Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Ovarian Neoplasms and ERCC4[original query] |
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| Nucleotide excision repair gene polymorphisms and risk of advanced colorectal adenoma: XPC polymorphisms modify smoking-related risk. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2006 Feb 15 (2): 306-11. Huang Wen-Yi, Berndt Sonja I, Kang Daehee, Chatterjee Nilanjan, Chanock Stephen J, Yeager Meredith, Welch Robert, Bresalier Robert S, Weissfeld Joel L, Hayes Richard |
| Xeroderma pigmentosum complementation group C single-nucleotide polymorphisms in the nucleotide excision repair pathway correlate with prolonged progression-free survival in advanced ovarian cancer. Cancer 2012 Feb 118 (3): 689-97. Fleming Nicole D, Agadjanian Hasmik, Nassanian Hoorig, Miller Carl W, Orsulic Sandra, Karlan Beth Y, Walsh Christine |
| Evaluation of rare variants in the new fanconi anemia gene ERCC4 (FANCQ) as familial breast/ovarian cancer susceptibility alleles. Human mutation 2013 Dec 34 (12): 1615-8. Osorio Ana, Bogliolo Massimo, Fernández Victoria, Barroso Alicia, de la Hoya Miguel, Caldés Trinidad, Lasa Adriana, Ramón y Cajal Teresa, Santamariña Marta, Vega Ana, Quiles Francisco, Lázaro Conxi, Díez Orland, Fernández Daniel, González-Sarmiento Rogelio, Durán Mercedes, Piqueras José Fernández, Marín Maria, Pujol Roser, Surrallés Jordi, Benítez Javi |
| The association of polymorphisms in nucleotide excision repair genes with ovarian cancer susceptibility. Bioscience reports 2018 Apr . Zhao Zhiguang, Zhang Anqi, Zhao Yuan, Xiang Junmiao, Yu Danyang, Liang Zongwen, Xu Chaoyi, Zhang Qiong, Li Jianmin, Duan Pi |
| Somatic variants of potential clinical significance in the tumors of BRCA phenocopies. Hereditary cancer in clinical practice 2019 7 17 21. Buckingham Lela, Mitchell Rachel, Maienschein-Cline Mark, Green Stefan, Hu Vincent Hong, Cobleigh Melody, Rotmensch Jacob, Burgess Kelly, Usha Lyd |
| Germline Genetic Findings Which May Impact Therapeutic Decisions in Families with a Presumed Predisposition for Hereditary Breast and Ovarian Cancer. Cancers 2020 8 12 (8): . Velázquez Carolina, K De Leeneer, Esteban-Cardeñosa Eva M, Avila Cobos Francisco, Lastra Enrique, Abella Luis E, de la Cruz Virginia, Lobatón Carmen D, Claes Kathleen B, Durán Mercedes, Infante M |
| Frequency of mutations in BRCA genes and other candidate genes in high-risk probands or probands with breast or ovarian cancer in the Czech Republic. Molecular biology reports 2020 3 47 (4): 2763-2769. Riedlova P, Janoutova J, Hermanova |
| Pathway-level mutation analysis in primary high-grade serous ovarian cancer and matched brain metastases. Scientific reports 2022 11 12 (1): 20537. Duchnowska Renata, Supernat Anna Maria, P?ksa Rafa?, ?ukasiewicz Marta, Stokowy Tomasz, Ronen Roy, Dutkowski Janusz, Umi?ska Monika, I?ycka-?wieszewska Ewa, Kowalczyk Anna, Och Waldemar, Ruci?ska Monika, Olszewski Wojciech P, Mandat Tomasz, Jarosz Bo?ena, Bie?kowski Micha?, Biernat Wojciech, Jassem Jac |
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