| 1 | APP, HCHWAD
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| A novel AbetaPP mutation exclusively associated with cerebral amyloid angiopathy.
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| Obici L, Demarchi A, de Rosa G, Bellotti V, Marciano S, Donadei S, Arbustini E, Palladini G, Diegoli M, Genovese E, Ferrari G, Coverlizza S, Merlini G.
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| Ann Neurol 58(4):639-44.
2005
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| 2 | APP, HCHWAD
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| Abeta is targeted to the vasculature in a mouse model of hereditary cerebral hemorrhage with amyloidosis.
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| Herzig MC, Winkler DT, Burgermeister P, Pfeifer M, Kohler E, Schmidt SD, Danner S, Abramowski D, Stürchler-Pierrat C, Bürki K, van Duinen SG, Maat-Schieman ML, Staufenbiel M, Mathews PM, Jucker M.
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| Nat Neurosci 7(9):954-60. Epub 2004 Aug 15.
2004
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| 3 | APP, HCHWAD
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| Dementia in hereditary cerebral hemorrhage with amyloidosis-Dutch type is associated with cerebral amyloid angiopathy but is independent of plaques and neurofibrillary tangles.
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| Natté R, Maat-Schieman ML, Haan J, Bornebroek M, Roos RA, van Duinen SG.
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| Ann Neurol 50(6):765-72.
2001
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| 4 | HCHWAD
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| Effects of the amyloid precursor protein Glu693-->Gln 'Dutch' mutation on the production and stability of amyloid beta-protein.
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| Watson DJ, et al.
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| Biochem J 340 ( Pt 3):703-9. 1999
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| 5 | APP, HCHWAD
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| The upstream promoter of the beta-amyloid precursor protein gene (APP) shows differential patterns of methylation in human brain.
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| Rogaev EI, et al.
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| Genomics 22 : 340-347. 1994
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| 6 | APP, HCHWAD
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| Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type.
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| Levy E, Carman MD, Fernandez-Madrid IJ, Power MD, Lieberburg I, van Duinen SG, Bots GT, Luyendijk W, Frangione B.
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| Science 248(4959):1124-6.
1990
|