Laminins von Durbeej, Madeleine

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A guide to the composition and functions of the extracellular matrix von Karamanos, Nikos K., Theocharis, Achilleas D., Piperigkou, Zoi, Manou, Dimitra, Passi, Alberto, Skandalis, Spyros S., Vynios, Demitrios H., Orian‐Rousseau, Véronique, Ricard‐Blum, Sylvie, Schmelzer, Christian E.H., Duca, Laurent, Durbeej, Madeleine, Afratis, Nikolaos A., Troeberg, Linda, Franchi, Marco, Masola, Valentina, Onisto, Maurizio

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Cell-matrix interactions in muscle disease von Carmignac, Virginie, Durbeej, Madeleine

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Dystroglycan is selectively cleaved at the parenchymal basement membrane at sites of leukocyte extravasation in experimental autoimmune encephalomyelitis von Agrawal, Smriti, Anderson, Per, Durbeej, Madeleine, van Rooijen, Nico, Ivars, Fredrik, Opdenakker, Ghislain, Sorokin, Lydia M

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A mutation-independent approach for muscular dystrophy via upregulation of a modifier gene von Kemaladewi, Dwi U., Bassi, Prabhpreet S., Erwood, Steven, Al-Basha, Dhekra, Gawlik, Kinga I., Lindsay, Kyle, Hyatt, Elzbieta, Kember, Rebekah, Place, Kara M., Marks, Ryan M., Durbeej, Madeleine, Prescott, Steven A., Ivakine, Evgueni A., Cohn, Ronald D.

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Bortezomib Does Not Reduce Muscular Dystrophy in the dy2J/dy2J Mouse Model of Laminin α2 Chain-Deficient Muscular Dystrophy von Körner, Zandra, Durbeej, Madeleine

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A Family of Laminin α2 Chain-Deficient Mouse Mutants: Advancing the Research on LAMA2-CMD von Gawlik, Kinga I, Durbeej, Madeleine

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Autophagy is increased in laminin α2 chain-deficient muscle and its inhibition improves muscle morphology in a mouse model of MDC1A von Carmignac, Virginie, Svensson, Martina, Körner, Zandra, Elowsson, Linda, Matsumura, Cintia, Gawlik, Kinga I., Allamand, Valerie, Durbeej, Madeleine

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Isobaric Tagging-Based Quantification for Proteomic Analysis: A Comparative Study of Spared and Affected Muscles from mdx Mice at the Early Phase of Dystrophy von Matsumura, Cintia Yuri, Menezes de Oliveira, Bruno, Durbeej, Madeleine, Marques, Maria Julia

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Skeletal muscle laminin and MDC1A: pathogenesis and treatment strategies von Gawlik, Kinga I, Durbeej, Madeleine

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Early skeletal muscle pathology and disease progress in the dy3K/dy3K mouse model of congenital muscular dystrophy with laminin α2 chain-deficiency von Gawlik, Kinga I., Körner, Zandra, Oliveira, Bruno M., Durbeej, Madeleine

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Absence of microRNA-21 does not reduce muscular dystrophy in mouse models of LAMA2-CMD von Moreira Soares Oliveira, Bernardo, Durbeej, Madeleine, Holmberg, Johan

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Muscular dystrophies involving the dystrophin–glycoprotein complex: an overview of current mouse models von Durbeej, Madeleine, Campbell, Kevin P.

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Laminin isoforms in development and disease von SCHEELE, Susanne, NYSTRÖM, Alexander, DURBEEJ, Madeleine, TALTS, Jan F, EKBLOM, Marja, EKBLOM, Peter

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Compositional Differences between Infant and Adult Human Corneal Basement Membranes von Kabosova, Andrea, Azar, Dimitri T, Bannikov, Gregory A, Campbell, Kevin P, Durbeej, Madeleine, Ghohestani, Reza F, Jones, Jonathan C. R, Kenney, M. Cristina, Koch, Manuel, Ninomiya, Yoshifumi, Patton, Bruce L, Paulsson, Mats, Sado, Yoshikazu, Sage, E. Helene, Sasaki, Takako, Sorokin, Lydia M, Steiner-Champliaud, Marie-France, Sun, Tung-Tien, SundarRaj, Nirmala, Timpl, Rupert, Virtanen, Ismo, Ljubimov, Alexander V

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Role of the extracellular matrix and its receptors in smooth muscle cell function: implications in vascular development and disease von Hultgårdh-Nilsson, Anna, Durbeej, Madeleine

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Distinct Roles for Laminin Globular Domains in Laminin α1 Chain Mediated Rescue of Murine Laminin α2 Chain Deficiency von Gawlik, Kinga I., Åkerlund, Mikael, Carmignac, Virginie, Elamaa, Harri, Durbeej, Madeleine

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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 activation von Oblander, Samantha A., Zhou, Zhongjun, Gálvez, Beatriz G., Starcher, Barry, Shannon, John M., Durbeej, Madeleine, Arroyo, Alicia G., Tryggvason, Karl, Apte, Suneel S.

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Laminin-211 in skeletal muscle function von Holmberg, Johan, Durbeej, Madeleine

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Brain and Eye Malformations Resembling Walker-Warburg Syndrome Are Recapitulated in Mice by Dystroglycan Deletion in the Epiblast von Satz, Jakob S, Barresi, Rita, Durbeej, Madeleine, Willer, Tobias, Turner, Amy, Moore, Steven A, Campbell, Kevin P

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