scholarly article | Q13442814 |
P356 | DOI | 10.1142/S0192415X01000307 |
P698 | PubMed publication ID | 11527070 |
P2093 | author name string | Chen SS | |
Chen TJ | |||
Yang SL | |||
Wang DC | |||
P2860 | cites work | Nitric oxide synthase complexed with dystrophin and absent from skeletal muscle sarcolemma in Duchenne muscular dystrophy | Q24307833 |
Dystroglycan-alpha, a dystrophin-associated glycoprotein, is a functional agrin receptor | Q28254849 | ||
Nitric oxide in skeletal muscle | Q28583418 | ||
X chromosome-linked muscular dystrophy (mdx) in the mouse | Q28589078 | ||
Mechanical function of dystrophin in muscle cells | Q36235185 | ||
Dystrophin protects the sarcolemma from stresses developed during muscle contraction | Q36259954 | ||
Neuronal nitric oxide synthase and dystrophin-deficient muscular dystrophy | Q37387484 | ||
The muscular dystrophies and dystrophin. | Q40807124 | ||
The potential for gene therapy in Duchenne muscular dystrophy and other genetic muscle diseases | Q40865653 | ||
Dystroglycan: an extracellular matrix receptor linked to the cytoskeleton. | Q41238978 | ||
Cloned human brain nitric oxide synthase is highly expressed in skeletal muscle | Q41578075 | ||
Direct visualization of the dystrophin network on skeletal muscle fiber membrane | Q42549173 | ||
Human dystrophin gene transfer: production and expression of a functional recombinant DNA-based gene | Q42825904 | ||
Immunolocalization of nitric oxide synthases at the postsynaptic domain of human and rat neuromuscular junctions--light and electron microscopic studies | Q43795325 | ||
Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface | Q44350613 | ||
Mini- and full-length dystrophin gene transfer induces the recovery of nitric oxide synthase at the sarcolemma of mdx4cv skeletal muscle fibers | Q45886323 | ||
A role for dystrophin-associated glycoproteins and utrophin in agrin-induced AChR clustering | Q46259714 | ||
Site and mechanics of failure in normal and dystrophin-deficient skeletal muscle | Q46270454 | ||
Muscular dystrophy in the mdx mouse: histopathology of the soleus and extensor digitorum longus muscles. | Q52255659 | ||
Immunoelectron microscopic localization of dystrophin in myofibres | Q59096146 | ||
Retroviral-mediated transfer of a dystrophin minigene into mdx mouse myoblasts in vitro | Q67737573 | ||
Dystrophin: Localization and presumed function | Q67897976 | ||
The mdx mouse skeletal muscle myopathy: II. Contractile properties | Q68025103 | ||
Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy | Q68137662 | ||
The molecular basis of muscular dystrophy in the mdx mouse: a point mutation | Q69514522 | ||
Nondystrophic myoblast transplantation into dystrophic muscle | Q69706327 | ||
Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy | Q69896114 | ||
Skeletal muscle pathology in X chromosome-linked muscular dystrophy (mdx) mouse | Q70039598 | ||
Muscle development in mdx mutant mice | Q70804155 | ||
Increased susceptibility of EDL muscles from mdx mice to damage induced by contractions with stretch | Q72102757 | ||
Muscular weakness in the mdx mouse | Q72726046 | ||
Nitric oxide synthase I (NOS-I) is deficient in the sarcolemma of striated muscle fibers in patients with Duchenne muscular dystrophy, suggesting an association with dystrophin | Q73118962 | ||
P433 | issue | 2 | |
P304 | page(s) | 281-292 | |
P577 | publication date | 2001-01-01 | |
P1433 | published in | The American Journal of Chinese Medicine | Q7713498 |
P1476 | title | Administration of chinese herbal medicines facilitates the locomotor activity in dystrophin-deficient mice. | |
P478 | volume | 29 |
Q91853463 | Characteristics of the traditional Liu-Wei-Di-Huang prescription reassessed in modern pharmacology |
Q44619135 | Detection of glucocorticoid-like activity in traditional Chinese medicine used for the treatment of Duchenne muscular dystrophy |
Q59808437 | Traditional Korean Medicine Treatment for Patients with Wilting Disorder: A Literature Review of In Vivo Studies |
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