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Mutation

FHA-Mediated Cell-Substrate and Cell-Cell Adhesions Are Critical for Bordetella pertussis Biofilm Formation on Abiotic Surfaces and in the Mouse Nose and the Trachea

Diego O. Serra, Matt S. Conover, [ ... ], Rajendar Deora

Identification of Sequence Variants in Genetic Disease-Causing Genes Using Targeted Next-Generation Sequencing

Xiaoming Wei, Xiangchun Ju, [ ... ], Jian Huang

Bacterial Niche-Specific Genome Expansion Is Coupled with Highly Frequent Gene Disruptions in Deep-Sea Sediments

Yong Wang, Jiang Ke Yang, [ ... ], Pei-Yuan Qian

Collagen XXVII Organises the Pericellular Matrix in the Growth Plate

Darren A. Plumb, Laila Ferrara, [ ... ], Raymond P. Boot-Handford

The Mutational Spectrum in a Cohort of Charcot-Marie-Tooth Disease Type 2 among the Han Chinese in Taiwan

Kon-Ping Lin, Bing-Wen Soong, [ ... ], Yi-Chung Lee

Inhibitors of Alphavirus Entry and Replication Identified with a Stable Chikungunya Replicon Cell Line and Virus-Based Assays

Leena Pohjala, Age Utt, [ ... ], Päivi Tammela

Comparison of Dysferlin Expression in Human Skeletal Muscle with That in Monocytes for the Diagnosis of Dysferlin Myopathy

Eduard Gallardo, Noemi de Luna, [ ... ], Isabel Illa

Clinical and Functional Characterization of URAT1 Variants

Velibor Tasic, Ann Marie Hynes, [ ... ], John A. Sayer

STAT1 Hyperphosphorylation and Defective IL12R/IL23R Signaling Underlie Defective Immunity in Autosomal Dominant Chronic Mucocutaneous Candidiasis

Sanne P. Smeekens, Theo S. Plantinga, [ ... ], Mihai G. Netea

Identification of a Novel Gene for Biosynthesis of a Bacteroid-Specific Electron Carrier Menaquinone

Fuli Xie, Guojun Cheng, [ ... ], Youguo Li

Reduced Selective Constraint in Endosymbionts: Elevation in Radical Amino Acid Replacements Occurs Genome-Wide

Jennifer J. Wernegreen

Heritable Targeted Inactivation of Myostatin Gene in Yellow Catfish (Pelteobagrus fulvidraco) Using Engineered Zinc Finger Nucleases

Zhangji Dong, Jiachun Ge, [ ... ], Qingshun Zhao

Cardiac Alpha-Myosin (MYH6) Is the Predominant Sarcomeric Disease Gene for Familial Atrial Septal Defects

Maximilian G. Posch, Stephan Waldmuller, [ ... ], Cemil Özcelik

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