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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2010
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Identification of 28 novel mutations in the Bardet-Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous disease
- Jean Muller
- Corinne Stoetzel
- Marie-Claire Vincent
- Carmen C Leitch
- Virginie Laurier
- Jean Marc Danse
- S. Hellé
- Vincent Marion
- V. Bennouna-Greene
- Serge Vicaire
- André Mégarbané
- Josseline Kaplan
- Valérie Drouin-Garraud
- M. Hamdani
- Sabine Sigaudy
- Christine Francannet
- Joëlle Roume
- P. Bitoun
- Alice Goldenberg
- Nicole Philip
- ...
Human Genetics ; Volume: 127 ; Page: 583-93
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Visualization of multiple alignments, phylogenies and gene family evolution.
- James B Procter
- Julie D. Thompson
- Ivica Letunic
- Chris Creevey
- Fabrice Jossinet
- Geoffrey J Barton
Nature Methods ; Volume: 7 ; Page: S16-25
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Poly(l-lysine) nanostructured particles for gene delivery and hormone stimulation
- Xin Zhang
- Mustapha Oulad-Abdelghani
- Alexander Zelkin
- Yajun Wang
- Youssef Haîkel
- Didier Mainard
- Jean-Claude Voegel
- Frank Caruso
- Nadia Benkirane-Jessel
Biomaterials ; Volume: 31 ; Page: 1699-1706
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Divergent roles of prokineticin receptors in the endothelial cells: angiogenesis and fenestration
- Célia Guilini
- Kyoji Urayama
- Gulen Turkeri
- Deniz B. Dedeoglu
- Hitoshi Kurose
- Nadia Messaddeq
- Canan G Nebigil
AJP - Heart and Circulatory Physiology ; Volume: 298 ; Page: H844-H852
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Sam68 sequestration and partial loss of function are associated with splicing alterations in FXTAS patients
- Chantal Sellier
- Frédérique Rau
- Yilei Liu
- Flora Tassone
- Renate Hukema
- Renata Gattoni
- Anne Schneider
- Stéphane Richard
- Rob Willemsen
- David Elliott
- Paul Hagerman
- Nicolas Charlet-Berguerand
EMBO Journal ; Volume: 29 ; Page: 1248-1261
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CRT-1/calreticulin and the E3 ligase EEL-1/HUWE1 control hemidesmosome maturation in C. elegans development.
- Hala Zahreddine
- Huimin Zhang
- Marie Diogon
- Yasuko Nagamatsu
- Michel Labouesse
Current Biology ; Volume: 20 ; Page: 322-7
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Vici syndrome associated with sensorineural hearing loss and evidence of neuromuscular involvement on muscle biopsy
- Verity Mcclelland
- Thomas Cullup
- Istvan Bodi
- Deborah Ruddy
- Anna Buj-Bello
- Valerie Biancalana
- J. Boehm
- Marc Bitoun
- Owen Miller
- Wajanat Jan
- Esse Menson
- Luis Amaya
- John Trounce
- Jocelyn Laporte
- Shehla Mohammed
- Caroline Sewry
- Julian Raiman
- Heinz Jungbluth
American Journal of Medical Genetics Part A ; Volume: 152A ; Page: 741-747
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Holoprosencephaly: An update on cytogenetic abnormalities.
- Claude Bendavid
- Valérie Dupé
- Lucie Rochard
- Isabelle Gicquel
- Christèle Dubourg
- Véronique David
American Journal of Medical Genetics Part C: Seminars in Medical Genetics ; Volume: 154C ; Page: 86-92
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Murine neonatal infection provides an efficient model for congenital ocular toxoplasmosis
- Ibtissem Lahmar
- Marie Guinard
- Arnaud Sauer
- Luc Marcellin
- Tamer Abdelrahman
- Michel Roux
- Marc Mousli
- Adnan Moussa
- Hamouda Babba
- Alexander Pfaff
- Ermanno Candolfi
Experimental Parasitology ; Volume: 124 ; Page: 190-196
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Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome.
- Vincent Laugel
- Cécile Dalloz
- M. Durand
- Florence Sauvanaud
- Hans-Ulrik Kristensen
- Marie-Claire Vincent
- Laurent Pasquier
- Sylvie Odent
- Valérie Cormier-Daire
- Blanca Gener
- Edward Spencer Tobias
- John Lorimer Tolmie
- Dominique Martin-Coignard
- Valérie Drouin-Garraud
- Delphine Heron
- Hubert Journel
- Emmanuel Raffo
- Jaqueline Vigneron
- Stanislas Lyonnet
- Victoria Alice Murday
- ...
Human Mutation ; Volume: 31 ; Page: 113-26
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