Scientific publications
Publications
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1995
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Genomic imprinting of Mash2, a mouse gene required for trophoblast development
- François Guillemot
- Tamara Caspary
- Shirley Tilghman
- Neal Copeland
- Debra Gilbert
- Nancy Jenkins
- David Anderson
- Alexandra Joyner
- Janet Rossant
- András Nagy
Nature Genetics ; Volume: 9 ; Page: 235-242
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Endogenous Retinoic Acid Receptor (RAR)-Retinoid X Receptor (RXR) Heterodimers Are the Major Functional Forms Regulating Retinoid-responsive Elements in Adult Human Keratinocytes
- Jia-Hao Xiao
- Beatrice Claude Durand
- Pierre Chambon
- John Voorhees
Journal of Biological Chemistry ; Volume: 270 ; Page: 3001-3011
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Mice deficient in cellular retinoic acid binding protein II (CRABPII) or in both CRABPI and CRABPII are essentially normal.
- M Lampron
- Cécile Rochette-Egly
- Philippe Gorry
- Pascal Dolle
- Manuel Mark
- T Lufkin
- Marianne Lemeur
- Pierre Chambon
Development (Cambridge, England) ; Volume: 121 ; Page: 539-48
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Proneural genes influence gliogenesis in Drosophila.
- A Giangrande
Development (Cambridge, England) ; Volume: 121 ; Page: 429-38
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Proneural genes influence gliogenesis in Drosophila.
- Angela Giangrande
Development (Cambridge, England) ; Volume: 121 ; Page: 429-38
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Proneural genes influence gliogenesis in Drosophila.
- A Giangrande
Development (Cambridge, England) ; Volume: 121 ; Page: 429-38
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Thrombin Does Not Alter Vascular Hyporeactivity in Models of Endotoxin-Induced Septic Shock in Rats
- Viviane Martin
- Marie-Louise Wiesel
- Anne Albert
- Alain Beretz
Clinical Science ; Volume: 88 ; Page: 149-157
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Roles of retinoic acid receptors and of Hox genes in the patterning of the teeth and of the jaw skeleton.
- Manuel Mark
- D Lohnes
- C Mendelsohn
- V Dupé
- J L Vonesch
- Philippe Kastner
- F Rijli
- Agnès Bloch-Zupan
- Pierre Chambon
International Journal of Developmental Biology ; Volume: 39 ; Page: 111-121
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Axial skeleton homeosis and forelimb malformations in Hoxd-11 mutant mice.
- Bertrand Favier
- Marianne Le Meur
- Pierre Chambon
- Pascal Dollé
Proceedings of the National Academy of Sciences of the United States of America ; Volume: 92 ; Page: 310-314
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Spectrum of mutations in the gene encoding the adrenoleukodystrophy protein.
- M Ligtenberg
- S Kemp
- Claude Olivier Sarde
- B van Geel
- W Kleijer
- P Barth
- Jean-Louis Mandel
- B van Oost
- P Bolhuis
American Journal of Human Genetics ; Volume: 56
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