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Hadas Newman

Showing results (11-20 of 37) with videos related to

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Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 4, 2020
Effect of light and diurnal variation on macular thickness in X-linked retinoschisis: a case seriesYair Rubinstein, Chen Weiner, Noa Chetrit, et al.
Retina (Philadelphia, Pa.)|January 8, 2014
The prevalence of retinal and optical coherence tomography findings in preeclamptic womenMeira Neudorfer, Oriel Spierer, Maya Goder, et al.
Protein Expression and Purification|February 8, 2017
Purification and characterization of human dehydrodolychil diphosphate synthase (DHDDS) overexpressed in E. coliMoshe Giladi, Ilan Edri, Michal Goldenberg, et al.
Investigative Ophthalmology & Visual Science|October 13, 2016
Homozygosity for a Recessive Loss-of-Function Mutation of the NRL Gene Is Associated With a Variant of Enhanced S-Cone SyndromeHadas Newman, Sergiu C Blumen, Itzhak Braverman, et al.
Journal of Visualized Experiments : Jove|August 16, 2017
Overexpression and Purification of Human Cis-prenyltransferase in Escherichia coliIlan Edri, Michal Goldenberg, Michal Lisnyansky, et al.
Current Eye Research|May 15, 2012
Involvement of CD24 in angiogenesis in a mouse model of oxygen-induced retinopathyHadas Newman, Shiran Shapira, Oriel Spierer, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|March 18, 2018
Prevalence of choroidal nevus and retinal pigment epithelial alterations in vitiligo patientsEfrat Fleissig, Mor Pavlovksy, Anat Loewenstein, et al.
Genetic Testing and Molecular Biomarkers|June 8, 2017
Oculopharyngeal Muscular Dystrophy and Inherited Retinal Dystrophy in Bukhara Jews Due to Linked Mutations in the PABPN1 and NRL GenesItzhak Braverman, Sergiu C Blumen, Hadas Newman, et al.
Biomolecules|October 31, 2019
Structural Characterization of Full-Length Human Dehydrodolichyl Diphosphate Synthase Using an Integrative Computational and Experimental ApproachMichal Lisnyansky Bar-El, Su Youn Lee, Ah Young Ki, et al.
European Journal of Human Genetics : EJHG|May 1, 2018
Carrier frequency analysis of mutations causing autosomal-recessive-inherited retinal diseases in the Israeli populationMor Hanany, Gilad Allon, Adva Kimchi, et al.
Pageof 4

Showing results (11-20 of 37) with videos related to

Sort By:
Pageof 4
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 4, 2020
Effect of light and diurnal variation on macular thickness in X-linked retinoschisis: a case seriesYair Rubinstein, Chen Weiner, Noa Chetrit, et al.
Retina (Philadelphia, Pa.)|January 8, 2014
The prevalence of retinal and optical coherence tomography findings in preeclamptic womenMeira Neudorfer, Oriel Spierer, Maya Goder, et al.
Protein Expression and Purification|February 8, 2017
Purification and characterization of human dehydrodolychil diphosphate synthase (DHDDS) overexpressed in E. coliMoshe Giladi, Ilan Edri, Michal Goldenberg, et al.
Investigative Ophthalmology & Visual Science|October 13, 2016
Homozygosity for a Recessive Loss-of-Function Mutation of the NRL Gene Is Associated With a Variant of Enhanced S-Cone SyndromeHadas Newman, Sergiu C Blumen, Itzhak Braverman, et al.
Journal of Visualized Experiments : Jove|August 16, 2017
Overexpression and Purification of Human Cis-prenyltransferase in Escherichia coliIlan Edri, Michal Goldenberg, Michal Lisnyansky, et al.
Current Eye Research|May 15, 2012
Involvement of CD24 in angiogenesis in a mouse model of oxygen-induced retinopathyHadas Newman, Shiran Shapira, Oriel Spierer, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|March 18, 2018
Prevalence of choroidal nevus and retinal pigment epithelial alterations in vitiligo patientsEfrat Fleissig, Mor Pavlovksy, Anat Loewenstein, et al.
Genetic Testing and Molecular Biomarkers|June 8, 2017
Oculopharyngeal Muscular Dystrophy and Inherited Retinal Dystrophy in Bukhara Jews Due to Linked Mutations in the PABPN1 and NRL GenesItzhak Braverman, Sergiu C Blumen, Hadas Newman, et al.
Biomolecules|October 31, 2019
Structural Characterization of Full-Length Human Dehydrodolichyl Diphosphate Synthase Using an Integrative Computational and Experimental ApproachMichal Lisnyansky Bar-El, Su Youn Lee, Ah Young Ki, et al.
European Journal of Human Genetics : EJHG|May 1, 2018
Carrier frequency analysis of mutations causing autosomal-recessive-inherited retinal diseases in the Israeli populationMor Hanany, Gilad Allon, Adva Kimchi, et al.
Pageof 4