Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Hanen Khabou"'
Autor:
Hanen Khabou, Elaine Orendorff, Francesco Trapani, Marco Rucli, Melissa Desrosiers, Pierre Yger, Deniz Dalkara, Olivier Marre
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 31, Iss , Pp 101107- (2023)
Most inherited retinal dystrophies display progressive photoreceptor cell degeneration leading to severe visual impairment. Optogenetic reactivation of inner retinal neurons is a promising avenue to restore vision in retinas having lost their photore
Externí odkaz:
https://doaj.org/article/b78a68eae9bd436db9cd81cc7fa020a7
Autor:
Marcela Garita-Hernandez, Antoine Chaffiol, Laure Guibbal, Fiona Routet, Hanen Khabou, Luisa Riancho, Lyes Toualbi, Serge Picaud, José-Alain Sahel, Olivier Goureau, Jens Duebel, Deniz Dalkara
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 15 (2021)
Human-induced pluripotent stem cell (hiPSC) derived organoids have become increasingly used systems allowing 3D-modeling of human organ development, and disease. They are also a reliable source of cells for transplantation in cell therapy and an exce
Externí odkaz:
https://doaj.org/article/d52cba0458fb442b986f0c8aa3494476
Autor:
Hanen Khabou, Elaine Orendorff, Francesco Trapani, Marco Rucli, Melissa Desrosiers, Pierre Yger, Deniz Dalkara, Olivier Marre
Most inherited retinal dystrophies display progressive photoreceptor cell degeneration leading to severe visual impairment. Optogenetic reactivation of inner retinal neurons is a promising avenue to restore vision in retinas having lost their photore
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc00ff4cbba86750cbb798a0f4505daf
https://doi.org/10.1101/2022.07.28.501925
https://doi.org/10.1101/2022.07.28.501925
Autor:
Giulia Lia Beatrice Spampinato, Emiliano Ronzitti, Valeria Zampini, Ulisse Ferrari, Francesco Trapani, Hanen Khabou, Anurag Agraval, Deniz Dalkara, Serge Picaud, Eirini Papagiakoumou, Olivier Marre, Valentina Emiliani
Publikováno v:
Cell reports methods. 2(8)
We developed a multi-unit microscope for all-optical inter-layers circuits interrogation. The system performs two-photon (2P) functional imaging and 2P multiplexed holographic optogenetics at axially distinct planes. We demonstrated the capability of
Autor:
Cardillia-Joe Simon, Hanen Khabou, Marion Finzi, Antoine Chaffiol, Kate Grieve, Nat Norberg, Anais Grimaud, Dennis Eickelbeck, Marco Rucli, Mélissa Desrosiers, Serge Sancho, Vera Bonilha, Saddek Mohand-Said, Jens Duebel, Michel paques, Serge Picaud, José-Alain Sahel, Isabelle Audo, Stefan Herlitze, Deniz Dalkara
Rod-cone dystrophy (RCD), also known as retinitis pigmentosa, is a group of inherited disorders characterized by rod degeneration followed by degeneration of peripheral cones, leaving patients with tunnel vision in mid stages and blindness in the lat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0d6a6e1032e8ed3c9e097448400d416
https://doi.org/10.21203/rs.3.rs-1189099/v1
https://doi.org/10.21203/rs.3.rs-1189099/v1
Autor:
Dora Fix Ventura, Deniz Dalkara, Anneka Joachimsthaler, Jan Kremers, Lucile Vignaud, Hanen Khabou, Ophélie Vacca, Alvaro Rendon, Mirella Telles Salgueiro Barboni, Cyrille Vaillend, Andre Liber, Michel Roux, Xavier Guillonneau
Publikováno v:
Investigative Ophthalmology & Visual Science
Investigative Ophthalmology & Visual Science, Association for Research in Vision and Ophthalmology, 2020, 61 (2), pp.11. ⟨10.1167/iovs.61.2.11⟩
Investigative Ophthalmology & Visual Science, 2020, 61 (2), pp.11. ⟨10.1167/iovs.61.2.11⟩
Investigative Ophthalmology & Visual Science, Association for Research in Vision and Ophthalmology, 2020, 61 (2), pp.11. ⟨10.1167/iovs.61.2.11⟩
Investigative Ophthalmology & Visual Science, 2020, 61 (2), pp.11. ⟨10.1167/iovs.61.2.11⟩
International audience; Purpose: To study the potential effect of a gene therapy, designed to rescue the expression of dystrophin Dp71 in the retinas of Dp71-null mice, on retinal physiology.Methods: We recorded electroretinograms (ERGs) in Dp71-null
AAV-Mediated Gene Delivery to 3D Retinal Organoids Derived from Human Induced Pluripotent Stem Cells
Autor:
Marcela Garita-Hernandez, Fiona Routet, Laure Guibbal, Hanen Khabou, Lyes Toualbi, Luisa Riancho, Sacha Reichman, Jens Duebel, Jose-Alain Sahel, Olivier Goureau, Deniz Dalkara
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, MDPI, 2020, 21 (3), pp.994. ⟨10.3390/ijms21030994⟩
Volume 21
Issue 3
International Journal of Molecular Sciences, Vol 21, Iss 3, p 994 (2020)
International Journal of Molecular Sciences, MDPI, 2020, 21 (3), pp.994. ⟨10.3390/ijms21030994⟩
Volume 21
Issue 3
International Journal of Molecular Sciences, Vol 21, Iss 3, p 994 (2020)
International audience; Human induced pluripotent stem cells (hiPSCs) promise a great number of future applications to investigate retinal development, pathophysiology and cell therapies for retinal degenerative diseases. Specific approaches to genet
All-optical interrogation of a direction selective retinal circuit by holographic wave front shaping
Autor:
Deniz Dalkara, Ulisse Ferrari, Emiliano Ronzitti, Emiliani, Serge Picaud, Eirini Papagiakoumou, Zampini, Trapani F, Hanen Khabou, Giulia Lb Spampinato, Olivier Marre
Direction selective (DS) ganglion cells (GC) in the retina maintain their tuning across a broad range of light levels. Yet very different circuits can shape their responses from bright to dim light, and their respective contributions are difficult to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9cf77be32d63e7f0e65cc33ead989911
https://doi.org/10.1101/513192
https://doi.org/10.1101/513192
Autor:
Deniz Dalkara, Alexis-Pierre Bemelmans, Hanen Khabou, José-Alain Sahel, Stéphane Fouquet, Céline Winckler, Gwenaëlle Auregan, Melissa Desrosiers
Publikováno v:
Biotechnology and Bioengineering. 113:2712-2724
Recently, we described a modified AAV2 vector—AAV2-7m8—having a capsid-displayed peptide insertion of 10 amino acids with enhanced retinal transduction properties. The insertion of the peptide referred to as 7m8 is responsible for high-level gene
Publikováno v:
Human Gene Therapy
Human Gene Therapy, Mary Ann Liebert, 2018, ⟨10.1089/hum.2018.144⟩
Human Gene Therapy, Mary Ann Liebert, 2018, 0, ⟨10.1089/hum.2018.144⟩
Human Gene Therapy, Mary Ann Liebert, 2018, ⟨10.1089/hum.2018.144⟩
Human Gene Therapy, Mary Ann Liebert, 2018, 0, ⟨10.1089/hum.2018.144⟩
International audience; Today, there are >500 published studies and 40 clinical trials to treat retinal disorders using gene therapy. The great majority of them rely on the use of adeno-associated virus vectors (AAV) for therapeutic gene delivery. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c63df2ea765c4bd1f25c805a75f3e84f
https://hal.sorbonne-universite.fr/hal-01927077
https://hal.sorbonne-universite.fr/hal-01927077