Scientific publications
Publications
-
2007
-
Histopathology in mouse metabolic investigations
- Manuel Mark
- Marius Teletin
- Cristina Antal
- Olivia Wendling
- Johan Auwerx
- Sami Heikkinen
- Konstantin Khetchoumian
- Carmena. Argmann
- Mounzer Dgheem
Current Protocols in Molecular Biology ; Volume: Chapter 29 ; Page: Unit-29B.4
-
Gene expression profiling in lung fibroblasts reveals new players in alveolarization
- Olivier Boucherat
- Marie-Laure Franco-Montoya
- Christelle Thibault
- Roberto Incitti
- Bernadette Chailley-Heu
- Christophe Delacourt
- Jacquesr. Bourbon
Physiological Genomics ; Volume: 32 ; Page: 128-141
-
Structural Basis of Spirolactone Recognition by the Mineralocorticoid Receptor
- Jessica Huyet
- Michel Fay
- Marie-Edith Rafestin-Oblin
Molecular Pharmacology
-
Structural Basis of Spirolactone Recognition by the Mineralocorticoid Receptor
- Jessica Huyet
- Michel Fay
- Marie-Edith Rafestin-Oblin
Molecular Pharmacology
-
Identification of a small TAF complex and its role in the assembly of TAF-containing complexes.
- Màté A Demény
- Evi Soutoglou
- Zita Nagy
- Elisabeth Scheer
- Agnes Jànoshàzi
- Magalie Richardot
- Manuela Argentini
- Pascal Kessler
- Laszlo Tora
PLoS ONE ; Volume: 2 ; Page: e316
-
Advancements in the pathophysiology of Friedreich's Ataxia and new prospects for treatments.
- Ngolela E Babady
- Nadege Carelle
- Robert D Wells
- Tracey A Rouault
- Michio Hirano
- David R Lynch
- Martin B Delatycki
- Robert B Wilson
- Grazia Isaya
- Hélène Puccio
Molecular Genetics and Metabolism ; Volume: 92 ; Page: 23-35
-
LRP1 functions as an atheroprotective integrator of TGFbeta and PDFG signals in the vascular wall: implications for Marfan syndrome.
- Philippe Boucher
- Wei-Ping Li
- Rachel L Matz
- Yoshiharu Takayama
- Johan Auwerx
- Richard G W Anderson
- Joachim Herz
PLoS ONE ; Volume: 2 ; Page: e448
-
Mutations de l’amphiphysine 2 (BIN1) dans les myopathies centronucléaires récessives [Mutations in amphiphysin 2 (BIN1) cause autosomal recessive centronuclear myopathy]
- Anne Toussaint
- Anne-Sophie Nicot
- Jean-Louis Mandel
- Jocelyn Laporte
Médecine/Sciences ; Volume: 23 ; Page: 1080-1082
-
Troubles neurologiques et trichothiodystrophie. Sans TFIIH, les hormones thyroïdiennes défaillent [Neurological disorders and trichothiodystrophy: when the transcription process is impaired]
- Emmanuel Compe
- Jean-Marc Egly
Médecine/Sciences ; Volume: 23 ; Page: 1171-1172
-
Contribution of targeted conditional somatic mutagenesis to deciphering retinoid X receptor functions and to generating mouse models of human diseases.
- Daniel Metzger
- Pierre Chambon
Handbook of Experimental Pharmacology ; Page: 511-524
-