المؤلفون: Steffen Emmert, Holger Thiele, Evelin Schröck, Eva Machackova, Karl Hackmann, Steffen Schubert, Filip Lhota, Luisa Mackenroth, Barbara Klink, Andreas Rump, Janin Lehmann, Romy Opitz, Karin Kast, Elitza Betcheva-Krajcir, Anna Benet-Pagès, Jan Dominik Kuhlmann, Petra Zemankova, Pauline Wimberger, Zdenek Kleibl, Nataliya DiDonato, Elke Holinski-Feder, Anke M. Nissen, Ramūnas Janavičius, Lenka Foretova

المساهمون: Eng, Charis

المصدر: PLoS Genetics
PLoS Genetics, Vol 12, Iss 8, p e1006248 (2016)

مصطلحات موضوعية: 0301 basic medicine, Cancer Research, DNA Repair, Breast cancer, Frameshift mutation, Mutation databases, Ovarian cancer, DNA transcription, DNA repair, Luciferase, Mutation, medicine.disease_cause, Biochemistry, Database and Informatics Methods, 0302 clinical medicine, Breast Tumors, Medicine and Health Sciences, Missense mutation, Frameshift Mutation, Genetics (clinical), Genetics, Ovarian Neoplasms, 3. Good health, Ovarian Cancer, Enzymes, Nucleic acids, Oncology, 030220 oncology & carcinogenesis, Female, Oxidoreductases, Research Article, Heterozygote, lcsh:QH426-470, Mutation, Missense, Breast Neoplasms, Biology, Research and Analysis Methods, 03 medical and health sciences, Germline mutation, Breast Cancer, medicine, Humans, Genetic Predisposition to Disease, Molecular Biology, Gene, Ecology, Evolution, Behavior and Systematics, Germ-Line Mutation, Xeroderma Pigmentosum Group D Protein, Biology and Life Sciences, Cancers and Neoplasms, Proteins, DNA, medicine.disease, lcsh:Genetics, 030104 developmental biology, Biological Databases, Mutation Databases, Enzymology, ERCC2, Gene expression, Gynecological Tumors

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74d68649e05d32f95dc4e1e4c86e62db
https://pubmed.ncbi.nlm.nih.gov/27504877