
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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2016
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Lymphopoiesis in transgenic mice over-expressing Artemis
- P. Rivera-Munoz
- V. Abramowski
- S. Jacquot
- P. Andre
- S. Charrier
- K. Lipson-Ruffert
- A. Fischer
- A. Galy
- M. Cavazzana
- J. P. De Villartay
Gene Ther ; Volume: 23 ; Page: 176-86
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Medications between psychiatric and addictive disorders
- Laurence Lalanne
- Pierre-Eric Lutz
- Benoit Trojak
- Jean-Philippe Lang
- Brigitte L. Kieffer
- Elisabeth Bacon
Progress in Neuro-Psychopharmacology and Biological Psychiatry ; Volume: 65 ; Page: 215-223
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CYP46A1, the rate-limiting enzyme for cholesterol degradation, is neuroprotective in Huntington’s disease
- Lydie Boussicault
- Sandro Alves
- Antonin Lamazière
- Anabelle Planques
- Nicolas Heck
- Lara Moumné
- Gaëtan Despres
- Susanne Bolte
- Amélie Hu
- Christiane Pagès
- Laurie Galvan
- Francoise Piguet
- Patrick Aubourg
- Nathalie Cartier
- Jocelyne Caboche
- Sandrine Betuing
Brain - A Journal of Neurology ; Volume: 139 ; Page: 953-970
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A phosphoinositide conversion mechanism for exit from endosomes
- K. Ketel
- M. Krauss
- Anne-Sophie Nicot
- D. Puchkov
- M. Wieffer
- R. Muller
- D. Subramanian
- C. Schultz
- Jocelyn Laporte
- V. Haucke
Nature ; Volume: 529 ; Page: 408-12
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In situ chemical behaviour of methylisothiazolinone (MI) and methylchloroisothiazolinone (MCI) in reconstructed human epidermis: a new approach to the cross-reactivity issue
- Camille Debeuckelaere
- Francois-Marie Moussallieh
- Karim El Bayed
- Izzie-Jacques Namer
- Valerie Berl
- Elena Giménez-Arnau
- Jean-Pierre Lepoittevin
Contact Dermatitis ; Volume: 74 ; Page: 159-167
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Identification of a novel mutation confirms the implication of IFT172 (BBS20) in Bardet-Biedl syndrome
- Elise Schaefer
- Corinne Stoetzel
- Sophie Scheidecker
- Véronique Geoffroy
- Megana Prasad
- Claire Redin
- I Missotte
- D Lacombe
- Jean-Louis Mandel
- Jean Muller
- Helene Dollfus
Journal of Human Genetics ; Volume: 61 ; Page: 447-450
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Homozygosity for the V377I mutation in mevalonate kinase causes distinct clinical phenotypes in two sibs with hyperimmunoglobulinaemia D and periodic fever syndrome (HIDS)
- Laurent Messer
- Ghada Alsaleh
- Philippe Georgel
- Raphael Carapito
- Hans Waterham
- Nassim Dali-Youcef
- Siamak Bahram
- Jean Sibilia
RMD Open : Rheumatic & Musculoskeletal Diseases ; Volume: 2 ; Page: e000196
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Gbp2 interacts with THO/TREX through a novel type of RRM domain
- Santiago Martínez-Lumbreras
- Valério Taverniti
- Silvia Zorrilla
- Bertrand Séraphin
- José Manuel Pérez-Cañadillas
Nucleic Acids Research ; Volume: 44 ; Page: 437-448
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Uncoiling collagen: a multidimensional mass spectrometry study
- H. J. Simon
- M. A. van Agthoven
- P. Y. Lam
- F. Floris
- L. Chiron
- Marc-André Delsuc
- C. Rolando
- M. P. Barrow
- P. B. O'Connor
Analyst ; Volume: 141 ; Page: 157-65
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