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Eric A Pierce

Showing results (41-50 of 131) with videos related to

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Advances in Experimental Medicine and Biology|December 30, 2019
In Vivo Assessment of Potential Therapeutic Approaches for USH2A-Associated DiseasesNachiket D Pendse, Veronica Lamas, Basil S Pawlyk, et al.
Molecular Vision|October 26, 2007
Characterization of retinal inosine monophosphate dehydrogenase 1 in several mammalian speciesCatherine J Spellicy, Stephen P Daiger, Lori S Sullivan, et al.
Molecular & Cellular Proteomics : MCP|May 15, 2007
The proteome of the mouse photoreceptor sensory cilium complexQin Liu, Glenn Tan, Natasha Levenkova, et al.
Advances in Experimental Medicine and Biology|December 30, 2019
Detection of Large Structural Variants Causing Inherited Retinal DiseasesStephen P Daiger, Lori S Sullivan, Sara J Bowne, et al.
Human Molecular Genetics|August 2, 2007
The R345W mutation in EFEMP1 is pathogenic and causes AMD-like deposits in miceLi Fu, Donita Garland, Zhenglin Yang, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 2, 2010
Retinal degeneration and failure of photoreceptor outer segment formation in mice with targeted deletion of the Joubert syndrome gene, Ahi1Jennifer E Westfall, Carlton Hoyt, Qin Liu, et al.
Human Molecular Genetics|March 12, 2021
Mutant Nmnat1 leads to a retina-specific decrease of NAD+ accompanied by increased poly(ADP-ribose) in a mouse model of NMNAT1-associated retinal degenerationScott H Greenwald, Emily E Brown, Michael J Scandura, et al.
Plos One|February 2, 2011
Temporal and tissue specific regulation of RP-associated splicing factor genes PRPF3, PRPF31 and PRPC8--implications in the pathogenesis of RPHuibi Cao, Jing Wu, Simon Lam, et al.
Advances in Experimental Medicine and Biology|March 19, 2010
Targeted high-throughput DNA sequencing for gene discovery in retinitis pigmentosaStephen P Daiger, Lori S Sullivan, Sara J Bowne, et al.
Genes|October 6, 2017
The Genetic Basis of Pericentral Retinitis Pigmentosa-A Form of Mild Retinitis PigmentosaJason Comander, Carol Weigel-DiFranco, Matthew Maher, et al.
Pageof 14

Showing results (41-50 of 131) with videos related to

Sort By:
Pageof 14
Advances in Experimental Medicine and Biology|December 30, 2019
In Vivo Assessment of Potential Therapeutic Approaches for USH2A-Associated DiseasesNachiket D Pendse, Veronica Lamas, Basil S Pawlyk, et al.
Molecular Vision|October 26, 2007
Characterization of retinal inosine monophosphate dehydrogenase 1 in several mammalian speciesCatherine J Spellicy, Stephen P Daiger, Lori S Sullivan, et al.
Molecular & Cellular Proteomics : MCP|May 15, 2007
The proteome of the mouse photoreceptor sensory cilium complexQin Liu, Glenn Tan, Natasha Levenkova, et al.
Advances in Experimental Medicine and Biology|December 30, 2019
Detection of Large Structural Variants Causing Inherited Retinal DiseasesStephen P Daiger, Lori S Sullivan, Sara J Bowne, et al.
Human Molecular Genetics|August 2, 2007
The R345W mutation in EFEMP1 is pathogenic and causes AMD-like deposits in miceLi Fu, Donita Garland, Zhenglin Yang, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 2, 2010
Retinal degeneration and failure of photoreceptor outer segment formation in mice with targeted deletion of the Joubert syndrome gene, Ahi1Jennifer E Westfall, Carlton Hoyt, Qin Liu, et al.
Human Molecular Genetics|March 12, 2021
Mutant Nmnat1 leads to a retina-specific decrease of NAD+ accompanied by increased poly(ADP-ribose) in a mouse model of NMNAT1-associated retinal degenerationScott H Greenwald, Emily E Brown, Michael J Scandura, et al.
Plos One|February 2, 2011
Temporal and tissue specific regulation of RP-associated splicing factor genes PRPF3, PRPF31 and PRPC8--implications in the pathogenesis of RPHuibi Cao, Jing Wu, Simon Lam, et al.
Advances in Experimental Medicine and Biology|March 19, 2010
Targeted high-throughput DNA sequencing for gene discovery in retinitis pigmentosaStephen P Daiger, Lori S Sullivan, Sara J Bowne, et al.
Genes|October 6, 2017
The Genetic Basis of Pericentral Retinitis Pigmentosa-A Form of Mild Retinitis PigmentosaJason Comander, Carol Weigel-DiFranco, Matthew Maher, et al.
Pageof 14