Laminin isoforms in development and disease. (2007)
Schéele, Susanne, Nystrom, Alexander, Durbeej, Madeleine, Talts, Jan, Ekblom, Marja, Ekblom, Peter
Abstract is not available
Hultgardh-Nilsson, Anna, Durbeej, Madeleine
Abstract is not available
Anderson, Per, Durbeej, Madeleine, Van Rooijen, Nico, Ivars, Fredrik, ...
The endothelial cell monolayer of cerebral vessels and its basement membrane (BM) are ensheathed by the astrocyte endfeet, the leptomeningeal cells, and their associated parenchymal BM, all of which...
Gawlik, Kinga I, Mayer, Ulrike, Blomberg, Kristina, Sonnenberg, Arnoud, Ekblom, Peter, Durbeej, Madeleine
Abstract is not available
Schéele, Susanne, Sasaki, Takako, Arnal-Estapé, Anna, Durbeej, Madeleine, Ekblom, Peter
Abstract is not available
Agrawal, Smriti, Anderson, Per, Durbeej, Madeleine, Van Rooijen, Nico, Ivars, Fredrik, Opdenakker, Ghislain, ...
Abstract is not available
Nystrom, Alexander, Holmblad, Johanna, Pedrosa-Domellof, Fatima, Sasaki, Takako, Durbeej, Madeleine
Abstract is not available
Laminin {alpha}1 chain improves laminin {alpha}2 chain deficient peripheral neuropathy. (2006)
Gawlik, Kinga I, Li, Jia-Yi, Petersén, Asa, Durbeej, Madeleine
Abstract is not available
Meszaros, Renata, Akerlund, Mikael, Hjalt, Tord, Durbeej, Madeleine, Ekblom, Peter
Abstract is not available
Laminin {alpha}1 chain improves laminin {alpha}2 chain deficient peripheral neuropathy (2006)
Gawlik, Kinga I., Li, Jia-Yi, Petersén, Åsa, Durbeej, Madeleine
Absence of laminin α2 chain leads to a severe form of congenital muscular dystrophy (MDC1A) associated with peripheral neuropathy. Hence, future therapies should be aimed at alleviating both muscle...
Laminin {alpha}1 chain improves laminin {alpha}2 chain deficient peripheral neuropathy (2006)
Gawlik, Kinga I., Li, Jia-Yi, Petersén, Åsa, Durbeej, Madeleine
Absence of laminin α2 chain leads to a severe form of congenital muscular dystrophy (MDC1A) associated with peripheral neuropathy. Hence, future therapies should be aimed at alleviating both muscle...
Laminin {alpha}1 Chain Corrects Male Infertility Caused by Absence of Laminin {alpha}2 Chain. (2005)
Häger, Mattias, Gawlik, Kinga, Nyström, Alexander, Sasaki, Takako, Durbeej, Madeleine
Abstract is not available
Laminin {alpha}1 chain reduces muscular dystrophy in laminin {alpha}2 chain deficient mice. (2004)
Gawlik, Kinga, Miyagoe-Suzuki, Yuko, Ekblom, Peter, Takeda, Shin'ichi, Durbeej, Madeleine
Abstract is not available
Laminin {alpha}1 chain reduces muscular dystrophy in laminin {alpha}2 chain deficient mice (2004)
Gawlik, Kinga, Miyagoe-Suzuki, Yuko, Ekblom, Peter, Takeda, Shin'ichi, Durbeej, Madeleine
Laminin α2 chain deficiency in humans and mice leads to severe forms of congenital muscular dystrophy. Here, we investigated whether laminin α1 chain in mice can compensate for the absence of...
Laminin {alpha}1 chain reduces muscular dystrophy in laminin {alpha}2 chain deficient mice (2004)
Gawlik, Kinga, Miyagoe-Suzuki, Yuko, Ekblom, Peter, Takeda, Shin'ichi, Durbeej, Madeleine
Laminin (LN) α2 chain deficiency in humans and mice leads to severe forms of congenital muscular dystrophy (CMD). Here, we investigated whether LNα1 chain in mice can compensate for the absence of...
Laminin {alpha}1 chain reduces muscular dystrophy in laminin {alpha}2 chain deficient mice (2004)
Gawlik, Kinga, Miyagoe-Suzuki, Yuko, Ekblom, Peter, Takeda, Shin'ichi, Durbeej, Madeleine
Laminin α2 chain deficiency in humans and mice leads to severe forms of congenital muscular dystrophy. Here, we investigated whether laminin α1 chain in mice can compensate for the absence of...
Ferletta, Maria, Kikkawa, Yamato, Yu, Hao, Talts, Jan F, Durbeej, Madeleine, Sonnenberg, Arnoud, ...
Abstract is not available
Olsson, Magnus, Durbeej, Madeleine, Ekblom, Peter, Hjalt, Tord
The basic helix-loop-helix (bHLH) proteins control differentiation and development of a variety of organs. We have isolated the complementary DNA (cDNA) of a novel class of bHLH transcription...
Ferletta, Maria, Kikkawa, Yamato, Yu, Hao, Talts, Jan F., Durbeej, Madeleine, Sonnenberg, Arnoud, ...
Laminin–integrin interactions can in some settings activate the extracellular signal-regulated kinases (ERKs) but the control mechanisms are poorly understood. Herein, we studied ERK activation in...
Durbeej, Madeleine, Sawatzki, Shanna M., Barresi, Rita, Schmainda, Kathleen M., Allamand, Valérie, Michele, Daniel E., ...
Limb-girdle muscular dystrophy types 2E and F are characterized by skeletal muscle weakness and often cardiomyopathy and are due to mutations in the genes encoding β- and δ-sarcoglycan. We...
Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complex
Cohn, Ronald D., Durbeej, Madeleine, Moore, Steven A., Coral-Vazquez, Ramón, Prouty, Sally, Campbell, Kevin P.
Cardiomyopathy is a multifactorial disease, and the dystrophin-glycoprotein complex has been implicated in the pathogenesis of both hereditary and acquired forms of the disease. Using mouse models of...
Ferletta, Maria, Kikkawa, Yamato, Yu, Hao, Talts, Jan F., Durbeej, Madeleine, Sonnenberg, Arnoud, ...
Laminin–integrin interactions can in some settings activate the extracellular signal-regulated kinases (ERKs) but the control mechanisms are poorly understood. Herein, we studied ERK activation in...
Durbeej, Madeleine, Sawatzki, Shanna M., Barresi, Rita, Schmainda, Kathleen M., Allamand, Valérie, Michele, Daniel E., ...
Limb-girdle muscular dystrophy types 2E and F are characterized by skeletal muscle weakness and often cardiomyopathy and are due to mutations in the genes encoding β- and δ-sarcoglycan. We...
Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complex
Cohn, Ronald D., Durbeej, Madeleine, Moore, Steven A., Coral-Vazquez, Ramón, Prouty, Sally, Campbell, Kevin P.
Cardiomyopathy is a multifactorial disease, and the dystrophin-glycoprotein complex has been implicated in the pathogenesis of both hereditary and acquired forms of the disease. Using mouse models of...
Laminin α1 Chain Corrects Male Infertility Caused by Absence of Laminin α2 Chain
Häger, Mattias, Gawlik, Kinga, Nyström, Alexander, Sasaki, Takako, Durbeej, Madeleine
Laminins are important for basement membrane structure and function. The laminin α2 chain is a major component of muscle basement membranes, and mutations in the laminin α2 gene lead to congenital...
Agrawal, Smriti, Anderson, Per, Durbeej, Madeleine, Van Rooijen, Nico, Ivars, Fredrik, Opdenakker, Ghislain, ...
The endothelial cell monolayer of cerebral vessels and its basement membrane (BM) are ensheathed by the astrocyte endfeet, the leptomeningeal cells, and their associated parenchymal BM, all of which...
Progressive Muscular Dystrophy in α-Sarcoglycan–deficient Mice
Duclos, Franck, Straub, Volker, Moore, Steven A., Venzke, David P., Hrstka, Ron F., Crosbie, Rachelle H., ...
Limb-girdle muscular dystrophy type 2D (LGMD 2D) is an autosomal recessive disorder caused by mutations in the α-sarcoglycan gene. To determine how α-sarcoglycan deficiency leads to muscle fiber...