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Results: 1 to 20 of 109

Similar articles for PubMed (Select 22977299)

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.

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.

3.

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.

PMID:
25479044
4.

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
5.

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.

6.

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.

7.

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.

8.

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.

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.

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.

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.

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
13.

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.

14.

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
15.

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
16.

A molecular phenotype atlas of the zebrafish retina.

Marc RE, Cameron D.

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

PMID:
12118163
17.

Double homozygous waltzer and Ames waltzer mice provide no evidence of retinal degeneration.

Ahmed ZM, Kjellstrom S, Haywood-Watson RJ, Bush RA, Hampton LL, Battey JF, Riazuddin S, Frolenkov G, Sieving PA, Friedman TB.

Mol Vis. 2008;14:2227-36. Epub 2008 Dec 8.

18.

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.

19.

Transgenic zebrafish expressing mutant human RETGC-1 exhibit aberrant cone and rod morphology.

Collery RF, Cederlund ML, Kennedy BN.

Exp Eye Res. 2013 Mar;108:120-8. doi: 10.1016/j.exer.2013.01.003. Epub 2013 Jan 15.

PMID:
23328348
20.

Retinal defects in the zebrafish bleached mutant.

Neuhauss SC, Seeliger MW, Schepp CP, Biehlmaier O.

Doc Ophthalmol. 2003 Jul;107(1):71-8.

PMID:
12906124
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