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- 2009
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Mark
E3 domain of laminin alpha 1 chain that binds to dystroglycan is not essential for survival and muscle regeneration in laminin alpha 1 chain mediated correction of laminin alpha 2 chain deficiency
2009) 14th International Congress of the World-Muscle-Society In Neuromuscular Disorders 19(8-9). p.598-599(
- Contribution to journal › Published meeting abstract
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Mark
Intrinsic laryngeal muscles are spared from degeneration in the dy(3k)/dy(3k) mouse model of congenital muscular dystrophy type 1A.
(
- Contribution to journal › Article
- 2008
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Mark
Cib2 binds integrin a7Bb1D and is reduced in laminin a2 chain deficient muscular dystrophy
(
- Contribution to journal › Article
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Mark
Expression of the novel gene Ened during mouse and Xenopus embryonic development.
(
- Contribution to journal › Article
- 2007
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Mark
Dystroglycan: a possible mediator for reducing congenital muscular dystrophy?
(
- Contribution to journal › Scientific review
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Mark
Role of the extracellular matrix and its receptors in smooth muscle cell function: implications in vascular development and disease
(
- Contribution to journal › Scientific review
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Mark
Laminin isoforms in development and disease.
(
- Contribution to journal › Scientific review
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Mark
Gene expression profiling of differentiating embryonic stem cells expressing dominant negative fibroblast growth factor receptor 2.
(
- Contribution to journal › Article
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Mark
Compositional differences between infant and adult human corneal basement membranes
(
- Contribution to journal › Article
- 2006
-
Mark
Laminin {alpha}1 chain improves laminin {alpha}2 chain deficient peripheral neuropathy.
(
- Contribution to journal › Article