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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2016
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Structural studies of protein arginine methyltransferase 2 reveal its interactions with potential substrates and inhibitors
- Vincent Cura
- Nils Marechal
- Nathalie Troffer‐Charlier
- Jean‐Marc Strub
- Matthijs J. Haren
- Nathaniel I. Martin
- Sarah Cianférani
- Luc Bonnefond
- Jean Cavarelli
Wiley ; Volume: 284 ; Page: 77-96
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Recessive mutations in the kinase ZAK cause a congenital myopathy with fibre type disproportion
- Nasim Vasli
- Elizabeth Harris
- Jason Karamchandani
- Eric Bareke
- Jacek Majewski
- Norma B. Romero
- Tanya Stojkovic
- Rita Barresi
- Hichem Tasfaout
- Richard Charlton
- Edoardo Malfatti
- Johann Böhm
- Chiara Marini-Bettolo
- Karine Choquet
- Marie-Josée Dicaire
- Yi-Hong Shao
- Ana Topf
- Erin O’ferrall
- Bruno Eymard
- Volker Straub
- ...
Brain - A Journal of Neurology ; Volume: 140 ; Page: 37-48
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ARID1B mutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability
- C. Mignot
- M. L. Moutard
- A. Rastetter
- L. Boutaud
- S. Heide
- T. Billette
- D. Doummar
- C. Garel
- A. Afenjar
- A. Jacquette
- D. Lacombe
- A. Verloes
- C. Bole-Feysot
- P. Nitschke
- C. Masson
- A. Faudet
- F. Lesne
- T. Bienvenu
- C. Alby
- T. Attie-Bitach
- ...
Brain - A Journal of Neurology ; Volume: 139
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Fragile X syndrome: Are signaling lipids the missing culprits?
- Ricardos Tabet
- Nicolas Vitale
- Hervé Moine
Biochimie ; Volume: 130 ; Page: 188-194
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Structure of the active form of Dcp1–Dcp2 decapping enzyme bound to m7GDP and its Edc3 activator
- Clément Charenton
- Valerio Taverniti
- Claudine Gaudon-Plesse
- Régis Back
- Bertrand Séraphin
- Marc Graille
Nature Structural and Molecular Biology ; Volume: 23 ; Page: 982-986
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Mutations in the HECT domain of NEDD4L lead to AKT–mTOR pathway deregulation and cause periventricular nodular heterotopia
- Loic Broix
- Hélène Jagline
- Ekaterina L Ivanova
- Stéphane Schmucker
- Nathalie Drouot
- Jill Clayton-Smith
- Alistair T. Pagnamenta
- Kay Metcalfe
- Bertrand Isidor
- Ulrike Walther Louvier
- Annapurna Poduri
- Jenny Taylor
- Peggy Tilly
- Karine Poirier
- Yoann Saillour
- Nicolas Lebrun
- Tristan Stemmelen
- Gabrielle Rudolf
- Giuseppe Muraca
- Benjamin Saintpierre
- ...
Nature Genetics ; Volume: 48 ; Page: 1349-1358
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Ribosomal 18S rRNA base pairs with mRNA during eukaryotic translation initiation
- Franck Martin
- Jean-François Ménétret
- Angelita Simonetti
- Alexander G. Myasnikov
- Quentin Vicens
- Lydia Prongidi-Fix
- S. Kundhavai Natchiar
- Bruno P. Klaholz
- Gilbert Eriani
Nature Communications ; Volume: 7 ; Page: 12622
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Eukaryotic Ribosome as a Target for Cardiovascular Disease
- Simone Pellegrino
- Gulnara Yusupova
Cell Chemical Biology ; Volume: 23 ; Page: 1319-1321
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Construction of a compatible Gateway-based co-expression vector set for expressing multiprotein complexes in E. coli
- Loubna Salim
- Claire Feger
- Didier Busso
Analytical Biochemistry ; Volume: 512 ; Page: 110-113
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