The early phenotype associated with the jimpy mutation of the proteolipid protein gene

Journal of Neurocytology

Volumn 28, Issue 3, 1999, Pages 207-221

  Thomson, C E ^a   Anderson, T J ^a   McCulloch, M C ^a   Dickinson, P ^a   Vouyiouklis, D A ^a   Griffiths, I R ^a  

^a UNIVERSITY OF GLASGOW   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; GLYCOPROTEIN; PROTEOLIPID;

ANIMAL CELL; ARTICLE; ASTROCYTOSIS; CELL DENSITY; CERVICAL SPINAL CORD; GENE EXPRESSION; GENE MUTATION; GLIA CELL; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; MALE; MOUSE; MYELIN DEFICIENCY; MYELINATION; NONHUMAN; OLIGODENDROGLIA; PHENOTYPE; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;

AGE FACTORS; ANIMALS; APOPTOSIS; ASTROCYTES; BIOLOGICAL MARKERS; CELL COUNT; CELL DIFFERENTIATION; CELLS, CULTURED; DEMYELINATING DISEASES; IN SITU HYBRIDIZATION; MALE; MICE; MICE, INBRED C3H; MICE, JIMPY; MICROSCOPY, ELECTRON; MYELIN PROTEOLIPID PROTEIN; MYELIN SHEATH; NERVE TISSUE PROTEINS; OLIGODENDROGLIA; PHENOTYPE; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SPINAL CORD; X CHROMOSOME;

ANIMALIA; RODENTIA;

EID: 0033499833     PISSN: 03004864     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1007024022663     Document Type: Article

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