Role for protein kinase C delta in the functional activity of human UGT1A6: implications for drug-drug interactions between PKC inhibitors and UGT1A6. (Q39733356)

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English	Role for protein kinase C delta in the functional activity of human UGT1A6: implications for drug-drug interactions between PKC inhibitors and UGT1A6.	scientific article

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scholarly article

1 reference

Europe PubMed Central

14 September 2017

Role for protein kinase C delta in the functional activity of human UGT1A6: implications for drug-drug interactions between PKC inhibitors and UGT1A6. (English)

1 reference

Europe PubMed Central

14 September 2017

drug interaction

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Michael H Court

2

object named as

M H Court

1 reference

Europe PubMed Central

14 September 2017

author name string

L P Volak

1

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Europe PubMed Central

14 September 2017

language of work or name

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publication date

1 May 2010

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Europe PubMed Central

14 September 2017

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Europe PubMed Central

14 September 2017

40

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Europe PubMed Central

14 September 2017

5

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Europe PubMed Central

14 September 2017

306-318

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Europe PubMed Central

14 September 2017

The major chemical-detoxifying system of UDP-glucuronosyltransferases requires regulated phosphorylation supported by protein kinase C

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Evidence for phosphorylation requirement for human bilirubin UDP-glucuronosyltransferase (UGT1A1) activity

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Phosphorylation of a UDP-glucuronosyltransferase regulates substrate specificity

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Gastrointestinally distributed UDP-glucuronosyltransferase 1A10, which metabolizes estrogens and nonsteroidal anti-inflammatory drugs, depends upon phosphorylation

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UDP-glucuronosyltransferase 1A6: structural, functional, and regulatory aspects

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Activation and translocation of PKCdelta is necessary for VEGF-induced ERK activation through KDR in HEK293T cells

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Short-chain fatty acids reduce expression of specific protein kinase C isoforms in human colonic epithelial cells

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Roles of specific isoforms of protein kinase C in the transcriptional control of cyclin D1 and related genes

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Rottlerin: an inappropriate and ineffective inhibitor of PKCdelta

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Curcuminoids inhibit multiple human cytochromes P450, UDP-glucuronosyltransferase, and sulfotransferase enzymes, whereas piperine is a relatively selective CYP3A4 inhibitor

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Drug-drug interactions for UDP-glucuronosyltransferase substrates: a pharmacokinetic explanation for typically observed low exposure (AUCi/AUC) ratios

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Rottlerin sensitizes colon carcinoma cells to tumor necrosis factor-related apoptosis-inducing ligand-induced apoptosis via uncoupling of the mitochondria independent of protein kinase C.

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Identifiers

10.3109/00498251003596817

1 reference

Europe PubMed Central

14 September 2017

0 references

1 reference

Europe PubMed Central

14 September 2017

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