Hôpital Necker-Enfants malades

Hospital


Location: Paris, France (FR) FR

ISNI: 0000000405939113

ROR: https://ror.org/05tr67282

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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

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Abstract

Journal

The human CIB1-EVER1-EVER2 complex governs keratinocyte-intrinsic immunity to beta-papillomaviruses (2018) De Jong SJ, Crequer A, Matos I, Hum D, Gunasekharan V, Lorenzo L, Jabot-Hanin F, et al. Journal article Epilepsy as a Network Disorder (2): What can we learn from other network disorders such as dementia and schizophrenia, and what are the implications for translational research? (2018) Scharfman HE, Kanner AM, Friedman A, Blümcke I, Crocker CE, Cendes F, Diaz-Arrastia R, et al. Journal article Mutations in KEOPS-complex genes cause nephritic syndrome with primary microcephaly (2017) Braun DA, Rao J, Mollet G, Schapiro D, Daugeron MC, Tan W, Gribouval O, et al. Journal article Contractile forces at tricellular contacts modulate epithelial organization and monolayer integrity (2017) Salomon J, Gaston C, Magescas J, Duvauchelle B, Canioni D, Sengmanivong L, Mayeux A, et al. Journal article Mutations in MDH2, Encoding a Krebs Cycle Enzyme, Cause Early-Onset Severe Encephalopathy (2017) Ait-El-Mkadem S, Dayem-Quere M, Gusic M, Chaussenot A, Bannwarth S, Francois B, Genin EC, et al. Journal article Standardized computer-based organized reporting of EEG: SCORE - Second version (2017) Beniczky S, Aurlien H, Brogger JC, Hirsch LJ, Schomer DL, Trinka E, Pressler RM, et al. Journal article Transduction of Herpesvirus saimiri-Transformed T Cells with Exogenous Genes of Interest (2016) Martínez-Barricarte R, De Jong SJ, Markle J, De Paus R, Boisson-Dupuis S, Bustamante J, Van de Vosse E, et al. Journal article Corrigendum: Evidence of innate lymphoid cell redundancy in humans (2016) Vely F, Barlogis V, Vallentin B, Neven B, Piperoglou C, Ebbo M, Perchet T, et al. Journal article, Erratum Evidence of innate lymphoid cell redundancy in humans (2016) Vely F, Barlogis V, Vallentin B, Neven B, Piperoglou C, Perchet T, Petit M, et al. Journal article A Multiplex Kindred with Hennekam Syndrome due to Homozygosity for a CCBE1 Mutation that does not Prevent Protein Expression (2016) Jackson CC, Best L, Lorenzo L, Casanova JL, Wacker J, Bertz S, Agaimy A, Harrer T Journal article