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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Retinoic acid receptors and muscle b-HLH proteins: partners in retinoid-induced myogenesis
- Anne Froeschlé
- Séverine Alric
- Magali Kitzmann
- Gilles Carnac
- Frédéric Auradé
- Cécile Rochette-Egly
- Anne Bonnieu
Oncogene ; Volume: 16 ; Page: 3369-3378
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pha-4, an HNF-3 homolog, specifies pharyngeal organ identity in Caenorhabditis elegans
- Michael A. Horner
- Sophie Quintin
- Mary Ellen Domeier
- Judith Kimble
- Michel Labouesse
- Susan E. Mango
Genes and Development ; Volume: 12 ; Page: 1947-1952
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DAX-1 Expression in Human Adrenocortical Neoplasms: Implications for Steroidogenesis
- M. Reincke
- F. Beuschlein
- E. Lalli
- W. Arlt
- S. Vay
- Paolo Sassone-Corsi
- B. Allolio
Journal of Clinical Endocrinology and Metabolism ; Volume: 83 ; Page: 2597-2600
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Doublecortin: the latest breakthrough in neuronal migration and cortical development
- J Chelly
Molecular Psychiatry ; Volume: 3 ; Page: 290-292
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Functional implications of the spectrum of mutations found in 234 cases with X-linked juvenile retinoschisis. The Retinoschisis Consortium
- Claudine Oudet
- Andre Hanauer
Human Molecular Genetics ; Volume: 7 ; Page: 1185-1192
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Differential expression of the TEF family of transcription factors in the murine placenta and during differentiation of primary human trophoblasts in vitro
- Patrick Jacquemin
- Vincent Sapin
- Eliane Alsat
- Danièle Evain-Brion
- Pascal Dollé
- Irwin Davidson
Developmental Dynamics ; Volume: 212 ; Page: 423-436
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Expression of DNA excision-repair-cross-complementing proteins p80 and p89 in brain of patients with Down Syndrome and Alzheimer's disease
- Michael Hermon
- Nigel Cairns
- Jean-Marc Egly
- Anabel Fery
- Olga Labudova
- Gert Lubec
Neuroscience Letters ; Volume: 251 ; Page: 45-48
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Mutation of the start codon in the FRDA1 gene: linkage analysis of three pedigrees with the ATG to ATT transversion points to a unique common ancestor
- Christine Zühlke
- Franco Laccone
- Mireille Cossée
- Alfried Kohlschütter
- Michel Koenig
- Eberhard Schwinger
Human Genetics ; Volume: 103 ; Page: 102-105
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Human TAFII28 and TAFII18 Interact through a Histone Fold Encoded by Atypical Evolutionary Conserved Motifs Also Found in the SPT3 Family
- Catherine Birck
- Olivier Poch
- Christophe Romier
- Marc Ruff
- Gabrielle Mengus
- Anne-Claire Lavigne
- Irwin Davidson
- Dino Moras
Cell ; Volume: 94 ; Page: 239-249
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