scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0065-1281(96)80051-1 |
P698 | PubMed publication ID | 9054190 |
P2093 | author name string | Gossrau R | |
Gosztonyi G | |||
Grozdanovic Z | |||
P2860 | cites work | Duchenne muscular dystrophy: deficiency of dystrophin-associated proteins in the sarcolemma | Q70651010 |
Demonstration of nitric oxide synthase (NOS) in marmosets by NADPH diaphorase (NADPH-d) histochemistry and NOS immunoreactivity | Q70797515 | ||
When NADPH diaphorase (NADPHd) works in the presence of formaldehyde, the enzyme appears to visualize selectively cells with constitutive nitric oxide synthase (NOS) | Q71673738 | ||
Endothelial type nitric oxide synthase in skeletal muscle fibers: mitochondrial relationships | Q71698647 | ||
The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle | Q24297845 | ||
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein | Q28118471 | ||
Glycoprotein complex anchoring dystrophin to sarcolemma | Q28292439 | ||
Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix | Q28296676 | ||
Nitric oxide in skeletal muscle | Q28583418 | ||
Membrane organization of the dystrophin-glycoprotein complex | Q29615149 | ||
Dystrophin: the protein product of the Duchenne muscular dystrophy locus | Q29618077 | ||
Dystrophin-glycoprotein complex: its role in the molecular pathogenesis of muscular dystrophies. | Q40792342 | ||
Deficiency of dystrophin-associated proteins: a common mechanism leading to muscle cell necrosis in severe childhood muscular dystrophies | Q40838945 | ||
Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptide | Q41429227 | ||
Cloned human brain nitric oxide synthase is highly expressed in skeletal muscle | Q41578075 | ||
Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface | Q44350613 | ||
Nitric oxide release is present from incubated skeletal muscle preparations | Q46492515 | ||
Demonstration of a unique population of neurons with NADPH-diaphorase histochemistry | Q48720909 | ||
Association of dystrophin and an integral membrane glycoprotein. | Q52485843 | ||
Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle | Q59089242 | ||
Immunoelectron microscopic localization of dystrophin in myofibres | Q59096146 | ||
Ultrastructural localization of dystrophin in human muscle by using gold immunolabelling | Q68091120 | ||
Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy | Q68137662 | ||
P433 | issue | 1 | |
P921 | main subject | Duchenne muscular dystrophy | Q1648484 |
P304 | page(s) | 61-69 | |
P577 | publication date | 1996-01-01 | |
P1433 | published in | Acta Histochemica | Q2690684 |
P1476 | title | 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 | |
P478 | volume | 98 |
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Q73330668 | Absence of nitric oxide synthase I despite the presence of the dystrophin complex in human striated muscle |
Q71668561 | Adhalin (alpha-sarcoglycan) is not required for anchoring of nitric oxide synthase I (NOS I) to the sarcolemma in non-mammalian skeletal (striated) muscle fibers |
Q53475327 | Administration of chinese herbal medicines facilitates the locomotor activity in dystrophin-deficient mice. |
Q74444837 | Caveolin-3 and nitric oxide synthase I in healthy and diseased skeletal muscle |
Q33644573 | Characteristics of skeletal muscle in mdx mutant mice |
Q73338676 | Differences in the localization of the postsynaptic nitric oxide synthase I and acetylcholinesterase suggest a heterogeneity of neuromuscular junctions in rat and mouse skeletal muscles |
Q31133021 | Early onset of lipofuscin accumulation in dystrophin-deficient skeletal muscles of DMD patients and mdx mice |
Q37088443 | Epigenetic drugs in the treatment of skeletal muscle atrophy. |
Q24538577 | Gene expression comparison of biopsies from Duchenne muscular dystrophy (DMD) and normal skeletal muscle |
Q71875157 | Histochemistry of therapeutically relevant enzymes in human tumours transplanted into severe combined immunodeficient (SCID) mice: nitric oxide synthase-associated diaphorase, beta-D-glucuronidase and non-specific alkaline phosphatase |
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Q77715320 | Inhibition of skeletal muscle sarcoplasmic reticulum Ca2+-ATPase by nitric oxide |
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Q34465013 | NO message from muscle |
Q36560597 | New insights in the regulation of calcium transfers by muscle dystrophin-based cytoskeleton: implications in DMD. |
Q73906319 | Nitric oxide synthase (NOS) I during postnatal development in rat and mouse skeletal muscle |
Q82394991 | Nitric oxide synthase activity in muscle foods |
Q36402599 | Sarcolemmal targeting of nNOSμ improves contractile function of mdx muscle |
Q43122388 | Skeletal muscle contraction-induced vasodilation in the microcirculation |
Q36820423 | Skeletal muscle function during exercise-fine-tuning of diverse subsystems by nitric oxide |
Q46303843 | Sparing of mdx extraocular muscles from dystrophic pathology is not attributable to normalized concentration or distribution of neuronal nitric oxide synthase |
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