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CORC

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Genetic analysis of TREM2 variants in Chinese Han patients with sporadic Parkinson's disease 期刊论文
Neuroscience Letters, 2016, 卷号: 612, 页码: 189-192
作者:  Tan, Ting;  Song, Zhi;  Yuan, Lamei;  Xiong, Wei;  Deng, Xiong
收藏  |  浏览/下载：14/0  |  提交时间：2019/12/03
PD  Parkinson’s disease  AD  Alzheimer’s disease  TREM2  the triggering receptor expressed on myeloid cells 2 gene  VPS35  the vacuolar protein sorting 35 gene  EIF4G1  the eukaryotic translation initiation factor 4-gamma 1 gene  S100B  the S100 calcium binding protein B gene  FBXO48  the F-box protein 48 gene  RAB39B  the RAB39B, member RAS oncogene family gene  TCEANC2  the transcription elongation factor A (SII) N-terminal and central domain containing 2 gene  MC1R  the melanocortin 1 receptor gene  SIFT  Sorting Intolerant from Tolerant  PolyPhen-2  Polymorphism Phenotyping v2  SNP  single nucleotide polymorphism  MAF  minor allele frequency  PCR  polymerase chain reaction  FTD  frontotemporal dementia  FTLD  frontotemporal lobar degeneration  ALS  amyotrophic lateral sclerosis  Sporadic Parkinson’s disease  TREM2 gene  rs75932628  rs2234253  Genetic analysis  Chinese Han  
Association of ABCB1 polymorphisms with prognostic outcomes of anthracycline and cytarabine in Chinese patients with acute myeloid leukemia 期刊论文
European Journal of Clinical Pharmacology, 2015, 卷号: 71, 期号: 3, 页码: 293-302
作者:  He, Hui;  Yin, Jiye;  Li, Xi;  Zhang, Yu;  Xu, Xiaojing
收藏  |  浏览/下载：7/0  |  提交时间：2019/12/03
Association of IL-1, IL-18, and IL-33 gene polymorphisms with late-onset Alzheimer's disease in a Hunan Han Chinese population 期刊论文
Brain Research, 2015, 卷号: 1596, 期号: Volume 1596, 页码: 136-145
作者:  Tian, M;  Deng, Y Y;  Hou, D R;  Li, W;  Feng, X L
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/03
AD  Alzheimer׳s disease  LOAD  late-onset Alzheimer׳s disease  EOAD  early-onset Alzheimer׳s disease  Aβ  amyloid-beta  APOE  apolipoprotein E  APP  amy1iod precursor protein  CAA  cerebral amyloid angiopathy  CNS  central nervous system  IL  interleukin  ACT  alpha1-antichymotrypsin  TNF  tumor necrosis factor  BMI  body mass index  TC  total cholesterol  TG  triglycerides  HDL-c  high-density lipoprotein cholesterol  LDL-c  low-density lipoprotein cholesterol  OR  odds ratio  CI  confidence interval  MMSE  Mini-Mental State Examination  ADL  activities of daily living scale  CDT  clock drawing task  HAMD  hamilton depression scale  SNP  single nucleotide polymorphism  PCR  polymerase chain reaction  MALDI-TOF-MS  Matrix Assisted Laser Desorption Ionization Time of Flight Mass Spectrometry  Alzheimer׳s disease  Inflammatory cytokines  IL-1 family  Single nucleotide polymorphism  
The single nucleotide polymorphism Rs12817488 is associated with Parkinson's disease in the Chinese population 期刊论文
Journal of Clinical Neuroscience, 2015, 卷号: 22, 期号: 6, 页码: 1002-1004
作者:  Yu, Ri-li;  Guo, Ji-feng;  Wang, Ya-qin;  Liu, Zhen-hua;  Sun, Zhan-fang
收藏  |  浏览/下载：5/0  |  提交时间：2019/12/03
A novel mutation of GATA4 (K300T) associated with familial atrial septal defect 期刊论文
Gene, 2015, 卷号: 575, 期号: 2, 页码: 473-477
作者:  Chen, Jia;  Qi, Bingyang;  Zhao, Juan;  Liu, Wei;  Duan, Ranhui*
收藏  |  浏览/下载：9/0  |  提交时间：2019/12/03
Association of platelet ITGA2B and ITGB3 polymorphisms with ex vivo antiplatelet effect of ticagrelor in healthy Chinese male subjects 期刊论文
International Journal of Hematology, 2014, 卷号: 99, 期号: 3, 页码: 263-271
作者:  Li, Mu-Peng;  Xiong, Yan;  Xu, An;  Zhou, Ji-Peng;  Tang, Jie
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/03
Effect of NR3C2 genetic polymorphisms on the blood pressure response to enalapril treatment 期刊论文
Pharmacogenomics, 2014, 卷号: 15, 期号: 2, 页码: 201-208
作者:  Luo, Jian-Quan;  Wang, Lu-Yan;  He, Fa-Zhong;  Sun, Ning-Ling;  Tang, Gen-Fu
收藏  |  浏览/下载：5/0  |  提交时间：2019/12/03
A novel mutation of GATA4 (K319E) is responsible for familial atrial septal defect and pulmonary valve stenosis 期刊论文
Gene, 2014, 卷号: 534, 期号: 2, 页码: 320-323
作者:  Xiang, Rong;  Fan, Liang-Liang;  Huang, Hao;  Cao, Bei-Bei;  Li, Xiang-Ping
收藏  |  浏览/下载：2/0  |  提交时间：2019/12/03
576 kb deletion in 1p36.33-p36.32 containing SKI is associated with limb malformation, congenital heart disease and epilepsy. 期刊论文
Gene, 2013, 卷号: 528, 期号: 2, 页码: 352-355
作者:  Zhu, Xin;  Zhang, Yi;  Wang, Jian;  Yang, Jin-Fu;  Yang, Yi-Feng
收藏  |  浏览/下载：2/0  |  提交时间：2019/12/03
The association of 5-HTR2A-1438A/G, COMTVal158Met, MAOA-LPR, DATVNTR and 5-HTTVNTR gene polymorphisms and antisocial personality disorder in male heroin-dependent Chinese subjects 期刊论文
Progress in Neuro-Psychopharmacology and Biological Psychiatry, 2012, 卷号: 36, 期号: 2, 页码: 282-289
作者:  Mei Yang;  Vasish Kavi;  Wenfu Wang;  Zhimei Wu;  Wei Hao
收藏  |  浏览/下载：2/0  |  提交时间：2019/12/03
APSD  antisocial personality disorder  bp  base-pair  COMT  catechol-O-methyltransferase gene  DA  dopamine  DAT  dopamine transporter gene  5-HT  5-hydroxytryptamine or serotonin  5-HTR2A  5-hydroxytryptamine receptor 2A gene  5-HTT  5-hydroxytryptamine transporter gene  5-HTTLPR  5-hydroxytryptamine transporter gene-linked polymorphic region  5-HTTVNTR  5-hydroxytryptamine transporter variable number of tandem repeats  LDR  ligase detection reaction  MAOA  monoamine oxidase A gene  MAOA-LPR  monoamine oxidase A gene-linked polymorphic region  NCS  National Comorbidity Survey  NE  norepinephrine  PCR  polymerase chain reaction  SNP  single nucleotide polymorphism  STin2VNTR  serotonin introns 2 variable number of tandem repeats  VNTR  variable number of tandem repeats  Antisocial personality disorder  Co-occurring disorders  Heroin dependence  Gene  Polymorphism  Association study  

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