(Q37378530)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19172427%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

review article

1 reference

title

The neurobiology of the dystrophin-associated glycoprotein complex (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19172427%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19172427%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

Matthew Locke

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19172427%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

author name string

Caroline L Tinsley

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19172427%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

Derek J Blake

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19172427%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

language of work or name

English

0 references

publication date

1 January 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19172427%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19172427%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

volume

41

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19172427%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19172427%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

page(s)

344-359

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19172427%20AND%20SRC:MED&resulttype=core&format=json

Molecular mechanisms of muscular dystrophies: old and new players

20 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Function and genetics of dystrophin and dystrophin-related proteins in muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Sparks, signals and shock absorbers: how dystrophin loss causes muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Dystrophin, its interactions with other proteins, and implications for muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Duchenne muscular dystrophy and dystrophin: pathogenesis and opportunities for treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Association between intellectual functioning and age in children and young adults with Duchenne muscular dystrophy: further results from a meta-analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Neuropsychiatric disorders in males with duchenne muscular dystrophy: frequency rate of attention-deficit hyperactivity disorder (ADHD), autism spectrum disorder, and obsessive--compulsive disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Social behavior problems in boys with Duchenne muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Behavior patterns in Duchenne muscular dystrophy: report on the Parent Project Muscular Dystrophy behavior workshop 8-9 of December 2006, Philadelphia, USA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Altered regional brain glucose metabolism in Duchenne muscular dystrophy: a pet study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Brain abnormalities in Duchenne muscular dystrophy: phosphorus-31 magnetic resonance spectroscopy and neuropsychological study

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Different dystrophin-like complexes are expressed in neurons and glia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Expression of four alternative dystrophin transcripts in brain regions regulated by different promoters

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Characterization of a 4.8kb transcript from the Duchenne muscular dystrophy locus expressed in Schwannoma cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

A housekeeping type promoter, located in the 3' region of the Duchenne muscular dystrophy gene, controls the expression of Dp71, a major product of the gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Localization of dystrophin to postsynaptic regions of central nervous system cortical neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Detection of dystrophin in the postsynaptic density of rat brain and deficiency in a mouse model of Duchenne muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Semiquantitative proteomic analysis of rat forebrain postsynaptic density fractions by mass spectrometry

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Influence of dystrophin-gene mutation on mdx mouse behavior. I. Retention deficits at long delays in spontaneous alternation and bar-pressing tasks.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Behavioral characterization of mdx3cv mice deficient in C-terminal dystrophins

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Spatial learning and hippocampal long-term potentiation are not impaired in mdx mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Impaired long-term spatial and recognition memory and enhanced CA1 hippocampal LTP in the dystrophin-deficient Dmd(mdx) mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Facilitated CA1 hippocampal synaptic plasticity in dystrophin-deficient mice: role for GABAA receptors?

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Long-term depression is reduced in cerebellar Purkinje cells of dystrophin-deficient mdx mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

SEA domain proteolysis determines the functional composition of dystroglycan

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

The effects of post-translational processing on dystroglycan synthesis and trafficking

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Dystroglycan: important player in skeletal muscle and beyond

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

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/10.1080%2F07853890802668522

Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

A homozygous nonsense mutation in the fukutin gene causes a Walker-Warburg syndrome phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Fukutin gene mutations cause dilated cardiomyopathy with minimal muscle weakness

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Protein glycosylation in disease: new insights into the congenital muscular dystrophies

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Congenital muscular dystrophies involving the O-mannose pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

FKRP gene mutations cause congenital muscular dystrophy, mental retardation, and cerebellar cysts

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

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/10.1080%2F07853890802668522

Mouse large can modify complex N- and mucin O-glycans on alpha-dystroglycan to induce laminin binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

The human LARGE gene from 22q12.3-q13.1 is a new, distinct member of the glycosyltransferase gene family

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Merosin-deficient congenital muscular dystrophy: the spectrum of brain involvement on magnetic resonance imaging

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Integrin-linked kinase is required for laminin-2-induced oligodendrocyte cell spreading and CNS myelination

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Skeletal, cardiac and tongue muscle pathology, defective retinal transmission, and neuronal migration defects in the Large(myd) mouse defines a natural model for glycosylation-deficient muscle - eye - brain disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

A stoichiometric complex of neurexins and dystroglycan in brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Neurexin-neuroligin signaling in synapse development

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Dystroglycan regulates structure, proliferation and differentiation of neuroepithelial cells in the developing vertebrate CNS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Coiled-coil regions in the carboxy-terminal domains of dystrophin and related proteins: potentials for protein-protein interactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

beta-dystrobrevin, a member of the dystrophin-related protein family

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Role of beta-dystrobrevin in nonmuscle dystrophin-associated protein complex-like complexes in kidney and liver

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Cerebellar synaptic defects and abnormal motor behavior in mice lacking alpha- and beta-dystrobrevin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Dystrobrevins in muscle and non-muscle tissues.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Schizophrenia genetics: dysbindin under the microscope

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Genetic variation in DTNBP1 influences general cognitive ability

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Neuronal and non-neuronal functions of the AP-3 sorting machinery

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Cloning of human basic A1, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Two forms of mouse syntrophin, a 58 kd dystrophin-associated protein, differ in primary structure and tissue distribution

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Gamma1- and gamma2-syntrophins, two novel dystrophin-binding proteins localized in neuronal cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Interaction of nitric oxide synthase with the postsynaptic density protein PSD-95 and alpha1-syntrophin mediated by PDZ domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Absence of alpha-syntrophin leads to structurally aberrant neuromuscular synapses deficient in utrophin

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Alpha1-syntrophin-deficient skeletal muscle exhibits hypertrophy and aberrant formation of neuromuscular junctions during regeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Dmd(mdx-beta geo): a new allele for the mouse dystrophin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

The role of utrophin and Dp71 for assembly of different dystrophin-associated protein complexes (DPCs) in the choroid plexus and microvasculature of the brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Dystroglycan in the cerebellum is a laminin alpha 2-chain binding protein at the glial-vascular interface and is expressed in Purkinje cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Aquaporin-4 deletion in mice reduces brain edema after acute water intoxication and ischemic stroke.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Delayed onset of brain edema and mislocalization of aquaporin-4 in dystrophin-null transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Dystrophin-dependent and -independent AQP4 pools are expressed in the mouse brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Molecular and cell biology of the sarcoglycan complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Zeta-sarcoglycan is a functional homologue of gamma-sarcoglycan in the formation of the sarcoglycan complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Phenotypic features of myoclonus-dystonia in three kindreds

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Myoclonus-dystonia: significance of large SGCE deletions

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

SGCE missense mutations that cause myoclonus-dystonia syndrome impair epsilon-sarcoglycan trafficking to the plasma membrane: modulation by ubiquitination and torsinA

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

The pathophysiological basis of dystonias.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Epsilon-sarcoglycan immunoreactivity and mRNA expression in mouse brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Identification and characterization of epsilon-sarcoglycans in the central nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Myoclonus, motor deficits, alterations in emotional responses and monoamine metabolism in epsilon-sarcoglycan deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

The beta-delta-core of sarcoglycan is essential for deposition at the plasma membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Processing and assembly of the dystrophin glycoprotein complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Molecular organization of sarcoglycan complex in mouse myotubes in culture

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

The sarcoglycan complex in Schwann cells and its role in myelin stability

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

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/10.1080%2F07853890802668522

Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, δ-sarcoglycan, in hamster: An animal model of disrupted dystrophin-associated glycoprotein complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

No muscle involvement in myoclonus-dystonia caused by epsilon-sarcoglycan gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Alpha-sarcoglycan is recycled from the plasma membrane in the absence of sarcoglycan complex assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Osprey: a network visualization system

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Cognitive impairment in Duchenne muscular dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Investigation of Poor Academic Achievement in Children with Duchenne Muscular Dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Cognitive and psychological profile of males with Becker muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Association of Duchenne muscular dystrophy with autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Interaction of alpha1-syntrophin with multiple isoforms of heterotrimeric G protein alpha subunits

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Neuroligins 3 and 4X interact with syntrophin-gamma2, and the interactions are affected by autism-related mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Regulation of capacitative calcium entries by alpha1-syntrophin: association of TRPC1 with dystrophin complex and the PDZ domain of alpha1-syntrophin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Syntrophins regulate alpha1D-adrenergic receptors through a PDZ domain-mediated interaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

The carboxyterminus of the ATP-binding cassette transporter A1 interacts with a beta2-syntrophin/utrophin complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

The phosphoinositol 3,4-bisphosphate-binding protein TAPP1 interacts with syntrophins and regulates actin cytoskeletal organization

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Interaction of gamma 1-syntrophin with diacylglycerol kinase-zeta. Regulation of nuclear localization by PDZ interactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Protein trafficking and anchoring complexes revealed by proteomic analysis of inward rectifier potassium channel (Kir2.x)-associated proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

The potassium channel Kir4.1 associates with the dystrophin-glycoprotein complex via alpha-syntrophin in glia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Interactions between beta 2-syntrophin and a family of microtubule-associated serine/threonine kinases

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Stress-activated protein kinase-3 interacts with the PDZ domain of alpha1-syntrophin. A mechanism for specific substrate recognition

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

The sarcolemmal calcium pump, alpha-1 syntrophin, and neuronal nitric-oxide synthase are parts of a macromolecular protein complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

α1‐Syntrophin has distinct binding sites for actin and calmodulin

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

Ca2+-calmodulin binding to mouse alpha1 syntrophin: syntrophin is also a Ca2+-binding protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

The C-terminus of human glutaminase L mediates association with PDZ domain-containing proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890802668522

10.1080/07853890802668522

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19172427%20AND%20SRC:MED&resulttype=core&format=json

release_zuala7xi7zgzzossr7riz76vem

20 January 2020

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/zuala7xi7zgzzossr7riz76vem

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference