Publications scientifiques

Publications

• 2013

  • 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

    HAL DOI

  • 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

    HAL DOI

  • 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

    HAL DOI

  • Reprogramming development

    • Olivier Pourquié

    Development (Cambridge, England) ; Volume: 140 ; Page: 1-2

    HAL DOI

  • 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

    HAL DOI

  • 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

    HAL DOI

  • 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

    HAL DOI

  • 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

    HAL DOI

  • TSLP Produced by Keratinocytes Promotes Allergen Sensitization through Skin and Thereby Triggers Atopic March in Mice

    • Juan Manuel Leyva-Castillo
    • Pierre Hener
    • Hua Jiang
    • Mei Li

    Journal of Investigative Dermatology ; Volume: 133 ; Page: 154-163

    HAL DOI

  • Iodinated α-tocopherol nano-emulsions as non-toxic contrast agents for preclinical X-ray imaging

    • Xiang Li
    • Nicolas Anton
    • Guy Zuber
    • Minjie Zhao
    • Nadia Messaddeq
    • François Hallouard
    • Hatem Fessi
    • Thierry F. Vandamme

    Biomaterials ; Volume: 34 ; Page: 481-491

    HAL DOI