(Q35056189)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12556455%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

review article

1 reference

title

Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12556455%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12556455%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

author name string

Daniel E Michele

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12556455%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

language of work or name

English

0 references

publication date

29 January 2003

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12556455%20AND%20SRC:MED&resulttype=core&format=json

Journal of Biological Chemistry

17 December 2019

number of pages

4

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12556455%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

volume

278

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12556455%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

page(s)

15457-15460

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12556455%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

issue

18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12556455%20AND%20SRC:MED&resulttype=core&format=json

Membrane organization of the dystrophin-glycoprotein complex

17 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

A stoichiometric complex of neurexins and dystroglycan in brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

A role for dystrophin-associated glycoproteins and utrophin in agrin-induced AChR clustering

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Dystroglycan-alpha, a dystrophin-associated glycoprotein, is a functional agrin receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Dystroglycan binds nerve and muscle agrin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Binding of the G domains of laminin alpha1 and alpha2 chains and perlecan to heparin, sulfatides, alpha-dystroglycan and several extracellular matrix proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2E

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Differential association of syntrophin pairs with the dystrophin complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Dystrobrevin and dystrophin: an interaction through coiled-coil motifs

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

alpha1-syntrophin gene disruption results in the absence of neuronal-type nitric-oxide synthase at the sarcolemma but does not induce muscle degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Role for alpha-dystrobrevin in the pathogenesis of dystrophin-dependent muscular dystrophies

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Syntrophin-dependent expression and localization of Aquaporin-4 water channel protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Caveolin-3 directly interacts with the C-terminal tail of beta -dystroglycan. Identification of a central WW-like domain within caveolin family members

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Molecular basis of muscular dystrophies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Purification of cranin, a laminin binding membrane protein. Identity with dystroglycan and reassessment of its carbohydrate moieties

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Dystroglycan is required for polarizing the epithelial cells and the oocyte in Drosophila.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Identification of the beta-dystroglycan binding epitope within the C-terminal region of alpha-dystroglycan.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Structures of sialylated O-linked oligosaccharides of bovine peripheral nerve alpha-dystroglycan. The role of a novel O-mannosyl-type oligosaccharide in the binding of alpha-dystroglycan with laminin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Structural analysis of sequences O-linked to mannose reveals a novel Lewis X structure in cranin (dystroglycan) purified from sheep brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

O-mannosyl glycans in mammals

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Tissue-specific heterogeneity in alpha-dystroglycan sialoglycosylation. Skeletal muscle alpha-dystroglycan is a latent receptor for Vicia villosa agglutinin b4 masked by sialic acid modification.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Structure of a WW domain containing fragment of dystrophin in complex with beta-dystroglycan

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Structure of the C-terminal laminin G-like domain pair of the laminin alpha2 chain harbouring binding sites for alpha-dystroglycan and heparin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Congenital muscular dystrophies: 1997 update

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Deficiency of alpha-dystroglycan in muscle-eye-brain disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Mutant glycosyltransferase and altered glycosylation of alpha-dystroglycan in the myodystrophy mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Identification of a human homolog of the Drosophila rotated abdomen gene (POMT1) encoding a putative protein O-mannosyl-transferase, and assignment to human chromosome 9q34.1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Mutations in the rotated abdomen locus affect muscle development and reveal an intrinsic asymmetry in Drosophila.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Matrix assembly, regulation, and survival functions of laminin and its receptors in embryonic stem cell differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Consequences of lack of beta 1 integrin gene expression in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Laminin polymerization induces a receptor-cytoskeleton network

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Enhanced expression of the alpha 7 beta 1 integrin reduces muscular dystrophy and restores viability in dystrophic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Chimaeric mice deficient in dystroglycans develop muscular dystrophy and have disrupted myoneural synapses

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Maturation and maintenance of the neuromuscular synapse: genetic evidence for roles of the dystrophin--glycoprotein complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

The dystroglycan complex is necessary for stabilization of acetylcholine receptor clusters at neuromuscular junctions and formation of the synaptic basement membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Dystroglycan is not required for localization of dystrophin, syntrophin, and neuronal nitric-oxide synthase at the sarcolemma but regulates integrin alpha 7B expression and caveolin-3 distribution

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

The complexities of dystroglycan

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Biochemical evidence for association of dystrobrevin with the sarcoglycan-sarcospan complex as a basis for understanding sarcoglycanopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200

Loss of Dp140 regulatory sequences is associated with cognitive impairment in dystrophinopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.R200031200