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deformities ultimately leaving them severely disabled. This lifelong disorder is currently incurable. The most prominent protein family implicated in the etiology of CMT are aminoacyl-tRNA synthetases (ARS
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include previous research in computational modeling, machine learning applications in genomics, protein structure, participation in bioinformatics projects, or hands-on experience with AI tools applied
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the genetic etiology and developing diagnostics and treatment methods for these diseases. Approaches range from human genetics, genomics, protein biochemistry and neuronal and glial cell biology to integrative
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