المؤلفون: A. Bersano, S. Lanfranconi, G.B. Boncoraglio, S. Corti, D. Ronchi, G.P. Comi, CANDELISE, LIVIA, H. S. Markus, S. Quaglini, E. Arbustini, G. Micieli, F. Taroni, C. Gellera, S. Baratta, S. Penco, L. Mosca, M. Grasso, P. Carrera, M. Ferrari, C. Cereda, G. Grieco, M. Teresa Bassi, L. Obici, E. A. Parati, A. Pezzini, M. L. De Lodovici, E. P. Verrengia, G. Bono, F. Mazucchelli, D. Zarcone, M. V. Calloni, P. Perrone, B. M. Bordo, A. Colombo, A. Padovani, A. Cavallini, S. Beretta, C. Ferrarese, C. Motto, E. Agostoni, G. Molini, F. Sasanelli, M. Corato, S. Marcheselli, M. Sessa, G. Comi, N. Checcarelli, M. Guidotti, D. Uccellini, E. Capitani, L. Tancredi, M. Arnaboldi, B. Incorvaia, C. S. Tadeo, L. Fusi, G. Grampa, G. Merlini, N. Trobia, M. Braga, P. Vitali, P. Baron, C. Grond Ginsbach

المساهمون: A. Bersano, H.S. Marku, S. Quaglini, E. Arbustini, S. Lanfranconi, G. Micieli, G.B. Boncoraglio, F. Taroni, C. Gellera, S. Baratta, S. Penco, L. Mosca, M. Grasso, P. Carrera, M. Ferrari, C. Cereda, G. Grieco, S. Corti, D. Ronchi, M. Teresa Bassi, L. Obici, E.A. Parati, A. Pezzini, M.L. De Lodovici, E.P. Verrengia, G. Bono, F. Mazucchelli, D. Zarcone, M.V. Calloni, P. Perrone, B.M. Bordo, A. Colombo, A. Padovani, A. Cavallini, S. Beretta, C. Ferrarese, C. Motto, E. Agostoni, G. Molini, F. Sasanelli, M. Corato, S. Marcheselli, M. Sessa, G. Comi, N. Checcarelli, M. Guidotti, D. Uccellini, E. Capitani, L. Tancredi, M. Arnaboldi, B. Incorvaia, C.S. Tadeo, L. Fusi, G. Grampa, G. Merlini, N. Trobia, G.P. Comi, M. Braga, P. Vitali, P. Baron, C. Grond-Ginsbach, L. Candelise

مصطلحات موضوعية: CADASIL, Fabry disease, MELAS syndrome, Marfan syndrome, cerebral amyloid angiopathy, familial, genetic, stroke, Settore MED/26 - Neurologia, Settore MED/03 - Genetica Medica

Relation: info:eu-repo/semantics/altIdentifier/pmid/27245348; info:eu-repo/semantics/altIdentifier/wos/WOS:000379844900017; volume:47; issue:7; firstpage:1702; lastpage:1709; numberofpages:8; journal:STROKE; http://hdl.handle.net/2434/398137; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84976592806

الاتاحة: http://hdl.handle.net/2434/398137
https://doi.org/10.1161/STROKEAHA.115.012281

المؤلفون: Cinzia Baschirotto, Andrea Ballabio, M. Vittoria Schiaffino, Cristina Colla, M. Teresa Bassi, Claudia Puri, Marilena d’Addio, Anna Alloni, Caterina Valetti, Carlo Tacchetti, Michele De Luca, Katia Cortese

المساهمون: Schiaffino, Mv, D'Addio, M, Alloni, A, Baschirotto, C, Valetti, C, Cortese, K, Puri, C, Bassi, Mt, Colla, C, DE LUCA, M, Tacchetti, C, Ballabio, Andrea, K., Cortese, Tacchetti, Carlo, Ballabio, A.

المصدر: Nature Genetics. 23:108-112

مصطلحات موضوعية: Ocular albinism, G protein, Molecular Sequence Data, Mutation, Missense, Biology, Transfection, Models, Biological, GTP-Binding Proteins, Heterotrimeric G protein, Genetics, medicine, Animals, Humans, Amino Acid Sequence, Eye Proteins, ocular albinism, melanocyte, cell signalling, G protein-coupled receptor, Membrane Glycoproteins, Sequence Homology, Amino Acid, Intracellular Membranes, Albinism, Ocular, medicine.disease, Recombinant Proteins, Cell biology, Intracellular signal transduction, Biochemistry, Membrane protein, COS Cells, Mutation, Mutagenesis, Site-Directed, Melanocytes, Ocular albinism type 1, sense organs, Signal transduction, Lysosomes, Signal Transduction

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba1e9e42f36ede7a8abbbc2472eafb43
https://doi.org/10.1038/12715