نتایج جستجو برای: merosin

تعداد نتایج: 173  

Journal: :Neuromuscular disorders : NMD 1995
E Arikawa-Hirasawa R Koga T Tsukahara I Nonaka A Mitsudome K Goto A H Beggs K Arahata

We report a 4-yr and 5-month-old boy with severe clinical features of an early-onset Duchenne muscular dystrophy, who had a very short (110 kDa) dystrophin at the sarcolemma. The patient had a large deletion (exons 2-44) of the dystrophin gene which was predicted to cause a reading frame shift. Sequence analysis of dystrophin mRNA in muscle revealed an alternatively spliced gene product from ex...

Journal: :The Journal of biological chemistry 1992
K Balbona H Tran S Godyna K C Ingham D K Strickland W S Argraves

Fibulin is a recently described extracellular matrix (ECM) and plasma glycoprotein (Argraves, W. S., Tran, H., Burgess, W. H., and Dickerson, K. (1990) J. Cell Biol. 111, 3155-3164). In this report, ligand affinity chromatography and solid-phase binding analyses were performed to determine which ECM protein(s) interact with fibulin. Fibulin-Sepharose bound two polypeptides of 240 and 100 kDa fr...

Journal: :Journal of medical genetics 1997
I S Naom M D'Alessandro H Topaloglu C Sewry A Ferlini A Helbling-Leclerc P Guicheney J Weissenbach K Schwartz K Bushby J Philpot V Dubowitz F Muntoni

About half of the children with classical congenital muscular dystrophy (CMD) show an absence in their skeletal muscle of laminin alpha2 chain, one of the components of the extracellular matrix protein, merosin. Linkage analysis implicated the laminin alpha2 chain gene (LAMA2) on chromosome 6q2, now confirmed by the discovery of mutations in the laminin alpha2 chain gene. We have further invest...

Journal: :The Journal of Cell Biology 2007
Sarina Meinen Patrizia Barzaghi Shuo Lin Hanns Lochmüller Markus A. Ruegg

Mutations in laminin-alpha2 cause a severe congenital muscular dystrophy, called MDC1A. The two main receptors that interact with laminin-alpha2 are dystroglycan and alpha7beta1 integrin. We have previously shown in mouse models for MDC1A that muscle-specific overexpression of a miniaturized form of agrin (mini-agrin), which binds to dystroglycan but not to alpha7beta1 integrin, substantially a...

Journal: :The Journal of clinical investigation 2008
Zia A Khan Elisa Boscolo Arnaud Picard Sarah Psutka Juan M Melero-Martin Tatianna C Bartch John B Mulliken Joyce Bischoff

Infantile hemangioma is a benign endothelial tumor composed of disorganized blood vessels. It exhibits a unique life cycle of rapid postnatal growth followed by slow regression to a fibrofatty residuum. Here, we have reported the isolation of multipotential stem cells from hemangioma tissue that give rise to hemangioma-like lesions in immunodeficient mice. Cells were isolated based on expressio...

Journal: :Neurosciences 2004
Nacim Louhichi Chahnez Triki Mariem Meziou Souad Rouis Hammadi Ayadi Faiza Fakhfakh

OBJECTIVE To minimize the uncertainty in clinical diagnosis and improve the classification of 14 Tunisian patients belonging to 12 families and affected with congenital muscular dystrophy (CMD). METHODS Fourteen patients belonging to 12 unrelated families originating from the south of Tunisia and affected with CMD were clinically examined between 1990 and 2001 in the neurology service of Chu ...

Journal: :The Journal of Cell Biology 1997
J.E. Sugiyama D.J. Glass G.D. Yancopoulos Z.W. Hall

The induction of acetylcholine receptor (AChR) clustering by neurally released agrin is a critical, early step in the formation of the neuromuscular junction. Laminin, a component of the muscle fiber basal lamina, also induces AChR clustering. We find that induction of AChR clustering in C2 myotubes is specific for laminin-1; neither laminin-2 (merosin) nor laminin-11 (a synapse-specific isofor...

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