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Items: 13


Animal modelling for inherited central vision loss.

Kostic C, Arsenijevic Y.

J Pathol. 2016 Jan;238(2):300-10. doi: 10.1002/path.4641. Epub 2015 Nov 13. Review.


Increased expression of MERTK is associated with a unique form of canine retinopathy.

Ahonen SJ, Arumilli M, Seppälä E, Hakosalo O, Kaukonen MK, Komáromy AM, Lohi H.

PLoS One. 2014 Dec 17;9(12):e114552. doi: 10.1371/journal.pone.0114552. eCollection 2014.


Genome-wide association and linkage analyses localize a progressive retinal atrophy locus in Persian cats.

Alhaddad H, Gandolfi B, Grahn RA, Rah HC, Peterson CB, Maggs DJ, Good KL, Pedersen NC, Lyons LA.

Mamm Genome. 2014 Aug;25(7-8):354-62. doi: 10.1007/s00335-014-9517-z. Epub 2014 Apr 29.


Cone specific promoter for use in gene therapy of retinal degenerative diseases.

Dyka FM, Boye SL, Ryals RC, Chiodo VA, Boye SE, Hauswirth WW.

Adv Exp Med Biol. 2014;801:695-701. doi: 10.1007/978-1-4614-3209-8_87.


Successful gene therapy in the RPGRIP1-deficient dog: a large model of cone-rod dystrophy.

Lhériteau E, Petit L, Weber M, Le Meur G, Deschamps JY, Libeau L, Mendes-Madeira A, Guihal C, François A, Guyon R, Provost N, Lemoine F, Papal S, El-Amraoui A, Colle MA, Moullier P, Rolling F.

Mol Ther. 2014 Feb;22(2):265-277. doi: 10.1038/mt.2013.232. Epub 2013 Oct 4.


A CNGB1 frameshift mutation in Papillon and Phalène dogs with progressive retinal atrophy.

Ahonen SJ, Arumilli M, Lohi H.

PLoS One. 2013 Aug 28;8(8):e72122. doi: 10.1371/journal.pone.0072122. eCollection 2013.


The genome of the heartworm, Dirofilaria immitis, reveals drug and vaccine targets.

Godel C, Kumar S, Koutsovoulos G, Ludin P, Nilsson D, Comandatore F, Wrobel N, Thompson M, Schmid CD, Goto S, Bringaud F, Wolstenholme A, Bandi C, Epe C, Kaminsky R, Blaxter M, Mäser P.

FASEB J. 2012 Nov;26(11):4650-61. doi: 10.1096/fj.12-205096. Epub 2012 Aug 13.


Gene delivery to the retina: from mouse to man.

Bennett J, Chung DC, Maguire A.

Methods Enzymol. 2012;507:255-74. doi: 10.1016/B978-0-12-386509-0.00013-2.


Gene therapy rescues photoreceptor blindness in dogs and paves the way for treating human X-linked retinitis pigmentosa.

Beltran WA, Cideciyan AV, Lewin AS, Iwabe S, Khanna H, Sumaroka A, Chiodo VA, Fajardo DS, Román AJ, Deng WT, Swider M, Alemán TS, Boye SL, Genini S, Swaroop A, Hauswirth WW, Jacobson SG, Aguirre GD.

Proc Natl Acad Sci U S A. 2012 Feb 7;109(6):2132-7. doi: 10.1073/pnas.1118847109. Epub 2012 Jan 23.


Spotlight on childhood blindness.

Sahel JA.

J Clin Invest. 2011 Jun;121(6):2145-9. doi: 10.1172/JCI58300. Epub 2011 May 23.


Achromatopsia as a potential candidate for gene therapy.

Pang JJ, Alexander J, Lei B, Deng W, Zhang K, Li Q, Chang B, Hauswirth WW.

Adv Exp Med Biol. 2010;664:639-46. doi: 10.1007/978-1-4419-1399-9_73.


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

Beltran WA.

Vet Ophthalmol. 2009 May-Jun;12(3):192-204. doi: 10.1111/j.1463-5224.2009.00694.x. Review. Erratum in: Vet Ophthalmol. 2011 Nov;14(6):423.


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.

Acland GM, Aguirre GD, Bennett J, Aleman TS, Cideciyan AV, Bennicelli J, Dejneka NS, Pearce-Kelling SE, Maguire AM, Palczewski K, Hauswirth WW, Jacobson SG.

Mol Ther. 2005 Dec;12(6):1072-82. Epub 2005 Oct 14.

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