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Department of Therapeutics,
Institut de la Vision,
Department of Therapeutics, Institut de la Vision
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Intracytoplasmic delivery of anionic proteins.
Molecular therapy : the journal of the American Society of Gene Therapy Jun, 2004 | Pubmed ID: 15194063
Cationic oligonucleotide-peptide conjugates with aggregating properties enter efficiently into cells while maintaining hybridization properties and enzymatic recognition.
Journal of the American Chemical Society Aug, 2006 | Pubmed ID: 16910671
Intracellular protein delivery with a dimerizable amphiphile for improved complex stability and prolonged protein release in the cytoplasm of adherent cell lines.
Journal of controlled release : official journal of the Controlled Release Society Dec, 2006 | Pubmed ID: 17097756
Suppression of cervical carcinoma cell growth by intracytoplasmic codelivery of anti-oncoprotein E6 antibody and small interfering RNA.
Molecular cancer therapeutics Jun, 2007 | Pubmed ID: 17575104
Molecular evolution of adeno-associated virus for enhanced glial gene delivery.
Molecular therapy : the journal of the American Society of Gene Therapy Dec, 2009 | Pubmed ID: 19672246
Inner limiting membrane barriers to AAV-mediated retinal transduction from the vitreous.
Molecular therapy : the journal of the American Society of Gene Therapy Dec, 2009 | Pubmed ID: 19672248
A novel adeno-associated viral variant for efficient and selective intravitreal transduction of rat Müller cells.
PloS one , 2009 | Pubmed ID: 19826483
Changes in adeno-associated virus-mediated gene delivery in retinal degeneration.
Human gene therapy May, 2010 | Pubmed ID: 20021232
Intravitreal injection of AAV2 transduces macaque inner retina.
Investigative ophthalmology & visual science Apr, 2011 | Pubmed ID: 21310920
AAV mediated GDNF secretion from retinal glia slows down retinal degeneration in a rat model of retinitis pigmentosa.
Molecular therapy : the journal of the American Society of Gene Therapy Sep, 2011 | Pubmed ID: 21522134
LiGluR restores visual responses in rodent models of inherited blindness.
Molecular therapy : the journal of the American Society of Gene Therapy Jul, 2011 | Pubmed ID: 21610698
Rapid optical control of nociception with an ion-channel photoswitch.
Nature methods Apr, 2012 | Pubmed ID: 22343342
Systemic scAAV9 variant mediates brain transduction in newborn rhesus macaques.
Scientific reports , 2012 | Pubmed ID: 22355765
Long-distance axonal regeneration induced by CNTF gene transfer is impaired by axonal misguidance in the injured adult optic nerve.
Neurobiology of disease Mar, 2013 | Pubmed ID: 23194670
Functional rescue of cone photoreceptors in retinitis pigmentosa.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie Jul, 2013 | Pubmed ID: 23575948
In vivo-directed evolution of a new adeno-associated virus for therapeutic outer retinal gene delivery from the vitreous.
Science translational medicine Jun, 2013 | Pubmed ID: 23761039
AAV-mediated gene delivery in Dp71-null mouse model with compromised barriers.
Glia Mar, 2014 | Pubmed ID: 24382652
Vertebrate cone opsins enable sustained and highly sensitive rapid control of Gi/o signaling in anxiety circuitry.
Neuron Mar, 2014 | Pubmed ID: 24656249
Gene therapy for inherited retinal degenerations.
Comptes rendus biologies Mar, 2014 | Pubmed ID: 24702845
Imaging light responses of foveal ganglion cells in the living macaque eye.
The Journal of neuroscience : the official journal of the Society for Neuroscience May, 2014 | Pubmed ID: 24806684
Targeting channelrhodopsin-2 to ON-bipolar cells with vitreally administered AAV Restores ON and OFF visual responses in blind mice.
Molecular therapy : the journal of the American Society of Gene Therapy Jan, 2015 | Pubmed ID: 25095892
Viral-mediated RdCVF and RdCVFL expression protects cone and rod photoreceptors in retinal degeneration.
The Journal of clinical investigation Jan, 2015 | Pubmed ID: 25415434
Intracisternal delivery of NFκB-inducible scAAV2/9 reveals locoregional neuroinflammation induced by systemic kainic acid treatment.
Frontiers in molecular neuroscience , 2014 | Pubmed ID: 25520614
Gene therapy for the eye focus on mutation-independent approaches.
Current opinion in neurology Feb, 2015 | Pubmed ID: 25545056
Sorbonne Universtés, UPMC Univ Paris 06, UMR_S 968
INSERM, U968
CNRS, UMR_7210
Ophélie Vacca1,2,3,
Brahim El Mathari1,2,3,
Marie Darche1,2,3,
José-Alain Sahel1,2,3,
Alvaro Rendon1,2,3,
Deniz Dalkara1,2,3
1Department of Therapeutics, Institut de la Vision, Sorbonne Universtés, UPMC Univ Paris 06, UMR_S 968,
2, INSERM, U968,
3, CNRS, UMR_7210
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