HuGE Literature Finder
Records
1
-
14
| Untangling the clinicopathological significance of MRE11-RAD50-NBS1 complex in sporadic breast cancers. NPJ breast cancer 2021 Nov 7 (1): 143. Alblihy Adel, Shoqafi Ahmed, Toss Michael S, Algethami Mashael, Harris Anna E, Jeyapalan Jennie N, Abdel-Fatah Tarek, Servante Juliette, Chan Stephen Y T, Green Andrew, Mongan Nigel P, Rakha Emad A, Madhusudan Srinivas |
| The spectrum of mutations predisposing to familial breast cancer in Poland. International journal of cancer 2019 Jun . Cybulski Cezary, Kluzniak Wojciech, Huzarski Tomasz, Wokolorczyk Dominika, Kashyap Aniruddh, Rusak Bogna, Stempa Klaudia, Gronwald Jacek, Szymiczek Agata, Bagherzadeh Maryam, Jakubowska Anna, Debniak Tadeusz, Lener Marcin, Rudnicka Helena, Szwiec Marek, Jarkiewicz-Tretyn Joanna, Stawicka Malgorzata, Domagala Pawel, Narod Steven A, Lubinski Jan, Akbari Mohammad R, |
| High frequency of pathogenic non-founder germline mutations in BRCA1 and BRCA2 in families with breast and ovarian cancer in a founder population. Hereditary cancer in clinical practice 2018 16 12. Maksimenko J, Irmejs A, Trofimovi?s G, B?rzi?a D, Skuja E, Purkalne G, Miklaševi?s E, Gardovskis |
| Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry. Breast cancer research : BCR 2017 Mar 19 (1): 30. Walker Logan C, Pearson John F, Wiggins George A R, Giles Graham G, Hopper John L, Southey Melissa |
| The risk for developing cancer in Israeli ATM, BLM, and FANCC heterozygous mutation carriers. Cancer genetics 2015 Dec . Laitman Yael, Boker-Keinan Lital, Berkenstadt Michal, Liphsitz Irena, Weissglas-Volkov Daphna, Ries-Levavi Liat, Sarouk Ifat, Pras Elon, Friedman Eit |
| Clinical evaluation of a multiple-gene sequencing panel for hereditary cancer risk assessment. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2014 Jul 32 (19): 2001-9. Kurian Allison W, Hare Emily E, Mills Meredith A, Kingham Kerry E, McPherson Lisa, Whittemore Alice S, McGuire Valerie, Ladabaum Uri, Kobayashi Yuya, Lincoln Stephen E, Cargill Michele, Ford James |
| Double heterozygotes among breast cancer patients analyzed for BRCA1, CHEK2, ATM, NBN/NBS1, and BLM germ-line mutations. Breast cancer research and treatment 2014 Jun 145 (2): 553-62. Sokolenko Anna P, Bogdanova Natalia, Kluzniak Wojciech, Preobrazhenskaya Elena V, Kuligina Ekatherina S, Iyevleva Aglaya G, Aleksakhina Svetlana N, Mitiushkina Natalia V, Gorodnova Tatiana V, Bessonov Alexandr A, Togo Alexandr V, Lubi?ski Jan, Cybulski Cezary, Jakubowska Anna, Dörk Thilo, Imyanitov Evgeny |
| BLM and RAD51 genes polymorphism and susceptibility to breast cancer. Pathology oncology research : POR 2013 Jul 19 (3): 451-9. Sassi Agnieszka, Popielarski Marcin, Synowiec Ewelina, Morawiec Zbigniew, Wozniak Katarzy |
| Nonsense mutation p.Q548X in BLM, the gene mutated in Bloom's syndrome, is associated with breast cancer in Slavic populations. Breast cancer research and treatment 2013 Jan 137 (2): 533-9. Prokofyeva Darya, Bogdanova Natalia, Dubrowinskaja Natalia, Bermisheva Marina, Takhirova Zalina, Antonenkova Natalia, Turmanov Nurzhan, Datsyuk Ihor, Gantsev Shamil, Christiansen Hans, Park-Simon Tjoung-Won, Hillemanns Peter, Khusnutdinova Elza, Dörk Thi |
| Exome sequencing identifies rare deleterious mutations in DNA repair genes FANCC and BLM as potential breast cancer susceptibility alleles. PLoS genetics 2012 Sep 8 (9): 9. Thompson ER, Doyle MA, Ryland GL, Rowley SM, Choong DY, Tothill RW, Thorne H, Barnes DR, Li J, Ellul J, Philip GK, Antill YC, James PA, Trainer AH, Mitchell G, Campbell IG |
| High prevalence and breast cancer predisposing role of the BLM c.1642 C>T (Q548X) mutation in Russia. International journal of cancer. Journal international du cancer 2012 Jun 130 (12): 2867-73. Sokolenko Anna P, Iyevleva Aglaya G, Preobrazhenskaya Elena V, Mitiushkina Nathalia V, Abysheva Svetlana N, Suspitsin Evgeny N, Kuligina Ekatherina Sh, Gorodnova Tatiana V, Pfeifer Werner, Togo Alexandr V, Turkevich Elena A, Ivantsov Alexandr O, Voskresenskiy Dmitry V, Dolmatov Georgy D, Bit-Sava Elena M, Matsko Dmitry E, Semiglazov Vladimir F, Fichtner Iduna, Larionov Alexey A, Kuznetsov Sergey G, Antoniou Antonis C, Imyanitov Evgeny |
| A polymorphism in Werner syndrome gene is associated with breast cancer susceptibility in Chinese women. Breast cancer research and treatment 2009 Nov 118 (1): 169-75. Wang Zhanwei, Xu Yan, Tang Jinhai, Ma Hongxia, Qin Jianwei, Lu Chen, Wang Xuechen, Hu Zhibin, Wang Xinru, Shen Hongbi |
| Genetic variants of BLM interact with RAD51 to increase breast cancer susceptibility. Carcinogenesis 2009 Jan 30 (1): 43-9. Ding Shian-Ling, Yu Jyh-Cherng, Chen Shou-Tung, Hsu Giu-Cheng, Kuo Shou-Jen, Lin Yu Hsin, Wu Pei-Ei, Shen Chen-Ya |
| Association between polymorphisms in RMI1, TOP3A, and BLM and risk of cancer, a case-control study. BMC cancer 2009 9 (1): 140. Broberg Karin, Huynh Elizabeth, Schläwicke Engström Karin, Björk Jonas, Albin Maria, Ingvar Christian, Olsson Håkan, Höglund Matti |
- Page last reviewed:Jul 25, 2022
- Page last updated:Jan 27, 2023
- Content source: