Ghent University Academic Bibliography

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An extended transcription factor regulatory network controls hepatocyte identity

Julie Dubois-Chevalier, Celine Gheeraert, Alexandre Berthier, Clemence Boulet, Vanessa Dubois (UGent) , Loic Guille, Marie Fourcot, Guillemette Marot, Karine Gauthier, Laurent Dubuquoy, et al.

(2023) EMBO REPORTS. 24(9).
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Perspectives on the use of super-enhancers as a defining feature of cell/tissue-identity genes

Julie Dubois-Chevalier, Vanessa Dubois (UGent) , Bart Staels, Philippe Lefebvre and Jerome Eeckhoute

(2020) EPIGENOMICS. 12(8). p.715-723
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Endoplasmic reticulum stress actively suppresses hepatic molecular identity in damaged liver

Vanessa Dubois (UGent) , Celine Gheeraert, Wouter Vankrunkelsven, Julie Dubois-Chevalier, Helene Dehondt, Marie Bobowski-Gerard, Manjula Vinod, Francesco Paolo Zummo, Fabian Guiza, Maheul Ploton, et al.

(2020) MOLECULAR SYSTEMS BIOLOGY. 16(5).
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The nuclear bile acid receptor FXR is a PKA- and FOXA2-sensitive activator of fasting hepatic gluconeogenesis

Maheul Ploton, Claire Mazuy, Celine Gheeraert, Vanessa Dubois (UGent) , Alexandre Berthier, Julie Dubois-Chevalier, Xavier Marechal, Kadiombo Bantubungi, Helene Diemer, Sarah Cianferani, et al.

(2018) JOURNAL OF HEPATOLOGY. 69(5). p.1099-1109
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The logic of transcriptional regulator recruitment architecture at cis-regulatory modules controlling liver functions

Julie Dubois-Chevalier, Vanessa Dubois (UGent) , Helene Dehondt, Parisa Mazrooei, Claire Mazuy, Aurelien A. Serandour, Celine Gheeraert, Penderia Guillaume, Eric Bauge, Bruno Derudas, et al.

(2017) GENOME RESEARCH. 27(6). p.985-996

Academic Bibliography

An extended transcription factor regulatory network controls hepatocyte identity

Perspectives on the use of super-enhancers as a defining feature of cell/tissue-identity genes

Endoplasmic reticulum stress actively suppresses hepatic molecular identity in damaged liver

The nuclear bile acid receptor FXR is a PKA- and FOXA2-sensitive activator of fasting hepatic gluconeogenesis

The logic of transcriptional regulator recruitment architecture at cis-regulatory modules controlling liver functions

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