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Madeleine Durbeej

Showing results (11-20 of 58) with videos related to

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Skeletal Muscle|July 30, 2011
Skeletal muscle laminin and MDC1A: pathogenesis and treatment strategiesKinga I Gawlik, Madeleine Durbeej
Scientific Reports|September 11, 2015
Deletion of integrin α7 subunit does not aggravate the phenotype of laminin α2 chain-deficient miceKinga I Gawlik, Madeleine Durbeej
Human Molecular Genetics|November 19, 2010
Proteasome inhibition improves the muscle of laminin α2 chain-deficient miceVirginie Carmignac, Ronan Quéré, Madeleine Durbeej
The American Journal of Pathology|January 8, 2014
Loss of dystrophin and β-sarcoglycan significantly exacerbates the phenotype of laminin α2 chain-deficient animalsKinga I Gawlik, Johan Holmberg, Madeleine Durbeej
Cell and Tissue Research|July 11, 2002
Nulp1, a novel basic helix-loop-helix protein expressed broadly during early embryonic organogenesis and prominently in developing dorsal root gangliaMagnus Olsson, Madeleine Durbeej, Peter Ekblom, et al.
The American Journal of Pathology|March 26, 2011
Transgenic expression of Laminin α1 chain does not prevent muscle disease in the mdx mouse model for Duchenne muscular dystrophyKinga I Gawlik, Bruno M Oliveira, Madeleine Durbeej
Cell and Tissue Research|August 7, 2009
Laminin alpha1 domains LG4-5 are essential for the complete differentiation of visceral endodermMikael Akerlund, Virginie Carmignac, Susanne Schéele, et al.
Plos One|August 4, 2017
Absence of microRNA-21 does not reduce muscular dystrophy in mouse models of LAMA2-CMDBernardo Moreira Soares Oliveira, Madeleine Durbeej, Johan Holmberg
The International Journal of Developmental Biology|October 29, 2008
Expression of the novel gene Ened during mouse and Xenopus embryonic developmentRenata Meszaros, Ina Strate, Edgar M Pera, et al.
Trends in Biotechnology|April 10, 2007
Dystroglycan: a possible mediator for reducing congenital muscular dystrophy?Francesca Sciandra, Kinga I Gawlik, Andrea Brancaccio, et al.
Pageof 6

Showing results (11-20 of 58) with videos related to

Sort By:
Pageof 6
Skeletal Muscle|July 30, 2011
Skeletal muscle laminin and MDC1A: pathogenesis and treatment strategiesKinga I Gawlik, Madeleine Durbeej
Scientific Reports|September 11, 2015
Deletion of integrin α7 subunit does not aggravate the phenotype of laminin α2 chain-deficient miceKinga I Gawlik, Madeleine Durbeej
Human Molecular Genetics|November 19, 2010
Proteasome inhibition improves the muscle of laminin α2 chain-deficient miceVirginie Carmignac, Ronan Quéré, Madeleine Durbeej
The American Journal of Pathology|January 8, 2014
Loss of dystrophin and β-sarcoglycan significantly exacerbates the phenotype of laminin α2 chain-deficient animalsKinga I Gawlik, Johan Holmberg, Madeleine Durbeej
Cell and Tissue Research|July 11, 2002
Nulp1, a novel basic helix-loop-helix protein expressed broadly during early embryonic organogenesis and prominently in developing dorsal root gangliaMagnus Olsson, Madeleine Durbeej, Peter Ekblom, et al.
The American Journal of Pathology|March 26, 2011
Transgenic expression of Laminin α1 chain does not prevent muscle disease in the mdx mouse model for Duchenne muscular dystrophyKinga I Gawlik, Bruno M Oliveira, Madeleine Durbeej
Cell and Tissue Research|August 7, 2009
Laminin alpha1 domains LG4-5 are essential for the complete differentiation of visceral endodermMikael Akerlund, Virginie Carmignac, Susanne Schéele, et al.
Plos One|August 4, 2017
Absence of microRNA-21 does not reduce muscular dystrophy in mouse models of LAMA2-CMDBernardo Moreira Soares Oliveira, Madeleine Durbeej, Johan Holmberg
The International Journal of Developmental Biology|October 29, 2008
Expression of the novel gene Ened during mouse and Xenopus embryonic developmentRenata Meszaros, Ina Strate, Edgar M Pera, et al.
Trends in Biotechnology|April 10, 2007
Dystroglycan: a possible mediator for reducing congenital muscular dystrophy?Francesca Sciandra, Kinga I Gawlik, Andrea Brancaccio, et al.
Pageof 6