B. Carr

发表

Comparison of Immortalized Fa2N-4 Cells and Human Hepatocytes as in Vitro Models for Cytochrome P450 Induction

X. Chu, R. Evers, N. Hariparsad, 2008, Drug Metabolism and Disposition.

Induction of drug metabolizing enzymes by 1,7‐phenanthroline and oltipraz in mice is unrelated to Ah‐responsiveness

B. Carr, M. Franklin, 1999 .

Drug-metabolizing enzyme induction by 2,2'-dipyridyl, 1,7-phenanthroline, 7,8-benzoquinoline and oltipraz in mouse.

B. Carr, M. Franklin, 1998, Xenobiotica; the fate of foreign compounds in biological systems.

Selective Inhibition of Dog Hepatic CYP 2 B 11 and CYP 3 A 12

A. D. Rodrigues, B. Carr, T. Rushmore, 2005 .

Selective Inhibition of Dog Hepatic CYP2B11 and CYP3A12

A. D. Rodrigues, B. Carr, T. Rushmore, 2005, Journal of Pharmacology and Experimental Therapeutics.

SELECTIVE INHIBITION OF DOG HEPATIC CYTOCHROMES P 450 2 B 11 AND 3 A 12

A. D. Rodrigues, B. Carr, T. Rushmore, 2005 .

siRNA-Mediated Knockdown of P450 Oxidoreductase in Rats: A Tool to Reduce Metabolism by CYPs and Increase Exposure of High Clearance Compounds

Marian E. Gindy, B. Carr, J. Hochman, 2014, Pharmaceutical Research.

Heterotropic modulation of sulfotransferase 2A1 activity by celecoxib: product ratio switching of ethynylestradiol sulfation.

B. Carr, E. Carlini, Catherine L. Booth-Genthe, 2004, Drug metabolism and disposition: the biological fate of chemicals.

3-methylindole-induced toxicity to human bronchial epithelial cell lines.

A. Pfeifer, S. Burchiel, B. Carr, 2003, Toxicological sciences : an official journal of the Society of Toxicology.

Angiotensin II reduces alcohol intake and choice in water- or food-restricted rats.

B. Carr, T. Allison, P. Kulkosky, 1996, Alcohol.

MK-329 blocks the inhibition of alcohol intake by CCK-8

B. Carr, J. Ballou, P. Kulkosky, 1993, Peptides.

siRNA-Mediated Knockdown of P450 Oxidoreductase in Rats: A Tool to Reduce Metabolism by CYPs and Increase Exposure of High Clearance Compounds

Marian E. Gindy, B. Carr, J. Hochman, 2014, Pharmaceutical Research.

SP1 AND SP3 REGULATE BASAL TRANSCRIPTION OF THE HUMAN CYP2F1 GENE

B. Carr, R. Hines, G. Yost, 2005, Drug Metabolism and Disposition.

SP 1 AND SP 3 REGULATE BASAL TRANSCRIPTION OF THE HUMAN CYP 2 F 1 GENE

B. Carr, R. Hines, G. Yost, 2005 .

Desmethionine-bombesin receptor antagonist blocks bombesin-induced inhibition of alcohol intake.

B. Carr, J. Ballou, P. Kulkosky, 1994, Alcohol.

Characterization of the Human Lung CYP2F1 Gene and Identification of a Novel Lung-specific Binding Motif*

B. Carr, R. Hines, G. Yost, 2003, The Journal of Biological Chemistry.

Monoclonal Antibodies with Identical Fc Sequences Can Bind to FcRn Differentially with Pharmacokinetic Consequences

B. Carr, J. Hochman, P. Lu, 2011, Drug Metabolism and Disposition.

Characterization of pulmonary CYP4B2, specific catalyst of methyl oxidation of 3-methylindole.

B. Carr, G. Yost, G. Dannan, 2003, Molecular pharmacology.

CYP2C75-Involved Autoinduction of Metabolism in Rhesus Monkeys of Methyl 3-Chloro-3′-fluoro-4′-{(1R)-1-[({1-[(trifluoroacetyl)amino]cyclopropyl}carbonyl)amino]ethyl}-1,1′-biphenyl-2-carboxylate (MK-0686), a Bradykinin B1 Receptor Antagonist

B. Ma, M. Bock, S. Kuduk, 2008, Journal of Pharmacology and Experimental Therapeutics.

CYP2C75-Involved Autoinduction of Metabolism in Rhesus Monkeys of Methyl 3-Chloro-3 (cid:1) -fluoro-4 (cid:1) -{(1 R -biphenyl-2-carboxylate (MK-0686), a Bradykinin B 1 Receptor Antagonist

B. Ma, M. Bock, S. Kuduk, 2008 .

Rhesus Monkeys of MK-0686, a Bradykinin B 1 Receptor Antagonist

B. Ma, M. Bock, S. Kuduk, 2008 .

Conditioned taste aversions induced by alcohol and lithium in rats selectively bred for ethanol neurosensitivity.

B. Carr, P. Kulkosky, R. Flores, 1995, Alcoholism, clinical and experimental research.

Development of a liver-targeted siRNA delivery platform with a broad therapeutic window utilizing biodegradable polypeptide-based polymer conjugates.

B. Carr, L. Sepp-Lorenzino, Rob S. Burke, 2014, Journal of controlled release : official journal of the Controlled Release Society.

Capsaicinoids cause inflammation and epithelial cell death through activation of vanilloid receptors.

B. Carr, C. Reilly, D. Crouch, 2003, Toxicological sciences : an official journal of the Society of Toxicology.

Diclofenac hydroxylation in monkeys: efficiency, regioselectivity, and response to inhibitors.

S. Kuduk, B. Carr, T. Rushmore, 2007, Biochemical pharmacology.

An in vivo evaluation of amphiphilic, biodegradable peptide copolymers as siRNA delivery agents.

B. Carr, K. Leander, L. Sepp-Lorenzino, 2014, International journal of pharmaceutics.

Endosomolytic bioreducible poly(amido amine disulfide) polymer conjugates for the in vivo systemic delivery of siRNA therapeutics.

B. Carr, K. Leander, L. Sepp-Lorenzino, 2013, Bioconjugate chemistry.

Characterization of the Rhesus Monkey CYP3A64 Enzyme: Species Comparisons of CYP3A Substrate Specificity and Kinetics Using Baculovirus-Expressed Recombinant Enzymes

A. D. Rodrigues, B. Carr, T. Rushmore, 2006, Drug Metabolism and Disposition.

Novel endosomolytic poly(amido amine) polymer conjugates for systemic delivery of siRNA to hepatocytes in rodents and nonhuman primates.

B. Carr, K. Leander, L. Sepp-Lorenzino, 2014, Bioconjugate chemistry.

Comparison of Immortalized Fa 2 N4 Cells and Human Hepatocytes as in Vitro Models for Cytochrome P 450 Induction

X. Chu, R. Evers, N. Hariparsad, 2008 .

In Vitro and in Vivo CYP3A64 Induction and Inhibition Studies in Rhesus Monkeys: A Preclinical Approach for CYP3A-Mediated Drug Interaction Studies

B. Carr, T. Prueksaritanont, Y. Qiu, 2006, Drug Metabolism and Disposition.

Rifampin Induces the in Vitro Oxidative Metabolism, but Not the in Vivo Clearance of Diclofenac in Rhesus Monkeys

B. Carr, T. Prueksaritanont, Chunze Li, 2006, Drug Metabolism and Disposition.