Human Genome Epidemiology Literature Finder
|
Records 1 - 24 (of 24 Records) |
| Query Trace: Disease and MSH3[original query] |
|---|
| Common germline variation in mismatch repair genes and survival after a diagnosis of colorectal cancer. International journal of cancer. Journal international du cancer 2009 Apr 124 (8): 1887-91. Koessler Thibaud, Azzato Elizabeth M, Perkins Barbara, Macinnis Robert J, Greenberg David, Easton Douglas F, Pharoah Paul D |
| Population genomics in a disease targeted primary cell model. Genome research 2009 Nov 19 (11): 1942-52. Grundberg Elin, Kwan Tony, Ge Bing, Lam Kevin C L, Koka Vonda, Kindmark Andreas, Mallmin Hans, Dias Joana, Verlaan Dominique J, Ouimet Manon, Sinnett Daniel, Rivadeneira Fernando, Estrada Karol, Hofman Albert, van Meurs Joyce M, Uitterlinden André, Beaulieu Patrick, Graziani Alexandru, Harmsen Eef, Ljunggren Osten, Ohlsson Claes, Mellström Dan, Karlsson Magnus K, Nilsson Olle, Pastinen To |
| Colorectal carcinomas with microsatellite instability display a different pattern of target gene mutations according to large bowel site of origin. BMC cancer 2010 10 (1): 587. Pinheiro Manuela, Ahlquist Terje, Danielsen Stine A, Lind Guro E, Veiga Isabel, Pinto Carla, Costa Vera, Afonso Luís, Sousa Olga, Fragoso Maria, Santos Lúcio, Henrique Rui, Lopes Paula, Lopes Carlos, Lothe Ragnhild A, Teixeira Manuel |
| DNA repair gene polymorphisms and risk of early onset colorectal cancer in Lynch syndrome. Cancer epidemiology 2012 Apr 36 (2): 183-9. Reeves Stuart G, Meldrum Cliff, Groombridge Claire, Spigelman Allan, Suchy Janina, Kurzawski Grzegorz, Lubinski Jan, Scott Rodney |
| DNA mismatch repair gene polymorphisms affect survival in pancreatic cancer. The oncologist 2011 16 (1): 61-70. Dong Xiaoqun, Li Yanan, Hess Kenneth R, Abbruzzese James L, Li Dongh |
| DNA repair gene variants are associated with an increased risk of myelodysplastic syndromes in a Czech population. Journal of hematology & oncology 2013 6 9. Belickova Monika, Merkerova Michaela Dostalova, Stara Eliska, Vesela Jitka, Sponerova Dana, Mikulenkova Dana, Brdicka Radim, Neuwirtova Radana, Jonasova Anna, Cermak Jarosl |
| Target gene mutational pattern in Lynch syndrome colorectal carcinomas according to tumour location and germline mutation. British journal of cancer 2015 Aug 113 (4): 686-92. Pinheiro Manuela, Pinto Carla, Peixoto Ana, Veiga Isabel, Lopes Paula, Henrique Rui, Baldaia Helena, Carneiro Fátima, Seruca Raquel, Tomlinson Ian, Kovac Michal, Heinimann Karl, Teixeira Manuel |
| A polymorphism in the MSH3 mismatch repair gene is associated with the levels of somatic instability of the expanded CTG repeat in the blood DNA of myotonic dystrophy type 1 patients. DNA repair 2016 Mar 40 57-66. Morales Fernando, Vásquez Melissa, Santamaría Carolina, Cuenca Patricia, Corrales Eyleen, Monckton Darren |
| Microsatellite Alterations With Allelic Loss at 9p24.2 Signify Less-Aggressive Colorectal Cancer Metastasis. Gastroenterology 2016 Apr 150 (4): 944-55. Koi Minoru, Garcia Melissa, Choi Chan, Kim Hyeong-Rok, Koike Junichi, Hemmi Hiromichi, Nagasaka Takeshi, Okugawa Yoshinaga, Toiyama Yuji, Kitajima Takahito, Imaoka Hiroki, Kusunoki Masato, Chen Yin-Hsiu, Mukherjee Bhramar, Boland C Richard, Carethers John |
| Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.
The Lancet. Neurology 2017 Jun . Moss Davina J Hensman, Pardiñas Antonio F, Langbehn Douglas, Lo Kitty, Leavitt Blair R, Roos Raymund, Durr Alexandra, Mead Simon, , , Holmans Peter, Jones Lesley, Tabrizi Sarah |
| Distinctive DNA mismatch repair and APC rare variants in African Americans with colorectal neoplasia. Oncotarget 2017 12 8 (59): 99966-99977. Ashktorab Hassan, Azimi Hamed, Varma Sudhir, Tavakoli Payaam, Nickerson Michael L, Brim Hass |
| Polymorphisms in DNA mismatch repair pathway genes predict toxicity and response to cisplatin chemoradiation in head and neck squamous cell carcinoma patients. Oncotarget 2018 07 9 (51): 29538-29547. Nogueira Guilherme Augusto Silva, Costa Ericka Francislaine Dias, Lopes-Aguiar Leisa, Lima Tathiane Regine Penna, Visacri Marília Berlofa, Pincinato Eder Carvalho, Lourenço Gustavo Jacob, Calonga Luciane, Mariano Fernanda Viviane, Altemani Albina Messias de Almeida Milani, Altemani João Maurício Carrasco, Moriel Patrícia, Chone Carlos Takahiro, Ramos Celso Dario, Lima Carmen Silvia Pass |
| Contribution of New Adenomatous Polyposis Predisposition Genes in an Unexplained Attenuated Spanish Cohort by Multigene Panel Testing. Scientific reports 2019 7 9 (1): 9814. Lorca Víctor, Rueda Daniel, Martín-Morales Lorena, Fernández-Aceñero María Jesús, Grolleman Judith, Poves Carmen, Llovet Patricia, Tapial Sandra, García-Barberán Vanesa, Sanz Julián, Pérez-Segura Pedro, de Voer Richarda M, Díaz-Rubio Eduardo, de la Hoya Miguel, Caldés Trinidad, Garre Pil |
| MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1. Brain : a journal of neurology 2019 6 142 (7): 1876-86. Flower Michael, Lomeikaite Vilija, Ciosi Marc, Cumming Sarah, Morales Fernando, Lo Kitty, Hensman Moss Davina, Jones Lesley, Holmans Peter, , , Monckton Darren G, Tabrizi Sarah |
| Genetic Profiling of Breast Cancer with and Without Preexisting Metabolic Disease. Translational oncology 2019 12 13 (2): 245-253. Jing Wenjiang, Li Ling, Zhang Xiumei, Wu Shouxin, Zhao Jiangman, Hou Qunxing, Wu Haotian, Ma Wu, Li Shuheng, Liu Huimin, Yang Binh |
| A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes. EBioMedicine 2019 Oct . Ciosi Marc, Maxwell Alastair, Cumming Sarah A, Hensman Moss Davina J, Alshammari Asma M, Flower Michael D, Durr Alexandra, Leavitt Blair R, Roos Raymund A C, , , Holmans Peter, Jones Lesley, Langbehn Douglas R, Kwak Seung, Tabrizi Sarah J, Monckton Darren |
| Genomic Profiling Comparison of Germline BRCA and Non-BRCA Carriers Reveals CCNE1 Amplification as a Risk Factor for Non-BRCA Carriers in Patients With Triple-Negative Breast Cancer. Frontiers in oncology 2020 11 10 583314. Huang Xin, Shao Di, Wu Huanwen, Zhu Changbin, Guo Dan, Zhou Yidong, Chen Chang, Lin Yan, Lu Tao, Zhao Bin, Wang Changjun, Sun Qia |
| Germline Alterations in Patients With IBD-associated Colorectal Cancer. Inflammatory bowel diseases 2021 8 28 (3): 447-454. Biscaglia Giuseppe, Latiano Anna, Castellana Stefano, Fontana Rosanna, Gentile Annamaria, Latiano Tiziana, Corritore Giuseppe, Panza Anna, Nardella Marianna, Martino Giuseppina, Bossa Fabrizio, Perri Francesco, Mazza Tommaso, Andriulli Angelo, Palmieri Oraz |
| Identifying genetic modifiers of age-associated penetrance in X-linked dystonia-parkinsonism. Nature communications 2021 5 12 (1): 3216. Laabs Björn-Hergen, Klein Christine, Pozojevic Jelena, Domingo Aloysius, Brüggemann Norbert, Grütz Karen, Rosales Raymond L, Jamora Roland Dominic, Saranza Gerard, Diesta Cid Czarina E, Wittig Michael, Schaake Susen, Dulovic-Mahlow Marija, Quismundo Jana, Otto Pia, Acuna Patrick, Go Criscely, Sharma Nutan, Multhaupt-Buell Trisha, Müller Ulrich, Hanssen Henrike, Kilpert Fabian, Franke Andre, Rolfs Arndt, Bauer Peter, Dobri?i? Valerija, Lohmann Katja, Ozelius Laurie J, Kaiser Frank J, König Inke R, Westenberger A |
| Filling the gap: A thorough investigation for the genetic diagnosis of unsolved polyposis patients with monoallelic MUTYH pathogenic variants. Molecular genetics & genomic medicine 2021 10 9 (12): e1831. Dell'Elice Anastasia, Cini Giulia, Fornasarig Mara, Armelao Franco, Barana Daniela, Bianchi Francesca, Casalis Cavalchini Guido Claudio, Maffè Antonella, Mammi Isabella, Pedroni Monica, Percesepe Antonio, Sorrentini Italo, Tibiletti Mariagrazia, Maestro Roberta, Quaia Michele, Viel Alessand |
| The Prevalence of Pathogenic or Likely Pathogenic Germline Variants in a Nationwide Cohort of Young Colorectal Cancer Patients Using a Panel of 18 Genes Associated with Colorectal Cancer. Cancers 2021 10 13 (20): . Frostberg Erik, Petersen Annabeth Høgh, Bojesen Anders, Rahr Hans Bjarke, Lindebjerg Jan, Rønlund Kari |
| Mosaic divergent repeat interruptions in XDP influence repeat stability and disease onset. Brain : a journal of neurology 2022 4 146 (3): 1075-1082. Trinh Joanne, Lüth Theresa, Schaake Susen, Laabs Björn-Hergen, Schlüter Kathleen, La? Joshua, Pozojevic Jelena, Tse Ronnie, König Inke, Jamora Roland Dominic, Rosales Raymond L, Brüggemann Norbert, Saranza Gerard, Diesta Cid Czarina E, Kaiser Frank J, Depienne Christel, Pearson Christopher E, Westenberger Ana, Klein Christi |
| Genetic variability in cisplatin metabolic pathways and outcome of locally advanced head and neck squamous cell carcinoma patients. Scientific reports 2023 10 13 (1): 16762. Ana Maria Castro Ferreira, João Maurício Carrasco Altemani, Ligia Traldi Macedo, Gustavo Jacob Lourenço, Carmen Silvia Passos Li |
| Microsatellite instability in mismatch repair proficient colorectal cancer: clinical features and underlying molecular mechanisms. EBioMedicine 2024 5 103 105142. Yun Xu, Kai Liu, Cong Li, Minghan Li, Xiaoyan Zhou, Menghong Sun, Liying Zhang, Sheng Wang, Fangqi Liu, Ye |
- Page last reviewed:Feb 1, 2024
- Content source:

