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Nitric Oxide : Biology and Chemistry|October 6, 2001
Titration of low K(d) binding sites: binding of arginine analogs to nitric oxide synthasesS M Smith, C Sham, L Roman, et al.Scandinavian Journal of Clinical and Laboratory Investigation|May 1, 1997
Molecular analysis of porphobilinogen (PBG) deaminase gene mutations in acute intermittent porphyria: first study in patients of Slavic originR Rosipal, H Puy, J Lamoril, et al.Hepatology (Baltimore, Md.)|September 1, 1989
Sensitivity of human tissue heme oxygenase to a new synthetic metalloporphyrinR J Chernick, P Martasek, R D Levere, et al.Bioorganic & Medicinal Chemistry|October 26, 1999
Imidazole-containing amino acids as selective inhibitors of nitric oxide synthasesY Lee, P Martasek, L J Roman, et al.Journal of Medicinal Chemistry|August 17, 1999
N(omega)-Nitroarginine-containing dipeptide amides. Potent and highly selective inhibitors of neuronal nitric oxide synthaseH Huang, P Martasek, L J Roman, et al.Acta Paediatrica (Oslo, Norway : 1992)|October 27, 2004
Clinical, biochemical and molecular analyses of six patients with isolated cytochrome c oxidase deficiency due to mutations in the SCO2 geneK Vesela, H Hansikova, M Tesarova, et al.Human Molecular Genetics|February 1, 1995
A molecular defect in coproporphyrinogen oxidase gene causing harderoporphyria, a variant form of hereditary coproporphyriaJ Lamoril, P Martasek, J C Deybach, et al.Physiological Research|February 15, 2007
De Novo mutation found in the porphobilinogen deaminase gene in Slovak acute intermittent porphyria patient: molecular biochemical studyD Ulbrichova, E Flachsova, M Hrdinka, et al.Biochemistry|September 9, 1997
Substrate binding-induced changes in the EPR spectra of the ferrous nitric oxide complexes of neuronal nitric oxide synthaseC T Migita, J C Salerno, B S Masters, et al.Bratislavske Lekarske Listy|January 7, 2005
A case of Rett syndrome from Ukraine--clinical diagnosis confirmed by mutation analysis of the MECP2 geneV Bzduch, D Zahorakova, E Grechanina, et al.Pageof 4