(Q52207469)

27 April 2018

title

Expression of laminin subunits in human fetal skeletal muscle (English)

1 reference

31 May 2024

author name string

C. A. Sewry

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7591842

31 May 2024

M. Chevallay

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7591842

31 May 2024

F. M. Tomé

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7591842

31 May 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7591842

31 May 2024

publication date

1 July 1995

1 reference

27 April 2018

full work available at URL

http://link.springer.com/content/pdf/10.1007/BF02388749.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF02388749/fulltext.html

31 May 2024

1 reference

http://link.springer.com/content/pdf/10.1007/BF02388749

31 May 2024

1 reference

The Histochemical Journal

31 May 2024

published in

1 reference

27 April 2018

volume

27

1 reference

27 April 2018

issue

7

1 reference

27 April 2018

page(s)

497-504

1 reference

27 April 2018

https://api.crossref.org/works/10.1007%2FBF00174322

1 reference

Abnormal localization of laminin subunits in muscular dystrophies

21 January 2018

1 reference

12 December 2020

A new nomenclature for the laminins

1 reference

12 December 2020

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

1 reference

12 December 2020

Merosin, a tissue-specific basement membrane protein, is a laminin-like protein

1 reference

12 December 2020

Congenital progressive muscular dystrophy of the Fukuyama type - clinical, genetic and pathological considerations

1 reference

12 December 2020

Prenatal diagnosis in congenital muscular dystrophy

1 reference

12 December 2020

Deficiency of merosin in dystrophic dy mice and genetic linkage of laminin M chain gene to dy locus

1 reference

12 December 2020

Congenital muscular dystrophy with merosin deficiency

1 reference

12 December 2020

Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33

1 reference

12 December 2020

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

1 reference

12 December 2020

Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping

1 reference

12 December 2020

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

1 reference

12 December 2020

Merosin, a protein specific for basement membranes of Schwann cells, striated muscle, and trophoblast, is expressed late in nerve and muscle development

1 reference

12 December 2020

Expression of dystrophin-associated glycoproteins during human fetal muscle development: a preliminary immunocytochemical study.

1 reference

12 December 2020

Contact and adhesive specificities in the associations, migrations, and targeting of cells and axons

1 reference

12 December 2020

Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse

1 reference

12 December 2020

Laminin variants: why, where and when?

1 reference

12 December 2020

Prenatal detection of merosin expression in human placenta

1 reference

12 December 2020

Molecular heterogeneity of basal laminae: isoforms of laminin and collagen IV at the neuromuscular junction and elsewhere

1 reference

12 December 2020

Expression of laminin subunits in congenital muscular dystrophy

1 reference

12 December 2020

Localization of the gene (LAMA4) to chromosome 6q21 and isolation of a partial cDNA encoding a variant laminin A chain

1 reference

12 December 2020

Characterisation of dystrophin during development of human skeletal muscle

1 reference

12 December 2020

Basal lamina assembly

1 reference

12 December 2020

Neural abnormalities in the dystrophic mouse

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00174322

1 reference

27 April 2018

1 reference

27 April 2018