Alain Hovnanian

chef d'équipe | Alain Hovnanian

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Alain Hovnanian

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Research: a scientific adventure

Our goal: to better understand genetic diseases to better treat them.

Resources & publications

Publications

Publication

Transgenic kallikrein 5 mice reproduce major cutaneous and systemic hallmarks...
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KLK5 Inactivation Reverses Cutaneous Hallmarks of Netherton Syndrome.
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Gene-Corrected Fibroblast Therapy for Recessive Dystrophic Epidermolysis Bull...
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Targeted Exon Skipping Restores Type VII Collagen Expression and Anchoring Fi...
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Selective Substrates and Inhibitors for Kallikrein-Related Peptidase 7 (KLK7)...
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Diacerein orphan drug development for epidermolysis bullosa simplex: A phase ...
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Intradermal Injection of Bone Marrow Mesenchymal Stromal Cells Corrects Reces...
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APOBEC mutation drives early-onset squamous cell carcinomas in recessive dyst...
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Ex Vivo COL7A1 Correction for Recessive Dystrophic Epidermolysis Bullosa Usin...
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Mutations in PERP Cause Dominant and Recessive Keratoderma.
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Mutations in PERP Cause Dominant and Recessive Keratoderma.
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EBGene trial: patient preselection outcomes for the European GENEGRAFT ex viv...
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Mutations in PERP Cause Dominant and Recessive Keratoderma.
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A TP63 mutation causes prominent alopecia with mild ectodermal dysplasia.
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A TP63 mutation causes prominent alopecia with mild ectodermal dysplasia.