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Mutation

Transgenic and Mutation-Based Suppression of a Berberine Bridge Enzyme-Like (BBL) Gene Family Reduces Alkaloid Content in Field-Grown Tobacco

Ramsey S. Lewis, Harry O. Lopez, [ ... ], Ralph E. Dewey

Significance of Four Methionine Sulfoxide Reductases in Staphylococcus aureus

Vineet K. Singh, Manisha Vaish, [ ... ], Jackob Moskovitz

Two Novel Mutations in Myosin Binding Protein C Slow Causing Distal Arthrogryposis Type 2 in Two Large Han Chinese Families May Suggest Important Functional Role of Immunoglobulin Domain C2

Xuefu Li, Bomeng Zhong, [ ... ], Miao Jiang

Affected Kindred Analysis of Human X Chromosome Exomes to Identify Novel X-Linked Intellectual Disability Genes

Tejasvi S. Niranjan, Cindy Skinner, [ ... ], Tao Wang

High Prevalence of the K65R Mutation in HIV-1 Subtype C Infected Patients Failing Tenofovir-Based First-Line Regimens in South Africa

Lindiwe Skhosana, Kim Steegen, [ ... ], Wendy S. Stevens

Single Site Suppressors of a Fission Yeast Temperature-Sensitive Mutant in cdc48 Identified by Whole Genome Sequencing

Irina N. Marinova, Jacob Engelbrecht, [ ... ], Rasmus Hartmann-Petersen

Characterization of RanBPM Molecular Determinants that Control Its Subcellular Localization

Louisa M. Salemi, Sandra O. Loureiro, Caroline Schild-Poulter

Homozygous STIL Mutation Causes Holoprosencephaly and Microcephaly in Two Siblings

Charlotte Mouden, Marie de Tayrac, [ ... ], Véronique David

Proteasome 19S RP Binding to the Sec61 Channel Plays a Key Role in ERAD

Marie-Luise Kaiser, Karin Römisch

Canine Disorder Mirrors Human Disease: Exonic Deletion in HES7 Causes Autosomal Recessive Spondylocostal Dysostosis in Miniature Schnauzer Dogs

Cali E. Willet, Mariano Makara, [ ... ], Claire M. Wade

Identification of Several Mutations in ATP2C1 in Lebanese Families: Insight into the Pathogenesis of Hailey-Hailey Disease

Waed Btadini, Ossama K. Abou Hassan, [ ... ], Mazen Kurban

An Efficient and Comprehensive Strategy for Genetic Diagnostics of Polycystic Kidney Disease

Tobias Eisenberger, Christian Decker, [ ... ], Carsten Bergmann

Whole Genome Sequencing Reveals a De Novo SHANK3 Mutation in Familial Autism Spectrum Disorder

Sergio I. Nemirovsky, Marta Córdoba, [ ... ], Marcelo A. Kauffman

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