Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: NDRG1[original query] |
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Mutation screening of the N-myc downstream-regulated gene 1 (NDRG1) in patients with Charcot-Marie-Tooth Disease. Human mutation 2003 Aug 22 (2): 129-35. Hunter Michael, Bernard Rafaëlle, Freitas Elizabeth, Boyer Amandine, Morar Bharti, Martins Ian J, Tournev Ivailo, Jordanova Albena, Guergelcheva Velina, Ishpekova Boryana, Kremensky Ivo, Nicholson Garth, Schlotter Beate, Lochmüller Hanns, Voit Thomas, Colomer Jaume, Thomas P K, Levy Nicolas, Kalaydjieva Lu |
[Update on hereditary neuropathy]. Rinsho shinkeigaku = Clinical neurology 2005 1 44 (11): 991-4. Nakagawa Masanori, Takashima Hiros |
Single nucleotide polymorphisms in Wnt signaling and cell death pathway genes and susceptibility to colorectal cancer. Carcinogenesis 2010 Aug 31 (8): 1381-6. Frank Bernd, Hoffmeister Michael, Klopp Norman, Illig Thomas, Chang-Claude Jenny, Brenner Herma |
Genotypic and phenotypic spectrum of the most common causative genes of Charcot-Marie-Tooth disease in Hungarian patients. Neuromuscular disorders : NMD 2017 11 28 (1): 38-43. Milley György Máté, Varga Edina Timea, Grosz Zoltán, Nemes Csilla, Arányi Zsuzsanna, Boczán Judit, Diószeghy Péter, Molnár Mária Judit, Gál Ani |
Network-directed cis-mediator analysis of normal prostate tissue expression profiles reveals downstream regulatory associations of prostate cancer susceptibility loci. Oncotarget 2017 Oct 8 (49): 85896-85908. Larson Nicholas B, McDonnell Shannon K, Fogarty Zach, Larson Melissa C, Cheville John, Riska Shaun, Baheti Saurabh, Weber Alexandra M, Nair Asha A, Wang Liang, O'Brien Daniel, Davila Jaime, Schaid Daniel J, Thibodeau Stephen |
Determination of the mutational landscape in Taiwanese patients with papillary thyroid cancer by whole-exome sequencing. Human pathology 2018 May . Chang Chun-Chi, Chang Ya-Sian, Huang Hsi-Yuan, Yeh Kun-Tu, Liu Ta-Chih, Chang Jan-Gow |
Genetic spectrum and clinical profiles in a southeast Chinese cohort of Charcot-Marie-Tooth disease. Clinical genetics 2019 Aug . Chen Cong-Xin, Dong Hai-Lin, Wei Qiao, Li Li-Xi, Yu Hao, Li Jia-Qi, Liu Gong-Lu, Li Hong-Fu, Bai Ge, Ma Huan, Wu Zhi-Yi |
Integrative Analysis of Hypoxia-Associated Signature in Pan-Cancer. iScience 2020 8 23 (9): 101460. Zhang Qian, Huang Rui, Hu Hanqing, Yu Lei, Tang Qingchao, Tao Yangbao, Liu Zheng, Li Jiaying, Wang Gui |
Investigation of Mutations in Exon 14 of SH3TC2 Gene and Exon 7 of NDRG1 Gene in Iranian Charcot-Marie-Tooth Disease Type 4 (CMT4D) Patients. Iranian journal of child neurology 2020 4 14 (2): 93-100. Moosavi Rahmaneh Sadat, Jahangir Sooltani Niloofar, Houshmand Masso |
The Importance of Multiple Gene Analysis for Diagnosis and Differential Diagnosis in Charcot Marie Tooth Disease. Turkish neurosurgery 2021 6 31 (6): 888-895. Yalcintepe Sinem, Gurkan Hakan, Dogan Ipek Gungor, Demir Selma, Sag Sebnem Ozemri, Kabayegit Zehra Manav, Atli Emine Ikbal, Atli Engin, Eker Damla, Temel Sehime Guls |
The Influence of NDRG1 Single Nucleotide Polymorphisms on Glioma Risk and Prognosis in Chinese Han Population. Cellular and molecular neurobiology 2021 Mar . Yang Yonghui, Cheng Yimin, Yang Liting, Shi Guangyao, Chen Peng, Li Liang, Fang Hangrong, Chen Chao, Jin Tian |
Tolerability of Eribulin and correlation between polymorphisms and neuropathy in an unselected population of female patients with metastatic breast cancer: results of the multicenter, single arm, phase IV PAINTER study. Breast cancer research : BCR 2022 10 24 (1): 71. La Verde Nicla, Damia Giovanna, Garrone Ornella, Santini Daniele, Fabi Alessandra, Ciccarese Mariangela, Generali Daniele Giulio, Nunzi Martina, Poletto Elena, Ferraris Elisa, Cretella Elisabetta, Scandurra Giuseppa, Meattini Icro, Bertolini Alessandro Stefano, Cavanna Luigi, Collovà Elena, Romagnoli Emanuela, Rulli Eliana, Legramandi Lorenzo, Guffanti Federica, Bramati Annalisa, Moretti Anna, Cassano Alessandra, Vici Patrizia, Torri Valter, Farina Gabriella, |
Inferring Homologous Recombination Deficiency of Ovarian Cancer From the Landscape of Copy Number Variation at Subchromosomal and Genetic Resolutions. Frontiers in oncology 2022 1 11 772604. Zhang Meng, Ma Si-Cong, Tan Jia-Le, Wang Jian, Bai Xue, Dong Zhong-Yi, Zhang Qing-X |
Genetic Polymorphisms Associated with Vincristine Pharmacokinetics and Vincristine-Induced Peripheral Neuropathy in Pediatric Oncology Patients. Cancers 2022 Jul 14 (14): . van de Velde Mirjam E, Uittenboogaard Aniek, Yang Wenjian, Bonten Erik, Cheng Cheng, Pei Deqing, van den Berg Marleen H, van der Sluis Inge M, van den Bos Cor, Abbink Floor C H, van den Heuvel-Eibrink Marry M, Segers Heidi, Chantrain Christophe, van der Werff Ten Bosch Jutte, Willems Leen, Evans William E, Kaspers Gertjan J |
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- Page last updated:Apr 22, 2024
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