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Journal Abstract Search

250 related items for PubMed ID: 9054190

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  • 2. Absence of nitric oxide synthase I despite the presence of the dystrophin complex in human striated muscle.
    Grozdanovic Z, Christova T, Gosztonyi G, Mellerowicz H, Blottner D, Gossrau R.
    Histochem J; 1997 Feb; 29(2):97-104. PubMed ID: 9147066
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  • 3. Nitric oxide synthase is up-regulated in muscle fibers in muscular dystrophy.
    Punkt K, Schering S, Löffler S, Minin EA, Samoilova VE, Hasselblatt M, Paulus W, Müller-Werdan U, Demus U, Koehler G, Boecker W, Buchwalow IB.
    Biochem Biophys Res Commun; 2006 Sep 15; 348(1):259-64. PubMed ID: 16876119
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  • 4. [Association between dystrophin and neuronal nitric oxide synthase in muscles of progressive muscular dystrophy].
    Wang S, Shen D.
    Zhonghua Yi Xue Za Zhi; 2002 Feb 10; 82(3):155-7. PubMed ID: 11953148
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  • 6. The specificity of the histochemical NADPH diaphorase reaction for nitric oxide synthase-1 in skeletal muscles is increased in the presence of urea.
    Baum O, Miethke A, Wöckel A, Willerding G, Planitzer G.
    Acta Histochem; 2002 Feb 10; 104(1):3-14. PubMed ID: 11993849
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  • 9. Fibre-related nitric oxide synthase (NOS) in Duchenne muscular dystrophy.
    Punkt K, Schering S, Fritzsche M, Asmussen G, Minin EA, Samoilova VE, Müller FU, Schmitz W, Hasselblatt M, Paulus W, Müller-Werdan U, Slezak J, Koehler G, Boecker W, Buchwalow IB.
    Acta Histochem; 2007 Feb 10; 109(3):228-36. PubMed ID: 17313973
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  • 10. Nitric oxide synthase complexed with dystrophin and absent from skeletal muscle sarcolemma in Duchenne muscular dystrophy.
    Brenman JE, Chao DS, Xia H, Aldape K, Bredt DS.
    Cell; 1995 Sep 08; 82(5):743-52. PubMed ID: 7545544
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  • 12. Nitric oxide synthase in the heterogeneous population of intramural striated muscle fibres of the human membranous urethral sphincter.
    Ho KM, McMurray G, Brading AF, Noble JG, Ny L, Andersson KE.
    J Urol; 1998 Mar 08; 159(3):1091-6. PubMed ID: 9474237
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  • 13. Co-localization of nitric oxide synthase I (NOS I) and NMDA receptor subunit 1 (NMDAR-1) at the neuromuscular junction in rat and mouse skeletal muscle.
    Grozdanovic Z, Gossrau R.
    Cell Tissue Res; 1998 Jan 08; 291(1):57-63. PubMed ID: 9394043
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  • 14. Mini- and full-length dystrophin gene transfer induces the recovery of nitric oxide synthase at the sarcolemma of mdx4cv skeletal muscle fibers.
    Decrouy A, Renaud JM, Lunde JA, Dickson G, Jasmin BJ.
    Gene Ther; 1998 Jan 08; 5(1):59-64. PubMed ID: 9536265
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  • 15. iNOS expression in dystrophinopathies can be reduced by somatic gene transfer of dystrophin or utrophin.
    Louboutin JP, Rouger K, Tinsley JM, Halldorson J, Wilson JM.
    Mol Med; 2001 May 08; 7(5):355-64. PubMed ID: 11474581
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  • 18. Constitutive properties, not molecular adaptations, mediate extraocular muscle sparing in dystrophic mdx mice.
    Porter JD, Merriam AP, Khanna S, Andrade FH, Richmonds CR, Leahy P, Cheng G, Karathanasis P, Zhou X, Kusner LL, Adams ME, Willem M, Mayer U, Kaminski HJ.
    FASEB J; 2003 May 08; 17(8):893-5. PubMed ID: 12670877
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