Works matching DE "PMS genes"

Results: 60

Mainstreaming genetics: the potential for miscommunication.

Published in:

2011

By:

McBride, Donna;
Lucassen, Anneke

Publication type:

Case Study

Fumarate in DNA repair.

Published in:

Nature Cell Biology, 2015, v. 17, n. 9, p. 1096, doi. 10.1038/ncb3232

By:

Lees-Miller, Susan P.

Publication type:

Article

Polymorphism discovery in 62 DNA repair genes and haplotype associations with risks for lung and head and neck cancers.

Published in:

Carcinogenesis, 2007, v. 28, n. 8, p. 1731, doi. 10.1093/carcin/bgm111

By:

Michiels, Stefan;
Danoy, Patrick;
Dessen, Philippe;
Bera, Alex;
Boulet, Thomas;
Bouchardy, Christine;
Lathrop, Mark;
Sarasin, Alain;
Benhamou, Simone

Publication type:

Article

Assessing Impairment of Executive Function and Psychomotor Speed in Premanifest and Manifest Huntington’s Disease Gene-expansion Carriers.

Published in:

Journal of the International Neuropsychological Society, 2015, v. 21, n. 3, p. 193, doi. 10.1017/S1355617715000090

By:

Unmack Larsen, Ida;
Vinther-Jensen, Tua;
Gade, Anders;
Nielsen, Jørgen Erik;
Vogel, Asmus

Publication type:

Article

EXAMINATION OF CHROMOSOME 7p22 CANDIDATE GENES RBaK, PMS2 AND GNA12 IN FAMILIAL HYPERALDOSTERONISM TYPE II.

Published in:

Clinical & Experimental Pharmacology & Physiology, 2008, v. 35, n. 4, p. 380, doi. 10.1111/j.1440-1681.2008.04882.x

By:

Jeske, YWA;
So, A;
Kelemen, L;
Sukor, N;
Willys, C;
Bulmer, B;
Gordon, RD;
Duffy, D;
Stowasser, M

Publication type:

Article

Loss of heterozygosity and point mutation at Aprt locus in T cells and fibroblasts of Pms2[sup-/-] mice.

Published in:

Oncogene, 2002, v. 21, n. 18, p. 2840, doi. 10.1038/sj.onc.1205358

By:

Changshun Shao;
Moying Yin;
Li Deng;
Stambrook, Peter J.;
Doetschman, Thomas;
Tischfield, Jay A.

Publication type:

Article

Elevated mutant frequencies and increased C : G→T : A transitions in Mlh1<sup>-/-</sup> versus Pms2<sup>-/-</sup> murine small intestinal epithelial cells.

Published in:

Oncogene, 2001, v. 20, n. 5, p. 619, doi. 10.1038/sj.onc.1204138

By:

Baross-Francis, Agnes;
Makhani, Naila;
Liskay, R Michael;
Jirik, Frank R

Publication type:

Article

Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene.

Published in:

Oncogene, 2000, v. 19, n. 13, p. 1719, doi. 10.1038/sj.onc.1203447

By:

De Rosa, Marina;
Fasano, Carlo;
Panariello, Luigi;
Scarano, Maria;
Belli, Giulio;
Iannelli, Antonio;
Ciciliano, Fabio;
Izzo, Paola

Publication type:

Article

Mouse models for colorectal cancer.

Published in:

Oncogene, 1999, v. 18, n. 38, p. 5325, doi. 10.1038/sj.onc.1203036

By:

Heyer, Joerg;
Yang, Kan;
Lipkin, Martin;
Edelmann, Winfried;
Kucherlapati, Raju

Publication type:

Article

Mice defective in the DNA mismatch gene PMS2 are hypersensitive to MNU induced thymic lymphoma and are partially protected by transgenic expression of human MGMT.

Published in:

Oncogene, 1999, v. 18, n. 30, p. 4394, doi. 10.1038/sj.onc.1202798

By:

Qin, Xiusheng;
Liu, Lili;
Gerson, Stanton L

Publication type:

Article

DNA Repair.

Published in:

Angewandte Chemie International Edition, 2015, v. 54, n. 51, p. 15330, doi. 10.1002/anie.201509770

By:

Carell, Thomas

Publication type:

Article

Genome-wide associated loci influencing interleukin (IL)-10, IL-1Ra, and IL-6 levels in African Americans.

Published in:

Immunogenetics, 2012, v. 64, n. 5, p. 351, doi. 10.1007/s00251-011-0596-7

By:

Tekola Ayele, Fasil;
Doumatey, Ayo;
Huang, Hanxia;
Zhou, Jie;
Charles, Bashira;
Erdos, Michael;
Adeleye, Jokotade;
Balogun, Williams;
Fasanmade, Olufemi;
Johnson, Thomas;
Oli, Johnnie;
Okafor, Godfrey;
Amoah, Albert;
Eghan, Benjamin;
Agyenim-Boateng, Kofi;
Acheampong, Joseph;
Adebamowo, Clement;
Herbert, Alan;
Gerry, Norman;
Christman, Michael

Publication type:

Article

Prediction of Lynch Syndrome in Consecutive Patients With Colorectal Cancer.

Published in:

JNCI: Journal of the National Cancer Institute, 2009, v. 101, n. 5, p. 331, doi. 10.1093/jnci/djn499

By:

Green, Roger C.;
Parfrey, Patrick S.;
Woods, Michael O.;
Younghusband, H. Banfield

Publication type:

Article

The Frequency of Muir-Torre Syndrome Among Lynch Syndrome Families.

Published in:

JNCI: Journal of the National Cancer Institute, 2008, v. 100, n. 4, p. 277, doi. 10.1093/jnci/djm291

By:

South, Christopher D.;
Hampel, Heather;
Comeras, Ilene;
Westman, Judith A.;
Frankel, Wendy L.;
de la Chapelle, Albert

Publication type:

Article

PMS2 Mutations in Childhood Cancer.

Published in:

JNCI: Journal of the National Cancer Institute, 2006, v. 98, n. 5, p. 358, doi. 10.1093/jnci/djj073

By:

De Vos, Michel;
Hayward, Bruce E.;
Chariton, Ruth;
Taylor, Graham R.;
Glaser, Adam W.;
Picton, Susan;
Cole, Trevor R.;
Maher, Eamonn R.;
McKeown, Carole M. E.;
Mann, Jill R.;
Yates, John R.;
Baralle, Diana;
Rankin, Julia;
Bonthron, David T.;
Sheridan, Eamonn

Publication type:

Article

Prognostic impact of molecular subgroups in grade 3 endometrioid endometrial carcinoma: a single cohort study in Northern China.

Published in:

European Journal of Gynaecological Oncology, 2025, v. 46, n. 1, p. 104, doi. 10.22514/ejgo.2025.010

By:

Wenxue Zhi;
Jing Zhang;
Yang Zhan;
Yulan Jin;
Honggang Liu

Publication type:

Article

Alleles of the Yeast PMS1 Mismatch-Repair Gene That Differentially Affect Recombinations and Replication-Related Processes.

Published in:

Genetics, 2002, v. 162, n. 3, p. 1131, doi. 10.1093/genetics/162.3.1131

By:

Welz-Voegele, Caroline;
Stone, Jana E.;
Tran, Phuoc T.;
Kearney, Hutton M.;
Liskay, R. Michael;
Petes, Thomas D.;
Jinks-Robertson, Sue

Publication type:

Article

Mismatch repair in Schizosaccharomyces pombe requires the mutL homologous gene pms1: Molecular...

Published in:

Genetics, 1997, v. 146, n. 4, p. 1275, doi. 10.1093/genetics/146.4.1275

By:

Schar, Primo;
Baur, Michel

Publication type:

Article

Mismatch correction acts a barrier to homeologous recombination in Saccharomyces cerevisiae.

Published in:

Genetics, 1995, v. 133, n. 3, p. 1175, doi. 10.1093/genetics/139.3.1175

By:

Selva, Erica M.;
New, Liguo

Publication type:

Article

White spot syndrome virus epizootic in cultured Pacific white shrimp Litopenaeus vannamei (Boone) in Taiwan.

Published in:

Journal of Fish Diseases, 2013, v. 36, n. 12, p. 977, doi. 10.1111/jfd.12027

By:

Cheng, L;
Lin, W‐H;
Wang, P‐C;
Tsai, M‐A;
Hsu, J‐P;
Chen, S‐C

Publication type:

Article

Molecular characteristics of mismatch repair genes in sporadic colorectal tumors in Czech patients.

Published in:

BMC Medical Genetics, 2014, v. 15, n. 1, p. 2, doi. 10.1186/1471-2350-15-17

By:

Veronika, Vymetalkova Polakova;
Jana, Slyskova;
Vlasta, Korenkova;
Ludovit, Bielik;
Lucie, Langerova;
Pavel, Prochazka;
Alexandra, Rejhova;
Lucie, Schwarzova;
Barbara, Pardini;
Alessio, Naccarati;
Pavel, Vodicka

Publication type:

Article

Novel pedigree analysis implicates DNA repair and chromatin remodeling in multiple myeloma risk.

Published in:

PLoS Genetics, 2018, v. 14, n. 2, p. 1, doi. 10.1371/journal.pgen.1007111

By:

Waller, Rosalie G.;
Darlington, Todd M.;
Wei, Xiaomu;
Madsen, Michael J.;
Thomas, Alun;
Curtin, Karen;
Coon, Hilary;
Rajamanickam, Venkatesh;
Musinsky, Justin;
Jayabalan, David;
Atanackovic, Djordje;
Rajkumar, S. Vincent;
Kumar, Shaji;
Slager, Susan;
Middha, Mridu;
Galia, Perrine;
Demangel, Delphine;
Salama, Mohamed;
Joseph, Vijai;
McKay, James

Publication type:

Article

Stabilization of mismatch repair gene PMS2 byglycogen synthase kinase 3β is implicated in thetreatment of cervical carcinoma.

Published in:

BMC Cancer, 2010, v. 10, p. 58, doi. 10.1186/1471-2407-10-58

By:

Yuan Zhang;
Yi Min Shu;
Shu Fang Wang;
Bang Hong Da;
Ze Hua Wang;
Hua Bin Li

Publication type:

Article

Isolation of chromosomal regions controlling intersex development in a marsupial.

Published in:

Cytogenetic & Genome Research, 2003, v. 101, n. 3/4, p. 224, doi. 10.1159/000074341

By:

Santucciu, C.;
Grützner, F.;
Carvalho-Silva, D. R.;
Graves, J. A. M.

Publication type:

Article

Human PMS2 gene family: Origin, molecular evolution, and biological implications.

Published in:

Doklady Biochemistry & Biophysics, 2006, v. 408, n. 1, p. 175, doi. 10.1134/S1607672906030185

By:

Shpakovskii, D.;
Shematorova, E.;
Shpakovskii, G.

Publication type:

Article

The relationship between serum vascular endothelial growth factor A and microsatellite instability in colorectal cancer.

Published in:

Colorectal Disease, 2011, v. 13, n. 9, p. 984, doi. 10.1111/j.1463-1318.2010.02357.x

By:

Hansen, T. F.;
Jensen, L. H.;
Spindler, K.-L. G.;
Lindebjerg, J.;
Brandslund, I.;
Jakobsen, A.

Publication type:

Article

PMS2 gene mutation results in DNA mismatch repair system failure in a case of adult granulosa cell tumor.

Published in:

Journal of Ovarian Research, 2017, v. 10, p. 1, doi. 10.1186/s13048-017-0317-4

By:

Wen-Chung Wang;
Ya-Ting Lee;
Yen-Chein Lai

Publication type:

Article

Specificity of signaling by STAT1 depends on SH2 and C-terminal domains that regulate Ser727 phosphorylation, differentially affecting specific target gene expression.

Published in:

EMBO Journal, 2001, v. 20, n. 1/2, p. 91, doi. 10.1093/emboj/20.1.91

By:

Kovarik, Pavel;
Mangold, Monika;
Ramsauer, Katrin;
Heidari, Hamid;
Steinborn, Ralf;
Zotter, Angelika;
Levy, David E.;
Müller, Mathias;
Decker, Thomas

Publication type:

Article

Type A microsatellite instability in pediatric gliomas as an indicator of Turcot syndrome.

Published in:

European Journal of Human Genetics, 2009, v. 17, n. 7, p. 919, doi. 10.1038/ejhg.2008.271

By:

Giunti, Laura;
Cetica, Valentina;
Ricci, Ugo;
Giglio, Sabrina;
Sardi, Iacopo;
Paglierani, Milena;
Andreucci, Elena;
Sanzo, Massimiliano;
Forni, Marco;
Buccoliero, Anna Maria;
Genitori, Lorenzo;
Genuardi, Maurizio

Publication type:

Article

Homozygous PMS2 germline mutations in two families with early-onset haematological malignancy, brain tumours, HNPCC-associated tumours, and signs of neurofibromatosis type 1.

Published in:

European Journal of Human Genetics, 2008, v. 16, n. 1, p. 62, doi. 10.1038/sj.ejhg.5201923

By:

Krüger, Stefan;
Kinzel, Miriam;
Walldorf, Constanze;
Gottschling, Sven;
Bier, Andrea;
Tinschert, Sigrid;
von Stackelberg, Arend;
Henn, Wolfram;
Görgens, Heike;
Boue, Stephanie;
Kölble, Konrad;
Büttner, Reinhard;
Schackert, Hans K.

Publication type:

Article

Compound heterozygosity for two MSH6 mutations in a patient with early onset of HNPCC-associated cancers, but without hematological malignancy and brain tumor.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 5, p. 561, doi. 10.1038/sj.ejhg.5201568

By:

Plaschke, Jens;
Linnebacher, Michael;
Kloor, Matthias;
Gebert, Johannes;
Cremer, Friedrich W;
Tinschert, Sigrid;
Aust, Daniela E;
von Knebel Doeberitz, Magnus;
Schackert, Hans K

Publication type:

Article

Inheritance of Partial Male-Sterility in Guar.

Published in:

Plant Breeding, 1989, v. 103, n. 1, p. 43, doi. 10.1111/j.1439-0523.1989.tb00349.x

By:

Stafford, R. E.

Publication type:

Article

Nine novel pathogenic germline mutations in MLH1, MSH2, MSH6 and PMS2 in families with Lynch syndrome.

Published in:

Acta Oncologica, 2007, v. 46, n. 6, p. 763, doi. 10.1080/02841860701230217

By:

Rahner, Nils;
Friedrichs, Nicolaus;
Wehner, Maria;
Steinke, Verena;
Aretz, Stefan;
Friedl, Waltraut;
Buettner, Reinhard;
Mangold, Elisabeth;
Propping, Peter;
Walldorf, Constanze

Publication type:

Article

Establishing cancer risks associated with PMS2 germline mutations in Lynch syndrome.

Published in:

Clinical Genetics, 2015, v. 87, n. 6, p. 533, doi. 10.1111/cge.12583

By:

Caron, N. S.

Publication type:

Article

High incidence of large deletions in the PMS2 gene in Spanish Lynch syndrome families.

Published in:

Clinical Genetics, 2014, v. 85, n. 6, p. 583, doi. 10.1111/cge.12232

By:

Brea‐Fernández, A.J.;
Cameselle‐Teijeiro, J.M.;
Alenda, C.;
Fernández‐Rozadilla, C.;
Cubiella, J.;
Clofent, J.;
Reñé, J.M.;
Anido, U.;
Milá, M.;
Balaguer, F.;
Castells, A.;
Castellvi‐Bel, S.;
Jover, R.;
Carracedo, A.;
Ruiz‐Ponte, C.

Publication type:

Article

Epigenetic mechanisms in the pathogenesis of Lynch syndrome.

Published in:

Clinical Genetics, 2014, v. 85, n. 5, p. 403, doi. 10.1111/cge.12349

By:

Peltomäki, P.

Publication type:

Article

Recurrent and founder mutations in the PMS2 gene.

Published in:

Clinical Genetics, 2013, v. 83, n. 3, p. 238, doi. 10.1111/j.1399-0004.2012.01898.x

By:

Tomsic, J;
Senter, L;
Liyanarachchi, S;
Clendenning, M;
Vaughn, C P;
Jenkins, M A;
Hopper, J L;
Young, J;
Samowitz, W;
Chapelle, A

Publication type:

Article

Genome-Wide Association Study Identifies Variants in PMS1 Associated with Serum Ferritin in a Chinese Population.

Published in:

PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0105844

By:

Liao, Ming;
Shi, Jianying;
Huang, Lirong;
Gao, Yong;
Tan, Aihua;
Wu, Chunlei;
Lu, Zheng;
Yang, Xiaobo;
Zhang, Shijun;
Hu, Yanlin;
Qin, Xue;
Li, Jianling;
Chen, Gang;
Xu, Jianfeng;
Mo, Zengnan;
Zhang, Haiying

Publication type:

Article

The Mutational Spectrum of Lynch Syndrome in Cyprus.

Published in:

PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0105501

By:

Loizidou, Maria A.;
Neophytou, Ioanna;
Papamichael, Demetris;
Kountourakis, Panteleimon;
Vassiliou, Vassilios;
Marcou, Yiola;
Kakouri, Eleni;
Ioannidis, Georgios;
Philippou, Chrystalla;
Spanou, Elena;
Tanteles, George A.;
Anastasiadou, Violetta;
Hadjisavvas, Andreas;
Kyriacou, Kyriacos

Publication type:

Article

Modulation of Chromatin Remodelling Induced by the Freshwater Cyanotoxin Cylindrospermopsin in Human Intestinal Caco-2 Cells.

Published in:

PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0099121

By:

Huguet, Antoine;
Hatton, Aurélie;
Villot, Romain;
Quenault, Hélène;
Blanchard, Yannick;
Fessard, Valérie

Publication type:

Article

Promoter Methylation of MLH1, PMS2, MSH2 and p16 Is a Phenomenon of Advanced-Stage HCCs.

Published in:

PLoS ONE, 2014, v. 9, n. 1, p. 1, doi. 10.1371/journal.pone.0084453

By:

Hinrichsen, Inga;
Kemp, Matthias;
Peveling-Oberhag, Jan;
Passmann, Sandra;
Plotz, Guido;
Zeuzem, Stefan;
Brieger, Angela

Publication type:

Article

Sporulation Genes Associated with Sporulation Efficiency in Natural Isolates of Yeast.

Published in:

PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0069765

By:

Tomar, Parul;
Bhatia, Aatish;
Ramdas, Shweta;
Diao, Liyang;
Bhanot, Gyan;
Sinha, Himanshu

Publication type:

Article

Exomic Sequencing of Immune-Related Genes Reveals Novel Candidate Variants Associated with Alopecia Universalis.

Published in:

PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0053613

By:

Seungbok Lee;
Seung Hwan Paik;
Hyun-Jin Kim;
Hyeong Ho Ryu;
Soeun Cha;
Seong Jin Jo;
Hee Chul Eun;
Jeong-Sun Seo;
Jong-Il Kim;
Oh Sang Kwon

Publication type:

Article

The Cumulative Effects of Polymorphisms in the DNA Mismatch Repair Genes and Tobacco Smoking in Oesophageal Cancer Risk.

Published in:

PLoS ONE, 2012, v. 7, n. 5, p. 1, doi. 10.1371/journal.pone.0036962

By:

Vogelsang, Matjaz;
Yabing Wang;
Veber, Nika;
Mwapagha, Lamech M.;
Parker, M. Iqbal

Publication type:

Article

Down-Regulation of DNA Mismatch Repair Enhances Initiation and Growth of Neuroblastoma and Brain Tumour Multicellular Spheroids.

Published in:

PLoS ONE, 2011, v. 6, n. 12, p. 1, doi. 10.1371/journal.pone.0028123

By:

Collins, Samuel L.;
Hervé, Rodolphe;
Keevil, C. W.;
Blaydes, Jeremy P.;
Webb, Jeremy S.

Publication type:

Article

Increased sensitivity of p53-deficient cells to anticancer agents due to loss of Pms2.

Published in:

2002

By:

Fedier, A.;
Ruefenacht, U.B.;
Schwarz, V.A.;
Haller, U.;
Fink, D.

Publication type:

journal article

Detecting clinically actionable variants in the 3′ exons of PMS2 via a reflex workflow based on equivalent hybrid capture of the gene and its pseudogene.

Published in:

BMC Medical Genetics, 2018, v. 19, n. 1, p. N.PAG, doi. 10.1186/s12881-018-0691-9

By:

Gould, Genevieve M;
Grauman, Peter V;
Theilmann, Mark R;
Spurka, Lindsay;
Wang, Irving E;
Melroy, Laura M;
Chin, Robert G;
Hite, Dustin H;
Chu, Clement S;
Maguire, Jared R;
Hogan, Gregory J;
Muzzey, Dale

Publication type:

Article

A Genetic Incompatibility Accelerates Adaptation in Yeast.

Published in:

PLoS Genetics, 2015, v. 11, n. 7, p. 1, doi. 10.1371/journal.pgen.1005407

By:

Bui, Duyen T.;
Dine, Elliot;
Anderson, James B.;
Aquadro, Charles F.;
Alani, Eric E.

Publication type:

Article

Germline mutation and protein expression analysis of mismatch repair genes MSH6 and PMS2 in Malaysian Lynch syndrome patients.

Published in:

2014

By:

Zahary, Mohd;
Kaur, Gurjeet;
Hassan, Muhammad;
Sidek, Ahmad;
Singh, Harjinder;
Yeh, Lee;
Ankathil, Ravindran

Publication type:

Letter

Colorectal cancer in Iran: immunohistochemical profiles of four mismatch repair proteins.

Published in:

International Journal of Colorectal Disease, 2010, v. 25, n. 1, p. 63, doi. 10.1007/s00384-009-0784-1

By:

Molaei, Mahsa;
Mansoori, Babak Khoshkrood;
Ghiasi, Somayeh;
Khatami, Fatemeh;
Attarian, Hamid;
Zali, MohammadReza

Publication type:

Article