HuGE Literature Finder
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| Mutations of TP53 and genes related to homologous recombination repair in breast cancer with germline BRCA1/2 mutations. Human genomics 2023 1 17 (1): 2. Kim Jinyong, Jeong Kyeonghun, Jun Hyeji, Kim Kwangsoo, Bae Jeong Mo, Song Myung Geun, Yi Hanbaek, Park Songyi, Woo Go-Un, Lee Dae-Won, Kim Tae-Yong, Lee Kyung-Hun, Im Seock- |
| Distinct Somatic Alteration Features Identified by Gene Panel Sequencing in Korean Triple-Negative Breast Cancer with High Ki67 Expression. Diagnostics (Basel, Switzerland) 2021 4 11 (3): . Sun Woo Young, Lee Jina, Kim Bong Kyun, Kim Jong Ok, Park Joonho |
| Frequency of heterozygous germline pathogenic variants in genes for Fanconi anemia in patients with non-BRCA1/BRCA2 breast cancer: a meta-analysis. Breast cancer research and treatment 2020 Jun . Alter Blanche P, Best Ana |
| Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer Patients. Cancers 2020 4 12 (4): . Del Valle Jesús, Rofes Paula, Moreno-Cabrera José Marcos, López-Dóriga Adriana, Belhadj Sami, Vargas-Parra Gardenia, Teulé Àlex, Cuesta Raquel, Muñoz Xavier, Campos Olga, Salinas Mónica, de Cid Rafael, Brunet Joan, González Sara, Capellá Gabriel, Pineda Marta, Feliubadaló Lídia, Lázaro Con |
| Analysis of polymorphisms in genes associated with the FA/BRCA pathway in three patients with multiple primary malignant neoplasms. Artificial cells, nanomedicine, and biotechnology 2019 Dec 47 (1): 1101-1112. Wang Le, Wang Hao, Wang Ting, Liu Jinhui, Chen Wei, Wang Yamin, Chen Chao, Zhu Hongli, Dai Pengg |
| Somatic mutations in early onset luminal breast cancer. Oncotarget 2018 Apr 9 (32): 22460-22479. Encinas Giselly, Sabelnykova Veronica Y, de Lyra Eduardo Carneiro, Hirata Katayama Maria Lucia, Maistro Simone, de Vasconcellos Valle Pedro Wilson Mompean, de Lima Pereira Gláucia Fernanda, Rodrigues Lívia Munhoz, de Menezes Pacheco Serio Pedro Adolpho, de Gouvêa Ana Carolina Ribeiro Chaves, Geyer Felipe Correa, Basso Ricardo Alves, Pasini Fátima Solange, Del Pilar Esteves Diz Maria, Brentani Maria Mitzi, Guedes Sampaio Góes João Carlos, Chammas Roger, Boutros Paul C, Koike Folgueira Maria Aparecida Azeve |
| Association of Single-Nucleotide Polymorphisms in Monoubiquitinated FANCD2-DNA Damage Repair Pathway Genes With Breast Cancer in the Chinese Population. Technology in cancer research & treatment 2018 Jan 17 1533033818819841. Chen Fei-Yu, Wang Hao, Li Hui, Hu Xue-Li, Dai Xu, Wang Shou-Man, Yan Guo-Jiao, Jiang Ping-Lan, Hu Yuan-Ping, Huang Juan, Tang Li- |
| Case-control analysis of truncating mutations in DNA damage response genes connects TEX15 and FANCD2 with hereditary breast cancer susceptibility. Scientific reports 2017 Apr 7 (1): 681. Mantere Tuomo, Tervasmäki Anna, Nurmi Anna, Rapakko Katrin, Kauppila Saila, Tang Jiangbo, Schleutker Johanna, Kallioniemi Anne, Hartikainen Jaana M, Mannermaa Arto, Nieminen Pentti, Hanhisalo Riitta, Lehto Sini, Suvanto Maija, Grip Mervi, Jukkola-Vuorinen Arja, Tengström Maria, Auvinen Päivi, Kvist Anders, Borg Åke, Blomqvist Carl, Aittomäki Kristiina, Greenberg Roger A, Winqvist Robert, Nevanlinna Heli, Pylkäs Kat |
| Biallelic truncating FANCM mutations cause early-onset cancer but not Fanconi anemia. Genetics in medicine : official journal of the American College of Medical Genetics 2017 8 20 (4): 458-463. Bogliolo Massimo, Bluteau Dominique, Lespinasse James, Pujol Roser, Vasquez Nadia, d'Enghien Catherine Dubois, Stoppa-Lyonnet Dominique, Leblanc Thierry, Soulier Jean, Surrallés Jor |
| AluY-mediated germline deletion, duplication and somatic stem cell reversion in UBE2T defines a new subtype of Fanconi anemia. Human molecular genetics 2015 Sep 24 (18): 5093-108. Virts Elizabeth L, Jankowska Anna, Mackay Craig, Glaas Marcel F, Wiek Constanze, Kelich Stephanie L, Lottmann Nadine, Kennedy Felicia M, Marchal Christophe, Lehnert Erik, Scharf Rüdiger E, Dufour Carlo, Lanciotti Marina, Farruggia Piero, Santoro Alessandra, Savasan Süreyya, Scheckenbach Kathrin, Schipper Jörg, Wagenmann Martin, Lewis Todd, Leffak Michael, Farlow Janice L, Foroud Tatiana M, Honisch Ellen, Niederacher Dieter, Chakraborty Sujata C, Vance Gail H, Pruss Dmitry, Timms Kirsten M, Lanchbury Jerry S, Alpi Arno F, Hanenberg Helm |
| Haplotype analysis of eight genes of the monoubiquitinated FANCD2-DNA damage-repair pathway in breast cancer patients. Cancer epidemiology 2013 Jun 37 (3): 311-7. Tang Li-Li, Chen Fei-Yu, Wang Hao, Hu Xue-Li, Dai Xu, Mao Jie, Shen Zheng-Tang, Wu Yu-Hui, Wang Shou-Man, Hai Jian, Yan Guo-Jiao, Li Hui, Huang Ju |
| Polymorphic variations in the FANCA gene in high-risk non-BRCA1/2 breast cancer individuals from the French Canadian population. Molecular oncology 2013 Feb 7 (1): 85-100. Litim Nadhir, Labrie Yvan, Desjardins Sylvie, Ouellette Geneviève, Plourde Karine, Belleau Pascal, , Durocher Franci |
| Genetic predictors of taxane-induced neurotoxicity in a SWOG phase III intergroup adjuvant breast cancer treatment trial (S0221). Breast cancer research and treatment 2011 Dec 130 (3): 993-1002. Sucheston Lara E, Zhao Hua, Yao Song, Zirpoli Gary, Liu Song, Barlow William E, Moore Halle C F, Thomas Budd G, Hershman Dawn L, Davis Warren, Ciupak Gregory L, Stewart James A, Isaacs Claudine, Hobday Timothy J, Salim Muhammad, Hortobagyi Gabriel N, Gralow Julie R, Livingston Robert B, Albain Kathy S, Hayes Daniel F, Ambrosone Christine |
| The Fanconi anemia family of genes and its correlation with breast cancer susceptibility and breast cancer features. Breast cancer research and treatment 2009 Jun . Barroso E, Pita G, Arias JI, Menendez P, Zamora P, Blanco M, Benitez J, Ribas G |
| FANCD2 associated with sporadic breast cancer risk. Carcinogenesis 2006 Sep 27 (9): 1930-7. Barroso E, Milne R L, Fernández L P, Zamora P, Arias J I, Benítez J, Ribas |
| Evaluation of Fanconi Anemia genes in familial breast cancer predisposition. Cancer research 2003 12 63 (24): 8596-9. Seal Sheila, Barfoot Rita, Jayatilake Hiran, Smith Paula, Renwick Anthony, Bascombe Linda, McGuffog Lesley, Evans D Gareth, Eccles Diana, Easton Douglas F, Stratton Michael R, Rahman Nazneen, |
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- Page last updated:Mar 28, 2023
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