HuGE Literature Finder
Records 1-20
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Lymph node metastasis in oral cancer is strongly associated with chromosomal instability and DNA repair defects.
International journal of cancer 2019 Mar . Biswas Nidhan K, Das Chitrarpita, Das Subrata, Maitra Arindam, Nair Sudhir, Gupta Tejpal, D'Cruz Anil K, Sarin Rajiv, Majumder Partha |
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Prevalence of BRCA1/2 large genomic rearrangements in Chinese women with sporadic triple-negative or familial breast cancer.
Clinical genetics 2018 Mar . Su L, Zhang J, Meng H, Ouyang T, Li J, Wang T, Fan Z, Fan T, Lin B, Xie |
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Can chimerism explain breast/ovarian cancers in BRCA non-carriers from BRCA-positive families?
PloS one 2018 13 (4): e0195497. Mitchell Rachel, Buckingham Lela, Cobleigh Melody, Rotmensch Jacob, Burgess Kelly, Usha Lyd |
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Analysis of chromosomal radiosensitivity of healthy BRCA2 mutation carriers and non-carriers in BRCA families with the G2 micronucleus assay.
Oncology reports 2017 Mar 37 (3): 1379-1386. Baert Annelot, Depuydt Julie, Van Maerken Tom, Poppe Bruce, Malfait Fransiska, Van Damme Tim, De Nobele Sylvia, Perletti Gianpaolo, De Leeneer Kim, Claes Kathleen B M, Vral An |
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Clinically Significant Unclassified Variants in BRCA1 and BRCA2 Genes Among Korean Breast Cancer Patients.
Cancer research and treatment : official journal of Korean Cancer Association 2016 Sep . Yoon Kyong-Ah, Park Boyoung, Lee Byung Il, Yang Moon Jung, Kong Sun-Young, Lee Eun So |
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Chromothripsis Is a Recurrent Genomic Abnormality in High-Risk Myelodysplastic Syndromes.
PloS one 2016 11 (10): e0164370. Abáigar María, Robledo Cristina, Benito Rocío, Ramos Fernando, Díez-Campelo María, Hermosín Lourdes, Sánchez-Del-Real Javier, Alonso Jose M, Cuello Rebeca, Megido Marta, Rodríguez Juan N, Martín-Núñez Guillermo, Aguilar Carlos, Vargas Manuel, Martín Ana A, García Juan L, Kohlmann Alexander, Del Cañizo M Consuelo, Hernández-Rivas Jesús |
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Integrated copy number and expression analysis identifies profiles of whole-arm chromosomal alterations and subgroups with favorable outcome in ovarian clear cell carcinomas.
PloS one 2015 10 (6): e0128066. Uehara Yuriko, Oda Katsutoshi, Ikeda Yuji, Koso Takahiro, Tsuji Shingo, Yamamoto Shogo, Asada Kayo, Sone Kenbun, Kurikawa Reiko, Makii Chinami, Hagiwara Otoe, Tanikawa Michihiro, Maeda Daichi, Hasegawa Kosei, Nakagawa Shunsuke, Wada-Hiraike Osamu, Kawana Kei, Fukayama Masashi, Fujiwara Keiichi, Yano Tetsu, Osuga Yutaka, Fujii Tomoyuki, Aburatani Hiroyu |
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Design and validation of an oligonucleotide microarray for the detection of genomic rearrangements associated with common hereditary cancer syndromes.
Journal of experimental & clinical cancer research : CR 2014 33 74. Mancini-DiNardo Debora, Judkins Thaddeus, Woolstenhulme Nick, Burton Collin, Schoenberger Jeremy, Ryder Matthew, Murray Adam, Gutin Natalia, Theisen Aaron, Holladay Jayson, Craft Jonathan, Arnell Christopher, Moyes Kelsey, Roa Benjam |
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Loss of heterozygosity at 13q13 and 14q32 predicts BRCA2 inactivation in luminal breast carcinomas.
International journal of cancer. Journal international du cancer 2013 Dec 133 (12): 2834-42. Pécuchet Nicolas, Popova Tatiana, Manié Elodie, Lucchesi Carlo, Battistella Aude, Vincent-Salomon Anne, Caux-Moncoutier Virginie, Bollet Marc, Sigal-Zafrani Brigitte, Sastre-Garau Xavier, Stoppa-Lyonnet Dominique, Stern Marc-Hen |
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Nonequivalent gene expression and copy number alterations in high-grade serous ovarian cancers with BRCA1 and BRCA2 mutations.
Clinical cancer research : an official journal of the American Association for Cancer Research 2013 Jul 19 (13): 3474-84. George Joshy, Alsop Kathryn, Etemadmoghadam Dariush, Hondow Heather, Mikeska Thomas, Dobrovic Alexander, deFazio Anna, , Smyth Gordon K, Levine Douglas A, Mitchell Gillian, Bowtell David |
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Tumor mutation burden forecasts outcome in ovarian cancer with BRCA1 or BRCA2 mutations.
PloS one 2013 8 (11): e80023. Birkbak Nicolai Juul, Kochupurakkal Bose, Izarzugaza Jose M G, Eklund Aron C, Li Yang, Liu Joyce, Szallasi Zoltan, Matulonis Ursula A, Richardson Andrea L, Iglehart J Dirk, Wang Zhigang |
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Clinical significance of large rearrangements in BRCA1 and BRCA2.
Cancer 2012 Nov 118 (21): 5210-6. Judkins Thaddeus, Rosenthal Eric, Arnell Christopher, Burbidge Lynn Anne, Geary Wade, Barrus Toby, Schoenberger Jeremy, Trost Jeffrey, Wenstrup Richard J, Roa Benjamin |
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Prediction of BRCA2-association in hereditary breast carcinomas using array-CGH.
Breast cancer research and treatment 2012 Apr 132 (2): 379-89. Joosse Simon A, Brandwijk Kim I M, Devilee Peter, Wesseling Jelle, Hogervorst Frans B L, Verhoef Senno, Nederlof Petra |
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Ionizing radiation or mitomycin-induced micronuclei in lymphocytes of BRCA1 or BRCA2 mutation carriers.
Breast cancer research and treatment 2011 Jun 127 (3): 611-22. Gutiérrez-Enríquez Sara, Ramón Y Cajal Teresa, Alonso Carmen, Corral Anna, Carrasco Pablo, Cornet Mónica, Sanz Judith, Ribas Montserrat, Baiget Montserrat, Diez Orla |
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Screening for common copy-number variants in cancer genes.
Cancer genetics and cytogenetics 2010 Dec 203 (2): 316-23. Tyson Jess, Majerus Tamsin M O, Walker Susan, Armour John A |
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Increased chromosomal radiosensitivity in women carrying BRCA1/BRCA2 mutations assessed with the G2 assay.
International journal of radiation oncology, biology, physics 2010 Mar 76 (4): 1199-205. Ernestos Beroukas, Nikolaos Pandis, Koulis Giannoukakos, Eleni Rizou, Konstantinos Beroukas, Alexandra Giatromanolaki, Michael Koukourak |
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Lymphocyte radiosensitivity in BRCA1 and BRCA2 mutation carriers and implications for breast cancer susceptibility.
International journal of cancer. Journal international du cancer 2007 Oct 121 (7): 1631-6. Barwell Julian, Pangon Laurent, Georgiou Anne, Kesterton Ian, Langman Caroline, Arden-Jones Audrey, Bancroft Elizabeth, Salmon Ashi, Locke Imogen, Kote-Jarai Zsofia, Morris Joanna R, Solomon Ellen, Berg Jonathan, Docherty Zoe, Camplejohn Richard, Eeles Rosalind, Hodgson Shirley |
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Large genomic rearrangement in BRCA1 and BRCA2 and clinical characteristics of men with breast cancer in the United States.
Clinical breast cancer 2007 Jun 7 (8): 627-33. Tchou Julia, Ward M Renee, Volpe Patricia, Palma Maurizia Dalla, Medina C Angelina, Sargen Michael, Sonnad Seema S, Godwin Andrew K, Daly Mary, Winchester David J, Garber Judy, Weber Barbara L, Domchek Susan, Nathanson Katherine |
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Polymorphisms in genes involved in DNA double-strand break repair pathway and susceptibility to benzene-induced hematotoxicity.
Carcinogenesis 2006 Oct 27 (10): 2083-9. Shen Min, Lan Qing, Zhang Luoping, Chanock Stephen, Li Guilan, Vermeulen Roel, Rappaport Stephen M, Guo Weihong, Hayes Richard B, Linet Martha, Yin Songnian, Yeager Meredith, Welch Robert, Forrest Matthew S, Rothman Nathaniel, Smith Martyn |
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[Bilateral breast carcinoma and local recurrence: prevalence of BRCA-1 and BRCA-2 gene mutations in an unselected patient sample].
Strahlentherapie und Onkologie : Organ der Deutschen Röntgengesellschaft ... [et al] 2001 Jul 177 (7): 325-9. Bremer M, Steinmann D, Dörk T, Börger J, Rades D, Karstens J |
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- Page last updated:Sep 18, 2020
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