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Items: 1 to 20 of 54

1.

Assessment of Rod, Cone, and Intrinsically Photosensitive Retinal Ganglion Cell Contributions to the Canine Chromatic Pupillary Response.

Yeh CY, Koehl KL, Harman CD, Iwabe S, Guzman JM, Petersen-Jones SM, Kardon RH, Komáromy AM.

Invest Ophthalmol Vis Sci. 2017 Jan 1;58(1):65-78. doi: 10.1167/iovs.16-19865.

2.

Safety and Biodistribution Evaluation in Cynomolgus Macaques of rAAV2tYF-PR1.7-hCNGB3, a Recombinant AAV Vector for Treatment of Achromatopsia.

Ye GJ, Budzynski E, Sonnentag P, Nork TM, Miller PE, Sharma AK, Ver Hoeve JN, Smith LM, Arndt T, Calcedo R, Gaskin C, Robinson PM, Knop DR, Hauswirth WW, Chulay JD.

Hum Gene Ther Clin Dev. 2016 Mar;27(1):37-48. doi: 10.1089/humc.2015.164.

3.

Safety and Biodistribution Evaluation in CNGB3-Deficient Mice of rAAV2tYF-PR1.7-hCNGB3, a Recombinant AAV Vector for Treatment of Achromatopsia.

Ye GJ, Budzynski E, Sonnentag P, Nork TM, Miller PE, McPherson L, Ver Hoeve JN, Smith LM, Arndt T, Mandapati S, Robinson PM, Calcedo R, Knop DR, Hauswirth WW, Chulay JD.

Hum Gene Ther Clin Dev. 2016 Mar;27(1):27-36. doi: 10.1089/humc.2015.163.

4.

The B3 Subunit of the Cone Cyclic Nucleotide-gated Channel Regulates the Light Responses of Cones and Contributes to the Channel Structural Flexibility.

Ding XQ, Thapa A, Ma H, Xu J, Elliott MH, Rodgers KK, Smith ML, Wang JS, Pittler SJ, Kefalov VJ.

J Biol Chem. 2016 Apr 15;291(16):8721-34. doi: 10.1074/jbc.M115.696138.

PMID:
26893377
5.

Canine CNGA3 Gene Mutations Provide Novel Insights into Human Achromatopsia-Associated Channelopathies and Treatment.

Tanaka N, Dutrow EV, Miyadera K, Delemotte L, MacDermaid CM, Reinstein SL, Crumley WR, Dixon CJ, Casal ML, Klein ML, Aguirre GD, Tanaka JC, Guziewicz KE.

PLoS One. 2015 Sep 25;10(9):e0138943. doi: 10.1371/journal.pone.0138943.

6.

A novel mutation in TTC8 is associated with progressive retinal atrophy in the golden retriever.

Downs LM, Wallin-Håkansson B, Bergström T, Mellersh CS.

Canine Genet Epidemiol. 2014 Apr 16;1:4. doi: 10.1186/2052-6687-1-4.

7.

The genetics of eye disorders in the dog.

Mellersh CS.

Canine Genet Epidemiol. 2014 Apr 16;1:3. doi: 10.1186/2052-6687-1-3. Review.

8.

Animal modelling for inherited central vision loss.

Kostic C, Arsenijevic Y.

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

9.

Loss of retinitis pigmentosa 2 (RP2) protein affects cone photoreceptor sensory cilium elongation in mice.

Li L, Rao KN, Zheng-Le Y, Hurd TW, Lillo C, Khanna H.

Cytoskeleton (Hoboken). 2015 Sep;72(9):447-54. doi: 10.1002/cm.21255.

10.

Inherited retinal diseases in dogs: advances in gene/mutation discovery.

Miyadera K.

Dobutsu Iden Ikushu Kenkyu. 2014;42(2):79-89.

11.

Gene Augmentation Therapy Restores Retinal Function and Visual Behavior in a Sheep Model of CNGA3 Achromatopsia.

Banin E, Gootwine E, Obolensky A, Ezra-Elia R, Ejzenberg A, Zelinger L, Honig H, Rosov A, Yamin E, Sharon D, Averbukh E, Hauswirth WW, Ofri R.

Mol Ther. 2015 Sep;23(9):1423-33. doi: 10.1038/mt.2015.114.

12.

Dog models for blinding inherited retinal dystrophies.

Petersen-Jones SM, Komáromy AM.

Hum Gene Ther Clin Dev. 2015 Mar;26(1):15-26. doi: 10.1089/humc.2014.155. Review.

13.

Genomic evidence for rod monochromacy in sloths and armadillos suggests early subterranean history for Xenarthra.

Emerling CA, Springer MS.

Proc Biol Sci. 2015 Feb 7;282(1800):20142192. doi: 10.1098/rspb.2014.2192.

14.

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.

15.

Clinical characteristics and current therapies for inherited retinal degenerations.

Sahel JA, Marazova K, Audo I.

Cold Spring Harb Perspect Med. 2014 Oct 16;5(2):a017111. doi: 10.1101/cshperspect.a017111. Review.

16.

A novel form of progressive retinal atrophy in Swedish vallhund dogs.

Cooper AE, Ahonen S, Rowlan JS, Duncan A, Seppälä EH, Vanhapelto P, Lohi H, Komáromy AM.

PLoS One. 2014 Sep 8;9(9):e106610. doi: 10.1371/journal.pone.0106610. Erratum in: PLoS One. 2015;10(2):e0118128.

17.

Microsatellite polymorphism and its association with body weight and selected morphometrics of farm red fox (Vulpes vulpes L.).

Zatoń-Dobrowolska M, Mucha A, Wierzbicki H, Morrice D, Moska M, Dobrowolski M, Przysiecki P.

J Appl Genet. 2014 Nov;55(4):475-84. doi: 10.1007/s13353-014-0217-x.

18.
19.

A cyclic nucleotide-gated channel mutation associated with canine daylight blindness provides insight into a role for the S2 segment tri-Asp motif in channel biogenesis.

Tanaka N, Delemotte L, Klein ML, Komáromy AM, Tanaka JC.

PLoS One. 2014 Feb 21;9(2):e88768. doi: 10.1371/journal.pone.0088768.

20.

Spectral-domain optical coherence tomography staging and autofluorescence imaging in achromatopsia.

Greenberg JP, Sherman J, Zweifel SA, Chen RW, Duncker T, Kohl S, Baumann B, Wissinger B, Yannuzzi LA, Tsang SH.

JAMA Ophthalmol. 2014 Apr 1;132(4):437-45. doi: 10.1001/jamaophthalmol.2013.7987.

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