (en anglès). Cancer Genetics and Cytogenetics, 155, 2, 2004-12, pàg. 149–151. DOI: 10.1016/j.cancergencyto.2004.03.012.

ensembl.org

May2017.archive.ensembl.org

GRCm38: Ensembl release 89: ENSMUSG00000005370 - Ensembl, May 2017

jamanetwork.com

jama.jamanetwork.com

Bonadona, Valérie «Cancer Risks Associated With Germline Mutations in MLH1, MSH2, and MSH6 Genes in Lynch Syndrome» (en anglès). JAMA, 305, 22, 08-06-2011, pàg. 2304. DOI: 10.1001/jama.2011.743. ISSN: 0098-7484.

lww.com

journals.lww.com

Mahalingam, Meera «MSH6, Past and Present and Muir–Torre Syndrome—Connecting the Dots» (en anglès). The American Journal of Dermatopathology, 39, 4, 2017-04, pàg. 239–249. DOI: 10.1097/DAD.0000000000000633. ISSN: 0193-1091.

nih.gov

ncbi.nlm.nih.gov

«Human PubMed Reference:». National Center for Biotechnology Information, U.S. National Library of Medicine.
«Mouse PubMed Reference:». National Center for Biotechnology Information, U.S. National Library of Medicine.
Edelbrock, Michael A.; Kaliyaperumal, Saravanan; Williams, Kandace J. «Structural, molecular and cellular functions of MSH2 and MSH6 during DNA mismatch repair, damage signaling and other noncanonical activities» (en anglès). Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 743-744, 2013-03, pàg. 53–66. DOI: 10.1016/j.mrfmmm.2012.12.008. PMC: PMC3659183. PMID: 23391514.
Wiesendanger, Margrit; Kneitz, Burkhard; Edelmann, Winfried; Scharff, Matthew D. «Somatic Hypermutation in Muts Homologue (Msh)3-, Msh6-, and Msh3/Msh6-Deficient Mice Reveals a Role for the Msh2–Msh6 Heterodimer in Modulating the Base Substitution Pattern» (en anglès). Journal of Experimental Medicine, 191, 3, 07-02-2000, pàg. 579–584. DOI: 10.1084/jem.191.3.579. ISSN: 0022-1007. PMC: PMC2195810. PMID: 10662804.

rupress.org

Wiesendanger, Margrit; Kneitz, Burkhard; Edelmann, Winfried; Scharff, Matthew D. «Somatic Hypermutation in Muts Homologue (Msh)3-, Msh6-, and Msh3/Msh6-Deficient Mice Reveals a Role for the Msh2–Msh6 Heterodimer in Modulating the Base Substitution Pattern» (en anglès). Journal of Experimental Medicine, 191, 3, 07-02-2000, pàg. 579–584. DOI: 10.1084/jem.191.3.579. ISSN: 0022-1007. PMC: PMC2195810. PMID: 10662804.

uniprot.org

«UniProt». [Consulta: 15 octubre 2022].

worldcat.org

Wiesendanger, Margrit; Kneitz, Burkhard; Edelmann, Winfried; Scharff, Matthew D. «Somatic Hypermutation in Muts Homologue (Msh)3-, Msh6-, and Msh3/Msh6-Deficient Mice Reveals a Role for the Msh2–Msh6 Heterodimer in Modulating the Base Substitution Pattern» (en anglès). Journal of Experimental Medicine, 191, 3, 07-02-2000, pàg. 579–584. DOI: 10.1084/jem.191.3.579. ISSN: 0022-1007. PMC: PMC2195810. PMID: 10662804.
Marsischky, G T; Filosi, N; Kane, M F; Kolodner, R «Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair.» (en anglès). Genes & Development, 10, 4, 15-02-1996, pàg. 407–420. DOI: 10.1101/gad.10.4.407. ISSN: 0890-9369.
Bonadona, Valérie «Cancer Risks Associated With Germline Mutations in MLH1, MSH2, and MSH6 Genes in Lynch Syndrome» (en anglès). JAMA, 305, 22, 08-06-2011, pàg. 2304. DOI: 10.1001/jama.2011.743. ISSN: 0098-7484.
Mahalingam, Meera «MSH6, Past and Present and Muir–Torre Syndrome—Connecting the Dots» (en anglès). The American Journal of Dermatopathology, 39, 4, 2017-04, pàg. 239–249. DOI: 10.1097/DAD.0000000000000633. ISSN: 0193-1091.