Aromatic hydrocarbon receptor interaction with the retinoblastoma protein potentiates repression of E2F-dependent transcription and cell cycle arrest (Q41715731)

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scientific article published on January 2000

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English	Aromatic hydrocarbon receptor interaction with the retinoblastoma protein potentiates repression of E2F-dependent transcription and cell cycle arrest	scientific article published on January 2000

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scholarly article

1 reference

Europe PubMed Central

7 October 2017

Aromatic hydrocarbon receptor interaction with the retinoblastoma protein potentiates repression of E2F-dependent transcription and cell cycle arrest (English)

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Europe PubMed Central

7 October 2017

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author name string

Puga A

1

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Europe PubMed Central

7 October 2017

Barnes SJ

2

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Europe PubMed Central

7 October 2017

Dalton TP

3

1 reference

Europe PubMed Central

7 October 2017

Chang C

4

1 reference

Europe PubMed Central

7 October 2017

Knudsen ES

5

1 reference

Europe PubMed Central

7 October 2017

Maier MA

6

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Europe PubMed Central

7 October 2017

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publication date

1 January 2000

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Europe PubMed Central

7 October 2017

Journal of Biological Chemistry

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Europe PubMed Central

7 October 2017

275

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Europe PubMed Central

7 October 2017

2943-2950

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Europe PubMed Central

7 October 2017

4

1 reference

Europe PubMed Central

7 October 2017

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A novel cytoplasmic protein that interacts with the Ah receptor, contains tetratricopeptide repeat motifs, and augments the transcriptional response to 2,3,7,8-tetrachlorodibenzo-p-dioxin

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The aryl hydrocarbon receptor complex

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Induction of the aromatic hydrocarbon receptor by trans-4-acetylaminostilbene in rat liver. Comparison with other aromatic amines

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Complementation of Ah receptor deficiency in hepatoma cells: negative feedback regulation and cell cycle control by the Ah receptor

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The aromatic hydrocarbon receptor modulates the Hepa 1c1c7 cell cycle and differentiated state independently of dioxin

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Constitutive activation of the aromatic hydrocarbon receptor

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Growth suppression by an E2F-binding-defective retinoblastoma protein (RB): contribution from the RB C pocket

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Dual mechanisms for the inhibition of E2F binding to RB by cyclin-dependent kinase-mediated RB phosphorylation

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Differential regulation of retinoblastoma protein function by specific Cdk phosphorylation sites

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Hyperphosphorylated p107 and p130 bind to T-antigen: identification of a critical regulatory sequence present in RB but not in p107/p130.

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The retinoblastoma protein and BRG1 form a complex and cooperate to induce cell cycle arrest

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TGF beta-induced growth inhibition in primary fibroblasts requires the retinoblastoma protein

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pRB plays an essential role in cell cycle arrest induced by DNA damage

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Control of pRB phosphorylation

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Modulation of Protein Kinase C-Related Signal Transduction by 2,3,7,8-Tetrachlorodibenzo-p-dioxin Exhibits Cell Cycle Dependence

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Identifiers

10.1074/JBC.275.4.2943

1 reference

Europe PubMed Central

7 October 2017

1 reference

Europe PubMed Central

7 October 2017

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