Intracellular detection of laminin alpha 2 chain in skin by electron microscopy immunocytochemistry: comparison between normal and laminin alpha 2 chain deficient subjects

scientific article (publication date: March 1997)

Intracellular detection of laminin alpha 2 chain in skin by electron microscopy immunocytochemistry: comparison between normal and laminin alpha 2 chain deficient subjects is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1016/S0960-8966(96)00420-8
P698PubMed publication ID9131649

P50authorStefano SquarzoniQ42412676
P2093author name stringA Pini
A Malandrini
L Merlini
P Sabatelli
S Squarzoni
N M Maraldi
P Toti
G C Guazzi
M Villanova
L. Merlini
P. Sabatelli
A. Pini
M. Villanova
N.M. Maraldi
A. Malandrini
G.C. Guazzi
P. Toti
P2860cites workMutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophyQ24308817
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Signal transduction from the extracellular matrixQ24675031
A hierarchy of ECM-mediated signalling regulates tissue-specific gene expressionQ34103381
Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.Q40612428
Dystrophin deficiency, altered cell signalling and fibre hypertrophyQ40644186
Localization of dystrophin COOH-terminal domain by the fracture-label techniqueQ41826854
Polarized expression of integrin receptors (alpha 6 beta 4, alpha 2 beta 1, alpha 3 beta 1, and alpha v beta 5) and their relationship with the cytoskeleton and basement membrane matrix in cultured human keratinocytesQ42470291
Localization of the laminin alpha 2 chain in normal human skeletal muscle and peripheral nerve: an ultrastructural immunolabeling studyQ42529199
Cloning and expression of laminin alpha 2 chain (M-chain) in the mouseQ48075129
Diagnosis of merosin (laminin-2) deficient congenital muscular dystrophy by skin biopsyQ70989173
Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletalQ71791406
Divergence of central nervous system involvement in 2 Italian sisters with congenital muscular dystrophy: a clinical and neuroradiological follow-upQ72051883
Somatosensory and visual evoked potentials in congenital muscular dystrophy: correlation with MRI changes and muscle merosin statusQ72337142
Coculture modulates laminin synthesis and mRNA levels in epidermal keratinocytes and dermal fibroblastsQ72753538
P433issue2
P407language of work or nameEnglishQ1860
P304page(s)91-98
91-8
P577publication date1997-03-01
P1433published inNeuromuscular DisordersQ1981326
P1476titleIntracellular detection of laminin alpha 2 chain in skin by electron microscopy immunocytochemistry: comparison between normal and laminin alpha 2 chain deficient subjects
Intracellular detection of laminin α2 chain in skin by electron microscopy immunocytochemistry: Comparison between normal and laminin α2 chain deficient subjects
P478volume7