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Mutation databases

Performance of TaqMan array card to detect TB drug resistance on direct specimens

Sayera Banu, Suporn Pholwat, Suporn Foongladda, Rattapha Chinli, Duangjai Boonlert, Sara Sabrina Ferdous, S. M. Mazidur Rahman, Arfatur Rahman, Shahriar Ahmed, Eric R. Houpt

published 04 May 2017

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Determining the role of missense mutations in the POU domain of HNF1A that reduce the DNA-binding affinity: A computational approach

Sneha P., Thirumal Kumar D., George Priya Doss C., Siva R., Hatem Zayed

published 14 Apr 2017

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Mobile Genome Express (MGE): A comprehensive automatic genetic analyses pipeline with a mobile device

Jun-Hee Yoon, Thomas W. Kim, Pedro Mendez, David M. Jablons, Il-Jin Kim

published 12 Apr 2017

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Investigation of mutations in the HBB gene using the 1,000 genomes database

Tânia Carlice-dos-Reis, Jaime Viana, Fabiano Cordeiro Moreira, Greice de Lemos Cardoso, João Guerreiro, Sidney Santos, Ândrea Ribeiro-dos-Santos

published 05 Apr 2017

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Epigenomic annotation of noncoding mutations identifies mutated pathways in primary liver cancer

Rebecca F. Lowdon, Ting Wang

published 23 Mar 2017

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The clinical features, outcomes and genetic characteristics of hypertrophic cardiomyopathy patients with severe right ventricular hypertrophy

Xiying Guo, Chaomei Fan, Lei Tian, Yanling Liu, Hongyue Wang, Shihua Zhao, Fujian Duan, Xiuling Zhang, Xing Zhao, Fengqi Wang, Hongguang Zhu, Aiqing Lin, Xia Wu, Yishi Li

published 21 Mar 2017

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The essential and downstream common proteins of amyotrophic lateral sclerosis: A protein-protein interaction network analysis

Yimin Mao, Su-Wei Kuo, Le Chen, C. J. Heckman, M. C. Jiang

published 10 Mar 2017

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Association of SMAD4 mutation with patient demographics, tumor characteristics, and clinical outcomes in colorectal cancer

Amir Mehrvarz Sarshekeh, Shailesh Advani, Michael J. Overman, Ganiraju Manyam, Bryan K. Kee, David R. Fogelman, Arvind Dasari, Kanwal Raghav, Eduardo Vilar, Shanequa Manuel, Imad Shureiqi, Robert A. Wolff, Keyur P. Patel, Raja Luthra, Kenna Shaw, Cathy Eng, Dipen M. Maru, Mark J. Routbort, Funda Meric-Bernstam, Scott Kopetz

published 07 Mar 2017

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Genomic variants reveal differential evolutionary constraints on human transglutaminases and point towards unrecognized significance of transglutaminase 2

Kiruphagaran Thangaraju, Róbert Király, Máté A. Demény, János András Mótyán, Mónika Fuxreiter, László Fésüs

published 01 Mar 2017

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A novel RNA sequencing data analysis method for cell line authentication

Erik Fasterius, Cinzia Raso, Susan Kennedy, Nora Rauch, Pär Lundin, Walter Kolch, Mathias Uhlén, Cristina Al-Khalili Szigyarto

published 13 Feb 2017

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Prognostic significance of SETBP1 mutations in myelodysplastic syndromes, chronic myelomonocytic leukemia, and chronic neutrophilic leukemia: A meta-analysis

Li-Hong Shou, Dan Cao, Xiao-Hui Dong, Qiu Fang, Ying Wu, Yan Zhang, Ju-Ping Fei, Bao-Lian Xu

published 03 Feb 2017

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No Evidence for Pathogenic Role of UBQLN2 Mutations in Sporadic Amyotrophic Lateral Sclerosis in the Mainland Chinese Population

Xiao Huang, Shen Shen, Dongsheng Fan

published 26 Jan 2017

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The Influence of BRAF and KRAS Mutation Status on the Association between Aspirin Use and Survival after Colon Cancer Diagnosis

Martine A. Frouws, Marlies S. Reimers, Marloes Swets, Esther Bastiaannet, Bianca Prinse, Ronald van Eijk, Valery E. P. P. Lemmens, Myrthe P. P. van Herk-Sukel, Tom van Wezel, Peter J. K. Kuppen, Hans Morreau, Cornelis J. H. van de Velde, Gerrit-Jan Liefers

published 26 Jan 2017

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