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迟发型阿兹海默病
迟发型阿兹海默病
发起讨论
迟发型阿兹海默病
40 个讨论
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老年痴呆症有救了？
能睡的CHST8基因
• 最后回复
WeGene_A48B8FF1
•
2024-05-20 22:55
1026
3
• 来自相关小组
有比我高的嘛？瑟瑟发抖！
名字刚好柒个字
• 最后回复
tia0804
•
2022-12-23 16:17
5355
20
• 来自相关小组
APOE基因型为ε1/ε4
ensomomo
• 最后回复
Scar2005
•
2022-09-15 22:52
4037
9
• 来自相关小组
今天是阿兹海默日
拍球的NTRK2基因
• 最后回复
摩羯的PDE1C基因
•
2022-08-29 23:15
2720
6
• 来自相关小组
有没有人觉得用脑过度才会阿兹海默的
洋气的ROBO1基因
• 最后回复
大灰狼
•
2022-08-29 12:02
2939
4
• 来自相关小组
如果有一天父母患上“老年痴呆”，你会怎么做？
lily
• 最后回复
west
•
2022-07-16 15:45
4503
5
• 来自相关小组
如何获得到携带有阿尔兹海默症风险基因的人但没有认知障碍的人的数据？
SevenSee
• 最后回复
an15001864256
•
2021-03-14 09:04
2215
1
• 来自相关小组
提前开始40Hz起来
Vacual
• 最后回复
zhengqiang
•
2020-08-18 09:55
2667
3
• 来自相关小组
TED演讲：跟老年痴呆说再见
费力科思
• 最后回复
chinallly
•
2020-03-30 22:19
4928
13
• 来自相关小组
阿兹海默症或可提前预测
无邪的KDM5D基因
• 最后回复
爽朗的FGF12基因
•
2019-08-29 15:24
2514
3
• 来自相关小组
爷爷的哥哥有阿兹海默
勤奋的ABCA1基因
• 最后回复
健壮的CHST8基因
•
2019-08-14 23:40
2659
2
• 来自相关小组
验血或可检测阿兹海默症 听说准确率达88%
欢快的CFTR基因
• 最后回复
欢快的CFTR基因
•
2019-08-13 15:13
3048
2
• 来自相关小组
有比我还高的嘛？
shi123yue123
• 最后回复
彷徨的ABCC1基因
•
2019-08-05 14:51
5829
17
• 来自相关小组
看看阿兹海默
Jpayne
• 最后回复
大灰狼
•
2019-05-06 20:04
3291
10
• 来自相关小组
家人已发病，且阿兹海默高风险的朋友可以来说下数值嘛？
生气的SAMD5基因
• 最后回复
an15001864256
•
2019-02-21 16:54
3249
5
• 来自相关小组
APOE基因型为ε2/ε2
朱先锋
• 最后回复
费力科思
•
2019-02-21 14:29
4610
5
• 来自相关小组
发起讨论
迟发型阿兹海默病
40 个讨论
相关基因
SLC24A4
位点：RS10498633
CELF1
位点：RS10838725
CD2AP
位点：RS10948363
SORL1
位点：RS11218343
位点：RS11218350
位点：RS1699103
位点：RS1784931
位点：RS1792113
位点：RS726601
EPHA1-AS1
位点：RS11771145
PLD3
位点：RS145999145
ZCWPW1
位点：RS1476679
FERMT2
位点：RS17125944
MEF2C-AS1
位点：RS190982
PTK2B
位点：RS28834970
PSEN2
位点：RS28936379
位点：RS63750048
INPP5D
位点：RS35349669
APOE
位点：RS429358
位点：RS7412
GRN
位点：RS5848
CETP
位点：RS5882
PSEN1
位点：RS63749824
位点：RS63749885
位点：RS63749891
位点：RS63750218
位点：RS63750526
位点：RS63750577
位点：RS63750590
位点：RS63750599
位点：RS63750815
位点：RS63750886
位点：RS63750900
位点：RS63751037
位点：RS63751141
位点：RS63751144
位点：RS63751163
位点：RS63751223
位点：RS63751229
位点：RS63751235
位点：RS63751320
CR1
位点：RS6656401
DISC1
位点：RS6675281
GAB2
位点：RS7101429
CASS4
位点：RS7274581
TREM2
位点：RS75932628
位点：RS143332484
DNM2
位点：RS892086
ABCA2
位点：RS908832
CLU
位点：RS9331896
KCNJ15
位点：RS928771
CNTNAP2
位点：RS802571
PICALM
位点：RS11234495
SPI1
位点：RS3740688
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Association between SORL1 and Alzheimer disease in a genome-wide study
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Rare coding variants in Phospholipase D3 (PLD3) confer risk for Alzheimer's disease
ZCWPW1 is associated with late-onset Alzheimer's disease in Han Chinese: a replication study and meta-analyses.
Association between SORL1 and Alzheimer disease in a genome-wide study
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Association between SORL1 and Alzheimer disease in a genome-wide study
Association between SORL1 and Alzheimer disease in a genome-wide study
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene.
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Pleiotropy in the presence of allelic heterogeneity: alternative genetic models for the influence of APOE on serum LDL, CSF Aβ42, and Dementia
Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia
Association of a functional polymorphism in the cholesteryl ester transfer protein (CETP) gene with memory decline and incidence of dementia.
Extreme cerebrospinal fluid amyloid beta levels identify family with late-onset Alzheimer's disease presenilin 1 mutation.
The acylation stimulating protein-adipsin system.
Two novel (M233T and R278T) presenilin-1 mutations in early-onset Alzheimer's disease pedigrees and preliminary evidence for association of presenilin-1 mutations with a novel phenotype.
A novel PSEN2 mutation associated with a peculiar phenotype.
A presenilin-1 mutation (Leu392Pro) in a familial AD kindred with psychiatric symptoms at onset.
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease.
Novel presenilin 1 mutation (S170F) causing Alzheimer disease with Lewy bodies in the third decade of life.
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease.
A novel presenilin-1 mutation (Leu85Pro) in early-onset Alzheimer disease with spastic paraparesis.
A novel mutation (V89L) in the presenilin 1 gene in a family with early onset Alzheimer's disease and marked behavioural disturbances.
Two novel (M233T and R278T) presenilin-1 mutations in early-onset Alzheimer's disease pedigrees and preliminary evidence for association of presenilin-1 mutations with a novel phenotype.
Clinical phenotypic heterogeneity of Alzheimer's disease associated with mutations of the presenilin-1 gene.
The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families.
The presenilin 1 C92S mutation increases abeta 42 production.
A novel presenilin 1 mutation (L174 M) in a large Cuban family with early onset Alzheimer disease.
Chromosome 14 familial Alzheimer's disease: the clinical and neuropathological characteristics of a family with a leucine-->serine (L250S) substitution at codon 250 of the presenilin 1 gene.
Missense mutations in the chromosome 14 familial Alzheimer's disease presenilin 1 gene.
The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families.
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease.
Two novel presenilin-1 mutations (Y256S and Q222H) are associated with early-onset Alzheimer's disease.
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Association of DISC1 Polymorphisms with Late-Onset Alzheimer's Disease in Northern Han Chinese.
GAB2 as an Alzheimer Disease Susceptibility Gene
Identifying genetic interactions associated with late-onset Alzheimer’s disease
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Pleiotropy in the presence of allelic heterogeneity: alternative genetic models for the influence of APOE on serum LDL, CSF Aβ42, and Dementia
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Dynamin 2 gene is a novel susceptibility gene for late-onset Alzheimer disease in non-APOE-epsilon4 carriers
Meta-Analyses of 8 Polymorphisms Associated with the Risk of the Alzheimer’s Disease
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Identification of genetic risk factors in the Chinese population implicates a role of immune system in Alzheimer’s disease pathogenesis
A genome-wide association study of late-onset Alzheimer's disease in a Japanese population.
Validating GWAS-Identified Risk Loci for Alzheimer's Disease in Han Chinese Populations.
Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing.
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
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