Loss of N-Glycanase 1 Alters Transcriptional and Translational Regulation in K562 Cell Lines

N-Glycanase 1 (NGLY1) deficiency is an ultra-rare, complex and devastating neuromuscular disease. Patients display multi-organ symptoms including developmental delays, movement disorders, seizures, constipation and lack of tear production. NGLY1 is a deglycosylating protein involved in the degradati...

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Dades bibliogràfiques
Publicat a:G3 (Bethesda)
Autors principals: Mueller, William F., Jakob, Petra, Sun, Han, Clauder-Münster, Sandra, Ghidelli-Disse, Sonja, Ordonez, Diana, Boesche, Markus, Bantscheff, Marcus, Collier, Paul, Haase, Bettina, Benes, Vladimir, Paulsen, Malte, Sehr, Peter, Lewis, Joe, Drewes, Gerard, Steinmetz, Lars M.
Format: Artigo
Idioma:Inglês
Publicat: Genetics Society of America 2020
Matèries:
Investigations
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7202010/
https://ncbi.nlm.nih.gov/pubmed/32265286
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/g3.119.401031
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