Scientific publications

Publications

• 2014

  • The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation

    • Martial Mallaret
    • Matthis Synofzik
    • Jaeho Lee
    • Cari Sagum
    • Muhammad Mahajnah
    • Rajech Sharkia
    • Nathalie Drouot
    • Mathilde Renaud
    • Fabrice A.C. Klein
    • Mathieu Anheim
    • Christine Tranchant
    • Cyril Mignot
    • Jean-Louis Mandel
    • Mark Bedford
    • Peter Bauer
    • Mustafa Am Salih
    • Rebecca Schüle
    • Ludger Schöls
    • C. Marcelo Aldaz
    • Michel Koenig

    Brain - A Journal of Neurology ; Volume: 137 ; Page: 411-419

    HAL DOI

  • A new system for naming ribosomal proteins

    • Nenad Ban
    • Roland Beckmann
    • Jamie Hd Cate
    • Jonathan Dinman
    • François Dragon
    • Steven Ellis
    • Denis Lj Lafontaine
    • Lasse Lindahl
    • Anders Liljas
    • Jeffrey Lipton
    • Michael Mcalear
    • Peter Moore
    • Harry Noller
    • Joaquin Ortega
    • Vikram Govind Panse
    • V Ramakrishnan
    • Christian Mt Spahn
    • Thomas Steitz
    • Marek Tchorzewski
    • David Tollervey
    • ...

    Current Opinion in Structural Biology ; Volume: 24 ; Page: 165-169

    HAL DOI

  • Characterization of the interaction between protein Snu13p/15.5K and the Rsa1p/NUFIP factor and demonstration of its functional importance for snoRNP assembly

    • Benjamin Rothé
    • Régis Back
    • Marc Quinternet
    • Jonathan Bizarro
    • Marie-Cécile Robert
    • Magali Blaud
    • Christophe Romier
    • Xavier Manival
    • Bruno Charpentier
    • Edouard Bertrand
    • Christiane Branlant

    Nucleic Acids Research ; Volume: 42 ; Page: 2015-2036

    HAL DOI

  • ANP32E is a histone chaperone that removes H2A.Z from chromatin

    • Ali Hamiche
    • Arnaud Obri
    • Khalid Ouararhni
    • Christophe Papin
    • Marie-Laure Diebold
    • Kiran Padmanabhan
    • Martin Marek
    • Isabelle Stoll
    • Ludovic Roy
    • Patrick Reilly
    • Tak Mak
    • Stefan Dimitrov
    • Christophe Romier

    Nature ; Volume: 505 ; Page: 648-653

    HAL DOI

  • Intracellular delivery of functionally active proteins using self-assembling pyridylthiourea-polyethylenimine

    • Viktoriia Postupalenko
    • Annie-Paule Sibler
    • Dominique Desplancq
    • Yves Nominé
    • Daniele Spehner
    • Patrick Schultz
    • Etienne Weiss
    • Guy Zuber

    Journal of Controlled Release ; Volume: 178 ; Page: 86-94

    HAL DOI

  • Lysine-specific demethylase 1 regulates differentiation onset and migration of trophoblast stem cells

    • Dongmei Zhu
    • Stefanie Hölz
    • Eric Metzger
    • Mihael Pavlovic
    • Anett Jandausch
    • Cordula Jilg
    • Petra Galgoczy
    • Corinna Herz
    • Markus Moser
    • Daniel Metzger
    • Thomas Günther
    • Sebastian Arnold
    • Roland Schüle

    Nature Communications ; Volume: 5 ; Page: 3174

    HAL DOI

  • Gene Therapy Prolongs Survival and Restores Function in Murine and Canine Models of Myotubular Myopathy

    • Martin Childers
    • Romain Joubert
    • Karine Poulard
    • Christel Moal
    • Robert Grange
    • Jonathan Doering
    • Michael Lawlor
    • Branden Rider
    • Thibaud Jamet
    • Nathalie Danièle
    • Samia Martin
    • Thomas Soker
    • Caroline Hammer
    • Laetitia van Wittenberghe
    • Mandy Lockard
    • Xuan Guan
    • Melissa Goddard
    • Erin Mitchell
    • Jane Barber
    • J Koudy Williams
    • ...

    Science Translational Medicine ; Volume: 6 ; Page: 220ra10-220ra10

    HAL DOI

  • Purification, characterization and crystallization of the human 80S ribosome

    • Heena Khatter
    • Alexander Myasnikov
    • Leslie Mastio
    • Isabelle Billas Massobrio
    • Catherine Birck
    • Stefano Stella
    • Bruno Klaholz

    Nucleic Acids Research ; Volume: 42 ; Page: e49

    HAL DOI

  • Fold change rank ordering statistics: a new method for detecting differentially expressed genes.

    • Doulaye Dembele
    • Philippe Kastner

    BMC Bioinformatics ; Volume: 15 ; Page: 14

    HAL DOI

  • The familial dementia gene revisited: a missense mutation revealed by whole-exome sequencing identifies ITM2B as a candidate gene underlying a novel autosomal dominant retinal dystrophy in a large family

    • Isabelle Audo
    • Kinga Bujakowska
    • Elise Orhan
    • Said El Shamieh
    • Florian Sennlaub
    • Xavier Guillonneau
    • Aline Antonio
    • Christelle Michiels
    • Marie-Elise Lancelot
    • Melanie Letexier
    • Jean-Paul Saraiva
    • Hoan Nguyen
    • Tien Luu
    • Thierry Léveillard
    • Olivier Poch
    • Hélène Dollfus
    • Michel Paques
    • Olivier Goureau
    • Saddek Mohand-Saïd
    • Shomi Bhattacharya
    • ...

    Human Molecular Genetics ; Volume: 23 ; Page: 491-501

    HAL DOI