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Regenerative Medicine
|
January 24, 2018
Autologous stem cell therapy for inherited and acquired retinal disease
Mary Ben L Apatoff, Jesse D Sengillo, Eugenia C White, et al.
Current Ophthalmology Reports
|
October 3, 2017
CRISPR-mediated Ophthalmic Genome Surgery
Galaxy 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 degeneration
Peter 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 defects
Ciprian 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 hypoplasia
Marcus A Toral, Gabriel Velez, Katherine Boudreault, et al.
Nature Communications
|
February 26, 2022
Investigation of Cas9 antibodies in the human eye
Marcus A Toral, Carsten T Charlesworth, Benjamin Ng, et al.
Nature Communications
|
April 13, 2022
Author Correction: Investigation of Cas9 antibodies in the human eye
Marcus 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 mice
Young 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 results
Ahra Cho, Jose Ronaldo Lima de Carvalho, Akemi J Tanaka, et al.
Page
of 16
Search research articles
Search
Showing results (71-80 of 156) with videos related to
Sort By:
Page
of 16
Regenerative Medicine
|
January 24, 2018
Autologous stem cell therapy for inherited and acquired retinal disease
Mary Ben L Apatoff, Jesse D Sengillo, Eugenia C White, et al.
Current Ophthalmology Reports
|
October 3, 2017
CRISPR-mediated Ophthalmic Genome Surgery
Galaxy 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 degeneration
Peter 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 defects
Ciprian 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 hypoplasia
Marcus A Toral, Gabriel Velez, Katherine Boudreault, et al.
Nature Communications
|
February 26, 2022
Investigation of Cas9 antibodies in the human eye
Marcus A Toral, Carsten T Charlesworth, Benjamin Ng, et al.
Nature Communications
|
April 13, 2022
Author Correction: Investigation of Cas9 antibodies in the human eye
Marcus 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 mice
Young 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 results
Ahra Cho, Jose Ronaldo Lima de Carvalho, Akemi J Tanaka, et al.
Page
of 16