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Journal Abstract Search

144 related items for PubMed ID: 16876119

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  • 4. 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.
    Grozdanovic Z, Gosztonyi G, Gossrau R.
    Acta Histochem; 1996 Jan; 98(1):61-9. PubMed ID: 9054190
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  • 6. Caveolin-3 and nitric oxide synthase I in healthy and diseased skeletal muscle.
    Gossrau R.
    Acta Histochem; 1998 Feb; 100(1):99-112. PubMed ID: 9542584
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  • 7. Absence of neuronal nitric oxide synthase (nNOS) as a pathological marker for the diagnosis of Becker muscular dystrophy with rod domain deletions.
    Torelli S, Brown SC, Jimenez-Mallebrera C, Feng L, Muntoni F, Sewry CA.
    Neuropathol Appl Neurobiol; 2004 Oct; 30(5):540-5. PubMed ID: 15488030
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  • 8. Utility of dystrophin and utrophin staining in childhood muscular dystrophy.
    Sundaram C, Vydehi B, Meena K, Murthy J.
    Indian J Pathol Microbiol; 2004 Jul; 47(3):367-9. PubMed ID: 16295426
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  • 10. Expression of Leu-19 (CD56, N-CAM) and nitric oxide synthase (NOS) I in denervated and reinnervated human skeletal muscle.
    Gosztonyi G, Naschold U, Grozdanovic Z, Stoltenburg-Didinger G, Gossrau R.
    Microsc Res Tech; 2001 Nov 01; 55(3):187-97. PubMed ID: 11747094
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  • 11. Role of nitric oxide in the pathogenesis of muscular dystrophies: a "two hit" hypothesis of the cause of muscle necrosis.
    Rando TA.
    Microsc Res Tech; 2001 Nov 15; 55(4):223-35. PubMed ID: 11748861
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  • 12. Oxidative stress and nitric oxide synthase in skeletal muscles of rats with post-infarction, compensated chronic heart failure.
    Rush JW, Green HJ, Maclean DA, Code LM.
    Acta Physiol Scand; 2005 Nov 15; 185(3):211-8. PubMed ID: 16218926
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  • 13. 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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  • 14. Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-alpha 2 deficient congenital muscular dystrophy; is congenital muscular dystrophy a primary fibrotic disease?
    Taniguchi M, Kurahashi H, Noguchi S, Sese J, Okinaga T, Tsukahara T, Guicheney P, Ozono K, Nishino I, Morishita S, Toda T.
    Biochem Biophys Res Commun; 2006 Apr 07; 342(2):489-502. PubMed ID: 16487936
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  • 15. Intermittent pneumatic compression regulates expression of nitric oxide synthases in skeletal muscles.
    Tan X, Qi WN, Gu X, Urbaniak JR, Chen LE.
    J Biomech; 2006 Apr 07; 39(13):2430-7. PubMed ID: 16225881
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  • 16. Upregulation of chemokines and their receptors in Duchenne muscular dystrophy: potential for attenuation of myofiber necrosis.
    De Paepe B, Creus KK, Martin JJ, De Bleecker JL.
    Muscle Nerve; 2012 Dec 07; 46(6):917-25. PubMed ID: 23225384
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  • 18. Heme oxygenase-2 is present in the sarcolemma region of skeletal muscle fibers and is non-continuously co-localized with nitric oxide synthase-1.
    Baum O, Feussner M, Richter H, Gossrau R.
    Acta Histochem; 2000 Aug 07; 102(3):281-98. PubMed ID: 10990066
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  • 19. Induction of hematopoietic prostaglandin D synthase in hyalinated necrotic muscle fibers: its implication in grouped necrosis.
    Okinaga T, Mohri I, Fujimura H, Imai K, Ono J, Urade Y, Taniike M.
    Acta Neuropathol; 2002 Oct 07; 104(4):377-84. PubMed ID: 12200624
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  • 20. Nitric oxide synthase in critically ischaemic muscle and alterations in isoform expression during revascularization surgery.
    Tsui JC, Baker DM, Shaw SG, Shi-Wen X, Dashwood MR.
    Br J Surg; 2008 Jan 07; 95(1):72-9. PubMed ID: 17849374
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