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Mouse Model Resources for Vision Research
Author(s) -
Jungyeon Won,
Lan Ying Shi,
Wanda L. Hicks,
Jieping Wang,
Ronald E. Hurd,
Jürgen Κ. Naggert,
Bo Chang,
Patsy M. Nishina
Publication year - 2010
Publication title -
journal of ophthalmology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.818
H-Index - 40
eISSN - 2090-0058
pISSN - 2090-004X
DOI - 10.1155/2011/391384
Subject(s) - medicine , optometry
The need for mouse models, with their well-developed genetics and similarity to human physiology and anatomy, is clear and their central role in furthering our understanding of human disease is readily apparent in the literature. Mice carrying mutations that alter developmental pathways or cellular function provide model systems for analyzing defects in comparable human disorders and for testing therapeutic strategies. Mutant mice also provide reproducible, experimental systems for elucidating pathways of normal development and function. Two programs, the Eye Mutant Resource and the Translational Vision Research Models, focused on providing such models to the vision research community are described herein. Over 100 mutant lines from the Eye Mutant Resource and 60 mutant lines from the Translational Vision Research Models have been developed. The ocular diseases of the mutant lines include a wide range of phenotypes, including cataracts, retinal dysplasia and degeneration, and abnormal blood vessel formation. The mutations in disease genes have been mapped and in some cases identified by direct sequencing. Here, we report 3 novel alleles of C r x t v r m 65 , R p 1 t v r m 64 , and R p e 65 t v r m 148 as successful examples of the TVRM program, that closely resemble previously reported knockout models.

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