Familial meningocerebrovascular amyloidosis, Hungarian type, with mutant transthyretin (TTR Asp18Gly)
about
Transthyretin and the brain re-visited: is neuronal synthesis of transthyretin protective in Alzheimer's disease?Human-murine transthyretin heterotetramers are kinetically stable and non-amyloidogenic. A lesson in the generation of transgenic models of diseases involving oligomeric proteinsEndoplasmic reticulum quality control and systemic amyloid disease: Impacting protein stability from the inside outEffects of chronic stress on prefrontal cortex transcriptome in mice displaying different genetic backgroundsOculoleptomeningeal Amyloidosis associated with transthyretin Leu12Pro in an African patient.Cerebral amyloidosis: amyloid subunits, mutants and phenotypes.Cerebral amyloid angiopathy and its relationship to Alzheimer's disease.Current and future treatment of amyloid diseases.APP Mutations in Cerebral Amyloid Angiopathy with or without Cortical Calcifications: Report of Three Families and a Literature Review.Liver transplantation as treatment for neurological disorders.Postmortem findings in a familial amyloid polyneuropathy patient with homozygosity of the mutant Val30Met transthyretin gene.Coexistence of familial transthyretin amyloidosis ATTR Val30Met and spinocerebellar ataxia type 1 in a Japanese family--a follow-up autopsy report.Cutaneous lymphatic amyloid deposits in "Hungarian-type" familial transthyretin amyloidosis: a case report.Unfolding and aggregation of transthyretin by the truncation of 50 N-terminal amino acids.Age-dependent cognitive dysfunction in untreated hereditary transthyretin amyloidosis.Suppression of choroid plexus transthyretin levels by antisense oligonucleotide treatment.A case of biopsy-proven leptomeningeal amyloidosis and intravenous Ig-responsive polyneuropathy associated with the Ala25Thr transthyretin gene mutation.Extended phenotype in the transthyretin Tyr77 familial amyloid polyneuropathy.FRET studies of various conformational states adopted by transthyretin.
P2860
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P2860
Familial meningocerebrovascular amyloidosis, Hungarian type, with mutant transthyretin (TTR Asp18Gly)
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年学术文章
@wuu
1996年学术文章
@zh
1996年学术文章
@zh-cn
1996年学术文章
@zh-hans
1996年学术文章
@zh-my
1996年学术文章
@zh-sg
1996年學術文章
@yue
1996年學術文章
@zh-hant
name
Familial meningocerebrovascula ...... t transthyretin (TTR Asp18Gly)
@en
Familial meningocerebrovascula ...... t transthyretin (TTR Asp18Gly)
@nl
type
label
Familial meningocerebrovascula ...... t transthyretin (TTR Asp18Gly)
@en
Familial meningocerebrovascula ...... t transthyretin (TTR Asp18Gly)
@nl
prefLabel
Familial meningocerebrovascula ...... t transthyretin (TTR Asp18Gly)
@en
Familial meningocerebrovascula ...... t transthyretin (TTR Asp18Gly)
@nl
P2093
P356
P1433
P1476
Familial meningocerebrovascula ...... t transthyretin (TTR Asp18Gly)
@en
P2093
P304
P356
10.1212/WNL.47.6.1562
P407
P577
1996-12-01T00:00:00Z