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Correction to: "Constitutive Androgen Receptor-Null Mice Are Sensitive to the Toxic Effects of Parathion: Association with Reduced Cytochrome P450-Mediated Parathion Metabolism".

Drug metabolism and disposition: the biological fate of chemicals

[No authors listed]
PMID: 26126545
Drug Metab Dispos. 2015 Aug;43(8):1285. doi: 10.1124/dmd.115.032961err.

No abstract available.

Cite
Correction to: "Constitutive Androgen Receptor-Null Mice Are Sensitive to the Toxic Effects of Parathion: Association with Reduced Cytochrome P450-Mediated Parathion Metabolism". Drug Metab Dispos. 2015;43(8):1285doi: 10.1124/dmd.115.032961err.
(2015). Correction to: "Constitutive Androgen Receptor-Null Mice Are Sensitive to the Toxic Effects of Parathion: Association with Reduced Cytochrome P450-Mediated Parathion Metabolism". Drug metabolism and disposition: the biological fate of chemicals, 43(8), 1285. https://doi.org/10.1124/dmd.115.032961err
"Correction to: "Constitutive Androgen Receptor-Null Mice Are Sensitive to the Toxic Effects of Parathion: Association with Reduced Cytochrome P450-Mediated Parathion Metabolism"." Drug metabolism and disposition: the biological fate of chemicals vol. 43,8 (2015): 1285. doi: https://doi.org/10.1124/dmd.115.032961err
Correction to: "Constitutive Androgen Receptor-Null Mice Are Sensitive to the Toxic Effects of Parathion: Association with Reduced Cytochrome P450-Mediated Parathion Metabolism". Drug Metab Dispos. 2015 Aug;43(8):1285. doi: 10.1124/dmd.115.032961err. PMID: 26126545; PMCID: PMC4518062.
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Correction to "p38 MAP Kinase Links CAR Activation and Inactivation in the Nucleus via Phosphorylation at Threonine 38 s".

Drug metabolism and disposition: the biological fate of chemicals

[No authors listed]
PMID: 28292786
Drug Metab Dispos. 2017 Apr;45(4):418. doi: 10.1124/dmd.115.070235err.

No abstract available.

Cite
Correction to "p38 MAP Kinase Links CAR Activation and Inactivation in the Nucleus via Phosphorylation at Threonine 38 s". Drug Metab Dispos. 2017;45(4):418doi: 10.1124/dmd.115.070235err.
(2017). Correction to "p38 MAP Kinase Links CAR Activation and Inactivation in the Nucleus via Phosphorylation at Threonine 38 s". Drug metabolism and disposition: the biological fate of chemicals, 45(4), 418. https://doi.org/10.1124/dmd.115.070235err
"Correction to "p38 MAP Kinase Links CAR Activation and Inactivation in the Nucleus via Phosphorylation at Threonine 38 s"." Drug metabolism and disposition: the biological fate of chemicals vol. 45,4 (2017): 418. doi: https://doi.org/10.1124/dmd.115.070235err
Correction to "p38 MAP Kinase Links CAR Activation and Inactivation in the Nucleus via Phosphorylation at Threonine 38 s". Drug Metab Dispos. 2017 Apr;45(4):418. doi: 10.1124/dmd.115.070235err. PMID: 28292786; PMCID: PMC5363698.
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Correction to "The Impact of Single Nucleotide Polymorphisms on Human Aldehyde Oxidase".

Drug metabolism and disposition: the biological fate of chemicals

[No authors listed]
PMID: 26842736
Drug Metab Dispos. 2016 Mar;44(3):365. doi: 10.1124/dmd.112.043828err.

No abstract available.

Cite
Correction to "The Impact of Single Nucleotide Polymorphisms on Human Aldehyde Oxidase". Drug Metab Dispos. 2016;44(3):365doi: 10.1124/dmd.112.043828err.
(2016). Correction to "The Impact of Single Nucleotide Polymorphisms on Human Aldehyde Oxidase". Drug metabolism and disposition: the biological fate of chemicals, 44(3), 365. https://doi.org/10.1124/dmd.112.043828err
"Correction to "The Impact of Single Nucleotide Polymorphisms on Human Aldehyde Oxidase"." Drug metabolism and disposition: the biological fate of chemicals vol. 44,3 (2016): 365. doi: https://doi.org/10.1124/dmd.112.043828err
Correction to "The Impact of Single Nucleotide Polymorphisms on Human Aldehyde Oxidase". Drug Metab Dispos. 2016 Mar;44(3):365. doi: 10.1124/dmd.112.043828err. PMID: 26842736.
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Phosphocholine conjugation: an unexpected in vivo conjugation pathway associated with hepatitis c ns5b inhibitors featuring a bicyclo[1.1.1]pentane.

Drug metabolism and disposition: the biological fate of chemicals

Zhuo X, Cantone JL, Wang Y, Leet JE, Drexler DM, Yeung KS, Huang XS, Eastman KJ, Parcella KE, Mosure KW, Soars MG, Kadow JF, Johnson BM.
PMID: 26961241
Drug Metab Dispos. 2016 Aug;44(8):1332-1340. doi: 10.1124/dmd.115.069062. Epub 2016 Mar 09.

During a medicinal chemistry campaign to identify inhibitors of the hepatitis C virus nonstructural protein 5B (RNA-dependent RNA polymerase), a bicyclo[1.1.1]pentane was introduced into the chemical scaffold to improve metabolic stability. The inhibitors bearing this feature, 5-(3-(bicyclo[1.1.1]pentan-1-ylcarbamoyl)-4-fluorophenyl)-2-(4-fluorophenyl)-N-methyl-6-(3,3,3-trifluoropropyl)furo[2,3-b]pyridine-3-carboxamide (1) and...

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Zhuo X, Cantone JL, Wang Y, et al. Phosphocholine conjugation: an unexpected in vivo conjugation pathway associated with hepatitis c ns5b inhibitors featuring a bicyclo[1.1.1]pentane. Drug Metab Dispos. 2016;44(8):1332-1340doi: 10.1124/dmd.115.069062.
Zhuo, X., Cantone, J. L., Wang, Y., Leet, J. E., Drexler, D. M., Yeung, K. S., Huang, X. S., Eastman, K. J., Parcella, K. E., Mosure, K. W., Soars, M. G., Kadow, J. F., & Johnson, B. M. (2016). Phosphocholine conjugation: an unexpected in vivo conjugation pathway associated with hepatitis c ns5b inhibitors featuring a bicyclo[1.1.1]pentane. Drug metabolism and disposition: the biological fate of chemicals, 44(8), 1332-1340. https://doi.org/10.1124/dmd.115.069062
Zhuo, Xiaoliang, et al. "Phosphocholine conjugation: an unexpected in vivo conjugation pathway associated with hepatitis c ns5b inhibitors featuring a bicyclo[1.1.1]pentane." Drug metabolism and disposition: the biological fate of chemicals vol. 44,8 (2016): 1332-1340. doi: https://doi.org/10.1124/dmd.115.069062
Zhuo X, Cantone JL, Wang Y, Leet JE, Drexler DM, Yeung KS, Huang XS, Eastman KJ, Parcella KE, Mosure KW, Soars MG, Kadow JF, Johnson BM. Phosphocholine conjugation: an unexpected in vivo conjugation pathway associated with hepatitis c ns5b inhibitors featuring a bicyclo[1.1.1]pentane. Drug Metab Dispos. 2016 Aug;44(8):1332-1340. doi: 10.1124/dmd.115.069062. Epub 2016 Mar 09. PMID: 26961241.
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Correction to: "hepatic uptake of atorvastatin: influence of variability in transporter expression on uptake clearance and drug-drug interactions".

Drug metabolism and disposition: the biological fate of chemicals

[No authors listed]
PMID: 25838404
Drug Metab Dispos. 2015 May;43(5):786-7. doi: 10.1124/dmd.114.056309err.

No abstract available.

Cite
Correction to: "hepatic uptake of atorvastatin: influence of variability in transporter expression on uptake clearance and drug-drug interactions". Drug Metab Dispos. 2015;43(5):786-7doi: 10.1124/dmd.114.056309err.
(2015). Correction to: "hepatic uptake of atorvastatin: influence of variability in transporter expression on uptake clearance and drug-drug interactions". Drug metabolism and disposition: the biological fate of chemicals, 43(5), 786-7. https://doi.org/10.1124/dmd.114.056309err
"Correction to: "hepatic uptake of atorvastatin: influence of variability in transporter expression on uptake clearance and drug-drug interactions"." Drug metabolism and disposition: the biological fate of chemicals vol. 43,5 (2015): 786-7. doi: https://doi.org/10.1124/dmd.114.056309err
Correction to: "hepatic uptake of atorvastatin: influence of variability in transporter expression on uptake clearance and drug-drug interactions". Drug Metab Dispos. 2015 May;43(5):786-7. doi: 10.1124/dmd.114.056309err. PMID: 25838404.
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The metabolic fate of stiripentol in the rat. Studies on cytochrome P-450-mediated methylenedioxy ring cleavage and side chain isomerism.

Drug metabolism and disposition: the biological fate of chemicals

Zhang K, Lepage F, Cuvier G, Astoin J, Rashed MS, Baillie TA.
PMID: 25989628
Drug Metab Dispos. 1990 Sep-Oct;18(5):794-803.

Following a single oral dose (200 mg Kg (-1) of stiripentol t (1) o adult male Sprague-Dawley rats, a total of 15 metabolites (accounting collectively for 44% of the administered dose collected over 48 hr) were identified in urine...

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Zhang K, Lepage F, Cuvier G, et al. The metabolic fate of stiripentol in the rat. Studies on cytochrome P-450-mediated methylenedioxy ring cleavage and side chain isomerism. Drug Metab Dispos. 1990;18(5):794-803
Zhang, K., Lepage, F., Cuvier, G., Astoin, J., Rashed, M. S., & Baillie, T. A. (1990). The metabolic fate of stiripentol in the rat. Studies on cytochrome P-450-mediated methylenedioxy ring cleavage and side chain isomerism. Drug metabolism and disposition: the biological fate of chemicals, 18(5), 794-803.
Zhang, K, et al. "The metabolic fate of stiripentol in the rat. Studies on cytochrome P-450-mediated methylenedioxy ring cleavage and side chain isomerism." Drug metabolism and disposition: the biological fate of chemicals vol. 18,5 (1990): 794-803.
Zhang K, Lepage F, Cuvier G, Astoin J, Rashed MS, Baillie TA. The metabolic fate of stiripentol in the rat. Studies on cytochrome P-450-mediated methylenedioxy ring cleavage and side chain isomerism. Drug Metab Dispos. 1990 Sep-Oct;18(5):794-803. PMID: 25989628.
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Correction to: Cytochrome P450 and Non-Cytochrome P450 Oxidative Metabolism: Contributions to the Pharmacokinetics, Safety, and Efficacy of Xenobiotics.

Drug metabolism and disposition: the biological fate of chemicals

[No authors listed]
PMID: 27511205
Drug Metab Dispos. 2016 Sep;44(9):1516. doi: 10.1124/dmd.115.071753err.

No abstract available.

Cite
Correction to: Cytochrome P450 and Non-Cytochrome P450 Oxidative Metabolism: Contributions to the Pharmacokinetics, Safety, and Efficacy of Xenobiotics. Drug Metab Dispos. 2016;44(9):1516doi: 10.1124/dmd.115.071753err.
(2016). Correction to: Cytochrome P450 and Non-Cytochrome P450 Oxidative Metabolism: Contributions to the Pharmacokinetics, Safety, and Efficacy of Xenobiotics. Drug metabolism and disposition: the biological fate of chemicals, 44(9), 1516. https://doi.org/10.1124/dmd.115.071753err
"Correction to: Cytochrome P450 and Non-Cytochrome P450 Oxidative Metabolism: Contributions to the Pharmacokinetics, Safety, and Efficacy of Xenobiotics." Drug metabolism and disposition: the biological fate of chemicals vol. 44,9 (2016): 1516. doi: https://doi.org/10.1124/dmd.115.071753err
Correction to: Cytochrome P450 and Non-Cytochrome P450 Oxidative Metabolism: Contributions to the Pharmacokinetics, Safety, and Efficacy of Xenobiotics. Drug Metab Dispos. 2016 Sep;44(9):1516. doi: 10.1124/dmd.115.071753err. PMID: 27511205.
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Notice of retraction.

Drug metabolism and disposition: the biological fate of chemicals

[No authors listed]
PMID: 25537846
Drug Metab Dispos. 2015 Feb;43(2):234. doi: 10.1124/dmd.114.045674err.

No abstract available.

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Notice of retraction. Drug Metab Dispos. 2015;43(2):234doi: 10.1124/dmd.114.045674err.
(2015). Notice of retraction. Drug metabolism and disposition: the biological fate of chemicals, 43(2), 234. https://doi.org/10.1124/dmd.114.045674err
"Notice of retraction." Drug metabolism and disposition: the biological fate of chemicals vol. 43,2 (2015): 234. doi: https://doi.org/10.1124/dmd.114.045674err
Notice of retraction. Drug Metab Dispos. 2015 Feb;43(2):234. doi: 10.1124/dmd.114.045674err. PMID: 25537846; PMCID: PMC4293400.
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The life and times of anthony Y. H. Lu .

Drug metabolism and disposition: the biological fate of chemicals

Miwa GT.
PMID: 9860922
Drug Metab Dispos. 1998 Dec;26(12):1174.

No abstract available.

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Miwa GT. The life and times of anthony Y. H. Lu . Drug Metab Dispos. 1998;26(12):1174
Miwa, G. T. (1998). The life and times of anthony Y. H. Lu . Drug metabolism and disposition: the biological fate of chemicals, 26(12), 1174.
Miwa. "The life and times of anthony Y. H. Lu ." Drug metabolism and disposition: the biological fate of chemicals vol. 26,12 (1998): 1174.
Miwa GT. The life and times of anthony Y. H. Lu . Drug Metab Dispos. 1998 Dec;26(12):1174. PMID: 9860922.
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Correction to "Mrp3 Transports Clopidogrel Acyl Glucuronide from the Hepatocytes into Blood".

Drug metabolism and disposition: the biological fate of chemicals

[No authors listed]
PMID: 29444909
Drug Metab Dispos. 2018 Mar;46(3):291. doi: 10.1124/dmd.117.078329err.

No abstract available.

Cite
Correction to "Mrp3 Transports Clopidogrel Acyl Glucuronide from the Hepatocytes into Blood". Drug Metab Dispos. 2018;46(3):291doi: 10.1124/dmd.117.078329err.
(2018). Correction to "Mrp3 Transports Clopidogrel Acyl Glucuronide from the Hepatocytes into Blood". Drug metabolism and disposition: the biological fate of chemicals, 46(3), 291. https://doi.org/10.1124/dmd.117.078329err
"Correction to "Mrp3 Transports Clopidogrel Acyl Glucuronide from the Hepatocytes into Blood"." Drug metabolism and disposition: the biological fate of chemicals vol. 46,3 (2018): 291. doi: https://doi.org/10.1124/dmd.117.078329err
Correction to "Mrp3 Transports Clopidogrel Acyl Glucuronide from the Hepatocytes into Blood". Drug Metab Dispos. 2018 Mar;46(3):291. doi: 10.1124/dmd.117.078329err. PMID: 29444909.
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Mrp3 Transports Clopidogrel Acyl Glucuronide from the Hepatocytes into Blood.

Drug metabolism and disposition: the biological fate of chemicals

Ji JZ, Tai T, Huang BB, Gu TT, Mi QY, Xie HG.
PMID: 29196299
Drug Metab Dispos. 2018 Feb;46(2):151-154. doi: 10.1124/dmd.117.078329. Epub 2017 Dec 01.

Clopidogrel acyl glucuronide (CLP-G) is a major phase II metabolite of clopidogrel generated in the liver for further excretion into urine; however, it is unclear whether CLP-G transports from hepatocytes into blood. Because multidrug resistance-associated protein 3 (MRP3) is...

Cite
Ji JZ, Tai T, Huang BB, et al. Mrp3 Transports Clopidogrel Acyl Glucuronide from the Hepatocytes into Blood. Drug Metab Dispos. 2017;46(2):151-154doi: 10.1124/dmd.117.078329.
Ji, J. Z., Tai, T., Huang, B. B., Gu, T. T., Mi, Q. Y., & Xie, H. G. (2018). Mrp3 Transports Clopidogrel Acyl Glucuronide from the Hepatocytes into Blood. Drug metabolism and disposition: the biological fate of chemicals, 46(2), 151-154. https://doi.org/10.1124/dmd.117.078329
Ji, Jin-Zi, et al. "Mrp3 Transports Clopidogrel Acyl Glucuronide from the Hepatocytes into Blood." Drug metabolism and disposition: the biological fate of chemicals vol. 46,2 (2018): 151-154. doi: https://doi.org/10.1124/dmd.117.078329
Ji JZ, Tai T, Huang BB, Gu TT, Mi QY, Xie HG. Mrp3 Transports Clopidogrel Acyl Glucuronide from the Hepatocytes into Blood. Drug Metab Dispos. 2018 Feb;46(2):151-154. doi: 10.1124/dmd.117.078329. Epub 2017 Dec 01. PMID: 29196299.
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Correction to "Metabolic Disposition of Luteolin Is Mediated by the Interplay of UDP-Glucuronosyltransferases and Catechol-.

Drug metabolism and disposition: the biological fate of chemicals

[No authors listed]
PMID: 29217536
Drug Metab Dispos. 2018 Jan;46(1):1. doi: 10.1124/dmd.116.073619err.

No abstract available.

Cite
Correction to "Metabolic Disposition of Luteolin Is Mediated by the Interplay of UDP-Glucuronosyltransferases and Catechol-. Drug Metab Dispos. 2018;46(1):1doi: 10.1124/dmd.116.073619err.
(2018). Correction to "Metabolic Disposition of Luteolin Is Mediated by the Interplay of UDP-Glucuronosyltransferases and Catechol-. Drug metabolism and disposition: the biological fate of chemicals, 46(1), 1. https://doi.org/10.1124/dmd.116.073619err
"Correction to "Metabolic Disposition of Luteolin Is Mediated by the Interplay of UDP-Glucuronosyltransferases and Catechol-." Drug metabolism and disposition: the biological fate of chemicals vol. 46,1 (2018): 1. doi: https://doi.org/10.1124/dmd.116.073619err
Correction to "Metabolic Disposition of Luteolin Is Mediated by the Interplay of UDP-Glucuronosyltransferases and Catechol-. Drug Metab Dispos. 2018 Jan;46(1):1. doi: 10.1124/dmd.116.073619err. PMID: 29217536; PMCID: PMC6041947.
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Showing 1 to 12 of 327 entries