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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

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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

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Calpena-Corpas, E.; Lopez Del Amo, V.; Chakraborty M; Llamusi, B.; Artero R; Espinos, C.; Galindo, MI. (2018). 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. Disease Models & Mechanisms. 11(1). https://doi.org/10.1242/dmm.029082

Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10251/143787

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Title: 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
Author: Calpena-Corpas, Eduardo Lopez del Amo, V Chakraborty M Llamusi, B Artero R Espinos, Carmen Galindo, Máximo Ibo
UPV Unit: Universitat Politècnica de València. Departamento de Biotecnología - Departament de Biotecnologia
Issued date:
Abstract:
[EN] Members of the Junctophilin (JPH) protein family have emerged as key actors in all excitable cells, with crucial implications for human pathophysiology. In mammals, this family consists of four members (JPH1-JPH4) ...[+]
Subjects: Junctophilin , Drosophila , Cardiomyopathy , Huntington's disease , Notch
Copyrigths: Reconocimiento (by)
Source:
Disease Models & Mechanisms. (issn: 1754-8403 )
DOI: 10.1242/dmm.029082
Publisher:
The Company of Biologists
Publisher version: https://doi.org/10.1242/dmm.029082
Project ID:
info:eu-repo/grantAgreement/MINECO//PI12%2F00453/ES/Investigación traslacional y mecanismos de enfermedad en neuropatías periféricas hereditarias/
...[+]
info:eu-repo/grantAgreement/MINECO//PI12%2F00453/ES/Investigación traslacional y mecanismos de enfermedad en neuropatías periféricas hereditarias/
info:eu-repo/grantAgreement/Association Française contre les Myopathies//AFM 18540/
info:eu-repo/grantAgreement/MINECO//PI15%2F00187/ES/Avanzar en el diagnóstico, la prognosis y la terapia de enfermedades neurodegenerativas raras/
info:eu-repo/grantAgreement/GVA//PROMETEOII%2F2014%2F067/
info:eu-repo/grantAgreement/ISCIII//IR11%2FTREAT-CMT/
info:eu-repo/grantAgreement/GVA//GRISOLIAP%2F2013%2FA%2F044/
info:eu-repo/grantAgreement/MINECO//CPII14%2F00002/ES/CPII14%2F00002/
info:eu-repo/grantAgreement/ISCIII//IR11%2FTREAT-CMT/ES/Translational research, experimental medicine and therapeutics on Charcot-Marie-Tooth disease/
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Thanks:
This work was supported by project grants from Association Francaise contre les Myopathies [AFM 18540 to M.I.G.], Instituto de Salud Carlos III (ISCIII) [PI12/000453 and PI15/000187 to C.E.], Generalitat Valenciana ...[+]
Type: Artículo

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