(Q28236824)

English

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 α2 chain in skin by electron microscopy immunocytochemistry: Comparison between normal and laminin α2 chain deficient subjects

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scholarly article

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

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Intracellular detection of laminin α2 chain in skin by electron microscopy immunocytochemistry: Comparison between normal and laminin α2 chain deficient subjects (English)

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Stefano Squarzoni

object named as

S. Squarzoni

1

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author name string

S Squarzoni

1

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M Villanova

2

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P Sabatelli

3

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A Malandrini

4

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P Toti

5

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A Pini

6

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L Merlini

7

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G C Guazzi

8

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N M Maraldi

9

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M. Villanova

2

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P. Sabatelli

3

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A. Malandrini

4

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P. Toti

5

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A. Pini

6

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L. Merlini

7

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G.C. Guazzi

8

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N.M. Maraldi

9

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language of work or name

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publication date

March 1997

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Neuromuscular Disorders

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7

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2

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91-8

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91-98

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Human laminin M chain (merosin): complete primary structure, chromosomal assignment, and expression of the M and A chain in human fetal tissues

1 reference

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Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.

1 reference

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7 January 2021

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Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal muscle

1 reference

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7 January 2021

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Divergence of central nervous system involvement in 2 Italian sisters with congenital muscular dystrophy: a clinical and neuroradiological follow-up

1 reference

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7 January 2021

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Somatosensory and visual evoked potentials in congenital muscular dystrophy: correlation with MRI changes and muscle merosin status

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900420-8

7 January 2021

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Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy

1 reference

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7 January 2021

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Cloning and expression of laminin alpha 2 chain (M-chain) in the mouse.

1 reference

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7 January 2021

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Coculture modulates laminin synthesis and mRNA levels in epidermal keratinocytes and dermal fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900420-8

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Diagnosis of merosin (laminin-2) deficient congenital muscular dystrophy by skin biopsy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900420-8

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Localization of the laminin alpha 2 chain in normal human skeletal muscle and peripheral nerve: an ultrastructural immunolabeling study

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900420-8

7 January 2021

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Localization of dystrophin COOH-terminal domain by the fracture-label technique

1 reference

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7 January 2021

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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 keratinocytes

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Signal transduction from the extracellular matrix

1 reference

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A hierarchy of ECM-mediated signalling regulates tissue-specific gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900420-8

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Dystrophin deficiency, altered cell signalling and fibre hypertrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900420-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0960-8966(96)00420-8

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