Keywords: Polygenic risk score; Sporadic late-onset Alzheimer's disease; Early-onset Alzheimer's disease; Early-onset autosomal dominant; Late-onset Alzheimer's disease; Dominantly inherited Alzheimer network; APOE; APP; PSEN1; PSEN2; Genetic architecture; Area und
مقالات ISI (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: PCA; Posterior Alzheimer's disease; Dementia; APOE; TREM2; PSEN2; NeuroX;
Keywords: Alzheimer's disease; PSEN1; PSEN2; APOE; Mutations; Ion sequencing technology;
Keywords: AD; Alzheimer's disease; Aβ; amyloid β; Aph-1; anterior pharynx defective 1; AP; adaptor protein; APOE; apolipoprotein E; APP; amyloid precursor protein; AICD; amyloid intracellular domain; BACE-1; β-secretase beta-site amyloid precursor protein-cleavi
Alzheimer's disease: How metal ions define β-amyloid function
Keywords: Aβ1â40; β-Amyloid, 40-residue isoform; Aβ1â42; β-Amyloid, 42-residue isoform; Aβ1â42/Aβ1â40; Ratio between levels of Aβ1â42 and Aβ1â40; ADAM; A Disintegrin And Metalloprotease, zinc peptidases, some being α-secretases; AICD; APP intra
Novel presenilin 1 mutation (Ile408Thr) in an Italian family with late-onset Alzheimer's disease
Keywords: DNA; Alzheimer's disease; PSEN1; PSEN2; APP;
Pilot whole-exome sequencing of a German early-onset Alzheimer's disease cohort reveals a substantial frequency of PSEN2 variants
Keywords: Early-onset dementia; Alzheimer's disease; Frontotemporal dementia; Volga German N141I; PSEN2; Exome sequencing;
Probable novel PSEN2 Pro123Leu mutation in a Chinese Han family of Alzheimer's disease
Keywords: Alzheimer's disease; PSEN2; P123L mutation; Positron emission tomography; ASL;
Epigenomics of Alzheimer's disease
Keywords: AD; Alzheimer's disease; APOE; apolipoprotein E; APP; amyloid precursor protein; BACE-1; beta-site APP-cleaving enzyme 1 gene; CG; cytosine-guanine dinucleotide; ChIP-Seq; chromatin immunoprecipitation-sequencing; CVD; cerebrovascular disease; GWAS; gen
A novel mutation in the PSEN2 gene (N141Y) associated with early-onset autosomal dominant Alzheimer's disease in a Chinese Han family
Keywords: Alzheimer's disease; PSEN2; APOE genotype; Chinese Han family; Target region sequencing; N141Y mutation;
Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's disease
Keywords: Alzheimer's disease; Neurodegenerative dementia; APP; PSEN1; PSEN2; MAPT; GRN; PRNP; Exome sequencing;
Exome sequencing identifies 2 novel presenilin 1 mutations (p.L166V and p.S230R) in British early-onset Alzheimer's disease
Keywords: Early-onset Alzheimer's disease; APP; PSEN1; PSEN2; British cohort;
Analysis of SNAP25 mRNA expression and promoter DNA methylation in brain areas of Alzheimer's Disease patients
Keywords: AD; Alzheimer's Disease; APOE; apolipoprotein E; APP; amyloid precursor protein; bp; base pair; CDR; clinical dementia rating; CT; cycle threshold; df; degrees of freedom; DSM-IV; IV Diagnostic and Statistical Manual of Mental Disorders; F; female; GLM;
Amyloid precursor protein (APP) processing genes and cerebrospinal fluid APP cleavage product levels in Alzheimer's disease
Keywords: APP; ADAM10; BACE1; BACE2; PSEN1; PSEN2; PEN2; NCSTN; APH1B; Alzheimer's; Cerebrospinal fluid;
Does the presenilin 2 gene predispose to schizophrenia?
Keywords: PSEN2; Schizophrenia; Case-control study; Gene expression; Clinical profiles
Review articleGenetics and dementia: Risk factors, diagnosis, and management
Keywords: Genetic counselling; Alzheimer's disease; Frontotemporal dementia; APOE; PSEN1; PSEN2; MAPT; PGRN;