The Gli3 hypomorphic mutation Pdn causes selective impairment in the growth, patterning, and axon guidance capability of the lateral ganglionic eminence

Journal of Neuroscience

Volumn 30, Issue 41, 2010, Pages 13883-13894

  Magnani, Dario ^a   Hasenpusch Theil, Kerstin ^a   Jacobs, Erin C ^b   Campagnoni, Anthony T ^b   Price, David J ^a   Theil, Thomas ^a  

^a UNIVERSITY OF EDINBURGH   (United Kingdom)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

NERVE PROTEIN; PROTEIN POLYDACTYLY NAGOYA; SONIC HEDGEHOG PROTEIN; TRANSCRIPTION FACTOR GLI3; UNCLASSIFIED DRUG; GLI3 PROTEIN, MOUSE; KRUPPEL LIKE FACTOR;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; GANGLION; GENE MUTATION; LATERAL GANGLION EMINENCE; MOUSE; NERVE CELL GROWTH; NERVE FIBER; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; THALAMOCORTICAL TRACT; UPREGULATION; ANIMAL; GENETICS; GROWTH, DEVELOPMENT AND AGING; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; METABOLISM; MORPHOGENESIS; NERVE CELL; PHYSIOLOGY; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; TELENCEPHALON; TRANSGENIC MOUSE; WESTERN BLOTTING;

ANIMALS; AXONS; BLOTTING, WESTERN; BODY PATTERNING; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; KRUPPEL-LIKE TRANSCRIPTION FACTORS; MICE; MICE, TRANSGENIC; NERVE TISSUE PROTEINS; NEURONS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; TELENCEPHALON;

EID: 77958058043     PISSN: 02706474     EISSN: 15292401     Source Type: Journal    
DOI: 10.1523/JNEUROSCI.3650-10.2010     Document Type: Article

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