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Adam P DeLuca

Showing results (1-10 of 41) with videos related to

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JAMA Ophthalmology|May 30, 2015
Apparent Usher Syndrome Caused by the Combination of BBS1-Associated Retinitis Pigmentosa and SLC26A4-Associated DeafnessAdam P DeLuca, Matthew C Weed, Christine M Haas, et al.
Human Molecular Genetics|May 27, 2017
Primary congenital and developmental glaucomasCarly J Lewis, Adam Hedberg-Buenz, Adam P DeLuca, et al.
Medical Research Archives|February 20, 2018
Keeping an Eye on Bardet-Biedl Syndrome: A Comprehensive Review of the Role of Bardet-Biedl Syndrome Genes in the EyeKatie Weihbrecht, Wesley A Goar, Thomas Pak, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 17, 2010
Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencingA Eliot Shearer, Adam P DeLuca, Michael S Hildebrand, et al.
Human Mutation|March 20, 2013
Prioritization of retinal disease genes: an integrative approachAlex H Wagner, Kyle R Taylor, Adam P DeLuca, et al.
Experimental Eye Research|September 10, 2020
Spectacle: An interactive resource for ocular single-cell RNA sequencing data analysisAndrew P Voigt, S Scott Whitmore, Nicholas D Lessing, et al.
Case Reports in Ophthalmology|October 9, 2025
Early-Onset Stargardt Disease Caused by Homozygosity of a Complex <i>ABCA4</i> Allele from Eastern Africa: Two Case ReportsSigrid Aslaksen, Eirik Bratland, Mari Hamre Bu, et al.
Cells|February 20, 2020
Single-Cell RNA Sequencing in Human Retinal Degeneration Reveals Distinct Glial Cell PopulationsAndrew P Voigt, Elaine Binkley, Miles J Flamme-Wiese, et al.
Scientific Reports|September 10, 2021
Label-free microfluidic enrichment of cancer cells from non-cancer cells in ascitesNicholas E Stone, Abhishek Raj, Katherine M Young, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 10, 2011
Exome sequencing and analysis of induced pluripotent stem cells identify the cilia-related gene male germ cell-associated kinase (MAK) as a cause of retinitis pigmentosaBudd A Tucker, Todd E Scheetz, Robert F Mullins, et al.
Pageof 5

Showing results (1-10 of 41) with videos related to

Sort By:
Pageof 5
JAMA Ophthalmology|May 30, 2015
Apparent Usher Syndrome Caused by the Combination of BBS1-Associated Retinitis Pigmentosa and SLC26A4-Associated DeafnessAdam P DeLuca, Matthew C Weed, Christine M Haas, et al.
Human Molecular Genetics|May 27, 2017
Primary congenital and developmental glaucomasCarly J Lewis, Adam Hedberg-Buenz, Adam P DeLuca, et al.
Medical Research Archives|February 20, 2018
Keeping an Eye on Bardet-Biedl Syndrome: A Comprehensive Review of the Role of Bardet-Biedl Syndrome Genes in the EyeKatie Weihbrecht, Wesley A Goar, Thomas Pak, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 17, 2010
Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencingA Eliot Shearer, Adam P DeLuca, Michael S Hildebrand, et al.
Human Mutation|March 20, 2013
Prioritization of retinal disease genes: an integrative approachAlex H Wagner, Kyle R Taylor, Adam P DeLuca, et al.
Experimental Eye Research|September 10, 2020
Spectacle: An interactive resource for ocular single-cell RNA sequencing data analysisAndrew P Voigt, S Scott Whitmore, Nicholas D Lessing, et al.
Case Reports in Ophthalmology|October 9, 2025
Early-Onset Stargardt Disease Caused by Homozygosity of a Complex <i>ABCA4</i> Allele from Eastern Africa: Two Case ReportsSigrid Aslaksen, Eirik Bratland, Mari Hamre Bu, et al.
Cells|February 20, 2020
Single-Cell RNA Sequencing in Human Retinal Degeneration Reveals Distinct Glial Cell PopulationsAndrew P Voigt, Elaine Binkley, Miles J Flamme-Wiese, et al.
Scientific Reports|September 10, 2021
Label-free microfluidic enrichment of cancer cells from non-cancer cells in ascitesNicholas E Stone, Abhishek Raj, Katherine M Young, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 10, 2011
Exome sequencing and analysis of induced pluripotent stem cells identify the cilia-related gene male germ cell-associated kinase (MAK) as a cause of retinitis pigmentosaBudd A Tucker, Todd E Scheetz, Robert F Mullins, et al.
Pageof 5