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Christina Zeitz

Showing results (21-30 of 155) with videos related to

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Human Mutation|April 4, 2007
Night blindness-associated mutations in the ligand-binding, cysteine-rich, and intracellular domains of the metabotropic glutamate receptor 6 abolish protein traffickingChristina Zeitz, Ursula Forster, John Neidhardt, et al.
Investigative Ophthalmology & Visual Science|September 9, 2024
Loss of ON-Pathway Function in Mice Lacking Lrit3 Decreases Recovery From Lens-Induced MyopiaBaptiste Wilmet, Christelle Michiels, Jingyi Zhang, et al.
American Journal of Human Genetics|February 29, 2008
Mutation of solute carrier SLC16A12 associates with a syndrome combining juvenile cataract with microcornea and renal glucosuriaBarbara Kloeckener-Gruissem, Kristof Vandekerckhove, Gudrun Nürnberg, et al.
Ophthalmic Genetics|May 10, 2021
Management of a case of Enhanced S-cone syndrome with massive foveoschisis treated with pars plana vitrectomy with silicone oil tamponadeLorane Bechet, Raphaël Atia, Christina Zeitz, et al.
Molecular Vision|April 10, 2014
Molecular profiling of complete congenital stationary night blindness: a pilot study on an Indian cohortSivasankar Malaichamy, Parveen Sen, Ramya Sachidanandam, et al.
Investigative Ophthalmology & Visual Science|December 12, 2025
Retinal Impairments in Mice Lacking Both Nxnl1 and Nxnl2 GenesZheng Li, Imen Harichane, Thérèse Cronin, et al.
Investigative Ophthalmology & Visual Science|April 26, 2003
Isolation of the mouse nyctalopin gene nyx and expression studies in mouse and rat retinaKatrin Pesch, Christina Zeitz, Julia E Fries, et al.
The British Journal of Ophthalmology|December 22, 2018
Macular sensitivity in patients with congenital stationary night-blindnessAntony William, Susanne Kohl, Christina Zeitz, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 15, 2019
Disinhibition of intrinsic photosensitive retinal ganglion cells in patients with X-linked congenital stationary night blindnessAndreas Schatz, Carina Kelbsch, Christina Zeitz, et al.
Stem Cell Research|July 20, 2023
Generation of gene corrected human isogenic iPSC lines (IDVi003-A_CR13, IDVi003-A_CR21, IDVi003-A_CR24) from an inherited retinal dystrophy patient-derived IPSC line ITM2B-5286-3 (IDVi003-A) carrying the ITM2B c.782A > C variant using CRISPR/Cas9Tasnim Ben Yacoub, Camille Letellier, Juliette Wohlschlegel, et al.
Pageof 16

Showing results (21-30 of 155) with videos related to

Sort By:
Pageof 16
Human Mutation|April 4, 2007
Night blindness-associated mutations in the ligand-binding, cysteine-rich, and intracellular domains of the metabotropic glutamate receptor 6 abolish protein traffickingChristina Zeitz, Ursula Forster, John Neidhardt, et al.
Investigative Ophthalmology & Visual Science|September 9, 2024
Loss of ON-Pathway Function in Mice Lacking Lrit3 Decreases Recovery From Lens-Induced MyopiaBaptiste Wilmet, Christelle Michiels, Jingyi Zhang, et al.
American Journal of Human Genetics|February 29, 2008
Mutation of solute carrier SLC16A12 associates with a syndrome combining juvenile cataract with microcornea and renal glucosuriaBarbara Kloeckener-Gruissem, Kristof Vandekerckhove, Gudrun Nürnberg, et al.
Ophthalmic Genetics|May 10, 2021
Management of a case of Enhanced S-cone syndrome with massive foveoschisis treated with pars plana vitrectomy with silicone oil tamponadeLorane Bechet, Raphaël Atia, Christina Zeitz, et al.
Molecular Vision|April 10, 2014
Molecular profiling of complete congenital stationary night blindness: a pilot study on an Indian cohortSivasankar Malaichamy, Parveen Sen, Ramya Sachidanandam, et al.
Investigative Ophthalmology & Visual Science|December 12, 2025
Retinal Impairments in Mice Lacking Both Nxnl1 and Nxnl2 GenesZheng Li, Imen Harichane, Thérèse Cronin, et al.
Investigative Ophthalmology & Visual Science|April 26, 2003
Isolation of the mouse nyctalopin gene nyx and expression studies in mouse and rat retinaKatrin Pesch, Christina Zeitz, Julia E Fries, et al.
The British Journal of Ophthalmology|December 22, 2018
Macular sensitivity in patients with congenital stationary night-blindnessAntony William, Susanne Kohl, Christina Zeitz, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 15, 2019
Disinhibition of intrinsic photosensitive retinal ganglion cells in patients with X-linked congenital stationary night blindnessAndreas Schatz, Carina Kelbsch, Christina Zeitz, et al.
Stem Cell Research|July 20, 2023
Generation of gene corrected human isogenic iPSC lines (IDVi003-A_CR13, IDVi003-A_CR21, IDVi003-A_CR24) from an inherited retinal dystrophy patient-derived IPSC line ITM2B-5286-3 (IDVi003-A) carrying the ITM2B c.782A > C variant using CRISPR/Cas9Tasnim Ben Yacoub, Camille Letellier, Juliette Wohlschlegel, et al.
Pageof 16