Scientific publications

Publications

• 2020

  • Ratchetaxis in Channels: Entry Point and Local Asymmetry Set Cell Directions in Confinement

    • Emilie Le Maout
    • Simon Lo Vecchio
    • Praveen Kumar Korla
    • Jim Jinn-Chyuan Sheu
    • Daniel Riveline

    Biophysical Journal ; Volume: 119 ; Page: 1301-1308

    HAL DOI

  • Functional microRNA screen uncovers O-linked N-acetylglucosamine transferase as a host factor modulating hepatitis C virus morphogenesis and infectivity

    • Katharina Herzog
    • Simonetta Bandiera
    • Sophie Pernot
    • Catherine Fauvelle
    • Frank Jühling
    • Amélie Weiss
    • Anne Bull
    • Sarah C. Durand
    • Béatrice Chane-Woon-Ming
    • Sébastien Pfeffer
    • Marion Mercey
    • Hervé Lerat
    • Jean-Christophe Meunier
    • Wolfgang Raffelsberger
    • Laurent Brino
    • Thomas Baumert
    • Mirjam B. Zeisel

    Gut ; Volume: 69 ; Page: 380-392

    HAL DOI

  • Impact of TP53 mutations in acute myeloid leukemia patients treated with azacitidine

    • Pierre Bories
    • Naïs Prade
    • Stéphanie Lagarde
    • Bastien Cabarrou
    • Laetitia Largeaud
    • Julien Plenecassagnes
    • Isabelle Luquet
    • Véronique de Mas
    • Thomas Filleron
    • Manon Cassou
    • Audrey Sarry
    • Luc-Matthieu Fornecker
    • Célestine Simand
    • Sarah Bertoli
    • Christian Recher
    • Eric Delabesse

    PLoS ONE ; Volume: 15 ; Page: e0238795

    HAL DOI

  • Follicular flushing versus direct aspiration in poor responder IVF patients a randomized prospective study.

    • Charline Calabre
    • Elodie Schuller
    • Marc André Goltzene
    • Catherine Rongières
    • Catherine Celebi
    • Nicolas Meyer
    • Marius Teletin
    • Olivier Pirrello

    European Journal of Obstetrics & Gynecology and Reproductive Biology ; Volume: 248 ; Page: 118-122

    HAL DOI

  • Attitudes towards Genetic Information Delivered by High-Throughput Sequencing among Molecular Geneticists, Genetic Counselors, Medical Advisors and Students in France

    • Vlad Titerlea
    • Doulaye Dembélé
    • Jean-Louis Mandel
    • Jocelyn Laporte

    European Journal of Medical Genetics ; Volume: 63

    HAL DOI

  • Deficiency of the SMOC2 matricellular protein impairs bone healing and produces age-dependent bone loss

    • Supawich Morkmued
    • François Clauss
    • Brigitte Schuhbaur
    • Valerie Fraulob
    • Eric Mathieu
    • Joseph Hemmerlé
    • Hans Clevers
    • Bon-Kyoung Koo
    • Pascal Dollé
    • Agnès Bloch-Zupan
    • Karen Niederreither

    Scientific Reports ; Volume: 10 ; Page: 14817

    HAL DOI

  • Callosal agenesis and congenital mirror movements: outcomes associated with DCC mutations

    • Megan Spencer-Smith
    • Jacquelyn Knight
    • Emmanuelle Lacaze
    • Christel Depienne
    • Paul J Lockhart
    • Linda J. Richards
    • Delphine Heron
    • Richard J. Leventer
    • Gail A. Robinson

    developmental medecine and child neurology ; Volume: 62 ; Page: 758-762

    HAL DOI

  • Benign hereditary chorea: From benign to serious

    • Anaide Lamiral
    • Salima El Chehadeh
    • Jameleddine Chelly
    • Mathieu Anheim
    • Vincent Laugel
    • Christine Tranchant

    Revue Neurologique ; Volume: 176 ; Page: 295-296

    HAL DOI

  • A Heterozygous Mutation in the Filamin C Gene Causes an Unusual Nemaline Myopathy With Ring Fibers

    • Teresinha Evangelista
    • Xavière Lornage
    • Pierre Carlier
    • Guillaume Bassez
    • Guy Brochier
    • Anaïs Chanut
    • Emmanuelle Lacène
    • Mai-Thao Bui
    • Corinne Metay
    • Ursula Oppermann
    • Johann Böhm
    • Jocelyn Laporte
    • Norma Romero

    Journal of Neurology, Neurosurgery and Psychiatry ; Volume: 79 ; Page: 908-914

    HAL DOI

  • Mutations in genes encoding regulators of mRNA decapping and translation initiation: links to intellectual disability

    • Dominique Weil
    • Amélie Piton
    • Davor Lessel
    • Nancy Standart

    Biochemical Society Transactions ; Volume: 48 ; Page: 1199-1211

    HAL DOI