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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2007
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ProMetIS 2.0: proteomics and metabolomics data analysis and integration, applied to the characterization of the Lat and Mx2 knock-out phenotypes
- Oneeb Nasir
- Alyssa Imbert
- Sylvain Dechaumet
- Pierrick Roger
- Thomas Burger
- Yves Vandenbrouck
- Marion Brandolini
- Florence Castelli
- Franck Giacomoni
- Magali Rompais
- Mohammed Selloum
- Emmanuelle Mouton-Barbosa
- Emeline Chu-Van
- Charlotte Joly
- Aurélie Hirschler
- Sophie Leblanc
- Tania Sorg
- Sadia Ouzia
- Claudine Médigue
- Christophe Junot
- ...
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Structural Basis of Spirolactone Recognition by the Mineralocorticoid Receptor
- Jessica Huyet
- Michel Fay
- Marie-Edith Rafestin-Oblin
Molecular Pharmacology
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Structural Basis of Spirolactone Recognition by the Mineralocorticoid Receptor
- Jessica Huyet
- Michel Fay
- Marie-Edith Rafestin-Oblin
Molecular Pharmacology
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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
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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
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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
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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
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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
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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
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Design and evaluation of Actichip, a thematic microarray for the study of the actin cytoskeleton.
- Jean Muller
- André Mehlen
- Guillaume Vetter
- Mikalai Yatskou
- Arnaud H. Muller
- Frédéric Chalmel
- Olivier Poch
- Evelyne Friederich
- Laurent Vallar
BMC Genomics ; Volume: 8 ; Page: 294
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