Severe disturbance in the Ca2+ signaling in astrocytes from mouse models of human infantile neuroaxonal dystrophy with mutated Pla2g6

Human Molecular Genetics

Volumn 21, Issue 12, 2012, Pages 2807-2814

  Strokin, Mikhail ^a   Seburn, Kevin L ^b   Cox, Gregory A ^b   Martens, Kimberly A ^b   Reiser, Georg ^a  

^a OTTO VON GUERICKE UNIVERSITY   (Germany)

^b JACKSON LABORATORY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATE; CALCIUM; PHOSPHOLIPASE A2 GROUP VI; PLA2G6 PROTEIN, HUMAN; PLA2G6 PROTEIN, MOUSE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; ASTROCYTE; CONTROLLED STUDY; FEMALE; GENE MUTATION; MALE; MOUSE; MOUSE MUTANT; MOUSE STRAIN; NEUROAXONAL DYSTROPHY; NONHUMAN; PATHOLOGY; POINT MUTATION; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; WILD TYPE; ANIMAL; C3H MOUSE; CALCIUM SIGNALING; CELL CULTURE; DISEASE MODEL; DRUG EFFECT; GENE EXPRESSION; GENETICS; GENOTYPE; HUMAN; METABOLISM; MUTATION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;

MUS;

ADENOSINE TRIPHOSPHATE; ANIMALS; ASTROCYTES; CALCIUM; CALCIUM SIGNALING; CELLS, CULTURED; DISEASE MODELS, ANIMAL; GENE EXPRESSION; GENOTYPE; GROUP VI PHOSPHOLIPASES A2; HUMANS; MICE; MICE, INBRED C3H; MICE, KNOCKOUT; MUTATION; NEUROAXONAL DYSTROPHIES; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION;

EID: 84861737424     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/dds108     Document Type: Article

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