Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Sciandra F. 3"'
Autor:
Signorino G (1), Covaceuszach S (2), Bozzi M (1), (3), Hübner W (4), Mönkemöller V (4), Konarev PV (5), Cassetta A (2), Brancaccio A (3), (6), Sciandra F (3).
Publikováno v:
Human mutation 39 (2018): 266–280.
info:cnr-pdr/source/autori:Signorino G (1), Covaceuszach S (2), Bozzi M (1),(3), Hübner W (4), Mönkemöller V (4), Konarev PV (5), Cassetta A (2), Brancaccio A (3),(6), Sciandra F (3)./titolo:A dystroglycan mutation (p.Cys66uPhe) associated to muscle-eye-brain disease with multicystic leukodystrophy results in ER-retention of the mutant protein/doi:/rivista:Human mutation/anno:2018/pagina_da:266/pagina_a:280/intervallo_pagine:266–280/volume:39
info:cnr-pdr/source/autori:Signorino G (1), Covaceuszach S (2), Bozzi M (1),(3), Hübner W (4), Mönkemöller V (4), Konarev PV (5), Cassetta A (2), Brancaccio A (3),(6), Sciandra F (3)./titolo:A dystroglycan mutation (p.Cys66uPhe) associated to muscle-eye-brain disease with multicystic leukodystrophy results in ER-retention of the mutant protein/doi:/rivista:Human mutation/anno:2018/pagina_da:266/pagina_a:280/intervallo_pagine:266–280/volume:39
Dystroglycan (DG) is a cell adhesion complex composed by two subunits, the highly glycosylated ?-DG and the transmembrane ?-DG. In skeletal muscle, DG is involved in dystroglycanopathies, a group of heterogeneous muscular dystrophies characterized by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::adbed9846b9650783ff2d45322dc2d02
http://www.cnr.it/prodotto/i/390142
http://www.cnr.it/prodotto/i/390142
Autor:
Gioia M (1, Fasciglione GF (1, Sbardella D (1, Sciandra F (3), Casella M (4), Camerini S (4), Crescenzi M (4), Gori A (5), Tarantino U (1), Cozza P (1), Brancaccio A (3, Coletta M (1, Bozzi M (3, 7).
Publikováno v:
Gioia, M, Fasciglione, G F, Sbardella, D, Sciandra, F, Casella, M, Camerini, S, Crescenzi, M, Gori, A, Tarantino, U, Cozza, P, Brancaccio, A, Coletta, M & Bozzi, M 2018, ' The enzymatic processing of α-dystroglycan by MMP-2 is controlled by two anchoring sites distinct from the active site ', PLoS ONE, vol. 13, no. 2, pp. e0192651 . https://doi.org/10.1371/journal.pone.0192651
PloS one 15 (2018).
info:cnr-pdr/source/autori:Gioia M (1,2), Fasciglione GF (1,2), Sbardella D (1,2), Sciandra F (3), Casella M (4), Camerini S (4), Crescenzi M (4), Gori A (5), Tarantino U (1), Cozza P (1), Brancaccio A (3,6), Coletta M (1,2), Bozzi M (3,7)./titolo:The enzymatic processing of ?-dystroglycan by MMP-2 is controller by two anchoring sites distinct from the active site/doi:/rivista:PloS one/anno:2018/pagina_da:/pagina_a:/intervallo_pagine:/volume:15
PLoS ONE
PLoS ONE, Vol 13, Iss 2, p e0192651 (2018)
PloS one 13 (2018). doi:10.1371/journal.pone.0192651
info:cnr-pdr/source/autori:Gioia M.; Fasciglione G.F.; Sbardella D.; Sciandra F.; Casella M.; Camerini S.; Crescenzi M.; Gori A.; Tarantino U.; Cozza P.; Brancaccio A.; Coletta M.; Bozzi M./titolo:The enzymatic processing of ?-dystroglycan by MMP-2 is controlled by two anchoring sites distinct from the active site/doi:10.1371%2Fjournal.pone.0192651/rivista:PloS one/anno:2018/pagina_da:/pagina_a:/intervallo_pagine:/volume:13
PloS one 15 (2018).
info:cnr-pdr/source/autori:Gioia M (1,2), Fasciglione GF (1,2), Sbardella D (1,2), Sciandra F (3), Casella M (4), Camerini S (4), Crescenzi M (4), Gori A (5), Tarantino U (1), Cozza P (1), Brancaccio A (3,6), Coletta M (1,2), Bozzi M (3,7)./titolo:The enzymatic processing of ?-dystroglycan by MMP-2 is controller by two anchoring sites distinct from the active site/doi:/rivista:PloS one/anno:2018/pagina_da:/pagina_a:/intervallo_pagine:/volume:15
PLoS ONE
PLoS ONE, Vol 13, Iss 2, p e0192651 (2018)
PloS one 13 (2018). doi:10.1371/journal.pone.0192651
info:cnr-pdr/source/autori:Gioia M.; Fasciglione G.F.; Sbardella D.; Sciandra F.; Casella M.; Camerini S.; Crescenzi M.; Gori A.; Tarantino U.; Cozza P.; Brancaccio A.; Coletta M.; Bozzi M./titolo:The enzymatic processing of ?-dystroglycan by MMP-2 is controlled by two anchoring sites distinct from the active site/doi:10.1371%2Fjournal.pone.0192651/rivista:PloS one/anno:2018/pagina_da:/pagina_a:/intervallo_pagine:/volume:13
Dystroglycan (DG) is a membrane receptor, belonging to the dystrophin-glycoprotein complex (DGC) and formed by two subunits, α-dystroglycan (α-DG) and β-dystroglycan (β -DG). The C-terminal domain of α-DG and the N-terminal extracellular domain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a90105657f5f2588120091d7187b47da
https://doi.org/10.1371/journal.pone.0192651
https://doi.org/10.1371/journal.pone.0192651
Autor:
Bozzi M. 1, Bianchi M. 2, Sciandra F. 3, Paci M. 4, Giardina B. 5, Brancaccio A. 6, Cicero D.O. 7.
Publikováno v:
Biochemistry (Easton) 42 (2003): 13717–13724.
info:cnr-pdr/source/autori:Bozzi M. 1, Bianchi M. 2, Sciandra F. 3, Paci M. 4, Giardina B. 5, Brancaccio A. 6, Cicero D.O. 7./titolo:Structural characterization by NMR of the natively unfolded extracellular domain of beta-dystroglycan: toward the identification of the binding epitope for alpha-dystroglycan/doi:/rivista:Biochemistry (Easton)/anno:2003/pagina_da:13717/pagina_a:13724/intervallo_pagine:13717–13724/volume:42
info:cnr-pdr/source/autori:Bozzi M. 1, Bianchi M. 2, Sciandra F. 3, Paci M. 4, Giardina B. 5, Brancaccio A. 6, Cicero D.O. 7./titolo:Structural characterization by NMR of the natively unfolded extracellular domain of beta-dystroglycan: toward the identification of the binding epitope for alpha-dystroglycan/doi:/rivista:Biochemistry (Easton)/anno:2003/pagina_da:13717/pagina_a:13724/intervallo_pagine:13717–13724/volume:42
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::910b3f0152bf2a0364cea2d2aca64155
http://www.cnr.it/prodotto/i/17308
http://www.cnr.it/prodotto/i/17308