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Christina Zeitz

Showing results (41-50 of 155) with videos related to

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The European Journal of Neuroscience|September 29, 2006
Nyctalopin is essential for synaptic transmission in the cone dominated zebrafish retinaRonja Bahadori, Oliver Biehlmaier, Christina Zeitz, et al.
Ophthalmology|May 10, 2018
Phenotypic Characteristics of a French Cohort of Patients with X-Linked RetinoschisisRaphaëlle Orès, Saddek Mohand-Said, Claire-Marie Dhaenens, et al.
Scientific Reports|August 21, 2019
TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli PopulationsAlaa AlTalbishi, Lina Zelinger, Christina Zeitz, et al.
International Journal of Biological Macromolecules|August 28, 2024
Differential pathogenetic mechanisms of mutations in helix 2 and helix 6 of rhodopsinAndrea Bighinati, Sara D'Alessandro, Angelo Felline, et al.
American Journal of Human Genetics|October 13, 2006
Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophyKatharina Agnes Wycisk, Christina Zeitz, Silke Feil, et al.
Investigative Ophthalmology & Visual Science|December 3, 2019
Peripapillary Sparing With Near Infrared Autofluorescence Correlates With Electroretinographic Findings in Patients With Stargardt DiseaseMarco Nassisi, Saddek Mohand-Saïd, Camille Andrieu, et al.
International Journal of Molecular Sciences|April 30, 2021
A New Mouse Model for Complete Congenital Stationary Night Blindness Due to <i>Gpr179</i> DeficiencyElise Orhan, Marion Neuillé, Miguel de Sousa Dias, et al.
JAMA Ophthalmology|October 20, 2022
Association of Missense Variants in VSX2 With a Peculiar Form of Congenital Stationary Night Blindness Affecting All Bipolar CellsVasily M Smirnov, Matthieu P Robert, Christel Condroyer, et al.
Retina (Philadelphia, Pa.)|August 23, 2020
DEEP PHENOTYPING AND FURTHER INSIGHTS INTO ITM2B-RELATED RETINAL DYSTROPHYMarco Nassisi, Juliette Wohlschlegel, Bingqian Liu, et al.
Investigative Ophthalmology & Visual Science|April 2, 2025
Phenotypic and Genotypic Characterization of RP1L1-Associated RetinopathyAlessio Antropoli, Lorenzo Bianco, Xavier Zanlonghi, et al.
Pageof 16

Showing results (41-50 of 155) with videos related to

Sort By:
Pageof 16
The European Journal of Neuroscience|September 29, 2006
Nyctalopin is essential for synaptic transmission in the cone dominated zebrafish retinaRonja Bahadori, Oliver Biehlmaier, Christina Zeitz, et al.
Ophthalmology|May 10, 2018
Phenotypic Characteristics of a French Cohort of Patients with X-Linked RetinoschisisRaphaëlle Orès, Saddek Mohand-Said, Claire-Marie Dhaenens, et al.
Scientific Reports|August 21, 2019
TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli PopulationsAlaa AlTalbishi, Lina Zelinger, Christina Zeitz, et al.
International Journal of Biological Macromolecules|August 28, 2024
Differential pathogenetic mechanisms of mutations in helix 2 and helix 6 of rhodopsinAndrea Bighinati, Sara D'Alessandro, Angelo Felline, et al.
American Journal of Human Genetics|October 13, 2006
Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophyKatharina Agnes Wycisk, Christina Zeitz, Silke Feil, et al.
Investigative Ophthalmology & Visual Science|December 3, 2019
Peripapillary Sparing With Near Infrared Autofluorescence Correlates With Electroretinographic Findings in Patients With Stargardt DiseaseMarco Nassisi, Saddek Mohand-Saïd, Camille Andrieu, et al.
International Journal of Molecular Sciences|April 30, 2021
A New Mouse Model for Complete Congenital Stationary Night Blindness Due to <i>Gpr179</i> DeficiencyElise Orhan, Marion Neuillé, Miguel de Sousa Dias, et al.
JAMA Ophthalmology|October 20, 2022
Association of Missense Variants in VSX2 With a Peculiar Form of Congenital Stationary Night Blindness Affecting All Bipolar CellsVasily M Smirnov, Matthieu P Robert, Christel Condroyer, et al.
Retina (Philadelphia, Pa.)|August 23, 2020
DEEP PHENOTYPING AND FURTHER INSIGHTS INTO ITM2B-RELATED RETINAL DYSTROPHYMarco Nassisi, Juliette Wohlschlegel, Bingqian Liu, et al.
Investigative Ophthalmology & Visual Science|April 2, 2025
Phenotypic and Genotypic Characterization of RP1L1-Associated RetinopathyAlessio Antropoli, Lorenzo Bianco, Xavier Zanlonghi, et al.
Pageof 16