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Edwin M Stone

Showing results (301-310 of 384) with videos related to

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Scientific Reports|July 30, 2016
cGMP production of patient-specific iPSCs and photoreceptor precursor cells to treat retinal degenerative blindnessLuke A Wiley, Erin R Burnight, Adam P DeLuca, et al.
Investigative Ophthalmology & Visual Science|May 17, 2017
Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 GeneSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Human Molecular Genetics|December 17, 2008
ABCA4 disease progression and a proposed strategy for gene therapyArtur V Cideciyan, Malgorzata Swider, Tomas S Aleman, et al.
Ophthalmology. Retina|April 25, 2019
Wide-Field Swept-Source OCT and Angiography in X-Linked RetinoschisisIan C Han, S Scott Whitmore, D Brice Critser, et al.
Ophthalmology Science|November 29, 2023
Using Goldmann Visual Field Volume to Track Disease Progression in ChoroideremiaAdam P DeLuca, S Scott Whitmore, Nicole J Tatro, et al.
Ophthalmology. Glaucoma|March 26, 2019
Histochemical Analysis of Glaucoma Caused by a Myocilin Mutation in a Human Donor EyeCarly J van der Heide, Wallace L M Alward, Miles Flamme-Wiese, et al.
Human Molecular Genetics|March 19, 2004
QRX, a novel homeobox gene, modulates photoreceptor gene expressionQing-liang Wang, Shiming Chen, Noriko Esumi, et al.
Human Gene Therapy|May 21, 2019
Development of a Molecularly Stable Gene Therapy Vector for the Treatment of <i>RPGR</i>-Associated X-Linked Retinitis PigmentosaJoseph C Giacalone, Jeaneen L Andorf, Qihong Zhang, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 13, 2003
Glaucoma phenotype in pedigrees with the myocilin Thr377Met mutationDavid A Mackey, Danielle L Healey, John H Fingert, et al.
Human Molecular Genetics|March 18, 2005
Mkks-null mice have a phenotype resembling Bardet-Biedl syndromeMelissa A Fath, Robert F Mullins, Charles Searby, et al.
Pageof 39

Showing results (301-310 of 384) with videos related to

Sort By:
Pageof 39
Scientific Reports|July 30, 2016
cGMP production of patient-specific iPSCs and photoreceptor precursor cells to treat retinal degenerative blindnessLuke A Wiley, Erin R Burnight, Adam P DeLuca, et al.
Investigative Ophthalmology & Visual Science|May 17, 2017
Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 GeneSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Human Molecular Genetics|December 17, 2008
ABCA4 disease progression and a proposed strategy for gene therapyArtur V Cideciyan, Malgorzata Swider, Tomas S Aleman, et al.
Ophthalmology. Retina|April 25, 2019
Wide-Field Swept-Source OCT and Angiography in X-Linked RetinoschisisIan C Han, S Scott Whitmore, D Brice Critser, et al.
Ophthalmology Science|November 29, 2023
Using Goldmann Visual Field Volume to Track Disease Progression in ChoroideremiaAdam P DeLuca, S Scott Whitmore, Nicole J Tatro, et al.
Ophthalmology. Glaucoma|March 26, 2019
Histochemical Analysis of Glaucoma Caused by a Myocilin Mutation in a Human Donor EyeCarly J van der Heide, Wallace L M Alward, Miles Flamme-Wiese, et al.
Human Molecular Genetics|March 19, 2004
QRX, a novel homeobox gene, modulates photoreceptor gene expressionQing-liang Wang, Shiming Chen, Noriko Esumi, et al.
Human Gene Therapy|May 21, 2019
Development of a Molecularly Stable Gene Therapy Vector for the Treatment of <i>RPGR</i>-Associated X-Linked Retinitis PigmentosaJoseph C Giacalone, Jeaneen L Andorf, Qihong Zhang, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 13, 2003
Glaucoma phenotype in pedigrees with the myocilin Thr377Met mutationDavid A Mackey, Danielle L Healey, John H Fingert, et al.
Human Molecular Genetics|March 18, 2005
Mkks-null mice have a phenotype resembling Bardet-Biedl syndromeMelissa A Fath, Robert F Mullins, Charles Searby, et al.
Pageof 39