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Jennifer A Thompson

Showing results (81-90 of 141) with videos related to

Pageof 15
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Trials|August 18, 2015
Five questions to consider before conducting a stepped wedge trialJames R Hargreaves, Andrew J Copas, Emma Beard, et al.
Stem Cell Research|May 7, 2019
Generation of an induced pluripotent stem cell line from a patient with retinitis pigmentosa caused by RP1 mutationXiao Zhang, Sang Yoon Moon, Dan Zhang, et al.
Stem Cell Research|August 19, 2020
Generation of two induced pluripotent stem cell lines from a patient with Stargardt Macular Dystrophy caused by the c.768G>T and c.6079C>T mutations in ABCA4Luke Jennings, Dan Zhang, Shang-Chih Chen, et al.
Investigative Ophthalmology & Visual Science|September 8, 2018
Development of High-Throughput Clinical Testing of RPGR ORF15 Using a Large Inherited Retinal Dystrophy CohortJohn P W Chiang, Tina M Lamey, Nicholas K Wang, et al.
Ophthalmology. Retina|July 6, 2022
Longitudinal Analysis of Functional and Structural Outcome Measures in PRPH2-Associated Retinal DystrophyRachael C Heath Jeffery, Jennifer A Thompson, Tina M Lamey, et al.
Stem Cell Research|May 25, 2021
Generation of two induced pluripotent stem cell lines from a retinitis pigmentosa patient with compound heterozygous mutations in CRB1Sang Yoon Moon, Dan Zhang, Shang-Chih Chen, et al.
Stem Cell Research|January 12, 2019
Generation of the induced pluripotent stem cell line from a patient with autosomal recessive ABCA4-mediated Stargardt Macular DystrophyJohann N Claassen, Dan Zhang, Shang-Chih Chen, et al.
Frontiers in Toxicology|October 31, 2022
Prenatal exposure to a low dose of BPS causes sex-dependent alterations to vascular endothelial function in adult offspringLiam T Connors, Hai-Lei Zhu, Manvir Gill, et al.
Molecular Genetics & Genomic Medicine|November 28, 2017
The genetic profile of Leber congenital amaurosis in an Australian cohortJennifer A Thompson, John N De Roach, Terri L McLaren, et al.
Molecular Genetics & Genomic Medicine|September 15, 2020
Characterization of CRB1 splicing in retinal organoids derived from a patient with adult-onset rod-cone dystrophy caused by the c.1892A>G and c.2548G>A variantsXiao Zhang, Jennifer A Thompson, Dan Zhang, et al.
Pageof 15

Showing results (81-90 of 141) with videos related to

Sort By:
Pageof 15
Trials|August 18, 2015
Five questions to consider before conducting a stepped wedge trialJames R Hargreaves, Andrew J Copas, Emma Beard, et al.
Stem Cell Research|May 7, 2019
Generation of an induced pluripotent stem cell line from a patient with retinitis pigmentosa caused by RP1 mutationXiao Zhang, Sang Yoon Moon, Dan Zhang, et al.
Stem Cell Research|August 19, 2020
Generation of two induced pluripotent stem cell lines from a patient with Stargardt Macular Dystrophy caused by the c.768G>T and c.6079C>T mutations in ABCA4Luke Jennings, Dan Zhang, Shang-Chih Chen, et al.
Investigative Ophthalmology & Visual Science|September 8, 2018
Development of High-Throughput Clinical Testing of RPGR ORF15 Using a Large Inherited Retinal Dystrophy CohortJohn P W Chiang, Tina M Lamey, Nicholas K Wang, et al.
Ophthalmology. Retina|July 6, 2022
Longitudinal Analysis of Functional and Structural Outcome Measures in PRPH2-Associated Retinal DystrophyRachael C Heath Jeffery, Jennifer A Thompson, Tina M Lamey, et al.
Stem Cell Research|May 25, 2021
Generation of two induced pluripotent stem cell lines from a retinitis pigmentosa patient with compound heterozygous mutations in CRB1Sang Yoon Moon, Dan Zhang, Shang-Chih Chen, et al.
Stem Cell Research|January 12, 2019
Generation of the induced pluripotent stem cell line from a patient with autosomal recessive ABCA4-mediated Stargardt Macular DystrophyJohann N Claassen, Dan Zhang, Shang-Chih Chen, et al.
Frontiers in Toxicology|October 31, 2022
Prenatal exposure to a low dose of BPS causes sex-dependent alterations to vascular endothelial function in adult offspringLiam T Connors, Hai-Lei Zhu, Manvir Gill, et al.
Molecular Genetics & Genomic Medicine|November 28, 2017
The genetic profile of Leber congenital amaurosis in an Australian cohortJennifer A Thompson, John N De Roach, Terri L McLaren, et al.
Molecular Genetics & Genomic Medicine|September 15, 2020
Characterization of CRB1 splicing in retinal organoids derived from a patient with adult-onset rod-cone dystrophy caused by the c.1892A>G and c.2548G>A variantsXiao Zhang, Jennifer A Thompson, Dan Zhang, et al.
Pageof 15