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Items: 4

1.

Corrigendum to "A Drosophila model of GDAP1 function reveals the involvement of insulin signalling in the mitochondria-dependent neuromuscular degeneration" [Biochim. Biophys. Acta 1863 (2017) 801-809].

López Del Amo V, Palomino-Schätzlein M, Seco-Cervera M, García-Giménez JL, Pallardó FV, Pineda-Lucena A, Galindo MI.

Biochim Biophys Acta Mol Basis Dis. 2019 Jan;1865(1):261. doi: 10.1016/j.bbadis.2018.11.001. Epub 2018 Nov 10. No abstract available.

PMID:
30424922
2.

The Drosophila junctophilin gene is functionally equivalent to its four mammalian counterparts and is a modifier of a Huntingtin poly-Q expansion and the Notch pathway.

Calpena E, López Del Amo V, Chakraborty M, Llamusí B, Artero R, Espinós C, Galindo MI.

Dis Model Mech. 2018 Jan 17;11(1). pii: dmm029082. doi: 10.1242/dmm.029082.

3.

A Drosophila model of GDAP1 function reveals the involvement of insulin signalling in the mitochondria-dependent neuromuscular degeneration.

López Del Amo V, Palomino-Schätzlein M, Seco-Cervera M, García-Giménez JL, Pallardó FV, Pineda-Lucena A, Galindo MI.

Biochim Biophys Acta Mol Basis Dis. 2017 Mar;1863(3):801-809. doi: 10.1016/j.bbadis.2017.01.003. Epub 2017 Jan 6. Erratum in: Biochim Biophys Acta Mol Basis Dis. 2019 Jan;1865(1):261.

4.

Mitochondrial defects and neuromuscular degeneration caused by altered expression of Drosophila Gdap1: implications for the Charcot-Marie-Tooth neuropathy.

López Del Amo V, Seco-Cervera M, García-Giménez JL, Whitworth AJ, Pallardó FV, Galindo MI.

Hum Mol Genet. 2015 Jan 1;24(1):21-36. doi: 10.1093/hmg/ddu416. Epub 2014 Aug 13.

PMID:
25122658

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