The T-box gene tbx-2, the homeobox gene egl-5 and the asymmetric cell division gene ham-1 specify neural fate in the HSN/PHB lineage

Genetics

Volumn 179, Issue 2, 2008, Pages 887-898

  Singhvi, Aakanksha ^a   Frank, C Andrew ^a,b   Garriga, Gian ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CELL CYCLE PROTEIN; CELL CYCLE PROTEIN HAM1; HOX PROTEIN; T BOX TRANSCRIPTION FACTOR; T BOX TRANSCRIPTION FACTOR TBX2; UNCLASSIFIED DRUG; CAENORHABDITIS ELEGANS PROTEIN; EGL 5 PROTEIN, C ELEGANS; EGL-5 PROTEIN, C ELEGANS; GREEN FLUORESCENT PROTEIN; HAM 1 PROTEIN, C ELEGANS; HAM-1 PROTEIN, C ELEGANS; HOMEODOMAIN PROTEIN; NERVE PROTEIN; RECOMBINANT PROTEIN; T BOX DOMAIN PROTEIN 2; T-BOX DOMAIN PROTEIN 2; TRANSCRIPTION FACTOR;

APOPTOSIS; ARTICLE; BRAIN CORTEX; CAENORHABDITIS ELEGANS; CELL DIFFERENTIATION; CELL DIVISION; CELL FATE; CELL LINEAGE; CELL MIGRATION; CONTROLLED STUDY; EGL5 GENE; GENE; GENE EXPRESSION; GENE FUNCTION; GENE INTERACTION; GENE MUTATION; GROWTH REGULATION; HOMEOBOX; NERVE CELL; NEURAL STEM CELL; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; TRANSGENE; AMINO ACID SEQUENCE; ANIMAL; BIOLOGICAL MODEL; CYTOLOGY; FEMALE; GENETIC COMPLEMENTATION; GENETIC EPISTASIS; GENETICS; MALE; MOTONEURON; MUTATION; PRENATAL DEVELOPMENT; SENSORY NERVE CELL; SEQUENCE HOMOLOGY; TRANSGENIC ANIMAL;

CAENORHABDITIS ELEGANS;

AMINO ACID SEQUENCE; ANIMALS; ANIMALS, GENETICALLY MODIFIED; APOPTOSIS; CAENORHABDITIS ELEGANS; CAENORHABDITIS ELEGANS PROTEINS; CELL DIFFERENTIATION; CELL DIVISION; EPISTASIS, GENETIC; FEMALE; GENES, HELMINTH; GENES, HOMEOBOX; GENETIC COMPLEMENTATION TEST; GREEN FLUORESCENT PROTEINS; HOMEODOMAIN PROTEINS; MALE; MODELS, GENETIC; MODELS, NEUROLOGICAL; MOTOR NEURONS; MUTATION; NERVE TISSUE PROTEINS; NEURONS, AFFERENT; RECOMBINANT PROTEINS; SEQUENCE HOMOLOGY, AMINO ACID; T-BOX DOMAIN PROTEINS; TRANSCRIPTION FACTORS;

EID: 49849099147     PISSN: 00166731     EISSN: 00166731     Source Type: Journal    
DOI: 10.1534/genetics.108.088948     Document Type: Article

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