(Q48881167)

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Congenital muscular dystrophy with laminin alpha 2 chain deficiency: identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry

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Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8911899

Congenital muscular dystrophy with laminin alpha 2 chain deficiency: identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry (English)

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8911899

immunohistochemistry

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based on heuristic

inferred from title

congenital muscular dystrophy

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author name string

R Herrmann

1

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8911899

V Straub

2

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8911899

K Meyer

3

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8911899

T Kahn

4

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8911899

M Wagner

5

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8911899

T Voit

6

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8911899

publication date

1 November 1996

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Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8911899

European Journal of Pediatrics

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Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8911899

155

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Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8911899

11

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Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8911899

968-976

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8911899

Laminin and other basement membrane components

1 reference

https://api.crossref.org/works/10.1007%2FBF02282889

21 January 2018

Abnormal localization of laminin subunits in muscular dystrophies

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https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin.

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https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

based on heuristic

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Two distinct cell-binding domains in laminin can independently promote nonneuronal cell adhesion and spreading

1 reference

https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Murine muscular dystrophy caused by a mutation in the laminin alpha 2 (Lama2) gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial concordance of brain magnetic resonance imaging changes in congenital muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

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22nd ENMC sponsored workshop on congenital muscular dystrophy held in Baarn, The Netherlands, 14-16 May 1993

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https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

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Proceedings of the 27th ENMC sponsored workshop on congenital muscular dystrophy. 22-24 April 1994, The Netherlands

1 reference

https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

based on heuristic

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Prenatal diagnosis in congenital muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

based on heuristic

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Congenital muscular dystrophy with merosin deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

based on heuristic

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Expression of laminin subunits in human fetal skeletal muscle

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https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

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

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https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

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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

https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Merosin promotes cell attachment and neurite outgrowth and is a component of the neurite-promoting factor of RN22 schwannoma cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

based on heuristic

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Laminin variants: why, where and when?

1 reference

https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal detection of merosin expression in human placenta

1 reference

https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of laminin subunits in congenital muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficiency of laminin α2‐Chain mRNA in muscle in a patient with merosin‐negative congenital muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Direct visualization of the dystrophin network on skeletal muscle fiber membrane

1 reference

https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

based on heuristic

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Preserved merosin M-chain (or laminin-alpha 2) expression in skeletal muscle distinguishes Walker-Warburg syndrome from Fukuyama muscular dystrophy and merosin-deficient congenital muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Xp21 dystrophin and 6q dystrophin-related protein. Comparative immunolocalization using multiple antibodies

1 reference

https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficiency of dystrophin-associated proteins: a common mechanism leading to muscle cell necrosis in severe childhood muscular dystrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/8911899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF02282889

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8911899

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8911899

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