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Peripheral myelin protein 22 modulates store-operated calcium channel activity, providing insights into Charcot-Marie-Tooth disease etiology

Charcot-Marie-Tooth (CMT) disease is a peripheral neuropathy associated with gene duplication and point mutations in the peripheral myelin protein 22 (PMP22) gene. However, the role of PMP22 in Schwann cell physiology and the mechanisms by which PMP22 mutations cause CMT are not well-understood. On...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Τόπος έκδοσης:J Biol Chem
Κύριοι συγγραφείς: Vanoye, Carlos G., Sakakura, Masayoshi, Follis, Rose M., Trevisan, Alexandra J., Narayan, Malathi, Li, Jun, Sanders, Charles R., Carter, Bruce D.
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: American Society for Biochemistry and Molecular Biology 2019
Θέματα:
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6690708/
https://ncbi.nlm.nih.gov/pubmed/31213528
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.RA118.006248
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