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Title:	Gene delivery to the eye using adeno-associated viral vectors
Source:	Methods [1046-2023] Martin, Keith R.G yr:2002

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description	1.	Thomas, Clare E E. "Progress and problems with the use of viral vectors for gene therapy." Nature reviews. Genetics 4.5 (2003): 346-58.
description	2.	Qiu, J. "Spinal Axon Regeneration Induced by Elevation of Cyclic AMP." Neuron 34.6 (2002): 895-903.
description	3.	Robinson, P. "Fireworks in the primate retina: in vitro photodynamics reveals diverse LGN-projecting ganglion cell types." Neuron 37.1 (2003): 15-27.
description	4.	Ali, R R R. "restoration of photoreceptor ultrastructure and function in retinal degeneration slow mice by gene therapy." Nature genetics 25.3 (2000): 306-310.
description	5.	Harvey, J. "Intravitreal injection of adeno-associated viral vectors results in the transduction of different types of retinal neurons in neonatal and adult rats: a comparison with lentiviral vectors." Molecular and cellular neurosciences 21.1 (2002): 141-57.
description	6.	Kay, M. "Viral vectors for gene therapy: the art of turning infectious agents into vehicles of therapeutics." Nature medicine 7.1 (2001): 33-40.
description	7.	Niidome, T. "Gene therapy progress and prospects: nonviral vectors." Gene therapy 10.24 (2003): 1647-52.
description	8.	Waehler, R. "Engineering targeted viral vectors for gene therapy." Nature reviews. Genetics 8.8 (2007): 573-87.
description	9.	Young, Lawrence S S. "Viral gene therapy strategies: from basic science to clinical application." The Journal of pathology 208.2 (2005): 299-318.
description	10.	O'Connor, Ronald G. "Genetic medicines: treatment strategies for hereditary disorders." Nature reviews. Genetics 7.4 (2006): 261-276.
description	11.	Jacobson, Samuel G G. "Long-term restoration of rod and cone vision by single dose rAAV-mediated gene transfer to the retina in a canine model of childhood blindness." Molecular therapy 12.6 (2006): 1072-82.
description	12.	Bennett, J. "Gene therapy restores vision in a canine model of childhood blindness." Nature genetics 28.1 (2001): 92-5.
description	13.	Lotery, Andrew J J. "Adeno-associated virus type 5: transduction efficiency and cell-type specificity in the primate retina." Human gene therapy 9.1 (2003): 1663-71.
description	14.	M Hellström; M J Ruitenberg; M A Pollett; E M E Ehlert; J Twisk; J Verhaagen; A R Harvey;, M. "Cellular tropism and transduction properties of seven adeno-associated viral vector serotypes in adult retina after intravitreal injection." Gene Therapy 16.4 (2009): 521-32.
description	15.	Dacey, D. "Melanopsin-expressing ganglion cells in primate retina signal colour and irradiance and project to the LGN." Nature 433.7027 (2005): 749-754.
description	16.	Grant, C A A. "Evaluation of recombinant adeno-associated virus as a gene transfer vector for the retina." Current eye research 16.9 (1997): 949-56.
description	17.	Doi, K. "Lentiviral transduction of green fluorescent protein in retinal epithelium: evidence of rejection." Vision Research 42.4 (2002): 551-8.
description	18.	Dacey, D M M. "The mosaic of midget ganglion cells in the human retina." The journal of neuroscience 13.12 (1994): 5334-55.
description	19.	Lin, B. "Retinal Ganglion Cell Type, Size, and Spacing Can Be Specified Independent of Homotypic Dendritic Contacts." Neuron 43.4 (2004): 475-85.
description	20.	Cai, D. "Neuronal cyclic AMP controls the developmental loss in ability of axons to regenerate." The journal of neuroscience 21.13 (2001): 4731-9.