Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: FANCB[original query] |
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Analysis of FANCB and FANCN/PALB2 fanconi anemia genes in BRCA1/2-negative Spanish breast cancer families. Breast cancer research and treatment 2009 Feb 113 (3): 545-51. García María J, Fernández Victoria, Osorio Ana, Barroso Alicia, Llort Gemma, Lázaro Conxi, Blanco Ignacio, Caldés Trinidad, de la Hoya Miguel, Ramón Y Cajal Teresa, Alonso Carmen, Tejada María-Isabel, San Román Carlos, Robles-Díaz Luis, Urioste Miguel, Benítez Javi |
Polymorphic variations in the FANCA gene in high-risk non-BRCA1/2 breast cancer individuals from the French Canadian population. Molecular oncology 2013 Feb 7 (1): 85-100. Litim Nadhir, Labrie Yvan, Desjardins Sylvie, Ouellette Geneviève, Plourde Karine, Belleau Pascal, , Durocher Franci |
Mutation screening and array comparative genomic hybridization using a 180K oligonucleotide array in VACTERL association. PloS one 2014 9 (1): e85313. Winberg Johanna, Gustavsson Peter, Papadogiannakis Nikos, Sahlin Ellika, Bradley Frideborg, Nordenskjöld Edvard, Svensson Pär-Johan, Annerén Göran, Iwarsson Erik, Nordgren Ann, Nordenskjöld Agne |
Genetic and Epigenetic Features of Rapidly Progressing IDH-Mutant Astrocytomas. Journal of neuropathology and experimental neurology 2018 5 77 (7): 542-548. Richardson Timothy E, Sathe Adwait Amod, Kanchwala Mohammed, Jia Gaoxiang, Habib Amyn A, Xiao Guanghua, Snuderl Matija, Xing Chao, Hatanpaa Kimmo |
Mutational and Functional Analysis of FANCB as a Candidate Gene for Sporadic Head and Neck Squamous Cell Carcinomas. Anticancer research 2018 3 38 (3): 1317-1325. Glaas Marcel F, Wiek Constanze, Wolter Linda-Maria, Roellecke Katharina, Balz Vera, Okpanyi Vera, Wagenmann Martin, Hoffmann Thomas Karl, Grässlin Rene, Plettenberg Christian, Schipper Jörg, Hanenberg Helmut, Scheckenbach Kathr |
Distinct homologous recombination gene expression profiles after neoadjuvant chemotherapy associated with clinical outcome in patients with ovarian cancer. Gynecologic oncology 2018 03 148 (3): 553-558. Kessous Roy, Octeau David, Klein Kathleen, Tonin Patricia N, Greenwood Celia M T, Pelmus Manuela, Laskov Ido, Kogan Liron, Salvador Shannon, Lau Susie, Yasmeen Amber, Gotlieb Walter |
Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresia. PloS one 2020 6 15 (6): e0234246. Zhang Rong, Gehlen Jan, Kawalia Amit, Melissari Maria-Theodora, Dakal Tikam Chand, Menon Athira M, Höfele Julia, Riedhammer Korbinian, Waffenschmidt Lea, Fabian Julia, Breuer Katinka, Kalanithy Jeshurun, Hilger Alina Christine, Sharma Amit, Hölscher Alice, Boemers Thomas M, Pauly Markus, Leutner Andreas, Fuchs Jörg, Seitz Guido, Ludwikowski Barbara M, Gomez Barbara, Hubertus Jochen, Heydweiller Andreas, Kurz Ralf, Leonhardt Johannes, Kosch Ferdinand, Holland-Cunz Stefan, Münsterer Oliver, Ure Beno, Schmiedeke Eberhard, Neser Jörg, Degenhardt Petra, Märzheuser Stefanie, Kleine Katharina, Schäfer Mattias, Spychalski Nicole, Deffaa Oliver J, Gosemann Jan-Hendrik, Lacher Martin, Heilmann-Heimbach Stefanie, Zwink Nadine, Jenetzky Ekkehart, Ludwig Michael, Grote Phillip, Schumacher Johannes, Thiele Holger, Reutter Hei |
Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer Patients. Cancers 2020 4 12 (4): . Del Valle Jesús, Rofes Paula, Moreno-Cabrera José Marcos, López-Dóriga Adriana, Belhadj Sami, Vargas-Parra Gardenia, Teulé Àlex, Cuesta Raquel, Muñoz Xavier, Campos Olga, Salinas Mónica, de Cid Rafael, Brunet Joan, González Sara, Capellá Gabriel, Pineda Marta, Feliubadaló Lídia, Lázaro Con |
Challenges in reporting pathogenic/potentially pathogenic variants in 94 cancer predisposing genes - in pediatric patients screened with NGS panels. Scientific reports 2020 1 10 (1): 223. Chirita-Emandi Adela, Andreescu Nicoleta, Zimbru Cristian G, Tutac Paul, Arghirescu Smaranda, Serban Margit, Puiu Mar |
A comprehensive molecular study identified 12 complementation groups with 56 novel FANC gene variants in Indian Fanconi anemia subjects. Human mutation 2021 Sep . George Merin, Solanki Avani, Chavan Niranjan, Rajendran Aruna, Raj Revathi, Mohan Sheila, Nemani Sandeep, Kanvinde Shailesh, Munirathnam Deendayalan, Rao Sudha, Radhakrishnan Nita, Lashkari Harsha Prasada, Ghildhiyal Radha Gulati, Manglani Mamta, Shanmukhaiah Chandrakala, Bhat Sunil, Ramesh Sowmyashree, Cherian Anchu, Junagade Pritesh, Vundinti Babu R |
[Association of CDH1, FANCB and APC Gene Polymorphisms ?with Lung Cancer Susceptibility in Chinese Population]. Zhongguo fei ai za zhi = Chinese journal of lung cancer 2022 Sep 25 (9): 658-664. Su Lianchun, Huang Hua, Gao Min, Li Yongwen, Shi Ruifeng, Chen Chen, Li Xuanguang, Zhu Guangsheng, Liu Hongyu, Chen J |
A comprehensive analysis of Fanconi anemia genes in Chinese patients with high-risk hereditary breast cancer. Journal of cancer research and clinical oncology 2023 8 . Qiao-Yan Zhu, Pu-Chun Li, Yi-Fan Zhu, Jia-Ni Pan, Rong Wang, Xiao-Lin Li, Wei-Wu Ye, Xiao-Wen Ding, Xiao-Jia Wang, Wen-Ming C |
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