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Items: 10

1.
Association between DNA mismatch repair gene polymorphisms and platinum-based chemotherapy toxicity in non-small cell lung cancer patients
Jun-Yan Liu, Chen-Yue Qian, Yuan-Feng Gao, Juan Chen, Hong-Hao Zhou, Ji-Ye Yin
Chin J Cancer. 2017; 36: 12. Published online 2017 Jan 16. doi: 10.1186/s40880-016-0175-2
PMCID:
PMC5238520
AbstractArticlePDF–1.0M
2.
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium
Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas
Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042
PMCID:
PMC3178059
AbstractArticlePDF–1.0M
3.
Differing patterns of genetic instability in mice deficient in the mismatch repair genes Pms2, Mlh1, Msh2, Msh3 and Msh6
Denise Campisi Hegan, Latha Narayanan, Frank R. Jirik, Winfried Edelmann, R. Michael Liskay, Peter M. Glazer
Carcinogenesis. Author manuscript; available in PMC 2008 Dec 31.
Published in final edited form as: Carcinogenesis. 2006 Dec; 27(12): 2402–2408. Published online 2006 May 25. doi: 10.1093/carcin/bgl079
PMCID:
PMC2612936
AbstractArticlePDF–656K
4.
Examination of Msh6- and Msh3-deficient Mice in Class Switching Reveals Overlapping and Distinct Roles of MutS Homologues in Antibody Diversification
Ziqiang Li, Stefan J. Scherer, Diana Ronai, Maria D. Iglesias-Ussel, Jonathan U. Peled, Philip D. Bardwell, Min Zhuang, KyeRyoung Lee, Alberto Martin, Winfried Edelmann, Matthew D. Scharff
J Exp Med. 2004 Jul 5; 200(1): 47–59. doi: 10.1084/jem.20040355
PMCID:
PMC2213317
AbstractArticlePDF–269K
5.
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
Margrit Wiesendanger, Burkhard Kneitz, Winfried Edelmann, Matthew D. Scharff
J Exp Med. 2000 Feb 7; 191(3): 579–584. doi: 10.1084/jem.191.3.579
PMCID:
PMC2195810
AbstractArticlePDF–66K
6.
Localization of MMR proteins on meiotic chromosomes in mice indicates distinct functions during prophase I
Nadine K. Kolas, Anton Svetlanov, Michelle L. Lenzi, Frank P. Macaluso, Steven M. Lipkin, R. Michael Liskay, John Greally, Winfried Edelmann, Paula E. Cohen
J Cell Biol. 2005 Nov 7; 171(3): 447–458. doi: 10.1083/jcb.200506170
PMCID:
PMC2171243
AbstractArticlePDF–4.2M
7.
Physical and functional interactions between Werner syndrome helicase and mismatch-repair initiation factors
Nurten Saydam, Radhakrishnan Kanagaraj, Tobias Dietschy, Patrick L. Garcia, Javier Peña-Diaz, Igor Shevelev, Igor Stagljar, Pavel Janscak
Nucleic Acids Res. 2007 Sep; 35(17): 5706–5716. Published online 2007 Aug 22. doi: 10.1093/nar/gkm500
PMCID:
PMC2034464
AbstractArticlePDF–2.3M
8.
Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences
Mammalian Gene Collection (MGC) Program Team
Proc Natl Acad Sci U S A. 2002 Dec 24; 99(26): 16899–16903. Published online 2002 Dec 11. doi: 10.1073/pnas.242603899
PMCID:
PMC139241
AbstractArticlePDF–118K
9.
hMutSα forms an ATP-dependent complex with hMutLα and hMutLβ on DNA
Guido Plotz, Jochen Raedle, Angela Brieger, Jörg Trojan, Stefan Zeuzem
Nucleic Acids Res. 2002 Feb 1; 30(3): 711–718. doi: 10.1093/nar/30.3.711
PMCID:
PMC100294
AbstractArticlePDF–384K
10.
hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6
Samir Acharya, Teresa Wilson, Scott Gradia, Michael F. Kane, Shawn Guerrette, Gerald T. Marsischky, Richard Kolodner, Richard Fishel
Proc Natl Acad Sci U S A. 1996 Nov 26; 93(24): 13629–13634. doi: 10.1073/pnas.93.24.13629
PMCID:
PMC19374
AbstractArticlePDF–357K

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