Transcription coactivator PRIP, the peroxisome proliferator-activated receptor (PPAR)-interacting protein, is redundant for the function of nuclear receptors PParalpha and CAR, the constitutive androstane receptor, in mouse liver. (Q50086459)

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scientific article published in January 2007

Language	Label	Description	Also known as
English	Transcription coactivator PRIP, the peroxisome proliferator-activated receptor (PPAR)-interacting protein, is redundant for the function of nuclear receptors PParalpha and CAR, the constitutive androstane receptor, in mouse liver.	scientific article published in January 2007

Statements

scholarly article

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1 January 2020

Transcription coactivator PRIP, the peroxisome proliferator-activated receptor (PPAR)-interacting protein, is redundant for the function of nuclear receptors PParalpha and CAR, the constitutive androstane receptor, in mouse liver (English)

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1 January 2020

author name string

Joy Sarkar

1

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1 January 2020

Chao Qi

2

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1 January 2020

Dongsheng Guo

3

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1 January 2020

Mohamed R Ahmed

4

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1 January 2020

Yuzhi Jia

5

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1 January 2020

Nobuteru Usuda

6

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1 January 2020

Navin Viswakarma

7

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1 January 2020

M Sambasiva Rao

8

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1 January 2020

Janardan K Reddy

9

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1 January 2020

publication date

1 January 2007

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1 January 2020

Gene Expression

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1 January 2020

13

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1 January 2020

4-5

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1 January 2020

255-269

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1 January 2020

Transcription coactivators for peroxisome proliferator-activated receptors

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Anatomical profiling of nuclear receptor expression reveals a hierarchical transcriptional network

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15 July 2018

Peroxisome proliferator-activated receptor (PPAR)-binding protein (PBP) but not PPAR-interacting protein (PRIP) is required for nuclear translocation of constitutive androstane receptor in mouse liver

1 reference

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Differential regulation of hepatic CYP2B6 and CYP3A4 genes by constitutive androstane receptor but not pregnane X receptor

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Critical roles of the p160 transcriptional coactivators p/CIP and SRC-1 in energy balance

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Serine 202 regulates the nuclear translocation of constitutive active/androstane receptor

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Transcription coactivator peroxisome proliferator-activated receptor-binding protein/mediator 1 deficiency abrogates acetaminophen hepatotoxicity

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Structural determinants of constitutive androstane receptor required for its glucocorticoid receptor interacting protein-1-mediated nuclear accumulation.

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Transcription coactivator PBP, the peroxisome proliferator-activated receptor (PPAR)-binding protein, is required for PPARalpha-regulated gene expression in liver

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CAR, driving into the future

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Activation of orphan nuclear constitutive androstane receptor requires subnuclear targeting by peroxisome proliferator-activated receptor gamma coactivator-1 alpha. A possible link between xenobiotic response and nutritional state

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Coactivator PRIP, the peroxisome proliferator-activated receptor-interacting protein, is a modulator of placental, cardiac, hepatic, and embryonic development

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Modulation of acetaminophen-induced hepatotoxicity by the xenobiotic receptor CAR

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Identification of a transcriptionally active peroxisome proliferator-activated receptor alpha -interacting cofactor complex in rat liver and characterization of PRIC285 as a coactivator

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Interaction of PIMT with transcriptional coactivators CBP, p300, and PBP differential role in transcriptional regulation

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Cloning and characterization of PIMT, a protein with a methyltransferase domain, which interacts with and enhances nuclear receptor coactivator PRIP function

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Dexamethasone enhances constitutive androstane receptor expression in human hepatocytes: consequences on cytochrome P450 gene regulation

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Mouse liver cell culture. I. Hepatocyte isolation

1 reference

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12 December 2020

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10.3727/000000006780666948

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1 January 2020

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1 January 2020

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1 January 2020

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