Literature DB >> 18188934

Gene therapy for mouse models of ADRP.

Marina S Gorbatyuk1, William W Hauswirth, Alfred S Lewin.   

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Year:  2008        PMID： 18188934     DOI： 10.1007/978-0-387-74904-4_11

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN： 0065-2598            Impact factor:   2.622


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  5 in total

1.  Long-term rescue of retinal structure and function by rhodopsin RNA replacement with a single adeno-associated viral vector in P23H RHO transgenic mice.

Authors:  Haoyu Mao; Marina S Gorbatyuk; Brian Rossmiller; William W Hauswirth; Alfred S Lewin
Journal:  Hum Gene Ther       Date:  2012-03-28       Impact factor: 5.695

2.  AAV delivery of wild-type rhodopsin preserves retinal function in a mouse model of autosomal dominant retinitis pigmentosa.

Authors:  Haoyu Mao; Thomas James; Alison Schwein; Arseniy E Shabashvili; William W Hauswirth; Marina S Gorbatyuk; Alfred S Lewin
Journal:  Hum Gene Ther       Date:  2011-03-07       Impact factor: 5.695

3.  Gene delivery of wild-type rhodopsin rescues retinal function in an autosomal dominant retinitis pigmentosa mouse model.

Authors:  Haoyu Mao; Marina S Gorbatyuk; William W Hauswirth; Alfred S Lewin
Journal:  Adv Exp Med Biol       Date:  2012       Impact factor: 2.622

Review 4.  The use of canine models of inherited retinal degeneration to test novel therapeutic approaches.

Authors:  William A Beltran
Journal:  Vet Ophthalmol       Date:  2009 May-Jun       Impact factor: 1.644

5.  Expression of wild-type Rp1 protein in Rp1 knock-in mice rescues the retinal degeneration phenotype.

Authors:  Qin Liu; Rob W J Collin; Frans P M Cremers; Anneke I den Hollander; L Ingeborgh van den Born; Eric A Pierce
Journal:  PLoS One       Date:  2012-08-21       Impact factor: 3.240
  5 in total

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