A mouse model of heritable cerebrovascular disease

PLoS ONE

Volumn 5, Issue 12, 2010, Pages

  Sproule, Thomas J ^a   Sled, John G ^b   Wentzell, Jill ^a   Wang, Bing ^a   Henkelman, R Mark ^b   Roopenian, Derry C ^a   Burgess, Robert W ^a  

^a JACKSON LABORATORY   (United States)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; ASTEROID HOMOLOG 1; GLIAL FIBRILLARY ACIDIC PROTEIN; MICRORNA; MITOCHONDRIAL RNA; NEVER IN MITOSIS GENE A; NUCLEOTIDE DIPHOSPHATE LINKED MOIETY X TYPE MOTIF 16; NUDIX HYDROLASE; RIBOSOME PROTEIN L3; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; ASTROCYTE; BODY WEIGHT; BRAIN BLOOD VESSEL; BRAIN ISCHEMIA; CEREBROVASCULAR DISEASE; CHROMOSOME 3Q; CHROMOSOME 9; CONTROLLED STUDY; FEMALE; GENE LOCUS; GENETIC DISTANCE; HERITABILITY; HISTOPATHOLOGY; HOMOZYGOSITY; MOUSE; MOUSE MUTANT; NERVE DEGENERATION; NONHUMAN; PHENOTYPE; PROTEIN EXPRESSION; SYNTENY; ANIMAL; CHROMOSOME MAP; COMPUTER ASSISTED TOMOGRAPHY; CONFOCAL MICROSCOPY; DISEASE MODEL; GENETIC RECOMBINATION; GENETICS; HOMOZYGOTE; HUMAN; IMMUNOHISTOCHEMISTRY; METHODOLOGY; MOLECULAR GENETICS; MUTATION; NUCLEOTIDE SEQUENCE; PATHOLOGY;

ANIMALIA; MUS;

ANIMALS; BASE SEQUENCE; CEREBROVASCULAR DISORDERS; CHROMOSOME MAPPING; DISEASE MODELS, ANIMAL; HOMOZYGOTE; HUMANS; IMMUNOHISTOCHEMISTRY; MICE; MICROSCOPY, CONFOCAL; MOLECULAR SEQUENCE DATA; MUTATION; RECOMBINATION, GENETIC; TOMOGRAPHY, X-RAY COMPUTED;

EID: 79251476543     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0015327     Document Type: Article

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