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Items: 1 to 20 of 131

1.

The Usher gene cadherin 23 is expressed in the zebrafish brain and a subset of retinal amacrine cells.

Glover G, Mueller KP, Söllner C, Neuhauss SC, Nicolson T.

Mol Vis. 2012;18:2309-22. Epub 2012 Sep 5.

2.

Identification of amacrine subtypes that express the atypical cadherin celsr3.

Lewis AA, Mahoney JT, Wilson N, Brockerhoff SE.

Exp Eye Res. 2015 Jan;130:51-7. doi: 10.1016/j.exer.2014.12.003. Epub 2014 Dec 3.

3.

Cdh23 mutations in the mouse are associated with retinal dysfunction but not retinal degeneration.

Libby RT, Kitamoto J, Holme RH, Williams DS, Steel KP.

Exp Eye Res. 2003 Dec;77(6):731-9.

PMID:
14609561
4.

Expression of cadherin 23 isoforms is not conserved: implications for a mouse model of Usher syndrome type 1D.

Lagziel A, Overlack N, Bernstein SL, Morell RJ, Wolfrum U, Friedman TB.

Mol Vis. 2009 Sep 12;15:1843-57.

5.

myosin 7aa(-/-) mutant zebrafish show mild photoreceptor degeneration and reduced electroretinographic responses.

Wasfy MM, Matsui JI, Miller J, Dowling JE, Perkins BD.

Exp Eye Res. 2014 May;122:65-76. doi: 10.1016/j.exer.2014.03.007. Epub 2014 Apr 1.

6.

Mutations in cadherin 23 affect tip links in zebrafish sensory hair cells.

Söllner C, Rauch GJ, Siemens J, Geisler R, Schuster SC, Müller U, Nicolson T; Tübingen 2000 Screen Consortium.

Nature. 2004 Apr 29;428(6986):955-9. Epub 2004 Mar 31.

7.

Cadherin-6 function in zebrafish retinal development.

Liu Q, Londraville R, Marrs JA, Wilson AL, Mbimba T, Murakami T, Kubota F, Zheng W, Fatkins DG.

Dev Neurobiol. 2008 Jul;68(8):1107-22. doi: 10.1002/dneu.20646.

8.

Expression of a 12-kb promoter element derived from the zebrafish enolase-2 gene in the zebrafish visual system.

Bai Q, Wei X, Burton EA.

Neurosci Lett. 2009 Jan 16;449(3):252-7. doi: 10.1016/j.neulet.2008.10.101. Epub 2008 Nov 5.

9.

Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes.

Schultz JM, Bhatti R, Madeo AC, Turriff A, Muskett JA, Zalewski CK, King KA, Ahmed ZM, Riazuddin S, Ahmad N, Hussain Z, Qasim M, Kahn SN, Meltzer MR, Liu XZ, Munisamy M, Ghosh M, Rehm HL, Tsilou ET, Griffith AJ, Zein WM, Brewer CC, Riazuddin S, Friedman TB.

J Med Genet. 2011 Nov;48(11):767-75. doi: 10.1136/jmedgenet-2011-100262. Epub 2011 Sep 22.

PMID:
21940737
10.

Duplicated genes with split functions: independent roles of protocadherin15 orthologues in zebrafish hearing and vision.

Seiler C, Finger-Baier KC, Rinner O, Makhankov YV, Schwarz H, Neuhauss SC, Nicolson T.

Development. 2005 Feb;132(3):615-23. Epub 2005 Jan 5.

11.

Celsr3 is required for normal development of GABA circuits in the inner retina.

Lewis A, Wilson N, Stearns G, Johnson N, Nelson R, Brockerhoff SE.

PLoS Genet. 2011 Aug;7(8):e1002239. doi: 10.1371/journal.pgen.1002239. Epub 2011 Aug 11.

12.

In vivo expression of Nurr1/Nr4a2a in developing retinal amacrine subtypes in zebrafish Tg(nr4a2a:eGFP) transgenics.

Goodings L, He J, Wood AJ, Harris WA, Currie PD, Jusuf PR.

J Comp Neurol. 2017 Jun 1;525(8):1962-1979. doi: 10.1002/cne.24185. Epub 2017 Mar 15.

PMID:
28177524
13.

Arl13b Interacts With Vangl2 to Regulate Cilia and Photoreceptor Outer Segment Length in Zebrafish.

Song P, Dudinsky L, Fogerty J, Gaivin R, Perkins BD.

Invest Ophthalmol Vis Sci. 2016 Aug 1;57(10):4517-26. doi: 10.1167/iovs.16-19898.

14.

Tryptophan hydroxylase and serotonin receptor 1A expression in the retina of the sea lamprey.

Cornide-Petronio ME, Anadón R, Barreiro-Iglesias A, Rodicio MC.

Exp Eye Res. 2015 Jun;135:81-7. doi: 10.1016/j.exer.2015.04.017. Epub 2015 Apr 26.

PMID:
25925848
15.

Lazy eyes zebrafish mutation affects Müller glial cells, compromising photoreceptor function and causing partial blindness.

Kainz PM, Adolph AR, Wong KY, Dowling JE.

J Comp Neurol. 2003 Aug 25;463(3):265-80.

PMID:
12820161
16.

Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.

Bolz H, von Brederlow B, Ramírez A, Bryda EC, Kutsche K, Nothwang HG, Seeliger M, del C-Salcedó Cabrera M, Vila MC, Molina OP, Gal A, Kubisch C.

Nat Genet. 2001 Jan;27(1):108-12.

PMID:
11138009
17.

Retinal function and morphology in two zebrafish models of oculo-renal syndromes.

Bahadori R, Huber M, Rinner O, Seeliger MW, Geiger-Rudolph S, Geisler R, Neuhauss SC.

Eur J Neurosci. 2003 Sep;18(6):1377-86.

PMID:
14511318
18.

Zebrafish Tg(7.2mab21l2:EGFP)ucd2 transgenics reveal a unique population of retinal amacrine cells.

Cederlund ML, Morrissey ME, Baden T, Scholz D, Vendrell V, Lagnado L, Connaughton VP, Kennedy BN.

Invest Ophthalmol Vis Sci. 2011 Mar 1;52(3):1613-21. doi: 10.1167/iovs.10-5376.

19.

A molecular phenotype atlas of the zebrafish retina.

Marc RE, Cameron D.

J Neurocytol. 2001 Jul;30(7):593-654.

PMID:
12118163
20.

CERKL knockdown causes retinal degeneration in zebrafish.

Riera M, Burguera D, Garcia-Fernàndez J, Gonzàlez-Duarte R.

PLoS One. 2013 May 9;8(5):e64048. doi: 10.1371/journal.pone.0064048. Print 2013.

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