
Publications scientifiques
Les scientifiques de l'IGBMC publient régulièrement dans des revues dédiées à la recherche. Vous trouverez la liste de ces publications ci-dessous.
Publications
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2013
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A general framework to characterize inhibitors of calmodulin: use of calmodulin inhibitors to study the interaction between calmodulin and its calmodulin binding domains
- Emilie Audran
- Rania Dagher
- Sophie Gioria
- Philipp Tsvetkov
- Alexandra A. Kulikova
- Bruno Didier
- Pascal Villa
- Alexander A. Makarov
- Marie-Claude Kilhoffer-Haiech
- Jacques Haiech
BBA - Biochimica et Biophysica Acta ; Volume: 1833 ; Page: 1720-1731
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Sirt1 suppresses RNA synthesis after UV irradiation in combined xeroderma pigmentosum group D/Cockayne syndrome (XP-D/CS) cells
- R. Velez-Cruz
- A. Zadorin
- Frédéric Coin
- J.-M. Egly
Proceedings of the National Academy of Sciences of the United States of America ; Volume: 110 ; Page: E212-E220
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A possible cranio-oro-facial phenotype in Cockayne syndrome.
- Agnès Bloch-Zupan
- Morgan Rousseaux
- Virginie Laugel
- Matthieu Schmittbuhl
- Rémy Mathis
- Emmanuelle Desforges
- Mériam Koob
- Ariane Zaloszyc
- Hélène Dollfus
- Vincent Laugel
Orphanet Journal of Rare Diseases ; Volume: 8 ; Page: 9
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Rapid purification of ribosomal particles assembled on histone H4 mRNA: a new method based on mRNA–DNA chimaeras
- Lydia Prongidi-Fix
- Laure Schaeffer
- Angelita Simonetti
- Sharief Barends
- Jean-François Ménétret
- Bruno P. Klaholz
- Gilbert Eriani
- Franck Martin
Biochemical Journal ; Volume: 449 ; Page: 719-728
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Neurons and cardiomyocytes derived from induced pluripotent stem cells as a model for mitochondrial defects in Friedreich's ataxia
- Aurore Hick
- Marie Wattenhofer-Donzé
- Satyan Chintawar
- Philippe Tropel
- Jodie Simard
- Nadège Vaucamps
- David Gall
- Laurie Lambot
- Cécile André
- Laurence Reutenauer
- Myriam Rai
- Marius Teletin
- Nadia Messaddeq
- Serge Schiffmann
- Stéphane Viville
- Christopher Pearson
- Massimo Pandolfo
- Hélène Puccio
Disease Models & Mechanisms ; Volume: 6 ; Page: 608-621
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Reprogramming development
- Olivier Pourquié
Development (Cambridge, England) ; Volume: 140 ; Page: 1-2
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STARD3/STARD3NL and VAP make a novel molecular tether between late endosomes and the ER
- Fabien Alpy
- Adrien Rousseau
- Yannick Schwab
- François Legueux
- Isabelle Stoll
- Corinne Wendling
- Coralie Spiegelhalter
- Pascal Kessler
- Carole Mathelin
- Marie-Christine Rio
- Timothy P Levine
- Catherine Tomasetto
Journal of Cell Science
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Conditional deletion of neurogenin-3 using Nkx2.1iCre results in a mouse model for the central control of feeding, activity and obesity
- Neal Anthwal
- Michelle Pelling
- Suzanne Claxton
- Georg Mellitzer
- Caitlin Collin
- Nicoletta Kessaris
- William D Richardson
- Gérard Gradwohl
- Siew-Lan Ang
Disease Models & Mechanisms
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Whole-Exome Sequencing Identifies LRIT3 Mutations as a Cause of Autosomal-Recessive Complete Congenital Stationary Night Blindness
- Christina Zeitz
- Samuel G. Jacobson
- Christian P. Hamel
- Kinga Bujakowska
- Marion Neuillé
- Elise Orhan
- Xavier Zanlonghi
- Marie-Elise Lancelot
- Christelle Michiels
- Sharon B. Schwartz
- Béatrice Bocquet
- Aline Antonio
- Claire Audier
- Mélanie Letexier
- Jean-Paul Saraiva
- Tien D. Luu
- Florian Sennlaub
- Hoan Nguyen
- Olivier Poch
- Hélène Dollfus
- ...
American Journal of Human Genetics ; Volume: 92 ; Page: 67-75
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The architecture of human general transcription factor TFIID core complex
- Christoph Bieniossek
- Gabor Papai
- Christiane Schaffitzel
- Frederic Garzoni
- Maxime Chaillet
- Elisabeth Scheer
- Petros Papadopoulos
- Laszlo Tora
- Patrick Schultz
- Imre Berger
Nature ; Volume: 493 ; Page: 699-702
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