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Lista de obras de 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).

artículo científico publicado en 2003

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

artículo científico publicado en 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 ⬇️

artículo científico publicado el 1 de agosto de 1997

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

artículo científico publicado en 2009

A dystroglycan mutation associated with limb-girdle muscular dystrophy.

artículo científico publicado en 2011

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

artículo científico publicado en 2006

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.

artículo científico publicado en 1998

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

artículo científico publicado en 2008

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

artículo científico publicado en 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.

artículo científico publicado en 1993

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

artículo científico publicado en 1995

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

artículo científico publicado en 2005

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

artículo científico publicado en 2003

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

artículo científico publicado en 1994

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

artículo científico publicado en 2010

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.

artículo científico publicado en 2003

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

artículo científico publicado en 1994

Alpha6beta4 integrin and dystroglycan cooperate to stabilize the myelin sheath

artículo científico publicado en 2008

An HMGA2-IGF2BP2 axis regulates myoblast proliferation and myogenesis

artículo científico publicado en 2012

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

artículo científico publicado en 1991

Analysis of the role of dystroglycan in early postimplantation mouse development

artículo científico publicado en 1998

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

artículo científico publicado en 1997

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

artículo científico publicado en 2011

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

artículo científico publicado en 2007

Assembly of the sarcoglycan complex. Insights for muscular dystrophy

artículo científico publicado en 1998

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

artículo científico publicado en 1994

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

artículo científico publicado en 1995

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

artículo científico publicado en 2003

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

artículo científico

Beta subunit heterogeneity in N-type Ca2+ channels.

artículo científico publicado en 1996

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

artículo científico publicado en 1998

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

artículo científico publicado en 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

artículo científico publicado en 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.

artículo científico publicado en 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

artículo científico publicado en 2006

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

artículo científico publicado en 2014

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

artículo científico publicado el 8 de mayo de 1998

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

artículo científico publicado en 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.

artículo científico publicado en 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.

artículo científico publicado en 1993

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

artículo científico publicado en 1980

Clinical heterogeneity of adhalin deficiency

artículo científico publicado en 1996

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

artículo científico publicado en 1993

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

artículo científico publicado en 2016

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

artículo científico publicado en 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

artículo científico publicado en 2013

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

artículo científico publicado el 19 de enero de 2011

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

artículo científico publicado en 2005

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

artículo científico publicado en 2000

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

artículo científico publicado el 1 de mayo de 1998

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

artículo científico publicado en 2000

Cortical localization of a calcium release channel in sea urchin eggs

artículo científico publicado en 1992

DIDS inhibition of sarcoplasmic reticulum anion efflux and calcium transport

artículo científico publicado en 1980

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

artículo científico publicado en 2010

Defective membrane repair in dysferlin-deficient muscular dystrophy

artículo científico publicado en 2003

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

artículo científico publicado en 1990

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

artículo científico publicado en 1994

Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy.

artículo científico publicado en 2002

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

artículo científico publicado en 1997

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

artículo científico publicado en 2002

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

artículo científico publicado en 2000

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

artículo científico publicado en 1999

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

artículo científico

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

artículo científico publicado en 1995

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.

artículo científico publicado en 1994

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

artículo científico publicado en 1996

Dysferlin and muscle membrane repair.

artículo científico publicado en 2007

Dystroglycan Function Requires Xylosyl- and Glucuronyltransferase Activities of LARGE ⬇️

artículo científico publicado el 6 de enero de 2012

Dystroglycan Maintains Inner Limiting Membrane Integrity to Coordinate Retinal Development

artículo científico publicado en 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.

artículo científico publicado en 2010

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.

artículo científico publicado en 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

artículo científico publicado en 2005

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

artículo científico publicado en 2006

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

artículo científico publicado en 2009

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

artículo científico publicado en 2012

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

artículo científico publicado en 2000

Dystroglycan: an extracellular matrix receptor linked to the cytoskeleton.

artículo científico publicado en 1996

Dystroglycan: from biosynthesis to pathogenesis of human disease.

artículo científico publicado en 2006

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

artículo científico publicado el 1 de diciembre de 2011

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

artículo científico publicado el 1 de diciembre de 1991

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

artículo científico publicado en 1994

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

artículo científico publicado en 2003

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

artículo científico publicado en 1991

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

artículo científico publicado en 2014

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

artículo científico publicado en 2011

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

artículo científico publicado en 1999

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 ⬇️

artículo científico publicado el 1 de abril de 1984

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

artículo científico publicado en 2010

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

artículo científico publicado en 1994

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

artículo científico publicado en 2019

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

artículo científico publicado en 2017

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

artículo científico publicado el 1 de junio de 1995

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

artículo científico publicado en 1994

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

artículo científico publicado en 1994

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

artículo científico publicado el 1 de agosto de 1995

Expression of sialidase and dystroglycan in human glomerular diseases

artículo científico publicado en 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 ⬇️

artículo científico publicado el 18 de julio de 1997

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

artículo científico publicado en 1996

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

artículo científico publicado en 1991

From adhalinopathies to alpha-sarcoglycanopathies: an overview.

artículo científico publicado en 1996

Fukutin gene mutations cause dilated cardiomyopathy with minimal muscle weakness

artículo científico publicado en 2006

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

artículo científico publicado el 1 de mayo de 1998

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

artículo científico publicado en 2010

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

artículo científico publicado en 2015

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

artículo científico publicado en 2003

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

artículo científico publicado en 2010

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

artículo científico publicado en 2015

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

artículo científico publicado en 1993

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

artículo científico publicado en 2013

Glycomic analyses of mouse models of congenital muscular dystrophy

artículo científico publicado en 2011

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

artículo científico publicado en 1993

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

artículo científico publicado en 2013

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

artículo científico publicado en 2012

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

artículo científico publicado en 1995

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

artículo científico publicado el 1 de junio de 1995

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

artículo científico publicado en 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.

artículo científico publicado en 2013

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

artículo científico publicado en 2007

Interactions of intermediate filament protein synemin with dystrophin and utrophin

artículo científico publicado en 2006

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

artículo científico publicado en 2001

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

artículo científico publicado en 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.

artículo científico publicado en 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.

artículo científico publicado en 2011

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.

artículo científico publicado en 2005

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

artículo científico publicado en 2002

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

artículo científico publicado en 2012

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

artículo científico publicado en 2009

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

artículo científico publicado en 2004

Loss of sarcolemma nNOS in sarcoglycan-deficient muscle.

artículo científico publicado en 2002

MG53's new identity.

artículo científico publicado en 2013

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

artículo científico

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.

artículo científico publicado en 2016

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

artículo científico publicado en 2001

Molecular basis of muscular dystrophies.

artículo científico publicado en 2000

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

artículo científico publicado en 2002

Mouse fukutin deletion impairs dystroglycan processing and recapitulates muscular dystrophy

artículo científico publicado en 2012

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.

artículo científico publicado en 2002

Muscular dystrophy associated with ?-dystroglycan deficiency

artículo científico publicado en 1996

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

artículo científico publicado en 2007

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

artículo científico publicado en 2013

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

artículo científico publicado en 2013

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

artículo científico publicado en 2011

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

artículo científico publicado en 2000

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

artículo científico publicado en 2016

Neurosensory hearing loss in secondary adhalinopathy.

artículo científico publicado en 1996

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

artículo científico publicado en 2010

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

artículo científico publicado en 2003

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

artículo científico publicado en 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.

artículo científico publicado en 2004

Phenotypic heterogeneity in the stargazin allelic series.

artículo científico publicado en 2003

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

artículo científico publicado en 1980

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

artículo científico publicado en 2011

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

artículo científico publicado en 2002

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

artículo científico publicado en 2005

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

artículo científico publicado en 1997

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

artículo científico publicado el 20 de febrero de 1992

Progressive Muscular Dystrophy in α-Sarcoglycan–deficient Mice ⬇️

artículo científico publicado el 21 de septiembre de 1998

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

artículo científico publicado en 1995

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

artículo científico publicado en 2004

Proteomic analysis of plasma membrane and secretory vesicles from human neutrophils

artículo científico publicado en 2007

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

artículo científico publicado en 1994

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

artículo científico publicado en 1993

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

artículo científico publicado en 1988

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

artículo científico publicado en 2007

Radioimmunoassay for the calcium release channel agonist ryanodine

scientific article published on 01 April 1994

Reactive oxygen species deglycosilate glomerular alpha-dystroglycan.

artículo científico publicado en 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.

artículo científico publicado en 2008

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

artículo científico publicado en 2011

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

artículo científico publicado en 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.

artículo científico publicado en 1989

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

artículo científico publicado en 1988

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

artículo científico publicado en 2013

SH3 domain-mediated interaction of dystroglycan and Grb2

artículo científico publicado en 1995

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

artículo científico publicado en 2010

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

artículo científico publicado el 12 de diciembre de 1997

Sarcospan-deficient mice maintain normal muscle function

artículo científico publicado en 2000

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.

artículo científico publicado en 1990

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

artículo científico publicado en 1993

Skeletal Muscle - one year on.

artículo científico publicado en 2012

Skeletal muscle's 3rd year anniversary

artículo científico publicado en 2014

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

artículo científico publicado en 2004

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

artículo científico publicado en 2016

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

artículo científico publicado en 2016

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

artículo científico publicado en 1989

Targeting Schwann cells by nonlytic arenaviral infection selectively inhibits myelination

artículo científico publicado en 2003

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

artículo científico publicado en 2009

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

artículo científico publicado en 1993

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

artículo científico publicado en 2009

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

artículo científico publicado el 1 de julio de 1991

The calcium signal and neutrophil activation.

artículo científico publicado en 1990

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

artículo científico publicado en 2016

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

artículo científico publicado en 2014

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

artículo científico publicado en 1998

The naming of voltage-gated calcium channels

artículo científico publicado en 1994

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

artículo científico publicado en 1993

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

artículo científico publicado en 2011

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.

artículo científico publicado en 1995

Training the next generation of biomedical investigators in glycosciences

artículo científico publicado en 2016

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

artículo científico publicado en 2008

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

artículo científico publicado en 1997

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

artículo científico publicado en 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

artículo científico publicado en 2018

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

scientific journal article

Unraveling the ribbon synapse.

artículo científico publicado en 2008

Utrophin to the rescue

artículo científico publicado en 1996

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

artículo científico publicado en 2011

Visual impairment in the absence of dystroglycan

artículo científico publicado en 2009

Welcome to Skeletal Muscle ⬇️

artículo científico publicado el 24 de enero de 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

artículo científico publicado en 1999

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

artículo científico publicado en 2007

mdx muscle pathology is independent of nNOS perturbation

artículo científico publicado en 1998

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

artículo científico publicado en 2002

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