Scientific publications
Publications
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1999
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HNF3 β and Lim1 interact in the visceral endoderm to regulate primitive streak formation and anterior-posterior polarity in the mouse embryo
- Aitana Perea-Gómez
- William Shawlot
- Hiroshi Sasaki
- Richard Behringer
- Siew-Lan Ang
Development (Cambridge, England) ; Volume: 126 ; Page: 4499-4511
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Expression of the transcriptional intermediary factor TIF1alpha during mouse development and in the reproductive organs
- Karen Niederreither
- Eumorphia Remboutsika
- Anne Gansmuller
- Regine Losson
- Pascal Dollé
Mechanisms of Development ; Volume: 88 ; Page: 111-117
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Positive selection of thymocytes induced by gene transfer: MHC class II-mediated selection of CD8 lineage cells
- Ronald Rooke
- Caroline Waltzinger
- Christophe Benoist
- Diane Mathis
International Immunology ; Volume: 11 ; Page: 1595-1600
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A novel peptide-SH3 interaction
- A. Mongiovi
- P Romano
- S Panni
- Manuel Mendoza
- W Wong
- A Musacchio
- G Cesareni
- P Di Fiore
EMBO Journal ; Volume: 18 ; Page: 5300-5309
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Gene targeting restricted to mouse striated muscle lineage
- Pierre Miniou
- Danilo Tiziano
- Tony Frugier
- Natacha Roblot
- Marianne Le Meur
- Judith Melki
Nucleic Acids Research ; Volume: 27 ; Page: 27-30
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Breakthroughs in molecular and cellular mechanisms underlying X-linked mental retardation
- Jamel Chelly
Human Molecular Genetics ; Volume: 8 ; Page: 1833-1838
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Physical and functional interactions between cellular retinoic acid binding protein II and the retinoic acid-dependent nuclear complex
- Laurent Delva
- J. N. Bastie
- Cécile Rochette-Egly
- R. Kraïba
- N. Balitrand
- G. Despouy
- Pierre Chambon
- C. Chomienne
Molecular and Cellular Biology ; Volume: 19 ; Page: 7158-7167
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Identification of novel mutations in theMTM1 gene causing severe and mild forms of X-linked myotubular myopathy
- Anna Buj-Bello
- Jocelyn Laporte
- Jean-Louis Mandel
Human Mutation ; Volume: 14 ; Page: 320-325
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Three Different noggin Genes Antagonize the Activity of Bone Morphogenetic Proteins in the Zebrafish Embryo
- Maximilian Fürthauer
- Bernard Thisse
- Christine Thisse
Developmental Biology ; Volume: 214 ; Page: 181-196
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G130V, a common FRDA point mutation, appears to have arisen from a common founder
- Martin B. Delatycki
- Melanie Knight
- Michel Koenig
- Mireille Cossée
- Robert Williamson
- Susan M. Forrest
Human Genetics ; Volume: 105 ; Page: 343-346
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