Cerebral amyloid angiopathy and parenchymal amyloid deposition in transgenic mice expressing the Danish mutant form of human BRI2

Brain Pathology

Volumn 19, Issue 1, 2009, Pages 58-68

  Vidal, Ruben ^a   Barbeito, Ana G ^a   Miravalle, Leticia ^a   Ghetti, Bernardino ^a  

^a INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

AD; Amyloid; CAA; FBD; FDD; Neurodegeneration

Indexed keywords

AMINO ACID; OLIGOMER; PRION PROTEIN; PROTEIN PRECURSOR;

ALZHEIMER DISEASE; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRI2 GENE; CATARACT; CEREBELLAR ATAXIA; CONTROLLED STUDY; DEGENERATIVE DISEASE; DEMENTIA; EMBRYO; FAMILIAL DANISH DEMENTIA; GAIT; GENE; GENE EXPRESSION; GENE INSERTION; GLIOSIS; GROOMING; HEARING IMPAIRMENT; INFLAMMATION; MOUSE; MUTANT; NEUROFIBRILLARY TANGLE; NEUROPATHOLOGY; NONHUMAN; PATHOGENESIS; PRNP GENE; PROMOTER REGION; TRANSGENIC MOUSE; VASCULAR AMYLOIDOSIS;

AGE FACTORS; AMYLOID BETA-PROTEIN; ANIMALS; BLOTTING, WESTERN; BRAIN; CEREBRAL AMYLOID ANGIOPATHY; DEMENTIA; DENMARK; DISEASE MODELS, ANIMAL; GENE EXPRESSION; GROOMING; HUMANS; IMMUNOHISTOCHEMISTRY; MEMBRANE PROTEINS; MICE; MICE, INBRED C57BL; MICE, TRANSGENIC; MUTATION; POLYMERASE CHAIN REACTION; PRIONS; WALKING;

EID: 57449090951     PISSN: 10156305     EISSN: 17503639     Source Type: Journal    
DOI: 10.1111/j.1750-3639.2008.00164.x     Document Type: Article

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