Kif14 Mutation Causes Severe Brain Malformation and Hypomyelination

PLoS ONE

Volumn 8, Issue 1, 2013, Pages

  Fujikura, Kohei ^a   Setsu, Tomiyoshi ^a   Tanigaki, Kenji ^b   Abe, Takaya ^c   Kiyonari, Hiroshi ^c   Terashima, Toshio ^a   Sakisaka, Toshiaki ^a  

^a KOBE UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^b Shiga Medical Center   (Japan)

^c RIKEN Center for Biosystems Dynamics Research   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ASPARTOACYLASE; CLAUDIN 11; COMPLEMENTARY DNA; CYTOCHROME P450 4A1; G PROTEIN COUPLED RECEPTOR; GELSOLIN; GUANINE NUCLEOTIDE BINDING PROTEIN; MAMMALIAN TARGET OF RAPAMYCIN; MEMBRANE PROTEIN; MITOGEN ACTIVATED PROTEIN KINASE KINASE KINASE 4; MYELIN; MYELIN AND LYMPHOCYTE PROTEIN; MYELIN BASIC PROTEIN; MYELIN OLIGODENDROCYTE GLYCOPROTEIN; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE 1; OLIGODENDROCYTE TRANSCRIPTION FACTOR 2; PHOSPHATIDYLINOSITOL 3 KINASE; PROTEIN KINASE B; PROTEOLIPID PROTEIN; SMALL NUCLEAR RIBONUCLEOPROTEIN; SPHINGOMYELIN PHOSPHODIESTERASE; TRANSCRIPTION FACTOR POU4F2; TRANSCRIPTION FACTOR SOX;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; APOPTOSIS; ARTICLE; ATAXIA; BODY WEIGHT; BRAIN CORTEX; BRAIN MALFORMATION; BRAIN SIZE; BRAIN WEIGHT; CONTROLLED STUDY; CYTOARCHITECTURE; EXON SKIPPING; FEMALE; GENE; GENE FREQUENCY; GENE FUNCTION; GENE MUTATION; GENE SEQUENCE; HIPPOCAMPUS; HISTOPATHOLOGY; HYPOMYELINATION; KIF14 GENE; LAGGARD GENE; LOCOMOTION; MALE; MICROARRAY ANALYSIS; MOUSE; MYELIN SHEATH; MYELINATION; NICK END LABELING; NONHUMAN; NORTHERN BLOTTING; NUCLEOTIDE SEQUENCE; PHENOTYPE; PROMOTER REGION; SIGNAL TRANSDUCTION; SINGLE NUCLEOTIDE POLYMORPHISM; STOP CODON; TREMOR;

AMINO ACID TRANSPORT SYSTEMS, ACIDIC; ANIMALS; ANTIPORTERS; APOPTOSIS; BASE SEQUENCE; CEREBELLAR ATAXIA; CEREBELLUM; CEREBRAL CORTEX; FEMALE; GENETIC COMPLEMENTATION TEST; HEREDITARY CENTRAL NERVOUS SYSTEM DEMYELINATING DISEASES; KINESIN; MALE; MICE; MICE, TRANSGENIC; MITOCHONDRIAL DISEASES; MOLECULAR SEQUENCE DATA; MUTATION; MYELIN SHEATH; PHENOTYPE; PROTEIN ISOFORMS; PSYCHOMOTOR DISORDERS;

MAMMALIA; MUS;

EID: 84871855606     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0053490     Document Type: Article

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