-
3
-
-
0029889353
-
Endothelial nitric oxide synthase. Expression in Escherichia coli, spectroscopic characterization, and role of tetrahydrobiopterin in dimer formation
-
Rodriguez-Crespo I., Gerber N.C., and Ortiz de Montellano P.R. Endothelial nitric oxide synthase. Expression in Escherichia coli, spectroscopic characterization, and role of tetrahydrobiopterin in dimer formation. J. Biol. Chem. 271 (1996) 11462-11467
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 11462-11467
-
-
Rodriguez-Crespo, I.1
Gerber, N.C.2
Ortiz de Montellano, P.R.3
-
4
-
-
0027320848
-
ω-hydroxyarginine to citrulline and nitrogen oxides and occurrence in NO synthases of a sequence very similar to the heme-binding sequence in P450s
-
ω-hydroxyarginine to citrulline and nitrogen oxides and occurrence in NO synthases of a sequence very similar to the heme-binding sequence in P450s. Biochem. Biophys. Res. Commun. 192 (1993) 53-60
-
(1993)
Biochem. Biophys. Res. Commun.
, vol.192
, pp. 53-60
-
-
Renaud, J.-P.1
Boucher, J.-L.2
Vadon, S.3
Delaforge, M.4
Mansuy, D.5
-
5
-
-
0028821761
-
On the mechanism of nitric oxide formation upon oxidative cleavage of C{double bond, long}N(OH) bonds by NO-synthases and cytochromes P450
-
Mansuy D., Boucher J.-L., and Clement B. On the mechanism of nitric oxide formation upon oxidative cleavage of C{double bond, long}N(OH) bonds by NO-synthases and cytochromes P450. Biochimie 77 (1995) 661-667
-
(1995)
Biochimie
, vol.77
, pp. 661-667
-
-
Mansuy, D.1
Boucher, J.-L.2
Clement, B.3
-
7
-
-
0027330180
-
ω-Hydroxy-l-arginine, a reactional intermediate in nitric oxide biosynthesis, induces cytostasis in human and murine tumor cells
-
ω-Hydroxy-l-arginine, a reactional intermediate in nitric oxide biosynthesis, induces cytostasis in human and murine tumor cells. Biochem. Biophys. Res. Commun. 196 (1993) 1558-1565
-
(1993)
Biochem. Biophys. Res. Commun.
, vol.196
, pp. 1558-1565
-
-
Chénais, B.1
Yapo, A.2
Lepoivre, M.3
Tenu, J.-P.4
-
9
-
-
0028170690
-
ω-Hydroxy-l-arginine, an intermediate in the l-arginine to nitric oxide pathway, is a strong inhibitor of liver and macrophage arginase
-
ω-Hydroxy-l-arginine, an intermediate in the l-arginine to nitric oxide pathway, is a strong inhibitor of liver and macrophage arginase. Biochem. Biophys. Res. Commun. 203 (1994) 1614-1621
-
(1994)
Biochem. Biophys. Res. Commun.
, vol.203
, pp. 1614-1621
-
-
Boucher, J.-L.1
Custot, J.2
Vadon, S.3
Delaforge, M.4
Lepoivre, M.5
Tenu, J.-P.6
Yapo, A.7
Mansuy, D.8
-
11
-
-
0030612791
-
G-hydroxy-l-arginine in patients with rheumatoid arthritis and systemic lupus erythematosus as an index of an increased nitric oxide synthase activity
-
G-hydroxy-l-arginine in patients with rheumatoid arthritis and systemic lupus erythematosus as an index of an increased nitric oxide synthase activity. Ann. Rheum. Dis. 56 (1997) 330-332
-
(1997)
Ann. Rheum. Dis.
, vol.56
, pp. 330-332
-
-
Wigand, R.1
Meyer, J.2
Busse, R.3
Hecker, M.4
-
12
-
-
0025883342
-
Nitric oxide: physiology, pathophysiology, and pharmacology
-
Moncada S., Palmer R.M.J., and Higgs E.A. Nitric oxide: physiology, pathophysiology, and pharmacology. Pharmacol. Rev. 43 (1991) 109-142
-
(1991)
Pharmacol. Rev.
, vol.43
, pp. 109-142
-
-
Moncada, S.1
Palmer, R.M.J.2
Higgs, E.A.3
-
13
-
-
0026629902
-
Nitric oxide as a secretory product of mammalian cells
-
Nathan C. Nitric oxide as a secretory product of mammalian cells. FASEB J. 6 (1992) 3051-3064
-
(1992)
FASEB J.
, vol.6
, pp. 3051-3064
-
-
Nathan, C.1
-
14
-
-
0024260683
-
Enzymatic reduction of benzamidoxime to benzamidine
-
Clement B., Schmitt S., and Zimmermann M. Enzymatic reduction of benzamidoxime to benzamidine. Arch. Pharm. 321 (1988) 955-956
-
(1988)
Arch. Pharm.
, vol.321
, pp. 955-956
-
-
Clement, B.1
Schmitt, S.2
Zimmermann, M.3
-
15
-
-
0036038490
-
Reduction of N-hydroxylated compounds: amidoximes (N-hydroxyamidines) as prodrugs of amidines
-
Clement B. Reduction of N-hydroxylated compounds: amidoximes (N-hydroxyamidines) as prodrugs of amidines. Drug Metab. Rev. 34 (2002) 565-579
-
(2002)
Drug Metab. Rev.
, vol.34
, pp. 565-579
-
-
Clement, B.1
-
16
-
-
0005260048
-
Oxidation and reduction of nitrogen via Cyp450: importance of the reduction of genotoxic N-hydroxylated functional groups
-
Clement B. Oxidation and reduction of nitrogen via Cyp450: importance of the reduction of genotoxic N-hydroxylated functional groups. Drug Metab.: Towards the Next Millenium (1998) 59-71
-
(1998)
Drug Metab.: Towards the Next Millenium
, pp. 59-71
-
-
Clement, B.1
-
17
-
-
0027141919
-
Cytochrome P450 dependent N-hydroxylation of a guanidine (debrisoquine), microsomal catalyzed reduction and further oxidation of the N-hydroxy-guanidine metabolite to the urea derivative
-
Clement B., Schultze-Mosgau M.-H., and Wohlers H. Cytochrome P450 dependent N-hydroxylation of a guanidine (debrisoquine), microsomal catalyzed reduction and further oxidation of the N-hydroxy-guanidine metabolite to the urea derivative. Biochem. Pharmacol. 46 (1993) 2249-2267
-
(1993)
Biochem. Pharmacol.
, vol.46
, pp. 2249-2267
-
-
Clement, B.1
Schultze-Mosgau, M.-H.2
Wohlers, H.3
-
18
-
-
0033787945
-
Reduction of amphetamine hydroxylamine and other aliphatic hydroxylamines by benzamidoxime reductase and human liver microsomes
-
Clement B., Behrens D., Möller W., and Cashman J.R. Reduction of amphetamine hydroxylamine and other aliphatic hydroxylamines by benzamidoxime reductase and human liver microsomes. Chem. Res. Toxicol. 13 (2000) 1037-1045
-
(2000)
Chem. Res. Toxicol.
, vol.13
, pp. 1037-1045
-
-
Clement, B.1
Behrens, D.2
Möller, W.3
Cashman, J.R.4
-
20
-
-
0029967158
-
Microsomal catalyzed N-hydroxylation of guanabenz and reduction of the N-hydroxylated metabolite: characterization of the two reactions and genotoxic potential of guanoxabenz
-
Clement B., Demesmaeker M., and Linne S. Microsomal catalyzed N-hydroxylation of guanabenz and reduction of the N-hydroxylated metabolite: characterization of the two reactions and genotoxic potential of guanoxabenz. Chem. Res. Toxicol. 9 (1996) 682-688
-
(1996)
Chem. Res. Toxicol.
, vol.9
, pp. 682-688
-
-
Clement, B.1
Demesmaeker, M.2
Linne, S.3
-
21
-
-
0025091897
-
Improved methods to isolate and subfractionate rat liver mitochondria. Lipid composition of the inner and outer membrane
-
Hovius R., Lambrechts H., Nicolay K., and deKruijff B. Improved methods to isolate and subfractionate rat liver mitochondria. Lipid composition of the inner and outer membrane. Biochim. Biophys. Acta 1021 (1990) 217-226
-
(1990)
Biochim. Biophys. Acta
, vol.1021
, pp. 217-226
-
-
Hovius, R.1
Lambrechts, H.2
Nicolay, K.3
deKruijff, B.4
-
22
-
-
0017088267
-
Some properties of a detergent-solubilized NADPH-cytochrome c (cytochrome P-450) reductase purified by biospecific affinity chromatography
-
Yasukochi Y., and Masters B.S.S. Some properties of a detergent-solubilized NADPH-cytochrome c (cytochrome P-450) reductase purified by biospecific affinity chromatography. J. Biol. Chem. 251 (1976) 5337-5344
-
(1976)
J. Biol. Chem.
, vol.251
, pp. 5337-5344
-
-
Yasukochi, Y.1
Masters, B.S.S.2
-
23
-
-
0022186670
-
Measurement of protein using bicinchoninic acid
-
Smith P.K., Krohn R.I., Hermanson G.T., Mallia A.K., Gartner F.H., Provenzano M.D., Fujimoto E.K., Goeke N.M., Olson B.J., and Klenk D.C. Measurement of protein using bicinchoninic acid. Anal. Biochem. 150 (1985) 76-85
-
(1985)
Anal. Biochem.
, vol.150
, pp. 76-85
-
-
Smith, P.K.1
Krohn, R.I.2
Hermanson, G.T.3
Mallia, A.K.4
Gartner, F.H.5
Provenzano, M.D.6
Fujimoto, E.K.7
Goeke, N.M.8
Olson, B.J.9
Klenk, D.C.10
-
24
-
-
78651165715
-
The carbon monoxide-binding pigment of liver microsomes, evidence for its hemoprotein nature
-
Omura T., and Sato R. The carbon monoxide-binding pigment of liver microsomes, evidence for its hemoprotein nature. J. Biol. Chem. 239 (1964) 2370-2378
-
(1964)
J. Biol. Chem.
, vol.239
, pp. 2370-2378
-
-
Omura, T.1
Sato, R.2
-
25
-
-
0017869007
-
The measurement of difference spectra: application to the cytochromes of microsomes
-
Estabrook R.W., and Werringloer J. The measurement of difference spectra: application to the cytochromes of microsomes. Methods Enzymol. 52 (1978) 212-221
-
(1978)
Methods Enzymol.
, vol.52
, pp. 212-221
-
-
Estabrook, R.W.1
Werringloer, J.2
|