Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M Lamey

Showing results (31-40 of 73) with videos related to

Pageof 8
Sort By:
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.
Genes|December 24, 2021
Genotype-Specific Lesion Growth Rates in Stargardt DiseaseRachael C Heath Jeffery, Jennifer A Thompson, Johnny Lo, 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.
Medical Physics|May 19, 2017
Poster - Thur Eve - 05: Safety systems and failure modes and effects analysis for a magnetic resonance image guided radiation therapy systemM Lamey, M Carlone, H Alasti, et al.
Stem Cell Research|December 6, 2024
Derivation of two induced pluripotent stem cell lines from a healthy control subjectDan Zhang, Di Huang, Leon M Larcher, et al.
Genes|July 2, 2021
Clinical Evidence for the Importance of the Wild-Type <i>PRPF31</i> Allele in the Phenotypic Expression of RP11Danial Roshandel, Jennifer A Thompson, Rachael C Heath Jeffery, et al.
Retina (Philadelphia, Pa.)|June 14, 2021
CLASSIFYING ABCA4 MUTATION SEVERITY USING AGE-DEPENDENT ULTRA-WIDEFIELD FUNDUS AUTOFLUORESCENCE-DERIVED TOTAL LESION SIZERachael C Heath Jeffery, Jennifer A Thompson, Tina M Lamey, et al.
Molecular Genetics & Genomic Medicine|January 26, 2021
Gene correction of the CLN3 c.175G>A variant in patient-derived induced pluripotent stem cells prevents pathological changes in retinal organoidsXiao Zhang, Dan Zhang, Jennifer A Thompson, et al.
Investigative Ophthalmology & Visual Science|January 6, 2023
Microperimetry and Adaptive Optics Imaging Reveal Localized Functional and Structural Changes in Asymptomatic RPGR Mutation CarriersDanial Roshandel, Tina M Lamey, Jason Charng, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|January 29, 2021
A novel phenotype in a family with autosomal dominant retinal dystrophy due to c.1430A > G in retinoid isomerohydrolase (RPE65) and c.37C > T in bestrophin 1 (BEST1)Juanita Pappalardo, Rachael C Heath Jeffery, Jennifer A Thompson, et al.
Pageof 8

Showing results (31-40 of 73) with videos related to

Sort By:
Pageof 8
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.
Genes|December 24, 2021
Genotype-Specific Lesion Growth Rates in Stargardt DiseaseRachael C Heath Jeffery, Jennifer A Thompson, Johnny Lo, 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.
Medical Physics|May 19, 2017
Poster - Thur Eve - 05: Safety systems and failure modes and effects analysis for a magnetic resonance image guided radiation therapy systemM Lamey, M Carlone, H Alasti, et al.
Stem Cell Research|December 6, 2024
Derivation of two induced pluripotent stem cell lines from a healthy control subjectDan Zhang, Di Huang, Leon M Larcher, et al.
Genes|July 2, 2021
Clinical Evidence for the Importance of the Wild-Type <i>PRPF31</i> Allele in the Phenotypic Expression of RP11Danial Roshandel, Jennifer A Thompson, Rachael C Heath Jeffery, et al.
Retina (Philadelphia, Pa.)|June 14, 2021
CLASSIFYING ABCA4 MUTATION SEVERITY USING AGE-DEPENDENT ULTRA-WIDEFIELD FUNDUS AUTOFLUORESCENCE-DERIVED TOTAL LESION SIZERachael C Heath Jeffery, Jennifer A Thompson, Tina M Lamey, et al.
Molecular Genetics & Genomic Medicine|January 26, 2021
Gene correction of the CLN3 c.175G>A variant in patient-derived induced pluripotent stem cells prevents pathological changes in retinal organoidsXiao Zhang, Dan Zhang, Jennifer A Thompson, et al.
Investigative Ophthalmology & Visual Science|January 6, 2023
Microperimetry and Adaptive Optics Imaging Reveal Localized Functional and Structural Changes in Asymptomatic RPGR Mutation CarriersDanial Roshandel, Tina M Lamey, Jason Charng, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|January 29, 2021
A novel phenotype in a family with autosomal dominant retinal dystrophy due to c.1430A > G in retinoid isomerohydrolase (RPE65) and c.37C > T in bestrophin 1 (BEST1)Juanita Pappalardo, Rachael C Heath Jeffery, Jennifer A Thompson, et al.
Pageof 8