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Sarah Hull

Showing results (31-40 of 66) with videos related to

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Investigative Ophthalmology & Visual Science|March 14, 2015
Lack of Interphotoreceptor Retinoid Binding Protein Caused by Homozygous Mutation of RBP3 Is Associated With High Myopia and Retinal DystrophyGavin Arno, Sarah Hull, Anthony G Robson, et al.
The Journal of Biological Chemistry|July 5, 2002
The Krüppel-like factor KLF15 regulates the insulin-sensitive glucose transporter GLUT4Susan Gray, Mark W Feinberg, Sarah Hull, et al.
Journal of Paediatrics and Child Health|July 25, 2024
Optic neuropathy from hypovitaminosis A in a series of children with severe dietary restrictionsJane Shi, James Caldwell, Leo Sheck, et al.
JAMA Ophthalmology|August 1, 2014
Clinical and molecular characterization of enhanced S-cone syndrome in childrenSarah Hull, Gavin Arno, Panagiotis I Sergouniotis, et al.
American Journal of Ophthalmology|November 10, 2019
GUCY2D-Associated Leber Congenital Amaurosis: A Retrospective Natural History Study in Preparation for Trials of Novel TherapiesZaina Bouzia, Michalis Georgiou, Sarah Hull, et al.
Stem Cells Translational Medicine|January 16, 2019
Corneal Wound Healing Effects of Mesenchymal Stem Cell Secretome Delivered Within a Viscoelastic Gel CarrierGabriella Maria Fernandes-Cunha, Kyung-Sun Na, Ilham Putra, et al.
JAMA Ophthalmology|July 9, 2016
Characterization of CDH3-Related Congenital Hypotrichosis With Juvenile Macular DystrophySarah Hull, Gavin Arno, Anthony G Robson, et al.
Investigative Ophthalmology & Visual Science|October 2, 2014
The phenotypic variability of retinal dystrophies associated with mutations in CRX, with report of a novel macular dystrophy phenotypeSarah Hull, Gavin Arno, Vincent Plagnol, et al.
JAMA Ophthalmology|January 6, 2017
Clinical Characterization of CNGB1-Related Autosomal Recessive Retinitis PigmentosaSarah Hull, Marcella Attanasio, Gavin Arno, et al.
JAMA Ophthalmology|July 9, 2016
Expanding the Phenotype of TRNT1-Related Immunodeficiency to Include Childhood Cataract and Inner Retinal DysfunctionSarah Hull, Aeesha N J Malik, Gavin Arno, et al.
Pageof 7

Showing results (31-40 of 66) with videos related to

Sort By:
Pageof 7
Investigative Ophthalmology & Visual Science|March 14, 2015
Lack of Interphotoreceptor Retinoid Binding Protein Caused by Homozygous Mutation of RBP3 Is Associated With High Myopia and Retinal DystrophyGavin Arno, Sarah Hull, Anthony G Robson, et al.
The Journal of Biological Chemistry|July 5, 2002
The Krüppel-like factor KLF15 regulates the insulin-sensitive glucose transporter GLUT4Susan Gray, Mark W Feinberg, Sarah Hull, et al.
Journal of Paediatrics and Child Health|July 25, 2024
Optic neuropathy from hypovitaminosis A in a series of children with severe dietary restrictionsJane Shi, James Caldwell, Leo Sheck, et al.
JAMA Ophthalmology|August 1, 2014
Clinical and molecular characterization of enhanced S-cone syndrome in childrenSarah Hull, Gavin Arno, Panagiotis I Sergouniotis, et al.
American Journal of Ophthalmology|November 10, 2019
GUCY2D-Associated Leber Congenital Amaurosis: A Retrospective Natural History Study in Preparation for Trials of Novel TherapiesZaina Bouzia, Michalis Georgiou, Sarah Hull, et al.
Stem Cells Translational Medicine|January 16, 2019
Corneal Wound Healing Effects of Mesenchymal Stem Cell Secretome Delivered Within a Viscoelastic Gel CarrierGabriella Maria Fernandes-Cunha, Kyung-Sun Na, Ilham Putra, et al.
JAMA Ophthalmology|July 9, 2016
Characterization of CDH3-Related Congenital Hypotrichosis With Juvenile Macular DystrophySarah Hull, Gavin Arno, Anthony G Robson, et al.
Investigative Ophthalmology & Visual Science|October 2, 2014
The phenotypic variability of retinal dystrophies associated with mutations in CRX, with report of a novel macular dystrophy phenotypeSarah Hull, Gavin Arno, Vincent Plagnol, et al.
JAMA Ophthalmology|January 6, 2017
Clinical Characterization of CNGB1-Related Autosomal Recessive Retinitis PigmentosaSarah Hull, Marcella Attanasio, Gavin Arno, et al.
JAMA Ophthalmology|July 9, 2016
Expanding the Phenotype of TRNT1-Related Immunodeficiency to Include Childhood Cataract and Inner Retinal DysfunctionSarah Hull, Aeesha N J Malik, Gavin Arno, et al.
Pageof 7