Increase of nitric oxide synthases and nitrotyrosine in inclusion‐body myositis
暂无分享,去创建一个
W. Engel | V. Askanas | V Askanas | W K Engel | R B Alvarez | C C Yang | RenateB. Alvarez | Valerie Askanas | Chih-Chao Yang
[1] C. Nathan,et al. Regulation of biosynthesis of nitric oxide. , 1994, The Journal of biological chemistry.
[2] W. Engel,et al. Abnormal accumulation of prion protein mRNA in muscle fibers of patients with sporadic inclusion-body myositis and hereditary inclusion-body myopathy. , 1994, The American journal of pathology.
[3] T. Dawson,et al. Gases as biological messengers: nitric oxide and carbon monoxide in the brain , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[4] Guy C. Brown. Nitric oxide regulates mitochondrial respiration and cell functions by inhibiting cytochrome oxidase , 1995, FEBS letters.
[5] W. Engel. Muscle biopsies in neuromuscular diseases. , 1967, Pediatric clinics of North America.
[6] W. Engel,et al. New advances in the understanding of sporadic inclusion‐body myositis and hereditary inclusion‐body myopathies , 1995, Current opinion in rheumatology.
[7] E. El-Fakahany,et al. beta-Amyloid 25-35 activates nitric oxide synthase in a neuronal clone. , 1993, Neuroreport.
[8] W. Engel,et al. Light and electron microscopic localization of beta-amyloid protein in muscle biopsies of patients with inclusion-body myositis. , 1992, The American journal of pathology.
[9] J. Beckman,et al. The role of peroxynitrite in nitric oxide-mediated toxicity. , 1995, Current topics in microbiology and immunology.