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Trials
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August 18, 2015
Five questions to consider before conducting a stepped wedge trial
James 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 mutation
Xiao 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 ABCA4
Luke 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 Cohort
John 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 Dystrophy
Rachael 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 CRB1
Sang 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 Dystrophy
Johann 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 offspring
Liam 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 cohort
Jennifer 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 variants
Xiao Zhang, Jennifer A Thompson, Dan Zhang, et al.
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of 15
Search research articles
Search
Showing results (81-90 of 141) with videos related to
Sort By:
Page
of 15
Trials
|
August 18, 2015
Five questions to consider before conducting a stepped wedge trial
James 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 mutation
Xiao 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 ABCA4
Luke 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 Cohort
John 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 Dystrophy
Rachael 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 CRB1
Sang 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 Dystrophy
Johann 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 offspring
Liam 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 cohort
Jennifer 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 variants
Xiao Zhang, Jennifer A Thompson, Dan Zhang, et al.
Page
of 15