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Insertion mutation

Targeted Exon Sequencing Successfully Discovers Rare Causative Genes and Clarifies the Molecular Epidemiology of Japanese Deafness Patients

Maiko Miyagawa, Takehiko Naito, [ ... ], Shin-ichi Usami

Identification of a Lifespan Extending Mutation in the Schizosaccharomyces pombe Cyclin Gene clg1⁺ by Direct Selection of Long-Lived Mutants

Bo-Ruei Chen, Yanhui Li, Jessica R. Eisenstatt, Kurt W. Runge

Heritable and Precise Zebrafish Genome Editing Using a CRISPR-Cas System

Woong Y. Hwang, Yanfang Fu, [ ... ], Jing-Ruey Joanna Yeh

A Reporter Screen in a Human Haploid Cell Line Identifies CYLD as a Constitutive Inhibitor of NF-κB

Clarissa C. Lee, Jan E. Carette, Thijn R. Brummelkamp, Hidde L. Ploegh

Trends in Genotypic HIV-1 Antiretroviral Resistance between 2006 and 2012 in South African Patients Receiving First- and Second-Line Antiretroviral Treatment Regimens

Gert U. Van Zyl, Tommy F. Liu, [ ... ], Robert W. Shafer

Mutational Analysis of Hedgehog Signaling Pathway Genes in Human Malignant Mesothelioma

Chuan Bian Lim, Cecilia M. Prêle, [ ... ], Steven E. Mutsaers

Longitudinal Analysis of CCR5 and CXCR4 Usage in a Cohort of Antiretroviral Therapy-Naïve Subjects with Progressive HIV-1 Subtype C Infection

Martin R. Jakobsen, Kieran Cashin, [ ... ], Paul R. Gorry

nfxB as a Novel Target for Analysis of Mutation Spectra in Pseudomonas aeruginosa

Mariela R. Monti, Natalia R. Morero, Virginia Miguel, Carlos E. Argaraña

Novel Mutations in the SCNN1A Gene Causing Pseudohypoaldosteronism Type 1

Jian Wang, Tingting Yu, [ ... ], Qihua Fu

The Role of Recombination in the Origin and Evolution of Alu Subfamilies

Ana Teixeira-Silva, Raquel M. Silva, [ ... ], Luísa Azevedo

Experimental Evolution Reveals Genome-Wide Spectrum and Dynamics of Mutations in the Rice Blast Fungus, Magnaporthe oryzae

Junhyun Jeon, Jaeyoung Choi, [ ... ], Yong-Hwan Lee

Prognostic and Predictive Value of KRAS Mutations in Advanced Non-Small Cell Lung Cancer

Jong-Mu Sun, Deok Won Hwang, [ ... ], Keunchil Park

Comprehensive Genetic Screening of KCNQ4 in a Large Autosomal Dominant Nonsyndromic Hearing Loss Cohort: Genotype-Phenotype Correlations and a Founder Mutation

Takehiko Naito, Shin-ya Nishio, [ ... ], Shin-ichi Usami

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