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Alexander G Bassuk

Showing results (71-80 of 156) with videos related to

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Regenerative Medicine|January 24, 2018
Autologous stem cell therapy for inherited and acquired retinal diseaseMary Ben L Apatoff, Jesse D Sengillo, Eugenia C White, et al.
Current Ophthalmology Reports|October 3, 2017
CRISPR-mediated Ophthalmic Genome SurgeryGalaxy Y Cho, Yazeed Abdulla, Jesse D Sengillo, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|November 7, 2014
Evaluating Familial Essential Tremor with Novel Genetic Approaches: Is it a Genotyping or Phenotyping Issue?Pedro Gonzalez-Alegre, Jorge Di Paola, Kai Wang, et al.
American Journal of Ophthalmology Case Reports|April 11, 2020
Phenotypic variance in Calpain-5 retinal degenerationPeter H Tang, Teja Chemudupati, Katherine J Wert, et al.
Human Mutation|September 9, 2011
Identification and characterization of novel rare mutations in the planar cell polarity gene PRICKLE1 in human neural tube defectsCiprian M Bosoi, Valeria Capra, Redouane Allache, et al.
Molecular Genetics & Genomic Medicine|May 27, 2017
Structural modeling of a novel <i>SLC38A8</i> mutation that causes foveal hypoplasiaMarcus A Toral, Gabriel Velez, Katherine Boudreault, et al.
Nature Communications|February 26, 2022
Investigation of Cas9 antibodies in the human eyeMarcus A Toral, Carsten T Charlesworth, Benjamin Ng, et al.
Nature Communications|April 13, 2022
Author Correction: Investigation of Cas9 antibodies in the human eyeMarcus A Toral, Carsten T Charlesworth, Benjamin Ng, et al.
The Journal of Clinical Investigation|April 12, 2021
Structure-based phylogeny identifies avoralstat as a TMPRSS2 inhibitor that prevents SARS-CoV-2 infection in miceYoung Joo Sun, Gabriel Velez, Dylan E Parsons, et al.
Orphanet Journal of Rare Diseases|February 1, 2020
Fundoscopy-directed genetic testing to re-evaluate negative whole exome sequencing resultsAhra Cho, Jose Ronaldo Lima de Carvalho, Akemi J Tanaka, et al.
Pageof 16

Showing results (71-80 of 156) with videos related to

Sort By:
Pageof 16
Regenerative Medicine|January 24, 2018
Autologous stem cell therapy for inherited and acquired retinal diseaseMary Ben L Apatoff, Jesse D Sengillo, Eugenia C White, et al.
Current Ophthalmology Reports|October 3, 2017
CRISPR-mediated Ophthalmic Genome SurgeryGalaxy Y Cho, Yazeed Abdulla, Jesse D Sengillo, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|November 7, 2014
Evaluating Familial Essential Tremor with Novel Genetic Approaches: Is it a Genotyping or Phenotyping Issue?Pedro Gonzalez-Alegre, Jorge Di Paola, Kai Wang, et al.
American Journal of Ophthalmology Case Reports|April 11, 2020
Phenotypic variance in Calpain-5 retinal degenerationPeter H Tang, Teja Chemudupati, Katherine J Wert, et al.
Human Mutation|September 9, 2011
Identification and characterization of novel rare mutations in the planar cell polarity gene PRICKLE1 in human neural tube defectsCiprian M Bosoi, Valeria Capra, Redouane Allache, et al.
Molecular Genetics & Genomic Medicine|May 27, 2017
Structural modeling of a novel <i>SLC38A8</i> mutation that causes foveal hypoplasiaMarcus A Toral, Gabriel Velez, Katherine Boudreault, et al.
Nature Communications|February 26, 2022
Investigation of Cas9 antibodies in the human eyeMarcus A Toral, Carsten T Charlesworth, Benjamin Ng, et al.
Nature Communications|April 13, 2022
Author Correction: Investigation of Cas9 antibodies in the human eyeMarcus A Toral, Carsten T Charlesworth, Benjamin Ng, et al.
The Journal of Clinical Investigation|April 12, 2021
Structure-based phylogeny identifies avoralstat as a TMPRSS2 inhibitor that prevents SARS-CoV-2 infection in miceYoung Joo Sun, Gabriel Velez, Dylan E Parsons, et al.
Orphanet Journal of Rare Diseases|February 1, 2020
Fundoscopy-directed genetic testing to re-evaluate negative whole exome sequencing resultsAhra Cho, Jose Ronaldo Lima de Carvalho, Akemi J Tanaka, et al.
Pageof 16