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Lack of GDAP1 induces neuronal calcium and mitochondrial defects in a knockout mouse model of charcot-marie-tooth neuropathy.
Barneo-Muñoz M, Juárez P, Civera-Tregón A, Yndriago L, Pla-Martin D, Zenker J, Cuevas-Martín C, Estela A, Sánchez-Aragó M, Forteza-Vila J, Cuezva JM, Chrast R, Palau F. Barneo-Muñoz M, et al. PLoS Genet. 2015 Apr 10;11(4):e1005115. doi: 10.1371/journal.pgen.1005115. eCollection 2015 Apr. PLoS Genet. 2015. PMID: 25860513 Free PMC article.
Silencing of the Charcot-Marie-Tooth disease-associated gene GDAP1 induces abnormal mitochondrial distribution and affects Ca2+ homeostasis by reducing store-operated Ca2+ entry.
Pla-Martín D, Rueda CB, Estela A, Sánchez-Piris M, González-Sánchez P, Traba J, de la Fuente S, Scorrano L, Renau-Piqueras J, Alvarez J, Satrústegui J, Palau F. Pla-Martín D, et al. Neurobiol Dis. 2013 Jul;55:140-51. doi: 10.1016/j.nbd.2013.03.010. Epub 2013 Mar 28. Neurobiol Dis. 2013. PMID: 23542510
Reshaping membranes to build mitochondrial DNA.
Pla-Martin D, Wiesner RJ. Pla-Martin D, et al. PLoS Genet. 2019 Jun 6;15(6):e1008140. doi: 10.1371/journal.pgen.1008140. eCollection 2019 Jun. PLoS Genet. 2019. PMID: 31170157 Free PMC article. No abstract available.
19 results