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Ophthalmic Genetics, ISSN 1381-6810, 03/2017, Volume 38, Issue 2, pp. 127 - 132
Journal Article
Molecular Vision, ISSN 1090-0535, 2010, Volume 16, Issue 44-46, pp. 378 - 391
Purpose: To characterize an N-ethyl-N-nitrosourea-induced dominant mouse mutant, M-1156, that exhibits progressive retinal degeneration and to investigate the... 
ENU MUTAGENESIS | SLOW RDS | PHOTORECEPTOR DISK MEMBRANES | GENE | RDS MUTANT MICE | ROD | BIOCHEMISTRY & MOLECULAR BIOLOGY | DIGENIC RETINITIS-PIGMENTOSA | PERIPHERIN-RDS | OPHTHALMOLOGY | GENOME-WIDE | MOUSE MODELS | Immunohistochemistry | Membrane Glycoproteins - metabolism | Molecular Sequence Data | Male | Retinal Degeneration - metabolism | Haplotypes - genetics | DNA Mutational Analysis | Mice, Mutant Strains | Base Sequence | Intermediate Filament Proteins - genetics | Ethylnitrosourea | Membrane Proteins - metabolism | Eye Proteins - genetics | Electroretinography | Peripherins | Photoreceptor Cells, Vertebrate - ultrastructure | Membrane Proteins - genetics | Retinal Degeneration - genetics | Mice, Inbred C57BL | Gene Expression Regulation | Mutation - genetics | Nerve Tissue Proteins - genetics | Membrane Glycoproteins - genetics | Nerve Tissue Proteins - metabolism | Phenotype | Animals | Eye Proteins - metabolism | Mutagenesis | Mice | Photoreceptor Cells, Vertebrate - metabolism | Retinal Degeneration - pathology | Fundus Oculi | Genes, Dominant - genetics | Intermediate Filament Proteins - metabolism | Photoreceptor Cells, Vertebrate - pathology | Index Medicus | chromosome 19 | Rhodopsin | retinal degeneration | Heterozygotes | Retina | mRNA | Rod outer segment membranes | Arteries | Western blotting | Electroretinograms | Homozygotes | Polymerase chain reaction | Ethyl nitrosourea | Missense mutation | Transmission electron microscopy | Peripherin | Photoreceptors | Genotypes | Linkage analysis
Journal Article
Genome, ISSN 0831-2796, 12/1998, Volume 41, Issue 6, pp. 789 - 796
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 10/2004, Volume 13, Issue 2, pp. R225 - R233
Journal Article
Genetics in Medicine, ISSN 1098-3600, 09/2003, Volume 5, Issue 5, pp. 347 - 352
Journal Article
EXPERIMENTAL ANIMALS, ISSN 1341-1357, 10/2013, Volume 62, Issue 4, pp. 333 - 346
The waltzer (v) mouse mutant harbors a mutation in Cadherin 23 (Cdh23) and is a model for Usher syndrome type ID, which is characterized by congenital... 
SENSORY HAIR-CELLS | SYNDROME TYPE 1D | CADHERIN GENE | hair cell | stereocilia | NONSYNDROMIC DEAFNESS | ZOOLOGY | USHER-SYNDROME | mouse mutant | age-related hearing loss | MOUSE MODEL | WALTZER MICE | DEAFNESS DFNB12 | DIGENIC INHERITANCE | VETERINARY SCIENCES | TIP LINKS | cadherin 23
Journal Article