Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type.
about
A decamer duplication in the 3' region of the BRI gene originates an amyloid peptide that is associated with dementia in a Danish kindredGenetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathiesFurin initiates gelsolin familial amyloidosis in the Golgi through a defect in Ca(2+) stabilizationMetalloendoprotease cleavage triggers gelsolin amyloidogenesisCutis laxa in hereditary gelsolin amyloidosis.Transthyretin Tyr77 familial amyloid polyneuropathy: a clinicopathological study of a large kindred.Degradation of proteins in the membrane-cytoskeleton complex in Alzheimer's disease. Might amyloidogenic APP processing be just the tip of the iceberg?Exclusion of the gelsolin gene on 9q32-34 as the cause of familial lattice corneal dystrophy type I.Lewy bodies are immunoreactive with antibodies raised to gelsolin related amyloid-Finnish type.Cerebral amyloidosis: amyloid subunits, mutants and phenotypes.Alzheimer's disease from the perspective of the systemic and localized forms of amyloidosis.Immunohistochemical analysis of lattice corneal dystrophies types I and II.Transgenic analysis of the anterior eye-specific enhancers of the zebrafish gelsolin-like 1 (gsnl1) gene.AAV9 delivered bispecific nanobody attenuates amyloid burden in the gelsolin amyloidosis mouse model.Unifying features of systemic and cerebral amyloidosis.Familial amyloid polyneuropathy.Peripheral nerve amyloidosis.Inherited amyloid polyneuropathy type IV (gelsolin variant) in a Japanese family.A 109-amino-acid C-terminal fragment of Alzheimer's-disease amyloid precursor protein contains a sequence, -RHDS-, that promotes cell adhesion.Renal Amyloidosis Associated With 5 Novel Variants in the Fibrinogen A Alpha Chain Protein.Familial amyloid polyneuropathy (Finnish type) presenting multiple cranial nerve deficits with carpal tunnel syndrome and orthostatic hypotension.Cells of the neuronal lineage play a major role in the generation of amyloid precursor fragments in gelsolin-related amyloidosis.Clinical characteristics and SAP scintigraphic findings in 10 patients with AGel amyloidosis.Functional consequences of amyloidosis mutation for gelsolin polypeptide -- analysis of gelsolin-actin interaction and gelsolin processing in gelsolin knock-out fibroblasts.Gelsolin-related familial amyloidosis, Finnish type, in a Portuguese family: clinical and neurophysiological studiesGelsolin–derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187CNS abnormalities in patients with familial amyloidosis, Finnish type (FAF)
P2860
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P2860
Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type.
description
1990 nî lūn-bûn
@nan
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
1990年论文
@zh
1990年论文
@zh-cn
name
Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type.
@en
type
label
Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type.
@en
prefLabel
Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type.
@en
P2093
P2860
P356
P1433
P1476
Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type.
@en
P2093
P2860
P304
P356
10.1042/BJ2720827
P407
P577
1990-12-01T00:00:00Z