Co-ordinating retinal histogenesis: Early cell cycle exit enhances early cell fate determination in the Xenopus retina

Development

Volumn 129, Issue 10, 2002, Pages 2435-2446

  Ohnuma, Shin Ichi ^a   Hopper, Susannah ^a   Wang, Kevin C ^a   Philpott, Anna ^a   Harris, William A ^a  

^a HARVARD MEDICAL SCHOOL   (United States)

Author keywords

Cell cycle regulation; Gliogenesis; Neurogenesis; Notch; Proneural gene; Xath5; Xenopus laevis

Indexed keywords

CYCLIN DEPENDENT KINASE INHIBITOR; CYCLIN E; HELIX LOOP HELIX PROTEIN; NOTCH RECEPTOR;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL ACTIVITY; CELL CYCLE; CELL FATE; CONTROLLED STUDY; HISTOGENESIS; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; RETINA DEVELOPMENT; RETINA GANGLION CELL; SENSORY NERVE CELL; XENOPUS;

ANIMALS; BASIC HELIX-LOOP-HELIX TRANSCRIPTION FACTORS; CELL CYCLE; CELL CYCLE PROTEINS; CYCLIN E; CYCLIN-DEPENDENT KINASE INHIBITOR P27; DROSOPHILA PROTEINS; EMBRYO, NONMAMMALIAN; EYE PROTEINS; FEMALE; GENE EXPRESSION REGULATION, DEVELOPMENTAL; MEMBRANE PROTEINS; NERVE TISSUE PROTEINS; NEUROGLIA; NEURONS; RECEPTORS, NOTCH; REPRESSOR PROTEINS; RETINA; TRANSCRIPTION FACTORS; TUMOR SUPPRESSOR PROTEINS; XENOPUS LAEVIS; XENOPUS PROTEINS;

ANIMALIA; VERTEBRATA; XENOPUS LAEVIS;

EID: 0036339911     PISSN: 09501991     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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