Human Genome Epidemiology Literature Finder
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Records 1 - 15 (of 15 Records) |
| Query Trace: Neoplasms and FANCG[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 |
| Germ line Fanconi anemia complementation group C mutations and pancreatic cancer. Cancer research 2005 Jan 65 (2): 383-6. Couch Fergus J, Johnson Michele R, Rabe Kari, Boardman Lisa, McWilliams Robert, de Andrade Mariza, Petersen Glor |
| The identification of pathogenic variants in BRCA1/2 negative, high risk, hereditary breast and/or ovarian cancer patients: High frequency of FANCM pathogenic variants. International journal of cancer 2018 11 144 (11): 2683-2694. Schubert Stephanie, van Luttikhuizen Jana L, Auber Bernd, Schmidt Gunnar, Hofmann Winfried, Penkert Judith, Davenport Colin F, Hille-Betz Ursula, Wendeburg Lena, Bublitz Janin, Tauscher Marcel, Hackmann Karl, Schröck Evelin, Scholz Caroline, Wallaschek Hannah, Schlegelberger Brigitte, Illig Thomas, Steinemann Dor |
| 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 |
| 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 |
| 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 |
| Prevalence of cancer susceptibility variants in patients with multiple Lynch syndrome related cancers. Scientific reports 2021 Jul 11 (1): 14807. Choi Yoon Young, Shin Su-Jin, Lee Jae Eun, Madlensky Lisa, Lee Seung-Tae, Park Ji Soo, Jo Jeong-Hyeon, Kim Hyunki, Nachmanson Daniela, Xu Xiaojun, Noh Sung Hoon, Cheong Jae-Ho, Harismendy Olivi |
| 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 |
| Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG. International journal of molecular sciences 2022 2 23 (4): . Reyes Pedro, García-de Teresa Benilde, Juárez Ulises, Pérez-Villatoro Fernando, Fiesco-Roa Moisés O, Rodríguez Alfredo, Molina Bertha, Villarreal-Molina María Teresa, Meléndez-Zajgla Jorge, Carnevale Alessandra, Torres Leda, Frias Sa |
| Next generation sequencing reveals a high prevalence of pathogenic mutations in homologous recombination DNA damage repair genes among patients with uterine sarcoma. Gynecologic oncology 2023 8 177 14-19. Dimitrios Nasioudis, Nawar A Latif, Emily M Ko, Lori Cory, Sarah H Kim, Lainie Martin, Fiona Simpkins, Robert Giunto |
| DNA damage response and repair gene mutations are associated with tumor mutational burden and outcomes to platinum-based chemotherapy/immunotherapy in advanced NSCLC patients. Diagnostic pathology 2023 11 18 (1): 119. Weiguang Gu, Wenya Zhuang, Mengxia Zhuang, Minhong He, Zhihua |
| 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- |
| Genomic alterations in two patients with esophageal carcinosarcoma identified by whole genome sequencing: a case report. Surgical case reports 2024 8 10 (1): 191. Masazumi Inoue, Yasuhiro Tsubosa, Sumiko Ohnami, Kazunori Tokizawa, Shuhei Mayanagi, Keiichi Ohshima, Kenichi Urakami, Shumpei Ohnami, Takeshi Nagashima, Ken Yamaguc |
| 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, |
- Page last reviewed:Feb 1, 2024
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