Results 241 to 250 of about 8,614,620 (399)
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Paroxysmal kinesigenic dyskinesia (PKD) is the most common hereditary paroxysmal movement disorder. The PRRT2 gene is the first identified causative gene and accounts for the majority of PKD. In this study, we investigated the pathogenicity of PRRT2 variants in the splice regions. Methods Patients with clinically suspected PKD and no
Jiao‐Jiao Xu +5 more
wiley +1 more source
NEAR: neural embeddings for amino acid relationships. [PDF]
BioinformaticsOlson D +5 more
europepmc +1 more source
Amino Acid Catabolism in Plants.
Molecular Plant, 2015 Tatjana M. Hildebrandt +3 more
semanticscholar +1 more source
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Epilepsy is increasingly associated with immune dysregulation and inflammation. The T cell receptor (TCR), a key mediator of adaptive immunity, shows repertoire alterations in various immune‐mediated diseases. The unique TCR sequence serves as a molecular barcode for T cells, and clonal expansion accompanied by reduced overall TCR ...
Yong‐Won Shin +12 more
wiley +1 more source
Editorial: Aromatic Amino Acid Metabolism
Frontiers in Molecular Biosciences, 2019 Qian Han +2 more
doaj +1 more source
Amino Acid Supplementation in Fish Nutrition and Welfare. [PDF]
Animals (Basel)Aragão C, Engrola S, Costas B.
europepmc +1 more source
Lysosomal amino acid transporter SLC38A9 signals arginine sufficiency to mTORC1
Science, 2015 Shuyu Wang +17 more
semanticscholar +1 more source