Matthias Titeux
7PUBLICATIONS
57CO-AUTHORS

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Publications (7)
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|Dec 05, 2024
Novel variants impairing Sp1 transcription factor binding in the COL7A1 promoter cause mild cases of recessive dystrophic epidermolysis bullosa.Nathalie Pironon, Artyom Gasparyan, María Joao Yubero
|Aug 19, 2024
Splice modulation strategy applied to deep intronic variants in <i>COL7A1</i> causing recessive dystrophic epidermolysis bullosa.Nathalie Pironon, Emmanuelle Bourrat, Catherine Prost
|Jul 13, 2024
Citrullinated Histone H3, a Marker for Neutrophil Extracellular Traps, Is Associated with Poor Prognosis in Cutaneous Squamous Cell Carcinoma Developing in Patients with Recessive Dystrophic Epidermolysis Bullosa.Hélène Ragot, Sonia Gaucher, Mathilde Bonnet des Claustres
|Sep 27, 2019
EBGene trial: patient preselection outcomes for the European GENEGRAFT ex vivo phase I/II gene therapy trial for recessive dystrophic epidermolysis bullosa.S Gaucher, S M Lwin, M Titeux
|Aug 24, 2018
APOBEC mutation drives early-onset squamous cell carcinomas in recessive dystrophic epidermolysis bullosa.Raymond J Cho, Ludmil B Alexandrov, Nicoline Y den Breems
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Frequent Collaborators
5 joint publications
Alain Hovnanian
3 joint publications
Nathalie Pironon
2 joint publications
Su M Lwin
2 joint publications
Emmanuelle Bourrat
1 joint publications
S Gaucher
1 joint publications
A Abdul-Wahab
1 joint publications
A Izmiryan
1 joint publications
S Miskinyte
1 joint publications
C Ganier
1 joint publications
S Duchatelet