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Tahleel Ali-Nasser

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

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Ophthalmic Genetics|February 18, 2021
Retinal dystrophy as part of <i>TTC21B</i>-associated ciliopathyTamar Ben-Yosef, Nurit Asia Batsir, Tahleel Ali Nasser, et al.
Molecular Vision|November 7, 2022
Autosomal dominant retinitis pigmentosa with incomplete penetrance due to an intronic mutation of the <i>PRPF31</i> geneTahleel Ali-Nasser, Shiri Zayit-Soudry, Eyal Banin, et al.
Journal of Molecular Biology|March 26, 2025
lncRNAlyzr: Enrichment Analysis for lncRNA SetsJohn Erol Evangelista, Tahleel Ali-Nasser, Lauren E Malek, et al.
Journal of Biomedical Science|February 28, 2024
Integration of transcription regulation and functional genomic data reveals lncRNA SNHG6's role in hematopoietic differentiation and leukemiaJoshua M Hazan, Raziel Amador, Tahleel Ali-Nasser, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 13, 2025
Biallelic null variants in C19orf44 cause a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophyMiriam Ehrenberg, Maayan Avraham, Sandeep Sarma Asodu, et al.
Pageof 1

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

Sort By:
Pageof 1
Ophthalmic Genetics|February 18, 2021
Retinal dystrophy as part of <i>TTC21B</i>-associated ciliopathyTamar Ben-Yosef, Nurit Asia Batsir, Tahleel Ali Nasser, et al.
Molecular Vision|November 7, 2022
Autosomal dominant retinitis pigmentosa with incomplete penetrance due to an intronic mutation of the <i>PRPF31</i> geneTahleel Ali-Nasser, Shiri Zayit-Soudry, Eyal Banin, et al.
Journal of Molecular Biology|March 26, 2025
lncRNAlyzr: Enrichment Analysis for lncRNA SetsJohn Erol Evangelista, Tahleel Ali-Nasser, Lauren E Malek, et al.
Journal of Biomedical Science|February 28, 2024
Integration of transcription regulation and functional genomic data reveals lncRNA SNHG6's role in hematopoietic differentiation and leukemiaJoshua M Hazan, Raziel Amador, Tahleel Ali-Nasser, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 13, 2025
Biallelic null variants in C19orf44 cause a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophyMiriam Ehrenberg, Maayan Avraham, Sandeep Sarma Asodu, et al.
Pageof 1