Differences in corneal phenotypes between destrin mutants are due to allelic difference and modified by genetic background

Molecular Vision

Volumn 18, Issue , 2012, Pages 606-616

  Kawakami Schulz, Sharolyn V ^a   Verdoni, Angela M ^a,b   Sattler, Shannon G ^a   Ikeda, Akihiro ^a   Ikeda, Sakae ^a  

^a UNIVERSITY OF WISCONSIN MADISON   (United States)

^b WASHINGTON UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIN DEPOLYMERIZING FACTOR; F ACTIN; SERUM RESPONSE FACTOR;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CAUSAL ATTRIBUTION; CELL COUNT; CELL PROLIFERATION; CONTROLLED STUDY; CORNEA DISEASE; CORNEA EPITHELIAL HYPERPROLIFERATION; CORNEA EPITHELIUM; CORNEA NEOVASCULARIZATION; DISEASE SEVERITY; DSTN GENE; GENE; GENE EXPRESSION; GENE FREQUENCY; GENE MUTATION; HOMOZYGOSITY; IMMUNOHISTOCHEMISTRY; KERATITIS; MOUSE; NONHUMAN; PHENOTYPIC VARIATION; POINT MUTATION; PRIORITY JOURNAL;

ACTINS; ALLELES; ANIMALS; CORNEA; CORNEAL NEOVASCULARIZATION; DESTRIN; FOUNDER EFFECT; GENE EXPRESSION; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; MICE; MICE, TRANSGENIC; MUTATION; PHENOTYPE; PROTEIN KINASES; SEVERITY OF ILLNESS INDEX;

EID: 84859074760     PISSN: None     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

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