Madeleine Durbeej-Hjalt
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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
Laminin isoforms in development and disease.
(
- 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
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- Contribution to journal › Scientific review
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Mark
Compositional differences between infant and adult human corneal basement membranes
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- Contribution to journal › Article
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Mark
Gene expression profiling of differentiating embryonic stem cells expressing dominant negative fibroblast growth factor receptor 2.
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- Contribution to journal › Article
- 2006
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Mark
Laminin {alpha}1 chain improves laminin {alpha}2 chain deficient peripheral neuropathy.
(
- Contribution to journal › Article
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Mark
Monoclonal anti-mouse laminin antibodies: AL-1 reacts with laminin alpha1 chain, AL-2 with laminin beta1 chain, and AL-4 with the coiled-coil domain of laminin beta1 chain.
(
- Contribution to journal › Article
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Mark
Laminin alpha1 chain mediated reduction of laminin alpha2 chain deficient muscular dystrophy involves integrin alpha7beta1 and dystroglycan.
(
- Contribution to journal › Article
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Mark
Extraocular muscle is spared upon complete laminin alpha2 chain deficiency: Comparative expression of laminin and integrin isoforms.
(
- Contribution to journal › Article
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Mark
Dystroglycan is selectively cleaved at the parenchymal basement membrane at sites of leukocyte extravasation in experimental autoimmune encephalomyelitis.
(
- Contribution to journal › Article
- 2005
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Mark
Laminin {alpha}1 Chain Corrects Male Infertility Caused by Absence of Laminin {alpha}2 Chain.
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- Contribution to journal › Article
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Mark
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
(
- Contribution to journal › Article
- 2004
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Mark
Laminin {alpha}1 chain reduces muscular dystrophy in laminin {alpha}2 chain deficient mice.
(
- Contribution to journal › Article
- 2003
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Mark
Gene transfer establishes primacy of striated vs. smooth muscle sarcoglycan complex in limb-girdle muscular dystrophy
(
- Contribution to journal › Article
- 2002
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Mark
Nulp1, a novel basic helix-loop-helix protein expressed broadly during early embryonic organogenesis and prominently in developing dorsal root ganglia.
(
- Contribution to journal › Article
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Mark
Muscular dystrophies involving the dystrophin-glycoprotein complex: an overview of current mouse models
(
- Contribution to journal › Article