Chromosome 13 dementia syndromes as models of neurodegeneration

Amyloid

Volumn 8, Issue 4, 2001, Pages 277-284

  Ghiso, J ^a   Revesz T ^a   Holton, J ^a   Rostagno, A ^a   Lashley, T ^a   Houlden, H ^a   Gibb, G ^a   Anderton, B ^a   Bek, T ^a   Bojsen Moller M ^a   Wood, N ^a   Vidal, R ^a   Braendgaard, H ^a   Plant, G ^a   Frangione, B ^a  

^a NEW YORK UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

ABri; ADan, familial British dementia; Amyloidosis; Familial Danish dementia; Neurofibrillary tangles; Perivascular lesions; Vascular amyloid

Indexed keywords

ALZHEIMER DISEASE; AMINO TERMINAL SEQUENCE; CELL DEATH; CENTRAL NERVOUS SYSTEM; CHROMOSOME 13; DENMARK; FAMILIAL DISEASE; GENETIC DISORDER; HUMAN; NERVE DEGENERATION; NEUROFIBRILLARY TANGLE; NEUROPATHOLOGY; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN PHOSPHORYLATION; REVIEW; SEQUENCE ANALYSIS; STOP CODON;

EID: 0035676453     PISSN: 13506129     EISSN: None     Source Type: Journal    
DOI: 10.3109/13506120108993826     Document Type: Review

References (23)

1. Nomenclature of amyloid fibril proteins
2. Cytokeratins in primary cutaneous amyloidosis
3. A stop-codon mutation in the BRI gene associated with familial British dementia
4. Medin: An integral fragment of aortic smooth muscle cell-produced lactadherin forms the most common human amyloid
5. A decamer duplication in the 3′ region of the BRI gene originates a new amyloid peptide that is associated with dementia in a Danish kindred
6. (110-131) peptides, and its relevance for lattice corneal amyloid dystrophy type 1
7. cDNA sequence analysis, chromosomal assignment and expression pattern of the gene coding for integral membrane protein 2B
8. Furin mediates enhanced production of fibrillogenic ABri peptides in familial British dementia
9. Mass spectrometry of purified amyloid beta protein in Alzheimer's disease
10. Amino- and carboxyl-terminal heterogeneity of beta-amyloid peptides deposited in human brain
11. N-terminal heterogeneity of parenchymal and cerebrovascular Aβ deposits
12. Amyloidogenesis in familial British dementia is associated with a genetic defect on chromosome 13
13. Familial presenile dementia with spastic paralysis
14. A form of familial presenile dementia with spastic paralysis (including the pathological examination of a case)
15. Congophilic angiopathy of the brain: A clinical and pathological report on two siblings
16. Familial cerebellar ataxia with cerebrovascular amyloid
17. Familial cerebral amyloid angiopathy with nonneuritic plaque formation
18. Familial British dementia with amyloid angiopathy: Early clinical, neuropsychological and imaging findings
19. Cytoskeletal pathology in familial cerebral amyloid angiopathy (British type) with non-neuritic plaque formation
20. Regional distribution of fibrillar and non-fibrillar ABri deposition and its association with neurofibrillary degeneration in familial British dementia
21. Heredopathia ophthalmo-oto-encephalica
22. Ocular changes in heredo-oto-ophtalmo-encephalopathy
23. Familial cerebral amyloid angiopathies