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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 death
Marijana Samardzija, Naoyuki Tanimoto, Corinne Kostic, et al.
EMBO Molecular Medicine
|
March 20, 2024
Fine-tuning FAM161A gene augmentation therapy to restore retinal function
Yvan 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 Efficacy
Martial 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 dystrophy
Corinne 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 RNA
Anne 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 characteristics
Virginie 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 myopia
Elisa Erjavec, Clémentine Angée, Djihad Hadjadj, et al.
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Search research articles
Search
Showing results (31-40 of 37) with videos related to
Sort By:
Page
of 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 death
Marijana Samardzija, Naoyuki Tanimoto, Corinne Kostic, et al.
EMBO Molecular Medicine
|
March 20, 2024
Fine-tuning FAM161A gene augmentation therapy to restore retinal function
Yvan 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 Efficacy
Martial 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 dystrophy
Corinne 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 RNA
Anne 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 characteristics
Virginie 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 myopia
Elisa Erjavec, Clémentine Angée, Djihad Hadjadj, et al.
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of 4