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Alexander G Bassuk

Showing results (61-70 of 156) with videos related to

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American Journal of Medical Genetics. Part A|August 28, 2010
Collagen XVIII mutation in Knobloch syndrome with acute lymphoblastic leukemiaVinit B Mahajan, Ann Haskins Olney, Penny Garrett, et al.
Retinal Cases & Brief Reports|October 10, 2018
PROGRESSION OF SCOTOPIC SINGLE-FLASH ELECTRORETINOGRAPHY IN THE STAGES OF CAPN5 VITREORETINOPATHYPeter H Tang, Tyson R Kinnick, James C Folk, et al.
Orphanet Journal of Rare Diseases|May 30, 2025
Structure-function analysis of CNGA3-associated achromatopsia patient variants complements clinical genomics in pathogenicity determinationDitte K Rasmussen, Young Joo Sun, Joel A Franco, et al.
Methods in Molecular Biology (Clifton, N.J.)|June 29, 2019
CRISPR Base Editing in Induced Pluripotent Stem CellsYa-Ju Chang, Christine L Xu, Xuan Cui, et al.
Trends in Molecular Medicine|May 31, 2022
Calpains as mechanistic drivers and therapeutic targets for ocular diseaseJennifer T Vu, Elena Wang, Jolan Wu, et al.
Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|March 15, 2018
Caring for Hereditary Childhood Retinal BlindnessRuben Jauregui, Galaxy Y Cho, Vitor K L Takahashi, et al.
Genetics Research|June 14, 2019
In trans variant calling reveals enrichment for compound heterozygous variants in genes involved in neuronal development and growthAllison J Cox, Fillan Grady, Gabriel Velez, et al.
Developmental Biology|August 28, 2007
Dual function of Sox1 in telencephalic progenitor cellsLixin Kan, Ali Jalali, Li-Ru Zhao, et al.
Human Mutation|August 13, 2019
CAPN5 genetic inactivation phenotype supports therapeutic inhibition trialsKatherine J Wert, Susanne F Koch, Gabriel Velez, et al.
Translational Vision Science & Technology|October 2, 2018
Personalized Proteomics for Precision Health: Identifying Biomarkers of Vitreoretinal DiseaseGabriel Velez, Peter H Tang, Thiago Cabral, et al.
Pageof 16

Showing results (61-70 of 156) with videos related to

Sort By:
Pageof 16
American Journal of Medical Genetics. Part A|August 28, 2010
Collagen XVIII mutation in Knobloch syndrome with acute lymphoblastic leukemiaVinit B Mahajan, Ann Haskins Olney, Penny Garrett, et al.
Retinal Cases & Brief Reports|October 10, 2018
PROGRESSION OF SCOTOPIC SINGLE-FLASH ELECTRORETINOGRAPHY IN THE STAGES OF CAPN5 VITREORETINOPATHYPeter H Tang, Tyson R Kinnick, James C Folk, et al.
Orphanet Journal of Rare Diseases|May 30, 2025
Structure-function analysis of CNGA3-associated achromatopsia patient variants complements clinical genomics in pathogenicity determinationDitte K Rasmussen, Young Joo Sun, Joel A Franco, et al.
Methods in Molecular Biology (Clifton, N.J.)|June 29, 2019
CRISPR Base Editing in Induced Pluripotent Stem CellsYa-Ju Chang, Christine L Xu, Xuan Cui, et al.
Trends in Molecular Medicine|May 31, 2022
Calpains as mechanistic drivers and therapeutic targets for ocular diseaseJennifer T Vu, Elena Wang, Jolan Wu, et al.
Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|March 15, 2018
Caring for Hereditary Childhood Retinal BlindnessRuben Jauregui, Galaxy Y Cho, Vitor K L Takahashi, et al.
Genetics Research|June 14, 2019
In trans variant calling reveals enrichment for compound heterozygous variants in genes involved in neuronal development and growthAllison J Cox, Fillan Grady, Gabriel Velez, et al.
Developmental Biology|August 28, 2007
Dual function of Sox1 in telencephalic progenitor cellsLixin Kan, Ali Jalali, Li-Ru Zhao, et al.
Human Mutation|August 13, 2019
CAPN5 genetic inactivation phenotype supports therapeutic inhibition trialsKatherine J Wert, Susanne F Koch, Gabriel Velez, et al.
Translational Vision Science & Technology|October 2, 2018
Personalized Proteomics for Precision Health: Identifying Biomarkers of Vitreoretinal DiseaseGabriel Velez, Peter H Tang, Thiago Cabral, et al.
Pageof 16