Scientific publications
Publications
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2016
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Characterization of non-canonical Polycomb Repressive Complex 1 subunits during early mouse embryogenesis
- André Eid
- Maria Elena Torres Padilla
Epigenetics ; Volume: 11 ; Page: 389-97
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The Substrate Specificity of Sirtuins
- Poonam Bheda
- Hui Jing
- Cynthia Wolberger
- Hening Lin
Annual Review of Biochemistry ; Volume: 85 ; Page: 405-429
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Nucleotide Excision Repair and Transcriptional Regulation: TFIIH and Beyond
- Emmanuel Compe
- Jean-Marc Egly
Annual Review of Biochemistry ; Volume: 85 ; Page: 265-90
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Effects of vitamin A deficiency in the postnatal mouse heart: role of hepatic retinoid stores
- Mary Ann Asson-Batres
- Sergey Ryzhov
- Oleg Tikhomirov
- Christine Duarte
- Clare Bates Congdon
- Craig Lessard
- Samuel Mcfarland
- Cecile Rochette-Egly
- Truc-Linh Tran
- Cristi Galindo
- Amanda Favreau-Lessard
- Douglas Sawyer
AJP - Heart and Circulatory Physiology ; Volume: 310 ; Page: H1773-H1789
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Biologie du développement
- Daniel Boujard
- Vincent Leclerc
- Stéphane Vincent
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SERMs have substance specific effects on bone and these effects are mediated via ERαAF-1 in female mice
- Anna E. Börjesson
- Helen H. Farman
- Sofia Movérare-Skrtic
- Cecilia Engdahl
- Maria Antal
- Antti Koskela
- Juha Tuukkanen
- Hans Carlsten
- Andrée Krust
- Pierre Chambon
- Klara Sjögren
- Marie K. Lagerquist
- Sara H. Windahl
- Claes Ohlsson
AJP - Endocrinology and Metabolism ; Volume: 310
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The MECP2 variant c.925C>T (p.Arg309Trp) causes intellectual disability in both males and females without classic features of Rett syndrome
- B. Schonewolf-Greulich
- M. I. Tejada
- K. Stephens
- K. Hadzsiev
- J. Gauthier
- K. Brondum-Nielsen
- R. Pfundt
- K. Ravn
- H. Maortua
- B. Gener
- C. Martinez-Bouzas
- Amélie Piton
- G. Rouleau
- J. Clayton-Smith
- T. Kleefstra
- A. M. Bisgaard
- Z. Tumer
Clinical Genetics ; Volume: 89 ; Page: 733-8
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Emerging Roles for the Unfolded Protein Response in the Developing Nervous System
- Juliette Godin
- Catherine Creppe
- Sophie Laguesse
- Laurent Nguyen
Trends in Neurosciences ; Volume: 39 ; Page: 394-404
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A new mutation identified in SPATA16 in two globozoospermic patients
- Elias Elinati
- Camille Fossard
- Ozlem Okutman
- Houda Ghédir
- Samira Ibala-Romdhane
- Pierre Ray
- Ali Saad
- Sylvianne Hennebicq
- Stéphane Viville
Journal of Assisted Reproduction and Genetics ; Volume: 33 ; Page: 815-820
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Novel de novo mutations in ZBTB20 in Primrose syndrome with congenital hypothyroidism
- Francesca Mattioli
- Amélie Piton
- Bénédicte Gerard
- Andrea Superti-Furga
- Jean-Louis Mandel
- Sheila Unger
Am J Med Genet A ; Volume: 170 ; Page: 1626-9
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