Lack of dystrophin but normal calcium homeostasis in smooth muscle from dystrophic mdx mice

scientific article published on 01 February 1993

Lack of dystrophin but normal calcium homeostasis in smooth muscle from dystrophic mdx mice is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1007/BF00132187
P698PubMed publication ID8478423

P2093author name stringJ M Gillis
B Boland
R Casteels
B Himpens
P2860cites workTwo dissociable phases in the contractile response of the guinea pig isolated vas deferens to adenosine triphosphateQ23922574
The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscleQ24297845
A new generation of Ca2+ indicators with greatly improved fluorescence propertiesQ27860793
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal proteinQ28118471
Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrixQ28296676
Pharmacological evidence that adenosine triphosphate and noradrenaline are co-transmitters in the guinea-pig vas deferensQ28384433
X chromosome-linked muscular dystrophy (mdx) in the mouseQ28589078
Decreased osmotic stability of dystrophin-less muscle cells from the mdx mouseQ35009267
Cytoplasmic free calcium, myosin light chain phosphorylation, and force in phasic and tonic smooth muscleQ36434266
The subcellular distribution of dystrophin in mouse skeletal, cardiac, and smooth muscleQ36530367
Increased calcium influx in dystrophic muscleQ36530501
Molecular genetics of Duchenne and Becker muscular dystrophyQ39514462
Gastrointestinal manifestations of the muscular dystrophiesQ40325881
Increased activity of calcium leak channels in myotubes of Duchenne human and mdx mouse originQ44177784
Increased protein degradation results from elevated free calcium levels found in muscle from mdx miceQ46266620
Evidence against adrenergic motor transmission in the guinea-pig vas deferensQ46286503
Calcium entry through stretch-inactivated ion channels in mdx myotubesQ46603395
Developmental regulation of mechanosensitive calcium channels in skeletal muscle from normal and mdx mice.Q52235615
Association of dystrophin and an integral membrane glycoprotein.Q52485843
Some properties of the smooth muscle of mouse vas deferensQ52709779
Monoclonal antibodies against defined regions of the muscular dystrophy protein, dystrophinQ67658194
Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophyQ68137662
Relationship between force and Ca2+ in anococcygeal and vas deferens smooth muscle cells of the mouseQ68207639
Free cytoplasmic Ca++ at rest and after cholinergic stimulus is increased in cultured muscle cells from Duchenne muscular dystrophy patientsQ68278618
Gastric hypomotility in Duchenne's muscular dystrophyQ68396395
Possible systemic smooth muscle layer dysfunction due to a deficiency of dystrophin in Duchenne muscular dystrophyQ69550785
Chronic intestinal pseudoobstruction as a complication of Duchenne's muscular dystrophyQ69609464
Small-caliber skeletal muscle fibers do not suffer deleterious consequences of dystrophic gene expressionQ69681281
Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophyQ69896114
Effects of calcium on protein turnover of incubated muscles from mdx miceQ70140519
P433issue1
P304page(s)133-139
P577publication date1993-02-01
P1433published inJournal of Muscle Research & Cell MotilityQ13739445
P1476titleLack of dystrophin but normal calcium homeostasis in smooth muscle from dystrophic mdx mice
P478volume14

Reverse relations

cites work (P2860)
Q54519217Cellular mechanism underlying the facilitation of contractile response of vas deferens smooth muscle by sodium orthovanadate.
Q33644573Characteristics of skeletal muscle in mdx mutant mice
Q44864203Immunohistochemical detection of neural cell adhesion molecule and laminin in X-linked dystrophic dogs and mdx mice
Q40500531The dystrophin superfamily: variability and complexity
Q33836366Understanding dystrophinopathies: an inventory of the structural and functional consequences of the absence of dystrophin in muscles of the mdx mouse

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