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Madeleine Durbeej

Showing results (41-50 of 58) with videos related to

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Npj Viruses|August 18, 2025
Lactoferricin enables adenovirus infection of human skeletal muscle cellsKatarina Danskog, Nitesh Mistry, Carin Årdahl, et al.
The Journal of Experimental Medicine|April 6, 2006
Dystroglycan is selectively cleaved at the parenchymal basement membrane at sites of leukocyte extravasation in experimental autoimmune encephalomyelitisSmriti Agrawal, Per Anderson, Madeleine Durbeej, et al.
Antioxidants (Basel, Switzerland)|March 22, 2020
Antioxidants Reduce Muscular Dystrophy in the <i>dy</i><sup>2J</sup><i>/dy</i><sup>2J</sup> Mouse Model of Laminin α2 Chain-Deficient Muscular DystrophyVahid M Harandi, Bernardo Moreira Soares Oliveira, Valérie Allamand, et al.
Human Molecular Genetics|September 17, 2011
Autophagy is increased in laminin α2 chain-deficient muscle and its inhibition improves muscle morphology in a mouse model of MDC1AVirginie Carmignac, Martina Svensson, Zandra Körner, et al.
Scientific Reports|March 11, 2017
Potent pro-inflammatory and pro-fibrotic molecules, osteopontin and galectin-3, are not major disease modulators of laminin α2 chain-deficient muscular dystrophyKinga I Gawlik, Johan Holmberg, Martina Svensson, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 17, 2008
Brain and eye malformations resembling Walker-Warburg syndrome are recapitulated in mice by dystroglycan deletion in the epiblastJakob S Satz, Rita Barresi, Madeleine Durbeej, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 10, 2003
Gene transfer establishes primacy of striated vs. smooth muscle sarcoglycan complex in limb-girdle muscular dystrophyMadeleine Durbeej, Shanna M Sawatzki, Rita Barresi, et al.
Molecular & Cellular Proteomics : MCP|July 5, 2014
Quantitative proteomic analysis reveals metabolic alterations, calcium dysregulation, and increased expression of extracellular matrix proteins in laminin α2 chain-deficient muscleBruno Menezes de Oliveira, Cintia Y Matsumura, Cibely C Fontes-Oliveira, et al.
Molecular Biology of the Cell|June 13, 2003
Opposing roles of integrin alpha6Abeta1 and dystroglycan in laminin-mediated extracellular signal-regulated kinase activationMaria Ferletta, Yamato Kikkawa, Hao Yu, et al.
Developmental Biology|December 2, 2004
Distinctive functions of membrane type 1 matrix-metalloprotease (MT1-MMP or MMP-14) in lung and submandibular gland development are independent of its role in pro-MMP-2 activationSamantha A Oblander, Zhongjun Zhou, Beatriz G Gálvez, et al.
Pageof 6

Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
Npj Viruses|August 18, 2025
Lactoferricin enables adenovirus infection of human skeletal muscle cellsKatarina Danskog, Nitesh Mistry, Carin Årdahl, et al.
The Journal of Experimental Medicine|April 6, 2006
Dystroglycan is selectively cleaved at the parenchymal basement membrane at sites of leukocyte extravasation in experimental autoimmune encephalomyelitisSmriti Agrawal, Per Anderson, Madeleine Durbeej, et al.
Antioxidants (Basel, Switzerland)|March 22, 2020
Antioxidants Reduce Muscular Dystrophy in the <i>dy</i><sup>2J</sup><i>/dy</i><sup>2J</sup> Mouse Model of Laminin α2 Chain-Deficient Muscular DystrophyVahid M Harandi, Bernardo Moreira Soares Oliveira, Valérie Allamand, et al.
Human Molecular Genetics|September 17, 2011
Autophagy is increased in laminin α2 chain-deficient muscle and its inhibition improves muscle morphology in a mouse model of MDC1AVirginie Carmignac, Martina Svensson, Zandra Körner, et al.
Scientific Reports|March 11, 2017
Potent pro-inflammatory and pro-fibrotic molecules, osteopontin and galectin-3, are not major disease modulators of laminin α2 chain-deficient muscular dystrophyKinga I Gawlik, Johan Holmberg, Martina Svensson, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 17, 2008
Brain and eye malformations resembling Walker-Warburg syndrome are recapitulated in mice by dystroglycan deletion in the epiblastJakob S Satz, Rita Barresi, Madeleine Durbeej, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 10, 2003
Gene transfer establishes primacy of striated vs. smooth muscle sarcoglycan complex in limb-girdle muscular dystrophyMadeleine Durbeej, Shanna M Sawatzki, Rita Barresi, et al.
Molecular & Cellular Proteomics : MCP|July 5, 2014
Quantitative proteomic analysis reveals metabolic alterations, calcium dysregulation, and increased expression of extracellular matrix proteins in laminin α2 chain-deficient muscleBruno Menezes de Oliveira, Cintia Y Matsumura, Cibely C Fontes-Oliveira, et al.
Molecular Biology of the Cell|June 13, 2003
Opposing roles of integrin alpha6Abeta1 and dystroglycan in laminin-mediated extracellular signal-regulated kinase activationMaria Ferletta, Yamato Kikkawa, Hao Yu, et al.
Developmental Biology|December 2, 2004
Distinctive functions of membrane type 1 matrix-metalloprotease (MT1-MMP or MMP-14) in lung and submandibular gland development are independent of its role in pro-MMP-2 activationSamantha A Oblander, Zhongjun Zhou, Beatriz G Gálvez, et al.
Pageof 6