L
Leila Abid
Publications - 2
Citations - 148
Leila Abid is an academic researcher. The author has contributed to research in topics: Congenital ichthyosis & Ceramide synthase 3. The author has an hindex of 2, co-authored 2 publications receiving 118 citations.
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Journal ArticleDOI
Mutations in CERS3 cause autosomal recessive congenital ichthyosis in humans.
Franz P.W. Radner,Slaheddine Marrakchi,Peter Kirchmeier,Peter Kirchmeier,Gwang-Jin Kim,Gwang-Jin Kim,Florence Ribierre,Bourane Kamoun,Leila Abid,Michael Leipoldt,Hamida Turki,Werner Schempp,Roland Heilig,Mark Lathrop,Mark Lathrop,Judith Fischer +15 more
TL;DR: Functional analysis of patient skin and in vitro differentiated keratinocytes demonstrated that mutations in CERS3 lead to a disturbed sphingolipid profile with reduced levels of epidermis-specific very long-chain ceramides that interferes with epidermal differentiation.
Journal ArticleDOI
Correction: Mutations in CERS3 Cause Autosomal Recessive Congenital Ichthyosis in Humans.
Franz P.W. Radner,Slaheddine Marrakchi,Peter Kirchmeier,Gwang-Jin Kim,Florence Ribierre,Bourane Kamoun,Leila Abid,Michael Leipoldt,Hamida Turki,Werner Schempp,Roland Heilig,Mark Lathrop,Judith Fischer +12 more
TL;DR: The following information was missing from the Funding section: "This work has been supported in part by grants to M. Lathrop from Genome Quebec, le Ministere de l'Enseignement superieur, de la Recherche, de the Science and de the Technologie (MESRST) Quebec, and from the ANR in France for the Labex project "Medical Genomics".