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Common Pathogenic Effects of Missense Mutations in the P-Type ATPase ATP13A2 (PARK9) Associated with Early-Onset Parkinsonism

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Common Pathogenic Effects of Missense Mutations in the P-Type ATPase ATP13A2 (PARK9) Associated with Early-Onset Parkinsonism

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Identification and Characterization of Tyrosine Kinase Nonreceptor 2 Mutations in Leukemia through Integration of Kinase Inhibitor Screening and Genomic Analysis

Joint mouse-human phenome-wide association to test gene function and disease risk

A Balance between Inhibitor Binding and Substrate Processing Confers Influenza Drug Resistance

The Black cells phenotype is caused by a point mutation in the Drosophila pro-phenoloxidase 1 gene that triggers melanization and hematopoietic defects

Whole Cell Target Engagement Identifies Novel Inhibitors of Mycobacterium tuberculosis Decaprenylphosphoryl-beta-D-ribose Oxidase

Probing the Unfolded Configurations of a β-Hairpin Using Sketch-Map

A Systematic Survey of an Intragenic Epistatic Landscape

From polymers to gene regulation

The H50Q Mutation Enhances alpha-Synuclein Aggregation, Secretion, and Toxicity

A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family