scholarly article | Q13442814 |
P356 | DOI | 10.1007/BF00132187 |
P698 | PubMed publication ID | 8478423 |
P2093 | author name string | J M Gillis | |
B Boland | |||
R Casteels | |||
B Himpens | |||
P2860 | cites work | Two dissociable phases in the contractile response of the guinea pig isolated vas deferens to adenosine triphosphate | Q23922574 |
The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle | Q24297845 | ||
A new generation of Ca2+ indicators with greatly improved fluorescence properties | Q27860793 | ||
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein | Q28118471 | ||
Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix | Q28296676 | ||
Pharmacological evidence that adenosine triphosphate and noradrenaline are co-transmitters in the guinea-pig vas deferens | Q28384433 | ||
X chromosome-linked muscular dystrophy (mdx) in the mouse | Q28589078 | ||
Decreased osmotic stability of dystrophin-less muscle cells from the mdx mouse | Q35009267 | ||
Cytoplasmic free calcium, myosin light chain phosphorylation, and force in phasic and tonic smooth muscle | Q36434266 | ||
The subcellular distribution of dystrophin in mouse skeletal, cardiac, and smooth muscle | Q36530367 | ||
Increased calcium influx in dystrophic muscle | Q36530501 | ||
Molecular genetics of Duchenne and Becker muscular dystrophy | Q39514462 | ||
Gastrointestinal manifestations of the muscular dystrophies | Q40325881 | ||
Increased activity of calcium leak channels in myotubes of Duchenne human and mdx mouse origin | Q44177784 | ||
Increased protein degradation results from elevated free calcium levels found in muscle from mdx mice | Q46266620 | ||
Evidence against adrenergic motor transmission in the guinea-pig vas deferens | Q46286503 | ||
Calcium entry through stretch-inactivated ion channels in mdx myotubes | Q46603395 | ||
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 deferens | Q52709779 | ||
Monoclonal antibodies against defined regions of the muscular dystrophy protein, dystrophin | Q67658194 | ||
Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy | Q68137662 | ||
Relationship between force and Ca2+ in anococcygeal and vas deferens smooth muscle cells of the mouse | Q68207639 | ||
Free cytoplasmic Ca++ at rest and after cholinergic stimulus is increased in cultured muscle cells from Duchenne muscular dystrophy patients | Q68278618 | ||
Gastric hypomotility in Duchenne's muscular dystrophy | Q68396395 | ||
Possible systemic smooth muscle layer dysfunction due to a deficiency of dystrophin in Duchenne muscular dystrophy | Q69550785 | ||
Chronic intestinal pseudoobstruction as a complication of Duchenne's muscular dystrophy | Q69609464 | ||
Small-caliber skeletal muscle fibers do not suffer deleterious consequences of dystrophic gene expression | Q69681281 | ||
Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy | Q69896114 | ||
Effects of calcium on protein turnover of incubated muscles from mdx mice | Q70140519 | ||
P433 | issue | 1 | |
P304 | page(s) | 133-139 | |
P577 | publication date | 1993-02-01 | |
P1433 | published in | Journal of Muscle Research & Cell Motility | Q13739445 |
P1476 | title | Lack of dystrophin but normal calcium homeostasis in smooth muscle from dystrophic mdx mice | |
P478 | volume | 14 |
Q54519217 | Cellular mechanism underlying the facilitation of contractile response of vas deferens smooth muscle by sodium orthovanadate. |
Q33644573 | Characteristics of skeletal muscle in mdx mutant mice |
Q44864203 | Immunohistochemical detection of neural cell adhesion molecule and laminin in X-linked dystrophic dogs and mdx mice |
Q40500531 | The dystrophin superfamily: variability and complexity |
Q33836366 | Understanding dystrophinopathies: an inventory of the structural and functional consequences of the absence of dystrophin in muscles of the mdx mouse |
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