Unusual laminin alpha2 processing in myoblasts from a patient with a novel variant of congenital muscular dystrophy.

Lattanzi, G; Muntoni, F; Sabatelli, P; Squarzoni, S; Maraldi, N M; Cenni, V; Villanova, M; Columbaro, M; Merlini, L; Marmiroli, S

Lattanzi, G; Muntoni, F; Sabatelli, P; Squarzoni, S; Maraldi, N M; Cenni, V; Villanova, M; Columbaro, M; Merlini, L; Marmiroli, S.

Affiliation

Lattanzi G; Institute of Normal and Pathological Cytomorphology, CNR, Bologna, Italy.

Biochem Biophys Res Commun ; 277(3): 639-42, 2000 Nov 02.

Article in En | MEDLINE | ID: mdl-11062006

Subject(s)

Laminin/metabolism; Muscular Dystrophies/metabolism; Cell Differentiation; Child, Preschool; Female; Humans; Matrix Metalloproteinase 2/metabolism; Matrix Metalloproteinases/metabolism; Matrix Metalloproteinases, Membrane-Associated; Metalloendopeptidases/metabolism; Muscular Dystrophies/enzymology; Muscular Dystrophies/pathology

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Collection: 01-internacional Database: MEDLINE Main subject: Laminin / Muscular Dystrophies Type of study: Prognostic_studies Limits: Child, preschool / Female / Humans Language: En Journal: Biochem Biophys Res Commun Year: 2000 Type: Article Affiliation country: Italy

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