Aurore Morlon

Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond–like features

Raphaël Carapito, Martina Konantz, Catherine Paillard et al. · Journal of Clinical Investigation · 2017 · 166 citations · Full text

Shwachman-diamond–like Features, Engineering, Genetics +17

The LIM-only protein FHL2 is a serum-inducible transcriptional coactivator of AP-1

Aurore Morlon, Paolo Sassone‐Corsi · Proceedings of the National Academy of Sciences · 2003 · 125 citations · Full text

TAB2, TRAF6 and TAK1 are involved in NF-κB activation induced by the TNF-receptor, Edar and its adaptator Edaradd

Aurore Morlon, Arnold Münnich, Asma Smahi · Human Molecular Genetics · 2005 · 105 citations · Full text

Transcription factor TEAD4 regulates expression of Myogenin and the unfolded protein response genes during C2C12 cell differentiation

Ataaillah Benhaddou, Céline Keime, Tao Ye et al. · Cell Death and Differentiation · 2011 · 89 citations · Full text

Transcriptional Regulation, Cell Regulation, Natural Sciences +12

ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder

Raphaël Carapito, Ekaterina L. Ivanova, Aurore Morlon et al. · The American Journal of Human Genetics · 2019 · 66 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +5