Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Juliette, Varin"'
Autor:
Aurélien Leray, Pierre-Alban Lalys, Juliette Varin, Mohammed Bouzelha, Audrey Bourdon, Dimitri Alvarez-Dorta, Karine Pavageau, Sébastien Depienne, Maia Marchand, Anthony Mellet, Joanna Demilly, Jean-Baptiste Ducloyer, Tiphaine Girard, Bodvaël Fraysse, Mireille Ledevin, Mickaël Guilbaud, Sébastien G. Gouin, Eduard Ayuso, Oumeya Adjali, Thibaut Larcher, Thérèse Cronin, Caroline Le Guiner, David Deniaud, Mathieu Mével
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 171, Iss , Pp 116148- (2024)
Decades of biological and clinical research have led to important advances in recombinant adeno-associated viruses rAAV-based gene therapy gene therapy. However, several challenges must be overcome to fully exploit the potential of rAAV vectors. Inno
Externí odkaz:
https://doaj.org/article/1ed978775aad41fbbbc3787da57c93b5
Autor:
Juliette Varin, Nassima Bouzidi, Gregory Gauvain, Corentin Joffrois, Melissa Desrosiers, Camille Robert, Miguel Miranda De Sousa Dias, Marion Neuillé, Christelle Michiels, Marco Nassisi, José-Alain Sahel, Serge Picaud, Isabelle Audo, Deniz Dalkara, Christina Zeitz
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 22, Iss , Pp 15-25 (2021)
Complete congenital stationary night blindness (cCSNB) due to mutations in TRPM1, GRM6, GPR179, NYX, or leucine-rich repeat immunoglobulin-like transmembrane domain 3 (LRIT3) is an incurable inherited retinal disorder characterized by an ON-bipolar c
Externí odkaz:
https://doaj.org/article/1f04f05b98504f5194e6bd3d6cde288d
Autor:
Marco Nassisi, Carlo Lavia, Saddek Mohand-Said, Vasily Smirnov, Aline Antonio, Christel Condroyer, Serge Sancho, Juliette Varin, Alain Gaudric, Christina Zeitz, José-Alain Sahel, Isabelle Audo
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Abstract Thirty-eight patients from 37 families with retinitis pigmentosa (RP) underwent macular 6 × 6-mm swept-source optical coherence tomography angiography (SS-OCTA) and 30° near-infrared fundus autofluorescence (NIR-FAF) acquisitions in one ey
Externí odkaz:
https://doaj.org/article/1f468fc60c014a278f92d298f1c7b90d
Autor:
Juliette Varin, Margaret M Reynolds, Nassima Bouzidi, Sarah Tick, Juliette Wohlschlegel, Ondine Becquart, Christelle Michiels, Olivier Dereure, Robert M Duvoisin, Catherine W Morgans, José-Alain Sahel, Quentin Samaran, Bernard Guillot, José S Pulido, Isabelle Audo, Christina Zeitz
Publikováno v:
PLoS ONE, Vol 15, Iss 4, p e0231750 (2020)
Melanoma-associated retinopathy (MAR) is a rare paraneoplastic retinal disorder usually occurring in the context of metastatic melanoma. Patients present with night blindness, photopsias and a constriction of the visual field. MAR is an auto-immune d
Externí odkaz:
https://doaj.org/article/7aa5b93b3b9e44f19da22f7f7d64c257
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 23, p 12818 (2021)
Gene therapy (GT) for ocular disorders has advanced the most among adeno-associated virus (AAV)-mediated therapies, with one product already approved in the market. The bank of retinal gene mutations carefully compiled over 30 years, the small retina
Externí odkaz:
https://doaj.org/article/416d58a39c6649e9b4c704152ca276c3
Autor:
Aurelien Leray, Pierre-Alban Lalys, Juliette Varin, Mohammed Bouzelha, Audrey Bourdon, Dimitri Alvarez-Dorta, Karine Pavageau, Sebastien Depienne, Maia Marchand, Anthony Mellet, Joanna Demilly, Jean-Baptiste Ducloyer, Tiphaine Girard, Bodval Fraysse, Mireille Ledevin, Mickael Guilbaud, Sebastien G. Gouin, Eduard Ayuso, Oumeya Adjali, Thibaut Larcher, Therese Cronin, Caroline Le Guiner, David Deniaud, Mathieu Mevel
Decades of biological and clinical research have led to important advances in recombinant adeno-associated viruses rAAV-based gene therapy gene therapy. However, several challenges must be overcome to fully exploit the potential of rAAV vectors. Inno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33fdeaf96dcd33201a922c4fba14ec65
https://doi.org/10.26434/chemrxiv-2023-6xnn8
https://doi.org/10.26434/chemrxiv-2023-6xnn8
Autor:
Christina Zeitz, Jerome E. Roger, Christelle Michiels, Nuria Sánchez‐Farías, Juliette Varin, Helen Frederiksen, Baptiste Wilmet, Marie‐Laure Gimenez, Nassima Bouzidi, Frederic Blond, Xavier Guilllonneau, Thierry Léveillard, José‐Alain Sahel, Serge Picaud, Isabelle Audo
Publikováno v:
Acta Ophthalmologica. 100
Autor:
Miguel Miranda de Sousa Dias, José-Alain Sahel, Serge Picaud, Christelle Michiels, Melissa Desrosiers, Isabelle Audo, Marco Nassisi, Camille Robert, Deniz Dalkara, Christina Zeitz, Marion Neuillé, Nassima Bouzidi, Corentin Joffrois, Juliette Varin, Gregory Gauvain
Publikováno v:
Molecular Therapy-Methods and Clinical Development
Molecular Therapy-Methods and Clinical Development, 2021, 22, pp.15-25. ⟨10.1016/j.omtm.2021.05.008⟩
Molecular Therapy-Methods and Clinical Development, Nature Publishing Group, 2021, 22, pp.15-25. ⟨10.1016/j.omtm.2021.05.008⟩
Molecular Therapy: Methods & Clinical Development, Vol 22, Iss, Pp 15-25 (2021)
Molecular Therapy. Methods & Clinical Development
Molecular Therapy-Methods and Clinical Development, 2021, 22, pp.15-25. ⟨10.1016/j.omtm.2021.05.008⟩
Molecular Therapy-Methods and Clinical Development, Nature Publishing Group, 2021, 22, pp.15-25. ⟨10.1016/j.omtm.2021.05.008⟩
Molecular Therapy: Methods & Clinical Development, Vol 22, Iss, Pp 15-25 (2021)
Molecular Therapy. Methods & Clinical Development
Complete congenital stationary night blindness (cCSNB) due to mutations in TRPM1, GRM6, GPR179, NYX, or leucine-rich repeat immunoglobulin-like transmembrane domain 3 (LRIT3) is an incurable inherited retinal disorder characterized by an ON-bipolar c
Autor:
Marco Nassisi, Saddek Mohand-Saïd, Camille Andrieu, Aline Antonio, Christel Condroyer, Cécile Méjécase, Juliette Varin, Juliette Wohlschlegel, Claire-Marie Dhaenens, José-Alain Sahel, Christina Zeitz, Isabelle Audo
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 20, p 5053 (2019)
We investigated the prevalence of reported deep-intronic variants in a French cohort of 70 patients with Stargardt disease harboring a monoallelic pathogenic variant on the exonic regions of ABCA4. Direct Sanger sequencing of selected intronic region
Externí odkaz:
https://doaj.org/article/7674c5ea151c4c3ca05349550bb3fdd2
Autor:
Christina Zeitz, Jérome E. Roger, Isabelle Audo, Christelle Michiels, Nuria Sánchez-Farías, Juliette Varin, Helen Frederiksen, Baptiste Wilmet, Jacques Callebert, Marie-Laure Gimenez, Nassima Bouzidi, Frederic Blond, Xavier Guilllonneau, Stéphane Fouquet, Thierry Léveillard, Vasily Smirnov, Ajoy Vincent, Elise Héon, José-Alain Sahel, Barbara Kloeckener-Gruissem, Florian Sennlaub, Catherine W. Morgans, Robert M. Duvoisin, Andrei V. Tkatchenko, Serge Picaud
Publikováno v:
Progress in Retinal and Eye Research. 93:101155