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Showing results (1091-1100 of 1,250) with videos related to

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Human Molecular Genetics|January 5, 2002
Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosaChristina F Chakarova, Matthew M Hims, Hanno Bolz, et al.
American Journal of Ophthalmology|September 11, 2012
Assessing retinal structure in complete congenital stationary night blindness and Oguchi diseasePooja Godara, Robert F Cooper, Panagiotis I Sergouniotis, et al.
Human Molecular Genetics|November 2, 2021
A large animal model of RDH5-associated retinopathy recapitulates important features of the human phenotypeLaurence M Occelli, Anahita Daruwalla, Samantha R De Silva, et al.
Investigative Ophthalmology & Visual Science|July 30, 2025
RHO-Associated Retinitis Pigmentosa: Genetics, Phenotype, Natural History, Functional Assays, and Animal Model - In Preparation for Clinical TrialsMalena Daich Varela, Juan Carlos Romo-Aguas, Rosellina Guarascio, et al.
Journal of the American College of Cardiology|January 20, 2010
National efforts to improve door-to-balloon time results from the Door-to-Balloon AllianceElizabeth H Bradley, Brahmajee K Nallamothu, Jeph Herrin, et al.
Investigative Ophthalmology & Visual Science|January 1, 2016
Disease Expression in Autosomal Recessive Retinal Dystrophy Associated With Mutations in the DRAM2 GenePanagiotis I Sergouniotis, Martin McKibbin, Anthony G Robson, et al.
Human Mutation|August 30, 2014
Three different cone opsin gene array mutational mechanisms with genotype-phenotype correlation and functional investigation of cone opsin variantsJessica C Gardner, Gerald Liew, Ying-Hua Quan, et al.
American Journal of Human Genetics|July 16, 2013
Mutations in ARL2BP, encoding ADP-ribosylation-factor-like 2 binding protein, cause autosomal-recessive retinitis pigmentosaAlice E Davidson, Nele Schwarz, Lina Zelinger, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 7, 2024
Highly enriched carbon and oxygen isotopes in carbonate-derived CO<sub>2</sub> at Gale crater, MarsDavid G Burtt, Jennifer C Stern, Christopher R Webster, et al.
Global Change Biology|January 1, 2017
Global synthesis of the temperature sensitivity of leaf litter breakdown in streams and riversJennifer J Follstad Shah, John S Kominoski, Marcelo Ardón, et al.
Pageof 125

Showing results (1091-1100 of 1,250) with videos related to

Sort By:
Pageof 125
Human Molecular Genetics|January 5, 2002
Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosaChristina F Chakarova, Matthew M Hims, Hanno Bolz, et al.
American Journal of Ophthalmology|September 11, 2012
Assessing retinal structure in complete congenital stationary night blindness and Oguchi diseasePooja Godara, Robert F Cooper, Panagiotis I Sergouniotis, et al.
Human Molecular Genetics|November 2, 2021
A large animal model of RDH5-associated retinopathy recapitulates important features of the human phenotypeLaurence M Occelli, Anahita Daruwalla, Samantha R De Silva, et al.
Investigative Ophthalmology & Visual Science|July 30, 2025
RHO-Associated Retinitis Pigmentosa: Genetics, Phenotype, Natural History, Functional Assays, and Animal Model - In Preparation for Clinical TrialsMalena Daich Varela, Juan Carlos Romo-Aguas, Rosellina Guarascio, et al.
Journal of the American College of Cardiology|January 20, 2010
National efforts to improve door-to-balloon time results from the Door-to-Balloon AllianceElizabeth H Bradley, Brahmajee K Nallamothu, Jeph Herrin, et al.
Investigative Ophthalmology & Visual Science|January 1, 2016
Disease Expression in Autosomal Recessive Retinal Dystrophy Associated With Mutations in the DRAM2 GenePanagiotis I Sergouniotis, Martin McKibbin, Anthony G Robson, et al.
Human Mutation|August 30, 2014
Three different cone opsin gene array mutational mechanisms with genotype-phenotype correlation and functional investigation of cone opsin variantsJessica C Gardner, Gerald Liew, Ying-Hua Quan, et al.
American Journal of Human Genetics|July 16, 2013
Mutations in ARL2BP, encoding ADP-ribosylation-factor-like 2 binding protein, cause autosomal-recessive retinitis pigmentosaAlice E Davidson, Nele Schwarz, Lina Zelinger, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 7, 2024
Highly enriched carbon and oxygen isotopes in carbonate-derived CO<sub>2</sub> at Gale crater, MarsDavid G Burtt, Jennifer C Stern, Christopher R Webster, et al.
Global Change Biology|January 1, 2017
Global synthesis of the temperature sensitivity of leaf litter breakdown in streams and riversJennifer J Follstad Shah, John S Kominoski, Marcelo Ardón, et al.
Pageof 125