Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Tornero-Écija A"'
Autor:
Olivier Vincent, Laura Antón-Esteban, Miranda Bueno-Arribas, Alba Tornero-Écija, María-Ángeles Navas, Ricardo Escalante
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
WIPIs are a conserved family of proteins with a characteristic 7-bladed β-propeller structure. They play a prominent role in autophagy, but also in other membrane trafficking processes. Mutations in human WIPI4 cause several neurodegenerative diseas
Externí odkaz:
https://doaj.org/article/6b779457268749cea266ff1a9f2b516a
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Publikováno v:
Disease Models & Mechanisms, Vol 12, Iss 2 (2019)
Members of the VPS13 family are associated with various human diseases. In particular, the loss of function of VPS13A leads to chorea-acanthocytosis (ChAc), a rare neurodegenerative disease without available curative treatments. Autophagy has been co
Externí odkaz:
https://doaj.org/article/ca1058b6efb64a2780de092cbc70e109
Publikováno v:
Journal of Cellular and Molecular Medicine.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eea92eeed7f0eb50877b6b6b1bb1510f
https://doi.org/10.1111/jcmm.17768
https://doi.org/10.1111/jcmm.17768
Autor:
Alba Tornero-Écija, Antonia Zapata-del-Baño, Laura Antón-Esteban, Olivier Vincent, Ricardo Escalante
Publikováno v:
Life Science Alliance. 6:e202201852
Human VPS13 proteins are implicated in severe neurological diseases. These proteins play an important role in lipid transport at membrane contact sites between different organelles. Identification of adaptors that regulate the subcellular localizatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fb59ac8b55cc6ff20f996cbc8e84b68
https://doi.org/10.26508/lsa.202201852
https://doi.org/10.26508/lsa.202201852
Autor:
Escalante, Ricardo, Tornero-Écija, Alba, Tábara, Luis-Carlos, Bueno Arribas, M., Antón-Esteban, Laura, Navarro-Gómez, Cristina, Sánchez, Irene, Blanca, Irene, Cruz-Cuevas, Celia, Navas, María-Angeles, Vincent, Olivier
Trabajo presentado en First BPAN disease symposium in France, celebrado en Lyon (Francia) del 13 al 14 de mayo de 2022.
WIPIs are a conserved family of proteins with a characteristic 7-bladed b-helix structure. Mutations in human WIPI4 cause BPA
WIPIs are a conserved family of proteins with a characteristic 7-bladed b-helix structure. Mutations in human WIPI4 cause BPA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1106::47c34e6db65f7608e847c1c1cd3e366a
http://hdl.handle.net/10261/304385
http://hdl.handle.net/10261/304385
Autor:
Miranda Bueno-Arribas, Ricardo Escalante, María-Angeles Navas, Alba Tornero-Écija, Laura Antón-Esteban, Olivier Vincent
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology
© 2021 Vincent, Antón-Esteban, Bueno-Arribas, Tornero-Écija, Navas and Escalante.
WIPIs are a conserved family of proteins with a characteristic 7-bladed β-propeller structure. They play a prominent role in autophagy, but also in other membr
WIPIs are a conserved family of proteins with a characteristic 7-bladed β-propeller structure. They play a prominent role in autophagy, but also in other membr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5879044591986e1e0c7719a6dd1743f1
http://hdl.handle.net/10261/265590
http://hdl.handle.net/10261/265590
Autor:
Laura Antón-Esteban, Olivier Vincent, Alba Tornero-Écija, Irene Sánchez, Cristina Navarro-Gómez, Luis-Carlos Tábara, Miranda Bueno-Arribas, Ricardo Escalante
Publikováno v:
Autophagy. 18(3)
PROPPINs are conserved PtdIns3P-binding proteins required for autophagosome biogenesis that fold into a characteristic group of seven-bladed beta-propellers. Mutations in WDR45/WIPI4, a human member of this family, lead to BPAN, a rare form of neurod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8425670d0ea4d12b19537dc872d1b8a
https://pubmed.ncbi.nlm.nih.gov/34328055
https://pubmed.ncbi.nlm.nih.gov/34328055
Akademický článek
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