Unusual Laminin α2 Processing in Myoblasts from a Patient with a Novel Variant of Congenital Muscular Dystrophy

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

Publisher： Elsevier

ISSN： 0006-291X

Source： Biochemical and Biophysical Research Communications, Vol.277, Iss.3, 2000-11, pp. : 639-642

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Muscular dystrophy linked to a mutation in laminin

By Xu H. Wu X.-R. Wewer U.M. Engvall E.

Trends in Cell Biology, Vol. 5, Iss. 2, 1995-02 ,pp. : 59-59

Elsevier

Access to resources Recommend Favorite

The incorporation of the novel histone variant H2AL2 confers unusual structural and functional properties of the nucleosome

By Syed Sajad Hussain

Nucleic Acids Research, Vol. 37, Iss. 14, 2009-08 ,pp. : 4684-4695

Oxford University Press

Access to resources Recommend Favorite

The role of defective glycosylation in congenital muscular dystrophy: SPECIAL ISSUE ON GLYCOCONJUGATES AND CELL SIGNALING, PART 3 (Guest Editor: Subhash Basu)

By Schachter Harry Vajsar Jiri Zhang Wenli

Glycoconjugate Journal, Vol. 20, Iss. 5, 2003-01 ,pp. : 291-300

Springer Publishing Company

Access to resources Recommend Favorite

Stem cell therapy for muscular dystrophy

By Sohn Regina Lee Gussoni Emanuela

Expert Opinion on Biological Therapy, Vol. 4, Iss. 1, 2004-01 ,pp. : 1-9

Informa Healthcare

Access to resources Recommend Favorite

Activation of Caspase-3 Apoptotic Pathways in Skeletal Muscle Fibers in Laminin α2-Deficient Mice

By Mukasa T. Momoi T. Momoi M.Y.

Biochemical and Biophysical Research Communications, Vol. 260, Iss. 1, 1999-06 ,pp. : 139-142

Elsevier

Access to resources Recommend Favorite