Additional file 3 of Protein signature of human skin fibroblasts allows the study of the molecular etiology of rare neurological diseases

Autor: Hentschel, Andreas, Czech, Artur, Münchberg, Ute, Freier, Erik, Schara-Schmidt, Ulrike, Sickmann, Albert, Reimann, Jens, Roos, Andreas
Rok vydání: 2021
DOI: 10.6084/m9.figshare.13843978.v1
Popis: Additional file 3: Table 3. List of proteins affected by bi-allelic c.762delC AAAS mutation in whole protein extracts of human skin fibroblasts identified by global proteomic profiling: 228 proteins were found to be increased whereas 156 were decreased in the nuclear fractions of patient-derived cells. For each protein, the predicted function as well as the subcellular localization ( www.uniprot.org ) is provided.
Databáze: OpenAIRE