Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: FANCF[original query] |
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Evaluation of Fanconi Anemia genes in familial breast cancer predisposition. Cancer research 2003 12 63 (24): 8596-9. Seal Sheila, Barfoot Rita, Jayatilake Hiran, Smith Paula, Renwick Anthony, Bascombe Linda, McGuffog Lesley, Evans D Gareth, Eccles Diana, Easton Douglas F, Stratton Michael R, Rahman Nazneen, |
Homozygous deletion of p16INK4a and tobacco carcinogen exposure in nonsmall cell lung cancer. International journal of cancer. Journal international du cancer 2006 Mar 118 (6): 1364-9. Kraunz Kim S, Nelson Heather H, Lemos Miriam, Godleski John J, Wiencke John K, Kelsey Karl |
A search for variants associated with young-onset type 2 diabetes in American Indians in a 100K genotyping array. Diabetes 2007 Dec 56 (12): 3045-52. Hanson Robert L, Bogardus Clifton, Duggan David, Kobes Sayuko, Knowlton Michele, Infante Aniello M, Marovich Leslie, Benitez Deb, Baier Leslie J, Knowler William |
Network Meta-Analysis on the Effects of DNA Damage Response-Related Gene Mutations on Overall Survival of Breast Cancer Based on TCGA Database. Journal of cellular biochemistry 2017 May . Liu Chang, Chang Hong, Li Xiao-Han, Qi Ya-Fei, Wang Jin-Ou, Zhang Ying, Yang Xiang-Ho |
Germline and Somatic DNA Damage Repair Gene Mutations and Overall Survival in Metastatic Pancreatic Adenocarcinoma Patients Treated with FOLFIRINOX. Clinical cancer research : an official journal of the American Association for Cancer Research 2018 8 24 (24): 6204-6211. Sehdev Amikar, Gbolahan Olumide, Hancock Brad A, Stanley Melissa, Shahda Safi, Wan Jun, Wu Howard H, Radovich Milan, O'Neil Bert |
Identification of mutations in patients with acquired pure red cell aplasia. Acta biochimica et biophysica Sinica 2018 5 50 (7): 685-692. Zhang Xinchao, Shi Yi, Song Lingjun, Shen Chang, Cai Qi, Zhang Zhou, Wu Jun, Fu Guohui, Shen Weiw |
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 |
Clinical importance of FANCD2, BRIP1, BRCA1, BRCA2 and FANCF expression in ovarian carcinomas. Cancer biology & therapy 2019 3 20 (6): 843-854. Moes-Sosnowska Joanna, Rzepecka Iwona K, Chodzynska Joanna, Dansonka-Mieszkowska Agnieszka, Szafron Lukasz M, Balabas Aneta, Lotocka Renata, Sobiczewski Piotr, Kupryjanczyk Jolan |
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 |
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 |
Genetic modulation of longitudinal change in neurocognitive function among adult glioma patients. Journal of neuro-oncology 2021 Nov . Wefel Jeffrey S, Zhou Renke, Sulman Erik P, Boehling Nicholas S, Armstrong Georgina N, Tsavachidis Spiridon, Liang Fu-Wen, Etzel Carol J, Kahalley Lisa S, Small Brent J, Scheurer Michael E, Bondy Melissa L, Liu Yanho |
Association of variations in the Fanconi anemia complementation group and prognosis in Non-small cell lung cancer patients with Platinum-based chemotherapy. Gene 2022 3 825 146398. Mo Jun-Luan, Liu Jia-Si, Xiao Qi, Hong Wen-Xu, Yin Ji-Ye, Chen Juan, Liu Zhao-Qi |
Next generation sequencing reveals a high prevalence of pathogenic mutations in homologous recombination DNA damage repair genes among patients with uterine sarcoma. Gynecologic oncology 2023 8 177 14-19. Dimitrios Nasioudis, Nawar A Latif, Emily M Ko, Lori Cory, Sarah H Kim, Lainie Martin, Fiona Simpkins, Robert Giunto |
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- Page last updated:Apr 22, 2024
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