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

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

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Lopez Del Amo, V.; Palomino-Schätzlein, M.; Seco-Cervera, M.; Garcia-Gimenez, JL.; Pallardó-Calatayud, FV.; Pineda-Lucena, A.; Galindo-Orozco, MI. (2017). A Drosophila model of GDAP1 function reveals the involvement of insulin signalling in the mitochondria-dependent neuromuscular degeneration. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1863(3):801-809. https://doi.org/10.1016/j.bbadis.2017.01.003

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Title: A Drosophila model of GDAP1 function reveals the involvement of insulin signalling in the mitochondria-dependent neuromuscular degeneration
Author: Lopez del Amo, V Palomino-Schätzlein, Martina Seco-Cervera, Marta Garcia-Gimenez, José Luis Pallardó-Calatayud, Federico V. Pineda-Lucena, Antonio Galindo-Orozco, Máximo Ibo
UPV Unit: Universitat Politècnica de València. Departamento de Biotecnología - Departament de Biotecnologia
Issued date:
Abstract:
[EN] Charcot-Marie-Tooth disease is a rare peripheral neuropathy for which there is no specific treatment. Some forms of Charcot-Marie-Tooth are due to mutations in the GDAP1 gene. A striking feature of mutations in GDAP1 ...[+]
Subjects: GDAP1 , Charcot-Marie-Tooth , Mitochondria , Insulin
Copyrigths: Reserva de todos los derechos
Source:
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. (issn: 0925-4439 )
DOI: 10.1016/j.bbadis.2017.01.003
Publisher:
Elsevier
Publisher version: https://doi.org/10.1016/j.bbadis.2017.01.003
Project ID:
ISCIII/IR11/TREAT-CMT
info:eu-repo/grantAgreement/MINECO//SAF2014-53977-R/ES/HERRAMIENTAS DE RMN PARA EL DESARROLLO DE UNA PLATAFORMA PARA LA IDENTIFIC. DE DIANAS, LA EVAL. DE FARMACOS Y LA PERSONAL. DE TRATAMIENTOS BASADA EN APROX. METABOLOMICAS/
Association Française contre les Myopathies/AFM 18540
IRDiRC/IR11/TREAT-CMT
Thanks:
This work was supported by a project grant from the Association Francaise contre les Myopathies [AFM 18540 to M.I.G]; a collaborative grant from International Rare Diseases Research consortium (IRDiRC) and Institute de ...[+]
Type: Artículo

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