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Matthias Titeux

Showing results (31-40 of 37) with videos related to

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Nature Communications|November 9, 2021
Transient mTOR inhibition rescues 4-1BB CAR-Tregs from tonic signal-induced dysfunctionBaptiste Lamarthée, Armance Marchal, Soëli Charbonnier, et al.
Journal of Medical Genetics|September 24, 2025
Sephardic origins revealed for rare skin disorder, recessive dystrophic epidermolysis bullosa, in individuals carrying the unique c.6527insC mutationEmily Mira Warshauer, Paul A Maier, Goran Runfeldt, et al.
Science (New York, N.Y.)|September 18, 2007
TLR3 deficiency in patients with herpes simplex encephalitisShen-Ying Zhang, Emmanuelle Jouanguy, Sophie Ugolini, et al.
JCI Insight|June 7, 2019
Safety and early efficacy outcomes for lentiviral fibroblast gene therapy in recessive dystrophic epidermolysis bullosaSu M Lwin, Farhatullah Syed, Wei-Li Di, et al.
Science Translational Medicine|August 24, 2018
APOBEC mutation drives early-onset squamous cell carcinomas in recessive dystrophic epidermolysis bullosaRaymond J Cho, Ludmil B Alexandrov, Nicoline Y den Breems, et al.
Science Immunology|June 17, 2018
A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activityVivien Béziat, Juan Li, Jian-Xin Lin, et al.
Cell|July 2, 2021
Humans with inherited T cell CD28 deficiency are susceptible to skin papillomaviruses but are otherwise healthyVivien Béziat, Franck Rapaport, Jiafen Hu, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Nature Communications|November 9, 2021
Transient mTOR inhibition rescues 4-1BB CAR-Tregs from tonic signal-induced dysfunctionBaptiste Lamarthée, Armance Marchal, Soëli Charbonnier, et al.
Journal of Medical Genetics|September 24, 2025
Sephardic origins revealed for rare skin disorder, recessive dystrophic epidermolysis bullosa, in individuals carrying the unique c.6527insC mutationEmily Mira Warshauer, Paul A Maier, Goran Runfeldt, et al.
Science (New York, N.Y.)|September 18, 2007
TLR3 deficiency in patients with herpes simplex encephalitisShen-Ying Zhang, Emmanuelle Jouanguy, Sophie Ugolini, et al.
JCI Insight|June 7, 2019
Safety and early efficacy outcomes for lentiviral fibroblast gene therapy in recessive dystrophic epidermolysis bullosaSu M Lwin, Farhatullah Syed, Wei-Li Di, et al.
Science Translational Medicine|August 24, 2018
APOBEC mutation drives early-onset squamous cell carcinomas in recessive dystrophic epidermolysis bullosaRaymond J Cho, Ludmil B Alexandrov, Nicoline Y den Breems, et al.
Science Immunology|June 17, 2018
A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activityVivien Béziat, Juan Li, Jian-Xin Lin, et al.
Cell|July 2, 2021
Humans with inherited T cell CD28 deficiency are susceptible to skin papillomaviruses but are otherwise healthyVivien Béziat, Franck Rapaport, Jiafen Hu, et al.
Pageof 4