المؤلفون: Fares Al-Ejeh, Ana Cristina Vargas, A. Hasson, Mariska Miranda, P. Kalita-de Croft, Peter T. Simpson, X. M. De Luca, Jamie R. Kutasovic, K. K. Khanna, Jonathan Beesley, Jodi M. Saunus, Emad A. Rakha, Ashwini Raghavendra, Georgia Chenevix-Trench, Julia Margaret Wendy Gee, Samir Lal, Emarene Kalaw, Irma Gresshoff, Korinne Northwood, Christopher J. Ormandy, Ian O. Ellis, Malcolm Lim, Andrew J. Dalley, A.E. McCart Reed, Andrew R. Green, Sunil R. Lakhani, Dan V. Nicolau

مصطلحات موضوعية: Breast cancer, SOX10, Cancer research, medicine, Cancer, Epigenome, Biology, medicine.disease, Reprogramming, Transcription factor, Triple-negative breast cancer, Chromatin

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::2f92ff5d4512d02716e3d46a042bfc3e
https://doi.org/10.1101/2021.03.30.437624

المؤلفون: Heather Thorne, A-M Patch, John F. Pearson, F Newell, Georgia Chenevix-Trench, Sriganesh Srihari, Vanessa Lakis, Katia Nones, Conrad Leonard, Sunil R. Lakhani, J Beasley, Peter T. Simpson, Michael T. Parsons, Mark A. Ragan, Aimee L Davidson, Amanda B. Spurdle, Andrea Degasperi, K. K. Khanna, Oliver Holmes, Julie K. Johnson, Kaltin Ferguson, Stephen H. Kazakoff, Serena Nik-Zainal, Scott Wood, Nick Waddell, Pamela Mukhopadhyay, Qinying Xu, X. M. De Luca, A.E. McCart Reed, Lynne Reid

المصدر: Cancer Research. 79:P5-10

مصطلحات موضوعية: Genetics, Whole genome sequencing, Cancer Research, Mutation, endocrine system diseases, PALB2, Cancer, Single-nucleotide polymorphism, Biology, medicine.disease, medicine.disease_cause, Germline mutation, Breast cancer, Oncology, medicine, skin and connective tissue diseases, CHEK2

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::317682359e8da6428f3291f702dbfddd
https://doi.org/10.1158/1538-7445.sabcs18-p5-10-01

المؤلفون: Stephen H. Kazakoff, Julie Johnson, Nicola Waddell, Oliver Holmes, Sunil R. Lakhani, K. K. Khanna, Conrad Leonard, Michael T. Parsons, Peter T. Simpson, Vanessa Lakis, Katia Nones, Serena Nik-Zainal, Aimee L Davidson, Scott Wood, Andrea Degasperi, Georgia Chenevix-Trench, A.E. McCart Reed, Lynne Reid, John V. Pearson, Ann-Marie Patch, Kaltin Ferguson, X. M. De Luca, Sriganesh Srihari, Jonathan M. Harris, Jonathan Beesley, Mark A. Ragan, David G. Barnes, Heather Thorne, Pamela Mukhopadhyay, Felicity Newell, Qinying Xu, Amanda B. Spurdle

المساهمون: Barnes, Daniel [0000-0002-3781-7570], Degasperi, Andrea [0000-0001-6879-0596], Nik-Zainal, Serena [0000-0001-5054-1727], Apollo - University of Cambridge Repository

المصدر: Ann Oncol

مصطلحات موضوعية: 0301 basic medicine, Adult, endocrine system diseases, mutation signatures, Somatic cell, PALB2, Breast Neoplasms, Germline, 03 medical and health sciences, 0302 clinical medicine, Germline mutation, MUTYH, Medicine, Humans, Genetic Predisposition to Disease, skin and connective tissue diseases, CHEK2, Germ-Line Mutation, Genetics, BRCA2 Protein, Whole Genome Sequencing, business.industry, BRCA1 Protein, Editorials, Hematology, DNA, Neoplasm, Middle Aged, BRCA1, Prognosis, BRCA2, 3. Good health, 030104 developmental biology, Oncology, whole-genome sequencing, 030220 oncology & carcinogenesis, PARP inhibitor, familial breast cancers, Female, business, Fanconi Anemia Complementation Group N Protein

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a412216dcef79f04224ef9da58a55a6a
https://pubmed.ncbi.nlm.nih.gov/31090898