Loss of adenomatous polyposis coli in Bergmann glia disrupts their unique architecture and leads to cell nonautonomous neurodegeneration of cerebellar Purkinje neurons

GLIA

Volumn 59, Issue 6, 2011, Pages 857-868

  Wang, Xiaohong ^a   Imura, Tetsuya ^a   Sofroniew, Michael V ^b   Fushiki, Shinji ^a  

^a KYOTO PREFECTURAL UNIVERSITY OF MEDICINE   (Japan)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Astrocytes; Ataxia; Beta catenin; Glial fibrillary acid protein; Wnt

Indexed keywords

APC PROTEIN; BETA CATENIN; GLIAL FIBRILLARY ACIDIC PROTEIN;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; ASTROCYTE; ATAXIA; BERGMANN GLIA LAYER; CEREBELLUM ATROPHY; CEREBELLUM CORTEX; CONTROLLED STUDY; GLIA; MOTOR COORDINATION; MOUSE; NONHUMAN; PERIKARYON; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PURKINJE CELL;

ADENOMATOUS POLYPOSIS COLI PROTEIN; ANIMALS; CEREBELLAR DISEASES; CEREBELLUM; DISEASE MODELS, ANIMAL; GENETIC PREDISPOSITION TO DISEASE; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; MICE, TRANSGENIC; NERVE DEGENERATION; NEUROGLIA; PURKINJE CELLS;

EID: 79954581516     PISSN: 08941491     EISSN: 10981136     Source Type: Journal    
DOI: 10.1002/glia.21154     Document Type: Article

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