Early onset familial Alzheimer's disease: Mutation frequency in 31 families.
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Genetics and phenotyping of urological chronic pelvic pain syndromeGenome-wide association studies in Alzheimer's diseaseTowards understanding the roles of heparan sulfate proteoglycans in Alzheimer's diseaseMutations, associated with early-onset Alzheimer's disease, discovered in Asian countriesClinical phenotypic heterogeneity of Alzheimer's disease associated with mutations of the presenilin-1 geneGenetic variants in Alzheimer disease - molecular and brain network approachesMolecular genetics and antisocial behavior: where do we stand?Creation of an open-access, mutation-defined fibroblast resource for neurological disease research.The presenilin 1 P264L mutation presenting as non-fluent/agrammatic primary progressive aphasia.The common dementias: a pictorial review.Aberrant amyloid precursor protein (APP) processing in hereditary forms of Alzheimer disease caused by APP familial Alzheimer disease mutations can be rescued by mutations in the APP GxxxG motif.The turn formation at positions 22 and 23 in the 42-mer amyloid beta peptide: the emerging role in the pathogenesis of Alzheimer's disease.Metals and cholesterol: two sides of the same coin in Alzheimer's disease pathology.Dissecting the Molecular Mechanisms of Neurodegenerative Diseases through Network BiologyIowa variant of familial Alzheimer's disease: accumulation of posttranslationally modified AbetaD23N in parenchymal and cerebrovascular amyloid depositsIntrinsic determinants of neurotoxic aggregate formation by the amyloid beta peptideInsensitivity of visual assessment of hippocampal atrophy in familial Alzheimer's diseaseOrdered-subsets linkage analysis detects novel Alzheimer disease loci on chromosomes 2q34 and 15q22.Effects of the English (H6R) and Tottori (D7N) familial Alzheimer disease mutations on amyloid beta-protein assembly and toxicity.Reexamining Alzheimer's disease: evidence for a protective role for amyloid-beta protein precursor and amyloid-betaPositive evolutionary selection of an HD motif on Alzheimer precursor protein orthologues suggests a functional role.The diagnosis of young-onset dementia.Modeling amyloid beta-peptide insertion into lipid bilayersMitochondrial genomic analysis of late onset Alzheimer's disease reveals protective haplogroups H6A1A/H6A1B: the Cache County Study on Memory in AgingInvestigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's disease.Genetics of Alzheimer diseaseGenetics of Alzheimer's disease: a centennial reviewDistinct effects of Zn2+, Cu2+, Fe3+, and Al3+ on amyloid-beta stability, oligomerization, and aggregation: amyloid-beta destabilization promotes annular protofibril formationYoung onset dementiaCortical and hippocampal atrophy in patients with autosomal dominant familial Alzheimer's disease.Amyloidosis associated with cerebral amyloid angiopathy: cell signaling pathways elicited in cerebral endothelial cells.Genetic counseling and testing for Alzheimer disease: joint practice guidelines of the American College of Medical Genetics and the National Society of Genetic CounselorsAlzheimer's disease: a clinical practice-oriented review.Biomarkers of neurodegenerative disorders: how good are they?Cerebral amyloidosis: amyloid subunits, mutants and phenotypes.Comparison of clinical characteristics between familial and non-familial early onset Alzheimer's disease.Genetics, transcriptomics, and proteomics of Alzheimer's diseaseConformation-dependent oligomers in cerebrospinal fluid of presymptomatic familial Alzheimer's disease mutation carriers.The structures of the E22Δ mutant-type amyloid-β alloforms and the impact of E22Δ mutation on the structures of the wild-type amyloid-β alloforms.Mutation-based structural modification and dynamics study of amyloid beta peptide (1-42): An in-silico-based analysis to cognize the mechanism of aggregation.
P2860
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P2860
Early onset familial Alzheimer's disease: Mutation frequency in 31 families.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
2003年學術文章
@zh
2003年學術文章
@zh-hant
name
Early onset familial Alzheimer's disease: Mutation frequency in 31 families.
@en
Early onset familial Alzheimer's disease: Mutation frequency in 31 families.
@nl
type
label
Early onset familial Alzheimer's disease: Mutation frequency in 31 families.
@en
Early onset familial Alzheimer's disease: Mutation frequency in 31 families.
@nl
prefLabel
Early onset familial Alzheimer's disease: Mutation frequency in 31 families.
@en
Early onset familial Alzheimer's disease: Mutation frequency in 31 families.
@nl
P2093
P1433
P1476
Early onset familial Alzheimer's disease: Mutation frequency in 31 families
@en
P2093
A Dickinson
J C Janssen
J Collinge
R J Harvey
T A Campbell
P304
P356
10.1212/01.WNL.0000042088.22694.E3
P407
P577
2003-01-01T00:00:00Z