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Tasnim Ben Yacoub

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Biomedical Optics Express|July 27, 2023
Interface self-referenced dynamic full-field optical coherence tomographyTual Monfort, Salvatore Azzollini, Tasnim Ben Yacoub, et al.
Stem Cell Research|July 20, 2023
Generation of gene corrected human isogenic iPSC lines (IDVi003-A_CR13, IDVi003-A_CR21, IDVi003-A_CR24) from an inherited retinal dystrophy patient-derived IPSC line ITM2B-5286-3 (IDVi003-A) carrying the ITM2B c.782A > C variant using CRISPR/Cas9Tasnim Ben Yacoub, Camille Letellier, Juliette Wohlschlegel, et al.
Stem Cell Research|September 18, 2024
Generation of human induced pluripotent stem cell lines from a subject with UBAP1L-associated retinal dystrophy and CRISPR/cas9-corrected isogenic iPSC linesAndréa Amprou, Tasnim Ben Yacoub, Camille Letellier, et al.
Scientific Reports|June 23, 2026
The ITM2B-associated retinal dystrophy mutation modifies BRI23 peptide interactions in the human retinaTasnim Ben Yacoub, Andréa Amprou, Camille Letellier, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 31, 2024
Variants in UBAP1L lead to autosomal recessive rod-cone and cone-rod dystrophyChristina Zeitz, Julien Navarro, Leila Azizzadeh Pormehr, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Biomedical Optics Express|July 27, 2023
Interface self-referenced dynamic full-field optical coherence tomographyTual Monfort, Salvatore Azzollini, Tasnim Ben Yacoub, et al.
Stem Cell Research|July 20, 2023
Generation of gene corrected human isogenic iPSC lines (IDVi003-A_CR13, IDVi003-A_CR21, IDVi003-A_CR24) from an inherited retinal dystrophy patient-derived IPSC line ITM2B-5286-3 (IDVi003-A) carrying the ITM2B c.782A > C variant using CRISPR/Cas9Tasnim Ben Yacoub, Camille Letellier, Juliette Wohlschlegel, et al.
Stem Cell Research|September 18, 2024
Generation of human induced pluripotent stem cell lines from a subject with UBAP1L-associated retinal dystrophy and CRISPR/cas9-corrected isogenic iPSC linesAndréa Amprou, Tasnim Ben Yacoub, Camille Letellier, et al.
Scientific Reports|June 23, 2026
The ITM2B-associated retinal dystrophy mutation modifies BRI23 peptide interactions in the human retinaTasnim Ben Yacoub, Andréa Amprou, Camille Letellier, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 31, 2024
Variants in UBAP1L lead to autosomal recessive rod-cone and cone-rod dystrophyChristina Zeitz, Julien Navarro, Leila Azizzadeh Pormehr, et al.
Pageof 1