Loss of Fyn tyrosine kinase on the C57BL/6 genetic background causes hydrocephalus with defects in oligodendrocyte development

Molecular and Cellular Neuroscience

Volumn 38, Issue 2, 2008, Pages 203-212

  Goto, June ^a   Tezuka, Tohru ^a   Nakazawa, Takanobu ^a   Sagara, Hiroshi ^b   Yamamoto, Tadashi ^a  

^a THE UNIVERSITY OF TOKYO   (Japan)

^b UNIVERSITY OF TOKYO   (Japan)

Author keywords

Axonal degeneration; Cortical development; Fyn; Oligodendrocyte

Indexed keywords

PROTEIN KINASE FYN;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BACKCROSSING; BRAIN CORTEX; BRAIN DEVELOPMENT; CELL MATURATION; CELL STRUCTURE; CONTROLLED STUDY; CORPUS CALLOSUM; HISTOPATHOLOGY; HYDROCEPHALUS; LATERAL BRAIN VENTRICLE; MORPHOGENESIS; MOUSE; MYELINATION; NERVE FIBER DEGENERATION; NONHUMAN; OLIGODENDROGLIA; PATHOGENESIS; PERINATAL PERIOD; PRIORITY JOURNAL; PROTEIN DEFICIENCY; PROTEIN DEPLETION;

ANIMALS; ANIMALS, NEWBORN; AXONS; CELL COMMUNICATION; CEREBRAL CORTEX; CEREBRAL VENTRICLES; GLIOSIS; HYDROCEPHALUS; LAC OPERON; MICE; MICE, INBRED C57BL; MICE, MUTANT STRAINS; MYELIN SHEATH; NERVE DEGENERATION; OLIGODENDROGLIA; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; SEVERITY OF ILLNESS INDEX; SRC-FAMILY KINASES;

MUS;

EID: 44749088016     PISSN: 10447431     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mcn.2008.02.009     Document Type: Article

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