Molecular genetics of Axenfeld-Rieger malformations

Human Molecular Genetics

Volumn 11, Issue 10, 2002, Pages 1177-1184

  Lines, Matthew A ^a   Kozlowski, Kathy ^a   Walter, Michael A ^a  

^a UNIVERSITY OF ALBERTA   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

MUTANT PROTEIN; TRANSCRIPTION FACTOR; DNA BINDING PROTEIN; EYE PROTEIN; FORKHEAD TRANSCRIPTION FACTOR; FOXC1 PROTEIN, HUMAN; FOXC1 PROTEIN, MOUSE; HOMEODOMAIN PROTEIN; NUCLEAR PROTEIN; PAIRED BOX TRANSCRIPTION FACTOR; REPRESSOR PROTEIN; TRANSCRIPTION FACTOR PAX6; TRANSCRIPTION FACTOR PITX2;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANTERIOR EYE SEGMENT; AUTOSOMAL DOMINANT INHERITANCE; BLINDNESS; CHROMOSOME 13Q; CHROMOSOME 16Q; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; DNA BINDING; EYE MALFORMATION; GENE FUNCTION; GENE IDENTIFICATION; GENE LOCUS; GENE MUTATION; GLAUCOMA; HUMAN; MOLECULAR CLONING; MOLECULAR GENETICS; MOUSE; NONHUMAN; NUCLEAR LOCALIZATION SIGNAL; ONTOGENY; PHENOTYPE; PRIORITY JOURNAL; PROTEIN DOMAIN; REVIEW; RIEGER SYNDROME; TRANSACTIVATION; ANIMAL; CONGENITAL MALFORMATION; GENETICS; METABOLISM; MULTIPLE MALFORMATION SYNDROME; NEURAL CREST; PRENATAL DEVELOPMENT;

ABNORMALITIES, MULTIPLE; ANIMAL; ANTERIOR EYE SEGMENT; HOMEODOMAIN PROTEINS; HUMAN; MICE; NEURAL CREST; SUPPORT, NON-U.S. GOV'T; TRANSCRIPTION FACTORS; ANIMALS; DNA-BINDING PROTEINS; EYE PROTEINS; FORKHEAD TRANSCRIPTION FACTORS; HUMANS; NUCLEAR PROTEINS; PAIRED BOX TRANSCRIPTION FACTORS; REPRESSOR PROTEINS;

ANIMALIA;

EID: 0037092595     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

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