Human Genome Epidemiology Literature Finder
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Records 1 - 12 (of 12 Records) |
| Query Trace: Disease and FANCD2[original query] |
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| Germline BRCA2 mutations and the risk of esophageal squamous cell carcinoma. Oncogene 2008 Feb 27 (9): 1290-6. Akbari M R, Malekzadeh R, Nasrollahzadeh D, Amanian D, Islami F, Li S, Zandvakili I, Shakeri R, Sotoudeh M, Aghcheli K, Salahi R, Pourshams A, Semnani S, Boffetta P, Dawsey S M, Ghadirian P, Narod S |
| Whole-exome sequencing of muscle-invasive bladder cancer identifies recurrent mutations of UNC5C and prognostic importance of DNA repair gene mutations on survival. Clinical cancer research : an official journal of the American Association for Cancer Research 2014 Dec 20 (24): 6605-17. Yap Kai Lee, Kiyotani Kazuma, Tamura Kenji, Antic Tatjana, Jang Miran, Montoya Magdeline, Campanile Alexa, Yew Poh Yin, Ganshert Cory, Fujioka Tomoaki, Steinberg Gary D, O'Donnell Peter H, Nakamura Yusu |
| 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 |
| Prevalence of DNA repair gene mutations in localized prostate cancer according to clinical and pathologic features: association of Gleason score and tumor stage. Prostate cancer and prostatic diseases 2018 Aug . Marshall Catherine Handy, Fu Wei, Wang Hao, Baras Alexander S, Lotan Tamara L, Antonarakis Emmanuel |
| 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 |
| Mutation Spectrum of Cancer-Associated Genes in Patients With Early Onset of Colorectal Cancer. Frontiers in oncology 2019 8 9 673. Zhunussova Gulnur, Afonin Georgiy, Abdikerim Saltanat, Jumanov Abai, Perfilyeva Anastassiya, Kaidarova Dilyara, Djansugurova Ley |
| 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 |
| 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 pan-cancer analysis of the oncogenic role of zinc finger protein 419 in human cancer. Frontiers in oncology 2022 12 12 1042118. Zhu Weizhen, Feng Dechao, Shi Xu, Li Dengxiong, Wei Qiang, Yang |
| 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 |
| Comprehensive laboratory diagnosis of Fanconi anaemia: comparison of cellular and molecular analysis. Journal of medical genetics 2023 3 . Joshi Gaurav, Arthur Nancy Beryl Janet, Geetha Thenral S, Datari Phaneendra Venkateswara Rao, Modak Kirti, Roy Debanjan, Chaudhury Anurag Dutta, Sundaraganesan Prasanth, Priyanka Sweety, Na Fouzia, Ramprasad Vedam, Abraham Aby, Srivastava Vivi M, Srivastava Alok, Kulkarni Uday Prakash, George Biju, Velayudhan Shaji |
| Identification of novel candidate predisposing genes in familial nonmedullary thyroid carcinoma implicating DNA damage repair pathways. International journal of cancer 2024 9 . Carolina Pires, Inês J Marques, Ana Saramago, Margarida M Moura, Marta Pojo, Rafael Cabrera, Catarina Santos, Francisco Rosário, Diana Lousa, João B Vicente, Tiago M Bandeiras, Manuel R Teixeira, Valeriano Leite, Branca M Cava |
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