使用本網(wǎng)站需要啟用 JavaScript, 請啟用后刷新頁面獲得更好的體驗
亚洲精品午夜精品,日本二手网站,国产AⅤ爽AV久久久久成人社区,日本一二三区不收费av
<form id="4vlv9"><strong id="4vlv9"></strong></form>
<ul id="4vlv9"><abbr id="4vlv9"></abbr></ul>
<center id="4vlv9"></center>
登錄
注冊
首頁
個人基因檢測
臨床應(yīng)用研究
科研合作項目
合作與服務(wù)
社區(qū)
純合片段分析
姓氏祖源
祖源平均臉
基因關(guān)系
基因保險助手
原始數(shù)據(jù)
使用 WeGene 需要啟用 Cookies, 請啟用后刷新頁面獲得更好的體驗
社區(qū)首頁
小組
遲發(fā)型阿茲海默病
遲發(fā)型阿茲海默病
發(fā)起討論
遲發(fā)型阿茲海默病
40 個討論
只看精華帖
按熱門排序
按最新排序
老年癡呆癥有救了？
能睡的CHST8基因
? 最后回復(fù)
WeGene_A48B8FF1
?
2024-05-20 22:55
1298
3
? 來自相關(guān)小組
有比我高的嘛？瑟瑟發(fā)抖！
名字剛好柒個字
? 最后回復(fù)
tia0804
?
2022-12-23 16:17
5622
20
? 來自相關(guān)小組
APOE基因型為ε1/ε4
ensomomo
? 最后回復(fù)
Scar2005
?
2022-09-15 22:52
4315
9
? 來自相關(guān)小組
今天是阿茲海默日
拍球的NTRK2基因
? 最后回復(fù)
摩羯的PDE1C基因
?
2022-08-29 23:15
2981
6
? 來自相關(guān)小組
有沒有人覺得用腦過度才會阿茲海默的
洋氣的ROBO1基因
? 最后回復(fù)
大灰狼
?
2022-08-29 12:02
3183
4
? 來自相關(guān)小組
如果有一天父母患上“老年癡呆”，你會怎么做？
lily
? 最后回復(fù)
west
?
2022-07-16 15:45
4811
5
? 來自相關(guān)小組
如何獲得到攜帶有阿爾茲海默癥風(fēng)險基因的人但沒有認知障礙的人的數(shù)據(jù)？
SevenSee
? 最后回復(fù)
an15001864256
?
2021-03-14 09:04
2497
1
? 來自相關(guān)小組
提前開始40Hz起來
Vacual
? 最后回復(fù)
zhengqiang
?
2020-08-18 09:55
3414
3
? 來自相關(guān)小組
TED演講：跟老年癡呆說再見
費力科思
? 最后回復(fù)
chinallly
?
2020-03-30 22:19
5221
13
? 來自相關(guān)小組
阿茲海默癥或可提前預(yù)測
無邪的KDM5D基因
? 最后回復(fù)
爽朗的FGF12基因
?
2019-08-29 15:24
2788
3
? 來自相關(guān)小組
爺爺?shù)母绺缬邪⑵澓Ｄ?/a>
勤奮的ABCA1基因
? 最后回復(fù)
健壯的CHST8基因
?
2019-08-14 23:40
2894
2
? 來自相關(guān)小組
驗血或可檢測阿茲海默癥 聽說準確率達88%
歡快的CFTR基因
? 最后回復(fù)
歡快的CFTR基因
?
2019-08-13 15:13
3289
2
? 來自相關(guān)小組
有比我還高的嘛？
shi123yue123
? 最后回復(fù)
彷徨的ABCC1基因
?
2019-08-05 14:51
6070
17
? 來自相關(guān)小組
看看阿茲海默
Jpayne
? 最后回復(fù)
大灰狼
?
2019-05-06 20:04
3733
10
? 來自相關(guān)小組
家人已發(fā)病，且阿茲海默高風(fēng)險的朋友可以來說下數(shù)值嘛？
生氣的SAMD5基因
? 最后回復(fù)
an15001864256
?
2019-02-21 16:54
3490
5
? 來自相關(guān)小組
APOE基因型為ε2/ε2
朱先鋒
? 最后回復(fù)
費力科思
?
2019-02-21 14:29
5035
5
? 來自相關(guān)小組
1
2
>
發(fā)起討論
遲發(fā)型阿茲海默病
40 個討論
相關(guān)基因
SLC24A4
位點：RS10498633
CELF1
位點：RS10838725
CD2AP
位點：RS10948363
SORL1
位點：RS11218343
位點：RS11218350
位點：RS1699103
位點：RS1784931
位點：RS1792113
位點：RS726601
EPHA1-AS1
位點：RS11771145
PLD3
位點：RS145999145
ZCWPW1
位點：RS1476679
FERMT2
位點：RS17125944
MEF2C-AS1
位點：RS190982
PTK2B
位點：RS28834970
PSEN2
位點：RS28936379
位點：RS63750048
INPP5D
位點：RS35349669
APOE
位點：RS429358
位點：RS7412
GRN
位點：RS5848
CETP
位點：RS5882
PSEN1
位點：RS63749824
位點：RS63749885
位點：RS63749891
位點：RS63750218
位點：RS63750526
位點：RS63750577
位點：RS63750590
位點：RS63750599
位點：RS63750815
位點：RS63750886
位點：RS63750900
位點：RS63751037
位點：RS63751141
位點：RS63751144
位點：RS63751163
位點：RS63751223
位點：RS63751229
位點：RS63751235
位點：RS63751320
CR1
位點：RS6656401
DISC1
位點：RS6675281
GAB2
位點：RS7101429
CASS4
位點：RS7274581
TREM2
位點：RS75932628
位點：RS143332484
DNM2
位點：RS892086
ABCA2
位點：RS908832
CLU
位點：RS9331896
KCNJ15
位點：RS928771
CNTNAP2
位點：RS802571
PICALM
位點：RS11234495
SPI1
位點：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
查看參考文獻
首頁
個人基因檢測
臨床應(yīng)用研究
科研合作項目
合作與服務(wù)
示例報告
下載 APP
社區(qū)
關(guān)于 WeGene
關(guān)于我們
媒體新聞
倫理委員會
隱私協(xié)議
加入我們
服務(wù)協(xié)議
價格保護
幫助中心
關(guān)于基因檢測
賬戶購買
樣本寄送
報告解讀
隱私安全
關(guān)于第三方數(shù)據(jù)
社區(qū)分享
開放平臺
申請成為開發(fā)者
開發(fā)文檔
客服微信公眾號
聯(lián)系我們
客服郵箱：
[email protected]
合作咨詢：
[email protected]
© 2025 WeGene. All Rights Reserved
深圳市市場監(jiān)督管理局企業(yè)主體身份公示
|
粵ICP備15012185號
| 互聯(lián)網(wǎng)藥品信息服務(wù)資格證書:（粵）-非經(jīng)營性-2023-0379
中文
English
<track id="ffr4e"></track>
<dfn id="ffr4e"></dfn>
主站蜘蛛池模板：
河南省
|
合肥市
|
东乡族自治县
|
武宣县
|
新化县
|
达拉特旗
|
正宁县
|
修水县
|
连州市
|
黄陵县
|
彭泽县
|
蒙山县
|
那曲县
|
合作市
|
略阳县
|
台江县
|
富宁县
|
昌都县
|
江北区
|
城口县
|
德阳市
|
普格县
|
北宁市
|
湟中县
|
开远市
|
通城县
|
甘孜县
|
乌兰浩特市
|
中阳县
|
安丘市
|
会宁县
|
青州市
|
扶沟县
|
佛冈县
|
习水县
|
夏邑县
|
新营市
|
成武县
|
青田县
|
大同市
|
开平市
|
<sup id="9hrjc"><span id="9hrjc"></span></sup>
<ul id="9hrjc"><em id="9hrjc"></em></ul>
深圳市市場監(jiān)督管理局企業(yè)主體身份公示
|
粵ICP備15012185號
|
互聯(lián)網(wǎng)藥品信息服務(wù)資格證書:（粵）-非經(jīng)營性-2023-0379
中文 
English
純合片段分析
姓氏祖源
祖源平均臉
基因關(guān)系
基因保險助手
原始數(shù)據(jù)
