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Adam P DeLuca

Showing results (31-40 of 41) with videos related to

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Hearing Research|September 15, 2012
Prediction of cochlear implant performance by genetic mutation: the spiral ganglion hypothesisRobert W Eppsteiner, A Eliot Shearer, Michael S Hildebrand, et al.
Human Molecular Genetics|August 7, 2013
Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt diseaseTerry A Braun, Robert F Mullins, Alex H Wagner, et al.
Stem Cells Translational Medicine|May 23, 2023
Propensity of Patient-Derived iPSCs for Retinal Differentiation: Implications for Autologous Cell ReplacementJessica A Cooke, Andrew P Voigt, Michael A Collingwood, et al.
Human Molecular Genetics|October 24, 2015
Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosisAdam P DeLuca, S Scott Whitmore, Jenna Barnes, et al.
The Annals of Otology, Rhinology, and Laryngology|November 5, 2015
Audioprofile Surfaces: The 21st Century AudiogramKyle R Taylor, Kevin T Booth, Hela Azaiez, et al.
Journal of Medical Genetics|June 28, 2013
Advancing genetic testing for deafness with genomic technologyA Eliot Shearer, E Ann Black-Ziegelbein, Michael S Hildebrand, et al.
Ophthalmology|October 29, 2015
North Carolina Macular Dystrophy Is Caused by Dysregulation of the Retinal Transcription Factor PRDM13Kent W Small, Adam P DeLuca, S Scott Whitmore, et al.
BMC Genomics|June 27, 2021
Exome-based investigation of the genetic basis of human pigmentary glaucomaCarly van der Heide, Wes Goar, Kacie J Meyer, et al.
Ophthalmology|February 3, 2024
A Retrospective Longitudinal Study of 460 Patients with ABCA4-Associated Retinal DiseaseBeau J Fenner, S Scott Whitmore, Adam P DeLuca, et al.
Human Mutation|April 27, 2011
DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing lossMichael S Hildebrand, Matías Morín, Nicole C Meyer, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Hearing Research|September 15, 2012
Prediction of cochlear implant performance by genetic mutation: the spiral ganglion hypothesisRobert W Eppsteiner, A Eliot Shearer, Michael S Hildebrand, et al.
Human Molecular Genetics|August 7, 2013
Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt diseaseTerry A Braun, Robert F Mullins, Alex H Wagner, et al.
Stem Cells Translational Medicine|May 23, 2023
Propensity of Patient-Derived iPSCs for Retinal Differentiation: Implications for Autologous Cell ReplacementJessica A Cooke, Andrew P Voigt, Michael A Collingwood, et al.
Human Molecular Genetics|October 24, 2015
Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosisAdam P DeLuca, S Scott Whitmore, Jenna Barnes, et al.
The Annals of Otology, Rhinology, and Laryngology|November 5, 2015
Audioprofile Surfaces: The 21st Century AudiogramKyle R Taylor, Kevin T Booth, Hela Azaiez, et al.
Journal of Medical Genetics|June 28, 2013
Advancing genetic testing for deafness with genomic technologyA Eliot Shearer, E Ann Black-Ziegelbein, Michael S Hildebrand, et al.
Ophthalmology|October 29, 2015
North Carolina Macular Dystrophy Is Caused by Dysregulation of the Retinal Transcription Factor PRDM13Kent W Small, Adam P DeLuca, S Scott Whitmore, et al.
BMC Genomics|June 27, 2021
Exome-based investigation of the genetic basis of human pigmentary glaucomaCarly van der Heide, Wes Goar, Kacie J Meyer, et al.
Ophthalmology|February 3, 2024
A Retrospective Longitudinal Study of 460 Patients with ABCA4-Associated Retinal DiseaseBeau J Fenner, S Scott Whitmore, Adam P DeLuca, et al.
Human Mutation|April 27, 2011
DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing lossMichael S Hildebrand, Matías Morín, Nicole C Meyer, et al.
Pageof 5