Evaluation of the dystrophin-glycoprotein complex, alpha-actinin, dysferlin and calpain 3 in an autosomal recessive muscular dystrophy in Labrador retrievers (Q31882212)

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Language	Label	Description	Also known as
English	Evaluation of the dystrophin-glycoprotein complex, alpha-actinin, dysferlin and calpain 3 in an autosomal recessive muscular dystrophy in Labrador retrievers	scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

Evaluation of the dystrophin-glycoprotein complex, alpha-actinin, dysferlin and calpain 3 in an autosomal recessive muscular dystrophy in Labrador retrievers (English)

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

muscular dystrophy

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based on heuristic

inferred from title

author name string

Olby NJ

1

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Europe PubMed Central

PubMed publication ID

4 July 2017

Sharp NJ

2

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

Anderson LV

3

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

Kunkel LM

4

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

Bönnemann CG

5

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

publication date

1 January 2001

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Europe PubMed Central

PubMed publication ID

4 July 2017

Neuromuscular Disorders

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Europe PubMed Central

PubMed publication ID

4 July 2017

11

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Europe PubMed Central

PubMed publication ID

4 July 2017

1

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Europe PubMed Central

PubMed publication ID

4 July 2017

41-49

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Europe PubMed Central

PubMed publication ID

4 July 2017

Generalised muscle weakness in the Labrador retriever

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https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Hereditary myopathy in Labrador retrievers: a morphologic study

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Glycoprotein complex anchoring dystrophin to sarcolemma

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https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the sarcoglycan genes in patients with myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E)

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Dysferlin is a plasma membrane protein and is expressed early in human development

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Dystrobrevin deficiency at the sarcolemma of patients with muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Isoform diversity of dystrobrevin, the murine 87-kDa postsynaptic protein

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Deficiency of a skeletal muscle isoform of α-actinin (α-actinin-3) in merosin-positive congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Characterization of monoclonal antibodies to calpain 3 and protein expression in muscle from patients with limb-girdle muscular dystrophy type 2A

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Multiplex Western blotting system for the analysis of muscular dystrophy proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Limb-girdle muscular dystrophy: a follow-up study of 79 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chain

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Muscular dystrophy in a litter of golden retriever dogs

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Dystrophin abnormalities in Duchenne/Becker muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

An error in dystrophin mRNA processing in golden retriever muscular dystrophy, an animal homologue of Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Caveolin-3 in muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900166-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0960-8966(00)00166-8

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

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