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Volumn 43, Issue 5, 2002, Pages 1350-1357
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Foxe3 haploinsufficiency in mice: A model for Peters' anomaly
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Author keywords
[No Author keywords available]
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Indexed keywords
ARGININE;
DNA BINDING PROTEIN;
LEUCINE;
TRANSCRIPTION FACTOR;
TRANSCRIPTION FACTOR FOXE3;
TRANSCRIPTION FACTOR PAX6;
UNCLASSIFIED DRUG;
ALLELE;
ANIMAL EXPERIMENT;
ANIMAL MODEL;
ANIMAL TISSUE;
ANTERIOR EYE SEGMENT;
ARTICLE;
CATARACT;
CONTROLLED STUDY;
CORNEA DISEASE;
CORNEA OPACITY;
GENE LOCUS;
GENE MUTATION;
GENE SEQUENCE;
GENETIC ANALYSIS;
GENETIC VARIABILITY;
HAPLOTYPE;
HETEROZYGOTE;
LENS DISEASE;
MOLECULAR CLONING;
MOUSE;
NONHUMAN;
NUCLEIC ACID BASE SUBSTITUTION;
PETERS ANOMALY;
PHENOTYPE;
POLYMERASE CHAIN REACTION;
PRIORITY JOURNAL;
PROTEIN DNA BINDING;
PROTEIN DOMAIN;
SEQUENCE ANALYSIS;
AMINO ACID SEQUENCE;
ANIMALS;
ANTERIOR EYE SEGMENT;
BASE SEQUENCE;
CATARACT;
CORNEAL OPACITY;
DISEASE MODELS, ANIMAL;
DNA PRIMERS;
DNA-BINDING PROTEINS;
EYE ABNORMALITIES;
FEMALE;
FORKHEAD TRANSCRIPTION FACTORS;
HAPLOTYPES;
HUMANS;
MALE;
MICE;
MICE, INBRED BALB C;
MICE, MUTANT STRAINS;
MOLECULAR SEQUENCE DATA;
MUTATION, MISSENSE;
PHENOTYPE;
RADIATION HYBRID MAPPING;
SEQUENCE HOMOLOGY, AMINO ACID;
TRANSCRIPTION FACTORS;
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EID: 0036237994
PISSN: 01460404
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (85)
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References (47)
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