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Eric A Pierce

Showing results (61-70 of 132) with videos related to

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The CRISPR Journal|April 26, 2019
Allele-Specific CRISPR-Cas9 Genome Editing of the Single-Base P23H Mutation for Rhodopsin-Associated Dominant Retinitis PigmentosaPingjuan Li, Benjamin P Kleinstiver, Mihoko Y Leon, et al.
Cold Spring Harbor Molecular Case Studies|November 14, 2022
Identification of a novel large multigene deletion and a frameshift indel in <i>PDE6B</i> as the underlying cause of early-onset recessive rod-cone degenerationRiccardo Sangermano, Pooja Biswas, Lori S Sullivan, et al.
Molecular Vision|June 23, 2020
Biallelic <i>RP1</i>-associated retinal dystrophies: Expanding the mutational and clinical spectrumRachel M Huckfeldt, Florin Grigorian, Emily Place, et al.
Discovery Medicine|January 1, 2013
Mitochondrial disease genetic diagnostics: optimized whole-exome analysis for all MitoCarta nuclear genes and the mitochondrial genomeMarni J Falk, Eric A Pierce, Mark Consugar, et al.
International Journal of Molecular Sciences|January 11, 2025
Optimized Prime Editing of Human Induced Pluripotent Stem Cells to Efficiently Generate Isogenic Models of Mendelian DiseasesRodrigo Cerna-Chavez, Alba Ortega-Gasco, Hafiz Muhammad Azhar Baig, et al.
Bioinformatics (Oxford, England)|July 22, 2011
Comparative analysis of RNA-Seq alignment algorithms and the RNA-Seq unified mapper (RUM)Gregory R Grant, Michael H Farkas, Angel D Pizarro, et al.
Ophthalmic Genetics|January 21, 2022
Novel <i>RCBTB1</i> variants causing later-onset non-syndromic retinal dystrophy with macular chorioretinal atrophyAndrew J Catomeris, Brian G Ballios, Riccardo Sangermano, et al.
Medrxiv : the Preprint Server for Health Sciences|July 18, 2023
Structure-based network analysis predicts mutations associated with inherited retinal diseaseBlake M Hauser, Yuyang Luo, Anusha Nathan, et al.
Investigative Ophthalmology & Visual Science|January 5, 2002
Identification and subcellular localization of the RP1 protein in human and mouse photoreceptorsQin Liu, Jie Zhou, Stephen P Daiger, et al.
Journal of Cell Science|June 16, 2004
Quantification of the cytoplasmic spaces of living cells with EGFP reveals arrestin-EGFP to be in disequilibrium in dark adapted rod photoreceptorsJon A Peet, Alvina Bragin, Peter D Calvert, et al.
Pageof 14

Showing results (61-70 of 132) with videos related to

Sort By:
Pageof 14
The CRISPR Journal|April 26, 2019
Allele-Specific CRISPR-Cas9 Genome Editing of the Single-Base P23H Mutation for Rhodopsin-Associated Dominant Retinitis PigmentosaPingjuan Li, Benjamin P Kleinstiver, Mihoko Y Leon, et al.
Cold Spring Harbor Molecular Case Studies|November 14, 2022
Identification of a novel large multigene deletion and a frameshift indel in <i>PDE6B</i> as the underlying cause of early-onset recessive rod-cone degenerationRiccardo Sangermano, Pooja Biswas, Lori S Sullivan, et al.
Molecular Vision|June 23, 2020
Biallelic <i>RP1</i>-associated retinal dystrophies: Expanding the mutational and clinical spectrumRachel M Huckfeldt, Florin Grigorian, Emily Place, et al.
Discovery Medicine|January 1, 2013
Mitochondrial disease genetic diagnostics: optimized whole-exome analysis for all MitoCarta nuclear genes and the mitochondrial genomeMarni J Falk, Eric A Pierce, Mark Consugar, et al.
International Journal of Molecular Sciences|January 11, 2025
Optimized Prime Editing of Human Induced Pluripotent Stem Cells to Efficiently Generate Isogenic Models of Mendelian DiseasesRodrigo Cerna-Chavez, Alba Ortega-Gasco, Hafiz Muhammad Azhar Baig, et al.
Bioinformatics (Oxford, England)|July 22, 2011
Comparative analysis of RNA-Seq alignment algorithms and the RNA-Seq unified mapper (RUM)Gregory R Grant, Michael H Farkas, Angel D Pizarro, et al.
Ophthalmic Genetics|January 21, 2022
Novel <i>RCBTB1</i> variants causing later-onset non-syndromic retinal dystrophy with macular chorioretinal atrophyAndrew J Catomeris, Brian G Ballios, Riccardo Sangermano, et al.
Medrxiv : the Preprint Server for Health Sciences|July 18, 2023
Structure-based network analysis predicts mutations associated with inherited retinal diseaseBlake M Hauser, Yuyang Luo, Anusha Nathan, et al.
Investigative Ophthalmology & Visual Science|January 5, 2002
Identification and subcellular localization of the RP1 protein in human and mouse photoreceptorsQin Liu, Jie Zhou, Stephen P Daiger, et al.
Journal of Cell Science|June 16, 2004
Quantification of the cytoplasmic spaces of living cells with EGFP reveals arrestin-EGFP to be in disequilibrium in dark adapted rod photoreceptorsJon A Peet, Alvina Bragin, Peter D Calvert, et al.
Pageof 14