'Forkhead' gene expression balanced on a knife-edge

Trends in Molecular Medicine

Volumn 7, Issue 2, 2000, Pages 51-

  Caplen, Natasha ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; PROTEIN VEGFR3; TRANSCRIPTION FACTOR FOXC1; TRANSCRIPTION FACTOR FOXC2; UNCLASSIFIED DRUG;

GENE DUPLICATION; GENE EXPRESSION; GENE MUTATION; GLAUCOMA; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN CELL; HUMAN TISSUE; LYMPHEDEMA; NOTE; TRANSCRIPTION REGULATION;

ANIMALS; DNA-BINDING PROTEINS; FORKHEAD TRANSCRIPTION FACTORS; GLAUCOMA; HETEROZYGOTE; HUMANS; LINKAGE (GENETICS); LYMPHEDEMA; MICE; MUTATION; NUCLEAR PROTEINS; PHENOTYPE; TRANSCRIPTION FACTORS;

EID: 0034472978     PISSN: 14714914     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Note

References (2)

1. Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma
2. Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome