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List of works by Kevin P Campbell

114th ENMC International Workshop on Congenital Muscular Dystrophy (CMD) 17-19 January 2003, Naarden, The Netherlands: (8th Workshop of the International Consortium on CMD; 3rd Workshop of the MYO-CLUSTER project GENRE).

scientific article published in September 2003

32,000-Dalton subunit of the 1,4-dihydropyridine receptor

scientific article published on 01 January 1989

A 5' dystrophin duplication mutation causes membrane deficiency of alpha-dystroglycan in a family with X-linked cardiomyopathy

scientific article published on 01 December 1997

A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey ⬇️

scientific article published on August 1, 1997

A comparative study of alpha-dystroglycan glycosylation in dystroglycanopathies suggests that the hypoglycosylation of alpha-dystroglycan does not consistently correlate with clinical severity

scientific article

A dystroglycan mutation associated with limb-girdle muscular dystrophy.

scientific article

A functional AMPA receptor-calcium channel complex in the postsynaptic membrane.

scholarly article

A monoclonal antibody to the Ca2+-ATPase of cardiac sarcoplasmic reticulum cross-reacts with slow type I but not with fast type II canine skeletal muscle fibers: an immunocytochemical and immunochemical study

scientific article published on 01 January 1988

A neuronal ryanodine receptor mediates light-induced phase delays of the circadian clock.

scientific article published in July 1998

A novel POMT2 mutation causes mild congenital muscular dystrophy with normal brain MRI.

scientific article published on 19 September 2008

A novel missense mutation in POMT1 modulates the severe congenital muscular dystrophy phenotype associated with POMT1 nonsense mutations.

scientific article published on 11 January 2014

A role for dystroglycan in basement membrane assembly

scientific article published on 01 December 1998

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

scientific article

A syntrophin gene maps to mouse chromosome 8 and is not the myodystrophy gene

scientific article published on 01 September 1995

Aberrant glycosylation of alpha-dystroglycan causes defective binding of laminin in the muscle of chicken muscular dystrophy

scientific article published on 01 April 2005

Abnormal coronary function in mice deficient in alpha1H T-type Ca2+ channels

scientific article

Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin.

scientific article

Adenosine A(3) receptor stimulation induces protection of skeletal muscle from eccentric exercise-mediated injury

scientific article

Adhalin gene mutations and autosomal recessive limb-girdle muscular dystrophy

scientific article published on 01 September 1995

Adhalin gene polymorphism

article

Alpha-dystroglycan can mediate arenavirus infection in the absence of beta-dystroglycan.

scientific article published on November 2003

Alpha-dystroglycan deficiency correlates with elevated serum creatine kinase and decreased muscle contraction tension in golden retriever muscular dystrophy

scientific article published on 01 August 1994

Alpha6beta4 integrin and dystroglycan cooperate to stabilize the myelin sheath

scientific article published on June 2008

An HMGA2-IGF2BP2 axis regulates myoblast proliferation and myogenesis

scientific article published on 21 November 2012

Analysis of excitation-contraction-coupling components in chronically stimulated canine skeletal muscle.

scientific article published in December 1991

Analysis of the role of dystroglycan in early postimplantation mouse development

scientific article published on 01 October 1998

Animal models for muscular dystrophy show different patterns of sarcolemmal disruption.

scientific article

Anti-epileptic drugs delay age-related loss of spiral ganglion neurons via T-type calcium channel

scientific article

Are voltage-dependent ion channels involved in the endothelial cell control of vasomotor tone?

scientific article published on 18 May 2007

Assembly of the sarcoglycan complex. Insights for muscular dystrophy

scientific article

Assessment of the 50-kDa dystrophin-associated glycoprotein in Brazilian patients with severe childhood autosomal recessive muscular dystrophy.

scientific article published in May 1994

Association of native Ca2+ channel beta subunits with the alpha 1 subunit interaction domain

scientific article published on 01 July 1995

Auxiliary subunits: essential components of the voltage-gated calcium channel complex.

scientific article

Basolateral entry and release of New and Old World arenaviruses from human airway epithelia

scientific article published on 16 April 2008

Beta subunit heterogeneity in N-type Ca2+ channels.

scientific article

Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate

scientific article

Biallelic Mutations in TMTC3, Encoding a Transmembrane and TPR-Containing Protein, Lead to Cobblestone Lissencephaly

scientific article published on 14 October 2016

Binding of Lassa virus perturbs extracellular matrix-induced signal transduction via dystroglycan.

scientific article published on 04 April 2012

Biochemical and pathological changes result from mutated Caveolin-3 in muscle

scholarly article by José Andrés González Coraspe published in August 2018

Biochemical characterization of the epithelial dystroglycan complex

scientific article published on 01 September 1999

Biosynthesis of dystroglycan: processing of a precursor propeptide

scientific article published on 01 February 2000

Both laminin and Schwann cell dystroglycan are necessary for proper clustering of sodium channels at nodes of Ranvier.

scientific article published on October 2005

Brief report: deficiency of a dystrophin-associated glycoprotein (adhalin) in a patient with muscular dystrophy and cardiomyopathy

scientific article published on 01 February 1996

Ca2+ channel regulation by a conserved beta subunit domain

scientific article published on 01 August 1994

CaV3.2 is the major molecular substrate for redox regulation of T-type Ca2+ channels in the rat and mouse thalamus

scientific article

Calcium channel β-subunit binds to a conserved motif in the I–II cytoplasmic linker of the α1-subunit

scientific article published in Nature

Cav3.2 T-type calcium channel is required for the NFAT-dependent Sox9 expression in tracheal cartilage

scientific article

Caveolin‐3 is not an integral component of the dystrophin glycoprotein complex ⬇️

scientific article published on May 8, 1998

Cell Therapy of  -Sarcoglycan Null Dystrophic Mice Through Intra-Arterial Delivery of Mesoangioblasts

scientific article (publication date: 25 July 2003)

Cell entry of Lassa virus induces tyrosine phosphorylation of dystroglycan

scientific article published on 20 December 2012

Cell stiffness and receptors: evidence for cytoskeletal subnetworks.

scientific article published on 22 September 2004

Centronuclear myopathy in mice lacking a novel muscle-specific protein kinase transcriptionally regulated by MEF2

scientific journal article

Characterization of the purified N-type Ca2+ channel and the cation sensitivity of omega-conotoxin GVIA binding.

scientific article published on November 1993

Chloride-induced release of actively loaded calcium from light and heavy sarcoplasmic reticulum vesicles

scientific article published on 01 January 1980

Clinical heterogeneity of adhalin deficiency

scientific article published on 01 February 1996

Clustering and immobilization of acetylcholine receptors by the 43-kD protein: a possible role for dystrophin-related protein.

scientific article

Collagen VI deficiency reduces muscle pathology, but does not improve muscle function, in the γ-sarcoglycan-null mouse

scientific article published on 24 January 2016

Combined deficiency of alpha and epsilon sarcoglycan disrupts the cardiac dystrophin complex

scientific article published on 2 September 2011

Common pathological mechanisms in mouse models for muscular dystrophies

article

Congenital disorder of glycosylation due to DPM1 mutations presenting with dystroglycanopathy-type congenital muscular dystrophy

scientific article

Congenital muscular dystrophy type 1D (MDC1D) due to a large intragenic insertion/deletion, involving intron 10 of the LARGE gene ⬇️

scientific article published on January 19, 2011

Congenital muscular dystrophy with glycosylation defects of alpha-dystroglycan in Japan.

scientific article published in May 2005

Congenital muscular dystrophy with rigid spine syndrome: a clinical, pathological, radiological, and genetic study

scientific article published on 01 February 2000

Contact-dependent regulation of N-type calcium channel subunits during synaptogenesis

scientific article published on May 1, 1998

Contrast agent-enhanced magnetic resonance imaging of skeletal muscle damage in animal models of muscular dystrophy

scientific article published on 01 October 2000

Cortical localization of a calcium release channel in sea urchin eggs

scientific article published on March 1992

DIDS inhibition of sarcoplasmic reticulum anion efflux and calcium transport

scientific article published on 01 January 1980

Decoding arenavirus pathogenesis: essential roles for alpha-dystroglycan-virus interactions and the immune response.

scientific article

Defective membrane repair in dysferlin-deficient muscular dystrophy

scientific article (publication date: 8 May 2003)

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

scientific article published in Nature

Deficiency of the 50 kDa dystrophin-associated glycoprotein and abnormal expression of utrophin in two south Asian cousins with variable expression of severe childhood autosomal recessive muscular dystrophy

scientific article published on 01 March 1994

Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy.

scientific article

Differential expression of dystrophin, utrophin and dystrophin-associated proteins in peripheral nerve

scientific article published on 01 November 1993

Direct binding of G-protein betagamma complex to voltage-dependent calcium channels

scientific article

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

scientific article published in September 2002

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

scientific article (publication date: 2000)

Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy

scientific article (publication date: 20 August 1999)

Distinct functions of glial and neuronal dystroglycan in the developing and adult mouse brain.

scientific article published on October 2010

Distribution of alpha-dystroglycan during embryonic nerve-muscle synaptogenesis.

scientific article

Distribution of dystroglycan in normal adult mouse tissues

scientific journal article

Dp71 can restore the dystrophin-associated glycoprotein complex in muscle but fails to prevent dystrophy.

scientific article published on December 1994

Dual function of the voltage-dependent Ca2+ channel alpha 2 delta subunit in current stimulation and subunit interaction.

scientific article published in February 1996

Dysferlin and muscle membrane repair.

scientific article

Dystroglycan Function Requires Xylosyl- and Glucuronyltransferase Activities of LARGE ⬇️

scientific article published on January 6, 2012

Dystroglycan Maintains Inner Limiting Membrane Integrity to Coordinate Retinal Development

scientific article published on 31 July 2017

Dystroglycan binding to laminin alpha1LG4 module influences epithelial morphogenesis of salivary gland and lung in vitro

scientific journal article

Dystroglycan controls signaling of multiple hormones through modulation of STAT5 activity.

scientific article

Dystroglycan expression in the wild type and mdx mouse neural retina: synaptic colocalization with dystrophin, dystrophin-related protein but not laminin

scientific article published on 01 November 1995

Dystroglycan in development and disease.

scientific article published in October 1998

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

scientific journal article

Dystroglycan is involved in laminin-1-stimulated motility of Müller glial cells: combined velocity and directionality analysis

scientific article published on 01 March 2005

Dystroglycan loss disrupts polarity and beta-casein induction in mammary epithelial cells by perturbing laminin anchoring.

scientific article

Dystroglycan matrix receptor function in cardiac myocytes is important for limiting activity-induced myocardial damage.

scientific article published on 24 September 2009

Dystroglycan on radial glia end feet is required for pial basement membrane integrity and columnar organization of the developing cerebral cortex.

scientific article

Dystroglycan overexpression in vivo alters acetylcholine receptor aggregation at the neuromuscular junction.

scientific article published in November 2000

Dystroglycan: an extracellular matrix receptor linked to the cytoskeleton.

scientific article published on October 1996

Dystroglycan: from biosynthesis to pathogenesis of human disease.

scientific article

Dystrophin deficiency exacerbates skeletal muscle pathology in dysferlin-null mice ⬇️

scientific article published on December 1, 2011

Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice ⬇️

scientific article published on December 1, 1991

Dystrophin-glycoprotein complex: its role in the molecular pathogenesis of muscular dystrophies.

scientific article

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

scientific article

Dystrophin-related protein is localized to neuromuscular junctions of adult skeletal muscle

scientific article published on 01 September 1991

Endogenous glucuronyltransferase activity of LARGE or LARGE2 required for functional modification of α-dystroglycan in cells and tissues

scientific article

Endpoint measures in the mdx mouse relevant for muscular dystrophy pre-clinical studies

scientific article published on 10 December 2011

Enteroviral protease 2A cleaves dystrophin: evidence of cytoskeletal disruption in an acquired cardiomyopathy.

scientific article

Evidence for the presence of calsequestrin in both peripheral and interior regions of sheep Purkinje fibers

scientific article published on 01 August 1984

Evidence for the presence of calsequestrin in two structurally different regions of myocardial sarcoplasmic reticulum ⬇️

scientific article published on April 1, 1984

Exercise-induced left ventricular systolic dysfunction in women heterozygous for dystrophinopathy

scientific article

Exogenous Dp71 restores the levels of dystrophin associated proteins but does not alleviate muscle damage in mdx mice

scientific article published on 01 December 1994

Exogenous expression of the glycosyltransferase LARGE1 restores α-dystroglycan matriglycan and laminin binding in rhabdomyosarcoma

scientific article published on 04 May 2019

Exome sequencing reveals independent SGCD deletions causing limb girdle muscular dystrophy in Boston terriers

scientific article published on 11 July 2017

Expression of Deletion-Containing Dystrophins in mdx Muscle: Implications for Gene Therapy and Dystrophin Function ⬇️

scientific article published on June 1, 1995

Expression of dystrophin-associated glycoproteins and utrophin in carriers of Duchenne muscular dystrophy.

scientific article

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

scientific article published in July 1994

Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy ⬇️

scientific article published on August 1, 1995

Expression of sialidase and dystroglycan in human glomerular diseases

scientific article published on 15 September 2009

Expression, localization and functions in acrosome reaction and sperm motility of CaV3.1 and CaV3.2 channels in sperm cells: An evaluation from CaV3.1 and CaV3.2 deficient mice

Extracellular Interaction of the Voltage-dependent Ca2+ Channel α2δ and α1 Subunits ⬇️

scientific article published on July 18, 1997

Forced expression of dystrophin deletion constructs reveals structure-function correlations.

scientific article

Frog cardiac calsequestrin. Identification, characterization, and subcellular distribution in two structurally distinct regions of peripheral sarcoplasmic reticulum in frog ventricular myocardium

scientific article published on 01 August 1991

From adhalinopathies to alpha-sarcoglycanopathies: an overview.

scientific article published on December 1996

Fukutin gene mutations cause dilated cardiomyopathy with minimal muscle weakness

scientific article

Functional Rescue of the Sarcoglycan Complex in the BIO 14.6 Hamster Using δ-Sarcoglycan Gene Transfer ⬇️

scientific article published on May 1, 1998

Functional glycosylation of dystroglycan is crucial for thymocyte development in the mouse

scientific article

Further characterization of light and heavy sarcoplasmic reticulum vesicles. Identification of the 'sarcoplasmic reticulum feet' associated with heavy sarcoplasmic reticulum vesicles

scientific article published on 01 October 1980

GMPPB-Associated Dystroglycanopathy: Emerging Common Variants with Phenotype Correlation

scientific article published on 27 August 2015

Gene transfer establishes primacy of striated vs. smooth muscle sarcoglycan complex in limb-girdle muscular dystrophy.

scientific article

Genetic ablation of complement C3 attenuates muscle pathology in dysferlin-deficient mice

scientific article

Genetic characterization and improved genotyping of the dysferlin-deficient mouse strain Dysf (tm1Kcam)

scientific article

Genetic heterogeneity for Duchenne-like muscular dystrophy (DLMD) based on linkage and 50 DAG analysis.

scientific article published on November 1993

Glial scaffold required for cerebellar granule cell migration is dependent on dystroglycan function as a receptor for basement membrane proteins

scientific article published on 6 September 2013

Glycomic analyses of mouse models of congenital muscular dystrophy

scientific article

Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization

scientific article (publication date: October 1993)

ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies

scientific article published on 3 January 2013

ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome

scientific article

Identification and characterization of proteins in sarcoplasmic reticulum from normal and failing human left ventricles

scientific article published on 01 December 1990

Identification and characterization of the dystrophin anchoring site on beta-dystroglycan

scientific article

Identification of a novel mutant transcript of laminin α2 chain gene responsible for muscular dystrophy and dysmyelination in dy2J mice ⬇️

scientific article published on June 1, 1995

Identification of alpha-syntrophin binding to syntrophin triplet, dystrophin, and utrophin

scientific article (publication date: 10 March 1995)

Identification of muscle-specific calpain and β-sarcoglycan genes in progressive autosomal recessive muscular dystrophies

article

Illuminating regeneration: noninvasive imaging of disease progression in muscular dystrophy.

scientific article published on 24 April 2013

Inhibition of recombinant N-type Ca(V) channels by the gamma 2 subunit involves unfolded protein response (UPR)-dependent and UPR-independent mechanisms.

scientific article published on March 2007

Interactions of intermediate filament protein synemin with dystrophin and utrophin

scientific article

Intramembrane charge movements and excitation- contraction coupling expressed by two-domain fragments of the Ca2+ channel.

scientific article

Involvement of Ca2+ channel synprint site in synaptic vesicle endocytosis.

scientific article published in January 2010

Ion pathways in proteins of the sarcoplasmic reticulum

scientific article published on 01 January 1980

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

scientific article published on 6 June 2004

LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophy

scientific journal article

Like-acetylglucosaminyltransferase (LARGE)-dependent modification of dystroglycan at Thr-317/319 is required for laminin binding and arenavirus infection.

scientific article

Limb-girdle muscular dystrophy in the United States

scientific article published on 01 October 2006

Localization of alpha-dystroglycan on the podocyte: from top to toe.

scientific article published on 13 June 2005

Long-term regulation of voltage-gated Ca(2+) channels by gabapentin

scientific article published in September 2002

Loss of LARGE2 disrupts functional glycosylation of α-dystroglycan in prostate cancer.

scientific article published on 6 December 2012

Loss of alpha-dystroglycan laminin binding in epithelium-derived cancers is caused by silencing of LARGE.

scientific article published on 24 February 2009

Loss of basement membrane, receptor and cytoskeletal lattices in a laminin-deficient muscular dystrophy

scientific article published on 20 January 2004

Loss of sarcolemma nNOS in sarcoglycan-deficient muscle.

scientific article published in November 2002

MG53's new identity.

scientific article published on November 2013

Matriglycan: a novel polysaccharide that links dystroglycan to the basement membrane.

scientific article published on 16 April 2015

Merosin-negative congenital muscular dystrophy associated with extensive brain abnormalities

scientific article published on 01 November 1995

Molecular Signatures of Membrane Protein Complexes Underlying Muscular Dystrophy.

scientific article published on 20 April 2016

Molecular analysis of the interaction of LCMV with its cellular receptor [alpha]-dystroglycan.

scientific article published on 15 October 2001

Molecular basis of muscular dystrophies.

scientific article

Molecular characterization of a two-domain form of the neuronal voltage-gated P/Q-type calcium channel alpha(1)2.1 subunit

scientific article published on December 2002

Mouse fukutin deletion impairs dystroglycan processing and recapitulates muscular dystrophy

scientific article

Muscles of mice deficient in alpha-sarcoglycan maintain large masses and near control force values throughout the life span

scientific article published on 10 May 2005

Muscular dystrophies involving the dystrophin-glycoprotein complex: an overview of current mouse models.

scientific article

Muscular dystrophy associated with ?-dystroglycan deficiency

scientific article published on 01 December 1996

Mutation associated with an autosomal dominant cone-rod dystrophy CORD7 modifies RIM1-mediated modulation of voltage-dependent Ca2+ channels.

scientific article

Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan

scientific article

Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan

scientific article

Myoglobinuria and muscle pain are common in patients with limb-girdle muscular dystrophy 2I.

scientific article

Neural regulation of alpha-dystroglycan biosynthesis and glycosylation in skeletal muscle

scientific article published on 01 January 2000

Neuronal Dystroglycan Is Necessary for Formation and Maintenance of Functional CCK-Positive Basket Cell Terminals on Pyramidal Cells.

scientific article published in October 2016

Neurosensory hearing loss in secondary adhalinopathy.

scientific article published in February 1996

O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin binding.

scientific article

Opposing roles of integrin alpha6Abeta1 and dystroglycan in laminin-mediated extracellular signal-regulated kinase activation

scientific article published on 6 February 2003

PGC-1alpha regulates the neuromuscular junction program and ameliorates Duchenne muscular dystrophy.

scientific article published on April 2007

POMK regulates dystroglycan function via LARGE-mediated elongation of matriglycan

scientific article published on 25 September 2020

POMT1 mutation results in defective glycosylation and loss of laminin-binding activity in alpha-DG.

scientific article

Phenotypic heterogeneity in the stargazin allelic series.

scientific article published in August 2003

Phosphorylation of heavy sarcoplasmic reticulum vesicles: identification and characterization of three phosphorylated proteins

scientific article published on 01 October 1980

Point mutation in the glycoprotein of lymphocytic choriomeningitis virus is necessary for receptor binding, dendritic cell infection, and long-term persistence.

scientific article

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

scientific article

Posttranslational modification of alpha-dystroglycan, the cellular receptor for arenaviruses, by the glycosyltransferase LARGE is critical for virus binding.

scientific article

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

scientific article published in May 1997

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

scientific article published on February 20, 1992

Progressive Muscular Dystrophy in α-Sarcoglycan–deficient Mice ⬇️

scientific article published on September 21, 1998

Properties of the alpha 1-beta anchoring site in voltage-dependent Ca2+ channels.

scientific article published in May 1995

Proteolytic enzymes and altered glycosylation modulate dystroglycan function in carcinoma cells.

scientific article published on September 2004

Proteomic analysis of plasma membrane and secretory vesicles from human neutrophils

scientific article

Purification and reconstitution of N-type calcium channel complex from rabbit brain

scientific article published on 01 January 1994

Purification of dystrophin-related protein (utrophin) from lung and its identification in pulmonary artery endothelial cells

scientific article published on 01 July 1993

Purified ryanodine receptor from rabbit skeletal muscle is the calcium-release channel of sarcoplasmic reticulum.

scientific article

RIM1 confers sustained activity and neurotransmitter vesicle anchoring to presynaptic Ca2+ channels.

scientific article published on 13 May 2007

Radioimmunoassay for the calcium release channel agonist ryanodine

scientific article published on 01 April 1994

Reactive oxygen species deglycosilate glomerular alpha-dystroglycan.

scientific article published in May 2006

Reduced expression of dystroglycan in breast and prostate cancer

scientific article published on 01 August 2001

Residual laminin-binding activity and enhanced dystroglycan glycosylation by LARGE in novel model mice to dystroglycanopathy.

scientific article

Response to the letter: “On the localization of ClC-1 in skeletal muscle fibers”.

scientific article published in March 2011

Restoration of dystrophin-associated proteins in skeletal muscle of mdx mice transgenic for dystrophin gene.

scientific article published in April 1993

Role of dystroglycan in limiting contraction-induced injury to the sarcomeric cytoskeleton of mature skeletal muscle.

scientific article published on 13 September 2016

Role of the ryanodine receptor of skeletal muscle in excitation-contraction coupling.

scientific article

Ryanodine receptor of skeletal muscle is a gap junction-type channel.

scientific article

SGK196 is a glycosylation-specific O-mannose kinase required for dystroglycan function

scientific article

SH3 domain-mediated interaction of dystroglycan and Grb2

scientific article

Sarcolemmal-restricted localization of functional ClC-1 channels in mouse skeletal muscle ⬇️

scientific article

Sarcospan, the 25-kDa Transmembrane Component of the Dystrophin-Glycoprotein Complex ⬇️

scientific article published on December 12, 1997

Sarcospan-deficient mice maintain normal muscle function

scientific article

Sequence similarity of calreticulin with a Ca2(+)-binding protein that co-purifies with an Ins(1,4,5)P3-sensitive Ca2+ store in HL-60 cells.

scientific article published on September 1990

Single base polymorphism in the DAG1 gene detected by DGGE and mismatch PCR.

scientific article published in November 1993

Skeletal Muscle - one year on.

scientific article published on 5 January 2012

Skeletal muscle's 3rd year anniversary

scientific article published on 24 January 2014

Structural analysis of the voltage-dependent calcium channel beta subunit functional core and its complex with the alpha 1 interaction domain

scientific article

Structural and functional correlates of a mutation in the malignant hyperthermia-susceptible pig ryanodine receptor

scientific article published on 01 April 1992

Structural basis of laminin binding to the LARGE glycans on dystroglycan

scientific article

Structure of protein O-mannose kinase reveals a unique active site architecture.

scientific article

Subcellular distribution of the 1,4-dihydropyridine receptor in rabbit skeletal muscle in situ: an immunofluorescence and immunocolloidal gold-labeling study.

scientific article

Targeting Schwann cells by nonlytic arenaviral infection selectively inhibits myelination

scientific article

The Ca(v)3.2 T-type Ca(2+) channel is required for pressure overload-induced cardiac hypertrophy in mice

scientific article published on 2 January 2009

The Ca2+-release channel/ryanodine receptor is localized in junctional and corbular sarcoplasmic reticulum in cardiac muscle.

scientific article

The alpha(2)delta subunit augments functional expression and modifies the pharmacology of Ca(V)1.3 L-type channels

scientific article published on 30 September 2009

The brain ryanodine receptor: A caffeine-sensitive calcium release channel ⬇️

scientific article published on July 1, 1991

The calcium signal and neutrophil activation.

scientific article published on April 1990

The functional O-mannose glycan on α-dystroglycan contains a phospho-ribitol primed for matriglycan addition

scientific article

The glucuronyltransferase B4GAT1 is required for initiation of LARGE-mediated α-dystroglycan functional glycosylation

scientific article

The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit.

scientific article published on August 1998

The naming of voltage-gated calcium channels

scientific article published on 01 September 1994

The role of the dystrophin-glycoprotein complex in the molecular pathogenesis of muscular dystrophies.

scientific article published on September 1993

The unfolded protein response mediates adaptation to exercise in skeletal muscle through a PGC-1α/ATF6α complex

scientific article

Third International Workshop for Glycosylation Defects in Muscular Dystrophies, 18-19 April 2013, Charlotte, USA

scientific article published on 03 March 2014

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

scientific article published on March 1995

Training the next generation of biomedical investigators in glycosciences

scientific article published on February 2016

Transcriptional upregulation of Cav3.2 mediates epileptogenesis in the pilocarpine model of epilepsy.

scientific article

Transient expression of Dp140, a product of the Duchenne muscular dystrophy locus, during kidney tubulogenesis.

scientific article published on January 1997

Two separate Ni(2+) -sensitive voltage-gated Ca(2+) channels modulate transretinal signalling in the isolated murine retina

scientific article published on 23 August 2011

Ultrastructural localization of calsequestrin in rat skeletal muscle by immunoferritin labeling of ultrathin frozen sections

scientific journal article

Uniparental disomy unveils a novel recessive mutation in POMT2

scientific article published on 10 April 2018

Unique role of dystroglycan in peripheral nerve myelination, nodal structure, and sodium channel stabilization

scientific journal article

Unraveling the ribbon synapse.

scientific article published in August 2008

Utrophin to the rescue

scientific article published in Nature

Variable disease severity in Saudi Arabian and Sudanese families with c.3924 + 2 T > C mutation of LAMA2.

scientific article

Visual impairment in the absence of dystroglycan

scientific article

Welcome to Skeletal Muscle ⬇️

scientific article published on January 24, 2011

Xylosyl- and glucuronyltransferase functions of LARGE in α-dystroglycan modification are conserved in LARGE2

scientific journal article

beta subunit reshuffling modifies N- and P/Q-type Ca2+ channel subunit compositions in lethargic mouse brain

scientific journal article

epsilon-sarcoglycan replaces alpha-sarcoglycan in smooth muscle to form a unique dystrophin-glycoprotein complex

scientific article published on 01 September 1999

gamma1-dependent down-regulation of recombinant voltage-gated Ca2+ channels

scientific article

mdx muscle pathology is independent of nNOS perturbation

scientific article published on 01 May 1998

γ1Subunit Interactions within the Skeletal Muscle L-type Voltage-gated Calcium Channels

scientific article published on 29 October 2002

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