Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: Anemia and FANCD2[original query] |
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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, |
The genetics of FANCC and FANCG in familial pancreatic cancer. Cancer biology & therapy 2004 1 3 (2): 167-9. Rogers Carmelle D, van der Heijden Michiel S, Brune Kieran, Yeo Charles J, Hruban Ralph H, Kern Scott E, Goggins Micha |
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 |
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 |
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 |
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 |
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 |
Assessing the spectrum of germline variation in Fanconi anemia genes among patients with head and neck carcinoma before age 50. Cancer 2017 Jul . Chandrasekharappa Settara C, Chinn Steven B, Donovan Frank X, Chowdhury Naweed I, Kamat Aparna, Adeyemo Adebowale A, Thomas James W, Vemulapalli Meghana, Hussey Caroline S, Reid Holly H, Mullikin James C, Wei Qingyi, Sturgis Erich |
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 |
Functional analysis of Fanconi anemia mutations in China. Experimental hematology 2018 7 66 32-41.e8. Li Niu, Ding Lixia, Li Benshang, Wang Jian, D'Andrea Alan D, Chen Ji |
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 |
Whole exome sequencing identifies a novel FANCD2 gene splice site mutation associated with disease progression in chronic myeloid leukemia: Implication in targeted therapy of advanced phase CML. Pakistan journal of pharmaceutical sciences 2020 12 33 (3(Special)): 1419-1426. Absar Muhammad, Mahmood Amer, Akhtar Tanveer, Basit Sulman, Ramzan Khushnooda, Jameel Abid, Afzal Sibtain, Ullah Anhar, Qureshi Kulsoom, Alanazi Nawaf, Iqbal Zaf |
A comprehensive molecular study identified 12 complementation groups with 56 novel FANC gene variants in Indian Fanconi anemia subjects. Human mutation 2021 Sep . George Merin, Solanki Avani, Chavan Niranjan, Rajendran Aruna, Raj Revathi, Mohan Sheila, Nemani Sandeep, Kanvinde Shailesh, Munirathnam Deendayalan, Rao Sudha, Radhakrishnan Nita, Lashkari Harsha Prasada, Ghildhiyal Radha Gulati, Manglani Mamta, Shanmukhaiah Chandrakala, Bhat Sunil, Ramesh Sowmyashree, Cherian Anchu, Junagade Pritesh, Vundinti Babu R |
Fanconi anemia gene-associated germline predisposition in aplastic anemia and hematologic malignancies. Frontiers of medicine 2021 Nov . Nie Daijing, Zhang Jing, Wang Fang, Li Xvxin, Liu Lili, Zhang Wei, Cao Panxiang, Chen Xue, Zhang Yang, Chen Jiaqi, Ma Xiaoli, Zhou Xiaosu, Wu Qisheng, Liu Ming, Liu Mingyue, Tian Wenjun, Liu Hongxi |
Phenotypic and genotypic correlation evaluation of 148 pediatric patients with Fanconi anemia in a Chinese rare disease cohort. Clinica chimica acta; international journal of clinical chemistry 2022 12 539 41-49. Chang Lixian, Zhang Li, An Wenbin, Wan Yang, Cai Yuli, Lan Yang, Zhang Aoli, Liu Lipeng, Ruan Min, Liu Xiaoming, Guo Ye, Yang Wenyu, Chen Xiaojuan, Chen Yumei, Wang Shuchun, Zou Yao, Yuan Weiping, Zhu Xiaof |
A comprehensive analysis of Fanconi anemia genes in Chinese patients with high-risk hereditary breast cancer. Journal of cancer research and clinical oncology 2023 8 . Qiao-Yan Zhu, Pu-Chun Li, Yi-Fan Zhu, Jia-Ni Pan, Rong Wang, Xiao-Lin Li, Wei-Wu Ye, Xiao-Wen Ding, Xiao-Jia Wang, Wen-Ming C |
A comprehensive study evaluating germline FANCG variants in predisposition to breast and ovarian cancer. Cancer medicine 2024 8 13 (16): e70103. Jana Soukupova, Barbora Stastna, Madiha Kanwal, Jan Hojny, Petra Zemankova, Marianna Borecka, Leona Cerna, Marta Cerna, Monika Cerna, Vaclava Curtisova, Tatana Dolezalova, Petra Duskova, Lenka Foretova, Ondrej Havranek, Klara Horackova, Milena Hovhannisyan, Lucie Hruskova, Stepan Chvojka, Marketa Janatova, Maria Janikova, Sandra Jelinkova, Pavel Just, Marta Kalousova, Petra Kleiblova, Marcela Kosarova, Monika Koudova, Jan Kral, Michaela Krausova, Vera Krutilkova, Eva Machackova, Katerina Matejkova, Renata Michalovska, Petr Nehasil, Barbora Nemcova, Jan Novotny, Matous Palek, Pavel Pesek, Marketa Safarikova, Ondrej Scheinost, Drahomira Springer, Lenka Stolarova, Viktor Stranecky, Ivan Subrt, Spiros Tavandzis, Eva Tureckova, Kamila Vesela, Zdenka Vlckova, Michal Vocka, Tomas Zima, Libor Macurek, Zdenek Kleibl, |
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