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Corinne Kostic

Showing results (31-40 of 37) with videos related to

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Human Molecular Genetics|January 17, 2009
In conditions of limited chromophore supply rods entrap 11-cis-retinal leading to loss of cone function and cell deathMarijana Samardzija, Naoyuki Tanimoto, Corinne Kostic, et al.
EMBO Molecular Medicine|March 20, 2024
Fine-tuning FAM161A gene augmentation therapy to restore retinal functionYvan Arsenijevic, Ning Chang, Olivier Mercey, et al.
International Journal of Molecular Sciences|September 10, 2021
Enhancer of Zeste Homolog 2 (EZH2) Contributes to Rod Photoreceptor Death Process in Several Forms of Retinal Degeneration and Its Activity Can Serve as a Biomarker for Therapy EfficacyMartial Mbefo, Adeline Berger, Karine Schouwey, et al.
Plos One|August 27, 2013
Rapid cohort generation and analysis of disease spectrum of large animal model of cone dystrophyCorinne Kostic, Simon Geoffrey Lillico, Sylvain Vincent Crippa, et al.
The Journal of Gene Medicine|October 20, 2012
Reduction of choroidal neovascularization in mice by adeno-associated virus-delivered anti-vascular endothelial growth factor short hairpin RNAAnne Louise Askou, Jean-Antoine C Pournaras, Maria Pihlmann, et al.
Molecular Brain|June 9, 2016
Amyloid Precursor-Like Protein 2 deletion-induced retinal synaptopathy related to congenital stationary night blindness: structural, functional and molecular characteristicsVirginie Dinet, Giuseppe D Ciccotosto, Kimberley Delaunay, et al.
American Journal of Human Genetics|September 18, 2024
Congenital microcoria deletion in mouse links Sox21 dysregulation to disease and suggests a role for TGFB2 in glaucoma and myopiaElisa Erjavec, Clémentine Angée, Djihad Hadjadj, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Human Molecular Genetics|January 17, 2009
In conditions of limited chromophore supply rods entrap 11-cis-retinal leading to loss of cone function and cell deathMarijana Samardzija, Naoyuki Tanimoto, Corinne Kostic, et al.
EMBO Molecular Medicine|March 20, 2024
Fine-tuning FAM161A gene augmentation therapy to restore retinal functionYvan Arsenijevic, Ning Chang, Olivier Mercey, et al.
International Journal of Molecular Sciences|September 10, 2021
Enhancer of Zeste Homolog 2 (EZH2) Contributes to Rod Photoreceptor Death Process in Several Forms of Retinal Degeneration and Its Activity Can Serve as a Biomarker for Therapy EfficacyMartial Mbefo, Adeline Berger, Karine Schouwey, et al.
Plos One|August 27, 2013
Rapid cohort generation and analysis of disease spectrum of large animal model of cone dystrophyCorinne Kostic, Simon Geoffrey Lillico, Sylvain Vincent Crippa, et al.
The Journal of Gene Medicine|October 20, 2012
Reduction of choroidal neovascularization in mice by adeno-associated virus-delivered anti-vascular endothelial growth factor short hairpin RNAAnne Louise Askou, Jean-Antoine C Pournaras, Maria Pihlmann, et al.
Molecular Brain|June 9, 2016
Amyloid Precursor-Like Protein 2 deletion-induced retinal synaptopathy related to congenital stationary night blindness: structural, functional and molecular characteristicsVirginie Dinet, Giuseppe D Ciccotosto, Kimberley Delaunay, et al.
American Journal of Human Genetics|September 18, 2024
Congenital microcoria deletion in mouse links Sox21 dysregulation to disease and suggests a role for TGFB2 in glaucoma and myopiaElisa Erjavec, Clémentine Angée, Djihad Hadjadj, et al.
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