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Eric A Pierce

Showing results (51-60 of 132) with videos related to

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The American Journal of Pathology|August 12, 2014
Mutations in pre-mRNA processing factors 3, 8, and 31 cause dysfunction of the retinal pigment epitheliumMichael H Farkas, Deborah S Lew, Maria E Sousa, et al.
Plos One|August 29, 2012
Expression of wild-type Rp1 protein in Rp1 knock-in mice rescues the retinal degeneration phenotypeQin Liu, Rob W J Collin, Frans P M Cremers, et al.
Investigative Ophthalmology & Visual Science|August 29, 2006
Why do mutations in the ubiquitously expressed housekeeping gene IMPDH1 cause retina-specific photoreceptor degeneration?Sara J Bowne, Qin Liu, Lori S Sullivan, et al.
Human Molecular Genetics|August 15, 2013
Mouse genetics and proteomic analyses demonstrate a critical role for complement in a model of DHRD/ML, an inherited macular degenerationDonita L Garland, Rosario Fernandez-Godino, Inderjeet Kaur, et al.
Discovery Medicine|February 29, 2012
Mitochondrial tRNA-serine (AGY) m.C12264T mutation causes severe multisystem disease with cataractsSamantha A Schrier, Lee-Jun Wong, Emily Place, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 30, 2025
Systematic empirical evaluation of individual base editing targets: Validating therapeutic targets in USH2A and comparison of methodsYuki Tachida, Kannan V Manian, Rossano Butcher, et al.
Molecular Therapy. Methods & Clinical Development|August 11, 2020
Gene Therapy Preserves Retinal Structure and Function in a Mouse Model of <i>NMNAT1</i>-Associated Retinal DegenerationScott H Greenwald, Emily E Brown, Michael J Scandura, et al.
Ophthalmology Science|June 17, 2024
Twelve-month Natural History Study of Centrosomal Protein 290 (CEP290)-associated Inherited Retinal DegenerationEric A Pierce, Bright S Ashimatey, Thiran Jayasundera, et al.
Molecular Vision|October 25, 2017
The importance of genetic testing as demonstrated by two cases of <i>CACNA1F</i>-associated retinal generation misdiagnosed as LCAClara J Men, Kinga M Bujakowska, Jason Comander, et al.
Investigative Ophthalmology & Visual Science|September 3, 2010
Three gene-targeted mouse models of RNA splicing factor RP show late-onset RPE and retinal degenerationJohn J Graziotto, Michael H Farkas, Kinga Bujakowska, et al.
Pageof 14

Showing results (51-60 of 132) with videos related to

Sort By:
Pageof 14
The American Journal of Pathology|August 12, 2014
Mutations in pre-mRNA processing factors 3, 8, and 31 cause dysfunction of the retinal pigment epitheliumMichael H Farkas, Deborah S Lew, Maria E Sousa, et al.
Plos One|August 29, 2012
Expression of wild-type Rp1 protein in Rp1 knock-in mice rescues the retinal degeneration phenotypeQin Liu, Rob W J Collin, Frans P M Cremers, et al.
Investigative Ophthalmology & Visual Science|August 29, 2006
Why do mutations in the ubiquitously expressed housekeeping gene IMPDH1 cause retina-specific photoreceptor degeneration?Sara J Bowne, Qin Liu, Lori S Sullivan, et al.
Human Molecular Genetics|August 15, 2013
Mouse genetics and proteomic analyses demonstrate a critical role for complement in a model of DHRD/ML, an inherited macular degenerationDonita L Garland, Rosario Fernandez-Godino, Inderjeet Kaur, et al.
Discovery Medicine|February 29, 2012
Mitochondrial tRNA-serine (AGY) m.C12264T mutation causes severe multisystem disease with cataractsSamantha A Schrier, Lee-Jun Wong, Emily Place, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 30, 2025
Systematic empirical evaluation of individual base editing targets: Validating therapeutic targets in USH2A and comparison of methodsYuki Tachida, Kannan V Manian, Rossano Butcher, et al.
Molecular Therapy. Methods & Clinical Development|August 11, 2020
Gene Therapy Preserves Retinal Structure and Function in a Mouse Model of <i>NMNAT1</i>-Associated Retinal DegenerationScott H Greenwald, Emily E Brown, Michael J Scandura, et al.
Ophthalmology Science|June 17, 2024
Twelve-month Natural History Study of Centrosomal Protein 290 (CEP290)-associated Inherited Retinal DegenerationEric A Pierce, Bright S Ashimatey, Thiran Jayasundera, et al.
Molecular Vision|October 25, 2017
The importance of genetic testing as demonstrated by two cases of <i>CACNA1F</i>-associated retinal generation misdiagnosed as LCAClara J Men, Kinga M Bujakowska, Jason Comander, et al.
Investigative Ophthalmology & Visual Science|September 3, 2010
Three gene-targeted mouse models of RNA splicing factor RP show late-onset RPE and retinal degenerationJohn J Graziotto, Michael H Farkas, Kinga Bujakowska, et al.
Pageof 14