Detalhe da pesquisa
1.
Restoration of cone vision in a mouse model of achromatopsia.
Nat Med
; 13(6): 685-7, 2007 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-17515894
2.
Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice.
Nat Genet
; 30(1): 81-5, 2002 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-11743578
3.
Age-related retinal degeneration (arrd2) in a novel mouse model due to a nonsense mutation in the Mdm1 gene.
Hum Mol Genet
; 17(24): 3929-41, 2008 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18805803
4.
Allelic variance between GRM6 mutants, Grm6nob3 and Grm6nob4 results in differences in retinal ganglion cell visual responses.
J Physiol
; 586(18): 4409-24, 2008 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18687716
5.
Dense nuclear cataract caused by the gammaB-crystallin S11R point mutation.
Invest Ophthalmol Vis Sci
; 49(1): 304-9, 2008 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-18172107
6.
Genetic background modifies inner ear and eye phenotypes of jag1 heterozygous mice.
Genetics
; 177(1): 307-11, 2007 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17890364
7.
Deficiency of SHP-1 protein-tyrosine phosphatase in "viable motheaten" mice results in retinal degeneration.
Invest Ophthalmol Vis Sci
; 47(3): 1201-9, 2006 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-16505059
8.
Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA).
Mol Vis
; 11: 152-62, 2005 Feb 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-15765048
9.
A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisis.
J Bone Miner Res
; 18(9): 1612-21, 2003 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-12968670
10.
Fierce: a new mouse deletion of Nr2e1; violent behaviour and ocular abnormalities are background-dependent.
Behav Brain Res
; 132(2): 145-58, 2002 May 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-11997145
11.
Iris phenotypes and pigment dispersion caused by genes influencing pigmentation.
Pigment Cell Melanoma Res
; 21(5): 565-78, 2008 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-18715234
12.
AAV-mediated gene therapy for retinal degeneration in the rd10 mouse containing a recessive PDEbeta mutation.
Invest Ophthalmol Vis Sci
; 49(10): 4278-83, 2008 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-18586879
13.
Early transposable element insertion in intron 9 of the Hsf4 gene results in autosomal recessive cataracts in lop11 and ldis1 mice.
Genomics
; 88(1): 44-51, 2006 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-16595169
14.
Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degeneration.
Am J Hum Genet
; 79(6): 1059-70, 2006 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-17186464
15.
Mouse model of subretinal neovascularization with choroidal anastomosis.
Retina
; 23(4): 518-22, 2003 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-12972764
16.
A Gja8 (Cx50) point mutation causes an alteration of alpha 3 connexin (Cx46) in semi-dominant cataracts of Lop10 mice.
Hum Mol Genet
; 11(5): 507-13, 2002 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-11875045
17.
Mfrp, a gene encoding a frizzled related protein, is mutated in the mouse retinal degeneration 6.
Hum Mol Genet
; 11(16): 1879-86, 2002 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-12140190
18.
Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene.
Hum Mol Genet
; 12(23): 3075-86, 2003 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-14519688
19.
CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retina.
Hum Mol Genet
; 12(17): 2179-89, 2003 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-12915475