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Jennifer A Thompson

Showing results (121-130 of 141) with videos related to

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Ophthalmology. Retina|June 27, 2024
Retinal Characteristics of Female Choroideremia Carriers: Multimodal Imaging, Microperimetry, and GeneticsSena A Gocuk, Thomas L Edwards, Jasleen K Jolly, et al.
Stem Cell Research|July 16, 2024
Generation of two induced pluripotent stem cell lines from an Usher syndrome type 1B patient with the homozygous c.496del MYO7A variantElaine Y M Wong, Xin E Khoh, Shang-Chih Chen, et al.
Stem Cell Research|July 2, 2021
Generation of an induced pluripotent stem cell line from a patient with Stargardt disease caused by biallelic c.[5461-10T>C;5603A>T];[6077T>C] mutations in the ABCA4 geneDi Huang, Dan Zhang, Shang-Chih Chen, et al.
Stem Cell Research|July 1, 2021
Generation of two induced pluripotent stem cell lines from a patient with Stargardt disease caused by compound heterozygous mutations in the ABCA4 geneDi Huang, Dan Zhang, Shang-Chih Chen, et al.
Antioxidants & Redox Signaling|May 8, 2023
Potentiation of Adipogenesis by Reactive Oxygen Species Is a Unifying Mechanism in the Proadipogenic Properties of Bisphenol A and Its New Structural AnaloguesRadha D Singh, Jessica L Wager, Taylor B Scheidl, et al.
Stem Cell Research|March 25, 2019
Generation of two induced pluripotent stem cell lines from a patient with compound heterozygous mutations in the USH2A geneSamuel McLenachan, Elaine Y M Wong, Xiao Zhang, et al.
Ophthalmic Genetics|September 28, 2020
Exploring microperimetry and autofluorescence endpoints for monitoring disease progression in <i>PRPF31</i>-associated retinopathyDanial Roshandel, Jennifer A Thompson, Jason Charng, et al.
Stem Cell Research|December 28, 2020
Generation of three induced pluripotent stem cell lines from a patient with Usher syndrome caused by biallelic c.949C > A and c.1256G > T mutations in the USH2A geneKhine Zaw, Elaine Y M Wong, Xiao Zhang, et al.
Ophthalmic Genetics|February 24, 2021
Deep clinical phenotyping and gene expression analysis in a patient with <i>RCBTB1</i>-associated retinopathyZhiqin Huang, Dan Zhang, Jennifer A Thompson, et al.
Molecular Genetics & Genomic Medicine|July 7, 2020
Phenotype-genotype correlations in a pseudodominant Stargardt disease pedigree due to a novel ABCA4 deletion-insertion variant causing a splicing defectDi Huang, Jennifer A Thompson, Jason Charng, et al.
Pageof 15

Showing results (121-130 of 141) with videos related to

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Pageof 15
Ophthalmology. Retina|June 27, 2024
Retinal Characteristics of Female Choroideremia Carriers: Multimodal Imaging, Microperimetry, and GeneticsSena A Gocuk, Thomas L Edwards, Jasleen K Jolly, et al.
Stem Cell Research|July 16, 2024
Generation of two induced pluripotent stem cell lines from an Usher syndrome type 1B patient with the homozygous c.496del MYO7A variantElaine Y M Wong, Xin E Khoh, Shang-Chih Chen, et al.
Stem Cell Research|July 2, 2021
Generation of an induced pluripotent stem cell line from a patient with Stargardt disease caused by biallelic c.[5461-10T>C;5603A>T];[6077T>C] mutations in the ABCA4 geneDi Huang, Dan Zhang, Shang-Chih Chen, et al.
Stem Cell Research|July 1, 2021
Generation of two induced pluripotent stem cell lines from a patient with Stargardt disease caused by compound heterozygous mutations in the ABCA4 geneDi Huang, Dan Zhang, Shang-Chih Chen, et al.
Antioxidants & Redox Signaling|May 8, 2023
Potentiation of Adipogenesis by Reactive Oxygen Species Is a Unifying Mechanism in the Proadipogenic Properties of Bisphenol A and Its New Structural AnaloguesRadha D Singh, Jessica L Wager, Taylor B Scheidl, et al.
Stem Cell Research|March 25, 2019
Generation of two induced pluripotent stem cell lines from a patient with compound heterozygous mutations in the USH2A geneSamuel McLenachan, Elaine Y M Wong, Xiao Zhang, et al.
Ophthalmic Genetics|September 28, 2020
Exploring microperimetry and autofluorescence endpoints for monitoring disease progression in <i>PRPF31</i>-associated retinopathyDanial Roshandel, Jennifer A Thompson, Jason Charng, et al.
Stem Cell Research|December 28, 2020
Generation of three induced pluripotent stem cell lines from a patient with Usher syndrome caused by biallelic c.949C > A and c.1256G > T mutations in the USH2A geneKhine Zaw, Elaine Y M Wong, Xiao Zhang, et al.
Ophthalmic Genetics|February 24, 2021
Deep clinical phenotyping and gene expression analysis in a patient with <i>RCBTB1</i>-associated retinopathyZhiqin Huang, Dan Zhang, Jennifer A Thompson, et al.
Molecular Genetics & Genomic Medicine|July 7, 2020
Phenotype-genotype correlations in a pseudodominant Stargardt disease pedigree due to a novel ABCA4 deletion-insertion variant causing a splicing defectDi Huang, Jennifer A Thompson, Jason Charng, et al.
Pageof 15