Mutational analysis in early-onset familial Alzheimer's disease in Mainland China-Reference-Cited by-同舟云学术

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Mutational analysis in early-onset familial Alzheimer's disease in Mainland China

Published:2014-08 Issue:8 Volume:35 Page:1957.e1-1957.e6
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Jiao Bin,Tang Beisha,Liu Xiaoyan,Xu Jun,Wang Yanjiang,Zhou Lin,Zhang Fufeng,Yan Xinxiang,Zhou Yafang,Shen Lu

Funder

National Basic Research Program

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Neurology (clinical),Aging,General Neuroscience

Reference29 articles.

1. Clinical features and APOE genotype of pathologically proven early-onset Alzheimer disease;Balasa;Neurology,2011

2. Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum;Campion;Am. J. Hum. Genet.,1999

3. Pathogenic APP mutations near the gamma-secretase cleavage site differentially affect Abeta secretion and APP C-terminal fragment stability;De Jonghe;Hum. Mol. Genet.,2001

4. Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS;DeJesus-Hernandez;Neuron,2011

5. Novel presenilin 1 mutations associated with early onset of dementia in a family with both early-onset and late-onset Alzheimer disease;Devi;Arch. Neurol.,2000

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1. Alzheimer-mutant γ-secretase complexes stall amyloid β-peptide production;2024-08-31

2. Revolutionizing Alzheimer's treatment: Harnessing human serum albumin for targeted drug delivery and therapy advancements;Ageing Research Reviews;2024-08

3. The presenilin 1 mutation P436S causes familial Alzheimer's disease with elevated Aβ43 and atypical clinical manifestations;Alzheimer's & Dementia;2024-06-02

4. Meta-analysis of the association between C9orf72 repeats and neurodegeneration diseases;Journal of Neurogenetics;2024-01-02

5. The presenilin 1 mutation P436S causes familial Alzheimer’s disease with elevated Aβ43 and atypical clinical manifestations;2023-12-06

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