Publications scientifiques
Les équipes de recherches de l'IGBMC publient régulièrement des articles qui font avancer les connaissances dans divers domaines de recherche. Vous trouverez sur cette page l'ensemble des publications dans lesquels les travaux de nos scientifiques sont cités.
Publications
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1998
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Introduction: Notch signalling and choice of cell fates in development
- Pat Simpson
Seminars in Cell and Developmental Biology ; Volume: 9 ; Page: 581-582
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Keratinocyte-specific retinoid regulation of human cellular retinoic acid binding protein-II (hCRABPII) gene promoter requires an evolutionarily conserved DR1 retinoic acid-responsive element
- Wen Di
- Xiao-Yan Li
- Subhash Datta
- Anders Aström
- Gary J. Fisher
- Pierre Chambon
- John J. Voorhees
- Jia-Hao Xiao
Journal of Investigative Dermatology ; Volume: 111 ; Page: 1109-1115
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Mutation analysis of the RSK2 gene in Coffin-Lowry patients: extensive allelic heterogeneity and a high rate of de novo mutations
- Sylvie Jacquot
- Karine Merienne
- Dario de Cesare
- S. Pannetier
- Jean-Louis Mandel
- Paolo Sassone-Corsi
- Andre Hanauer
American Journal of Human Genetics ; Volume: 63 ; Page: 1631-1640
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Natural dietary polyphenolic compounds cause endothelium-dependent vasorelaxation in rat thoracic aorta.
- E Andriambeloson
- C Magnier
- Gisele Haan-Archipoff
- Annelise Lobstein
- R Anton
- Alain Beretz
- Jc Stoclet
- R Andriantsitohaina
The Journal of Nutrition
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Visual sensations produced by optic nerve stimulation using an implanted self-sizing spiral cuff electrode.
- C. Veraart
- C. Raftopoulos
- J. T. Mortimer
- J. Delbeke
- D. Pins
- G. Michaux
- A. Vanlierde
- S. Parrini
- M. C. Wanet-Defalque
Brain Research ; Volume: 813 ; Page: 181-6
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Positive autoregulation of the glial promoting factor glide/gcm
- Alita Miller
- Roberto Bernardoni
- Angela Giangrande
The EMBO Journal ; Volume: 17 ; Page: 6316-6326
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Exon organisation of the mouse gene encoding the Adrenoleukodystrophy related protein (ALDRP)
- Cyril Broccardo
- Nathalie Troffer-Charlier
- Stephane Savary
- Jean-Louis Mandel
- Giovanna Chimini
European Journal of Human Genetics ; Volume: 6 ; Page: 638-641
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Spatio-temporally-controlled somatic mutations in the mouse
- Jacques Brocard Brocard
- Xavier Warot
- Olivia Wendling
- Nadia Messaddeq
- Jean-Luc Vonesch
- Pierre Chambon
- Daniel Metzger
Pathologie Biologie ; Volume: 46 ; Page: 671-673
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Mutations in XPD helicase prevent its interaction and regulation by p44, another subunit of TFIIH, resulting in Xeroderma pigmentosum (XP) and trichothiodystrophy (TTD) phenotypes
- Frédéric Coin
- J. C. Marinoni
- Jean-Marc Egly
Pathologie Biologie ; Volume: 46 ; Page: 679-680
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Rapid immunoblot and kinase assay tests for a syndromal form of X linked mental retardation: Coffin-Lowry syndrome
- Karine Merienne
- Sylvie Jacquot
- E. Trivier
- S. Pannetier
- A. Rossi
- C. Scott
- A. Schinzel
- C. Castellan
- W. Kress
- Andre Hanauer
Journal of Medical Genetics ; Volume: 35 ; Page: 890-894
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Page 641 sur 694