Bromodomain Protein BRD4 Accelerates Glucocorticoid Dysregulation of Bone Mass and Marrow Adiposis by Modulating H3K9 and Foxp1

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: In: 10.3390/cells9061500

Event: Veröffentlichung

(where): Aachen

(who): Universitätsbibliothek der RWTH Aachen

(when): 2020

Creator: Wang, Feng-Sheng
Chen, Yu-Shan
Ko, Jih-Yang
Kuo, Chung-Wen
Ke, Huei-Jing
Hsieh, Chin-Kuei
Wang, Shao-Yu
Kuo, Pei-Chen
Jahr, Holger
Lian, Wei-Shiung

DOI: 10.18154/RWTH-CONV-243630

URN: urn:nbn:de:101:1-2023112300340465467609

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:20 AM CEST

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Associated

Wang, Feng-Sheng
Chen, Yu-Shan
Ko, Jih-Yang
Kuo, Chung-Wen
Ke, Huei-Jing
Hsieh, Chin-Kuei
Wang, Shao-Yu
Kuo, Pei-Chen
Jahr, Holger
Lian, Wei-Shiung
Universitätsbibliothek der RWTH Aachen

Time of origin

2020

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The interaction between the papillomaviral protein E2 and the cellular bromodomain protein Brd4 is important for the viral life cycle and viral oncogenesis

Dysregulation of hypoxia-inducible factor 1α in the sympathetic nervous system accelerates diabetic cardiomyopathy

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Selectively Binding a Bromodomain

Hochschulschrift

The interaction between the papillomaviral protein E2 and the cellular bromodomain protein Brd4 is important for the viral life cycle and viral oncogenesis

Dysregulation of hypoxia-inducible factor 1α in the sympathetic nervous system accelerates diabetic cardiomyopathy

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Bromodomain Protein BRD4 Accelerates Glucocorticoid Dysregulation of Bone Mass and Marrow Adiposis by Modulating H3K9 and Foxp1

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Other Objects (12)

BRD3 and BRD4 BET Bromodomain Proteins Differentially Regulate Skeletal Myogenesis

Epigenetic targeting of bromodomain protein BRD4 counteracts cancer cachexia and prolongs survival

Bromodomain protein BRD4 is a transcriptional repressor of autophagy and lysosomal function

Targeting bromodomain-containing protein 4 (BRD4) inhibits MYC expression in colorectal cancer cells

Dissecting the role of BET bromodomain proteins BRD2 and BRD4 in human NK cell function

Bromodomain-containing protein 4 (BRD4) as an epigenetic regulator of fatty acid metabolism genes and ferroptosis

Ferritinophagy is required for the induction of ferroptosis by the bromodomain protein BRD4 inhibitor (+)-JQ1 in cancer cells

Neonatal overfeeding induced glucocorticoid overexposure accelerates hepatic lipogenesis in male rats

Bromodomain-Containing Protein 4 (BRD4) Inhibition Sensitizes Palomid 529-Induced Anti-Renal Cell Carcinoma Cell Activity in Vitro and in Vivo

Selectively Binding a Bromodomain

The interaction between the papillomaviral protein E2 and the cellular bromodomain protein Brd4 is important for the viral life cycle and viral oncogenesis

Dysregulation of hypoxia-inducible factor 1α in the sympathetic nervous system accelerates diabetic cardiomyopathy

BRD3 and BRD4 BET Bromodomain Proteins Differentially Regulate Skeletal Myogenesis

Epigenetic targeting of bromodomain protein BRD4 counteracts cancer cachexia and prolongs survival

Bromodomain protein BRD4 is a transcriptional repressor of autophagy and lysosomal function

Targeting bromodomain-containing protein 4 (BRD4) inhibits MYC expression in colorectal cancer cells

Dissecting the role of BET bromodomain proteins BRD2 and BRD4 in human NK cell function

Bromodomain-containing protein 4 (BRD4) as an epigenetic regulator of fatty acid metabolism genes and ferroptosis

Ferritinophagy is required for the induction of ferroptosis by the bromodomain protein BRD4 inhibitor (+)-JQ1 in cancer cells

Neonatal overfeeding induced glucocorticoid overexposure accelerates hepatic lipogenesis in male rats

Bromodomain-Containing Protein 4 (BRD4) Inhibition Sensitizes Palomid 529-Induced Anti-Renal Cell Carcinoma Cell Activity in Vitro and in Vivo

Selectively Binding a Bromodomain

The interaction between the papillomaviral protein E2 and the cellular bromodomain protein Brd4 is important for the viral life cycle and viral oncogenesis

Dysregulation of hypoxia-inducible factor 1α in the sympathetic nervous system accelerates diabetic cardiomyopathy

BRD3 and BRD4 BET Bromodomain Proteins Differentially Regulate Skeletal Myogenesis

Epigenetic targeting of bromodomain protein BRD4 counteracts cancer cachexia and prolongs survival

Bromodomain protein BRD4 is a transcriptional repressor of autophagy and lysosomal function

Targeting bromodomain-containing protein 4 (BRD4) inhibits MYC expression in colorectal cancer cells

Dissecting the role of BET bromodomain proteins BRD2 and BRD4 in human NK cell function

Bromodomain-containing protein 4 (BRD4) as an epigenetic regulator of fatty acid metabolism genes and ferroptosis

Ferritinophagy is required for the induction of ferroptosis by the bromodomain protein BRD4 inhibitor (+)-JQ1 in cancer cells

Neonatal overfeeding induced glucocorticoid overexposure accelerates hepatic lipogenesis in male rats

Bromodomain-Containing Protein 4 (BRD4) Inhibition Sensitizes Palomid 529-Induced Anti-Renal Cell Carcinoma Cell Activity in Vitro and in Vivo

Selectively Binding a Bromodomain

The interaction between the papillomaviral protein E2 and the cellular bromodomain protein Brd4 is important for the viral life cycle and viral oncogenesis

Dysregulation of hypoxia-inducible factor 1α in the sympathetic nervous system accelerates diabetic cardiomyopathy

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