Widespread defects in the primary olfactory pathway caused by loss of Mash1 function

Journal of Neuroscience

Volumn 23, Issue 5, 2003, Pages 1769-1780

  Murray, Richard C ^a   Navi, Daniel ^a   Fesenko, John ^a   Lander, Arthur D ^a   Calof, Anne L ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

BHLH transcription factor; Granule cell; Lineage; Neural progenitor; Olfactory bulb; Olfactory epithelium; Olfactory receptor neuron; Rostral migratory stream; Subventricular zone; Supporting cell; Transgenic mouse; Vomeronasal organ

Indexed keywords

BIOLOGICAL MARKER; TAU PROTEIN; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR MASH1; UNCLASSIFIED DRUG;

ALLELE; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL COUNT; CELL DEATH; CELL FATE; CELL PROLIFERATION; CELL SUBPOPULATION; CELL TYPE; CENTRAL NERVOUS SYSTEM; CONTROLLED STUDY; EMBRYO; FEMALE; GLIA CELL; INTERNEURON; MORPHOLOGY; NERVE CELL; NERVE FIBER; NERVOUS SYSTEM DEVELOPMENT; NONHUMAN; NUCLEOTIDE SEQUENCE; OLFACTORY BULB; OLFACTORY EPITHELIUM; OLFACTORY NERVE DISEASE; OLFACTORY RECEPTOR; OLFACTORY SYSTEM; PERIPHERAL NERVOUS SYSTEM; PRIORITY JOURNAL; PROTEIN DETERMINATION; PROTEIN EXPRESSION; PROTEIN FUNCTION; QUANTITATIVE ANALYSIS; REGULATORY MECHANISM; REPORTER GENE; SENSORY NERVE; STEM CELL; TRANSGENIC MOUSE; VOMERONASAL ORGAN;

EID: 0037338154     PISSN: 02706474     EISSN: None     Source Type: Journal    
DOI: 10.1523/jneurosci.23-05-01769.2003     Document Type: Article

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