Publications
1999
Article in a journal
Characterization of the DNA-binding and dimerization properties of the nuclear orphan receptor germ cell nuclear factor
- Holger Greschik
- Jean-Marie Wurtz
- Philip Hublitz
- Fabian Köhler
- Dino Moras
- Roland Schüle
Molecular and Cellular Biology ; Volume: 19 ; Page: 690-703
Article in a journal
T-cell development: A new marker of differentiation state
- Christophe Benoist
- Diane Mathis
Current Biology ; Volume: 9 ; Page: R59-R61
Article in a journal
Novel mutations in Rsk-2, the gene for Coffin-Lowry syndrome (CLS)
- Fatima Abidi
- Sylvie Jacquot
- Christopher Lassiter
- Elizabeth Trivier
- Andre Hanauer
- Charles E. Schwartz
European Journal of Human Genetics ; Volume: 7 ; Page: 20-26
Article in a journal
Frequent factor II G20210A mutation in idiopathic portal vein thrombosis
- Patrick Chamouard
- Erwan Pencreach
- Frédéric Maloisel
- Lélia Grunebaum
- Jean-François Ardizzone
- Alice Meyer
- Marie-Pierre Gaub
- Joëlle Goetz
- René Baumann
- Béatrice Uring-Lambert
- Salomon Levy
- Patrick Dufour
- Georges Hauptmann
- Pierre Oudet
Gastroenterology ; Volume: 116 ; Page: 144-148
Article in a journal
BAliBASE: a benchmark alignment database for the evaluation of multiple alignment programs
- Julie Thompson
- Frederic Plewniak
- Olivier Poch
Bioinformatics ; Volume: 15 ; Page: 87-88
Article in a journal
High level expression of expanded full-length ataxin-3 in vitro causes cell death and formation of intranuclear inclusions in neuronal cells
- B. Evert
- Ullrich Wüllner
- Jörg B Schulz
- Michael N Weller
- Peter Groscurth
- Yvon Trottier
- Alexis Brice
- Thomas Klockgether
Human Molecular Genetics ; Volume: 8 ; Page: 1169-1176
Article in a journal
Differential expression of retinoid receptors in the adult mouse central nervous system
- Wojciech Krężel
- Philippe Kastner
- Pierre Chambon
Neuroscience ; Volume: 89 ; Page: 1291-1300
Article in a journal
In utero fetal muscle biopsy: a precious aid for the prenatal diagnosis of Duchenne muscular dystrophy
- Sergine Heckel
- Romain Favre
- Jean Flori
- Michel Koenig
- Jean-Louis Mandel
- Bernard Gasser
- Denis Chaigne
Fetal Diagnosis and Therapy ; Volume: 14 ; Page: 127-132
Article in a journal
Unreported RSK2 missense mutation in two male sibs with an unusually mild form of Coffin-Lowry syndrome
- S. Manouvrier-Hanu
- J. Amiel
- Sylvie Jacquot
- Karine Merienne
- A. Moerman
- A. Coëslier
- F. Labarriere
- L. Vallée
- M. F. Croquette
- Andre Hanauer
Journal of Medical Genetics ; Volume: 36 ; Page: 775-778
Article in a journal
Rhythmic Transcription: The Molecular Basis of Circadian Melatonin Synthesis
- Paolo Sassone-Corsi
- David Whitmore
- Nicolas Cermakian
- Nicholas Foulkes
Novartis Foundation symposium ; Page: 3-10