[PDF][PDF] Mineralocorticoid receptor gene-2G/C polymorphism in central serous chorioretinopathy and relation of polymorphism with plasma cortisol levels

A Yazici, ES Sari, B Eser, G Sahin… - International Eye …, 2016 - researchgate.net
… Additionally the racial predilection to white, Hispanic and Asian populations also supports
a genetic tendency. However, the genetic background of the disease was not exclusively …

[PDF][PDF] D-serine and Serine Racemases

YQ Feng, H Xiao, YW Shi - Hans J. Biomed, 2013 - pdf.hanspub.org
… Serine racemase may be a new target for the neurological and psychiatric diseases. In this
review, the recent advances in D-serine and serine racemase with the aspects of structure, …

[PDF][PDF] 1d sequence based 3d chromatin phase separation: Forces, processes, and functions

S Liu, H Quan, H Tian, R Zhou, L Yang… - Acta Physico-Chimica …, 2020 - researchgate.net
The high-order chromatin structure plays a nonnegligible role in gene regulation. The formation
of chromatin structure and its regulatory mechanisms have been studied intensely. To …

[HTML][HTML] Retrospective Study of Idiopathic Paroxysmal Kinesigenic Dyskinesia in Children: A Rare and Benign Neurological Disorder Commonly Being Misdiagnosed …

B Chan, KY Chan - HK J Paediatr (new series), 2009 - hkjpaed.org
Objective: To investigate the clinical characteristics and treatment outcome of idiopathic
paroxysmal kinesigenic dyskinesia (PKD) in Chinese paediatric patients. Method: This was a …

為生命的語言開一扇窗: 遺傳護理學的契機

陳煥華, 洪志秀 - 高雄護理雜誌, 2014 - airitilibrary.com
genetics and genomics, the roles and functions of nursing professionals in genetic nursing
applications of geneticgenetic nursing in Taiwan and Western countries. The myth of medical …

利用全基因體關聯掃描探討與多發性思覺失調症及其較早發病年齡相關之遺傳變異

AL Woolston - 國立臺灣大學流行病學與預防醫學研究所學位論文, 2017 - airitilibrary.com
… Third, family-based association tests on genome-wide common and rare variants, utilizing
genotyping microarray designed for psychiatric diseases, were performed among multiplex …

注意缺陷多动障碍遗传易感性的生物信息学研究

常素华 - 2012 - ir.psych.ac.cn
… First, we made multi-dimension data integration analyses for the genetic data, genomic
data and phenotype data for ADHD and developed the first ADHD genetic database (ADHDgene…

[HTML][HTML] 基于转录组的肝豆状核变性调控网络的构建和分析

杨晓曦, 何松, 李潇瑾, 周冬虎, 伯晓晨, 黄坚 - 生物工程学报, 2022 - cjb.ijournals.cn
… 筛选由铜诱导产生的差异表达基因(differentially expressed genes, DEGs) 后进行基因本体论
(gene ontology, GO), 京都基因和基因组百科全书(Kyoto encyclopedia of genes and genomes, …

尼曼匹克症轉錄體學研究

MH Liu - 2022 - ir.lib.ncu.edu.tw
… After the analysis, we also grouped these Niemann-Pick disease type C patients with …
diseases from the differentially expressed genes of patients with Niemann-Pick disease type C. We …

脑组织的表达数量性状遗传位点定位方法解析精神疾病遗传基础

C Liu - Neuroscience Bulletin, 2011 - Springer
Genome-wide association study (GWAS) can be used to identify genes that increase the
risk of psychiatric diseases… explain the genetic component of complex psychiatric diseases. …