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作品数：161被引量：414H指数：11
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LncRNA AFAP1-AS1/miR-27b-3p/VEGF-C axis modulates stemness characteristics in cervical cancer cells被引量：6
《Chinese Medical Journal》2021年第17期2091-2101,共11页Meng Xia Li-Jun Duan Bi-Nan Lu Yu-Zhou Pang Zong-Ran Pang 
Background:Long non-coding RNA(lncRNA)actin filament-associated protein 1 antisense RNA 1(AFAP1-AS1)functions as a competing endogenous RNA to regulate target genes expression by sponging microRNAs(miRs)to play cancer...
关键词：Hyaluronic acid receptor cluster of differentiation 44 variant exon 6 Cell stemness Cervical cancer Long non-coding RNA actin filament-associated protein 1 antisense RNA 1 MicroRNA-27b-3p 
A novel missense mutation of the TYR gene in a pedigree with oculocutaneous albinism type 1 from China被引量：5
《Chinese Medical Journal》2011年第20期3358-3361,共4页LIN Yu-ying WEI Ai-hua ZHOU Zhi-yong ZHU Wei HE Xin LIAN Shi 
This study was supported in part by grants from the Natural Science Foundation of Beijing （No. 7092040）, the Capital Medical Development Foundation （No. 2007-3111）, and the National Natural Science Foundation of China （No. 31071252）.
Background The mutation of the tyrosinase （TYR） gene results in oculocutaneous albinism type 1 （OCA1）, an autosomal recessive genetic disorder. OCA1 is the most common type of OCA in the Chinese population. Hence,...
关键词：oculocutaneous albinism type 1 MUTATION TYR gene EXON HOMOZYGOUS 
Functional polymorphism in exon 5 and variant haplotype of the interleukin-1 receptor-associated kinase 1 gene are associated with susceptibility to and severity of sepsis in the Chinese population
《Chinese Medical Journal》2011年第15期2248-2253,共6页FANG Yu ZHANG Lu ZHOU Gang-qiao WANG Zhi-fu ZENG Zhao-shu LUO Zhi-yi LI Lei LIU Bao-chi 
This study was supported by the grants from the Chinese National Basic Research Program （No. 2005CB522602）, Beijing Science ＆ Technology NOVA Program （No. 2006A54） and National Natural Science Foundation of China （No. 31071100）.
Background The interleukin-1 （IL-1） receptor-associated kinase 1 （IRAK1） is believed to play an important role in the pathogenesis of sepsis. Recent studies have suggested that the I RAK1 functional genetic varian...
关键词：SEPSIS interleukin-1 receptor-associated kinase 1 haplotype tagging single nucleotide polymorphisms linkage disequilibrium genetic association 
Effects of single nucleotide polymorphisms 869 T/C and 915 G/C in the exon 1 locus of transforming growth factor-β1 gene on chronic obstructive pulmonary disease susceptibility in Chinese被引量：9
《Chinese Medical Journal》2010年第4期390-394,共5页LIU Dai-shun LI Xiao-ou YING Bin-wu CHEN Lei WANG Tao XU Dan WEN Fu-qiang 
This study was supported by the grants from the National Natural Science Foundation of China （No. 30425007 and No. 30370627）.Acknowledgement： We are grateful to LIAO Ga for the haplotype analysis, to YUN Li-bing and ZHOU Bin for the DHPLC analysis, and to JIA Zheng for helpful discussions. We are deeply grateful to the patients and families for their cooperation.
Background The main risk factor for chronic obstructive pulmonary disease （COPD） is cigarette smoking. However, only 10%-20% of chronic heavy smokers develop systematic COPD. We hypothesized that the inheritance of ...
关键词：chronic obstructive pulmonary disease transforming growth factor-ill gene polymorphism 
R25G mutation in exon 1 of LMNA gene is associated with dilated cardiomyopathy and limb-girdle muscular dystrophy 1B被引量：5
《Chinese Medical Journal》2009年第23期2840-2845,共6页YUAN Wo-liang HUANG Chun-yan WANG Jing-feng XIE Shuang-lun NIE Ru-qiong LIU Ying-mei LIU Pin-ming ZHOU Shu-xian CHEN Su-qin HUANG Wei-jun 
This study was supported by the grant from Natural Science Foundation of Guangdong Province, China, 2005 （No. 5001673）.
Background Mutations of the LMNA gene encoding lamin A and C are associated with dilated cardiomyopathy （DCM）, conduction system defects and skeletal muscle dystrophy. Here we report a family with a mutation of the ...
关键词：lamin A/C dilated cardiomyopathy limb-girdle muscular dystrophy MUTATION sudden death 
Polymorphism of the second exon of human leukocyte antigen-DQA1, -DQB1 gene and genetic susceptibility to idiopathic dilated cardiomyopathy in people of the Han nationality in northern China被引量：2
《Chinese Medical Journal》2005年第3期238-241,共4页LIUWei LIWei-min SUNNing-ling 
Idiopathic dilated cardiomyopathy ( IDC) is characterized by dilation andimpaired contraction of the left ventricle or both, and it is a relevant cause of heart failure anda common indication for heart transplantation...
关键词：idiopathic dilated cardiomyopathy human leukocyte antigen GENEPOLYMORPHISM genetic susceptibility 
Expression of exon 13 from the Ki-67 gene in human cells and tissues by digoxigenin-labelled mRNA in situ hybridization被引量：2
《Chinese Medical Journal》2001年第1期48-53,共6页吴育连 彭承宏 沈宏伟 
boththeNationalNaturalScienceFoundationofChina (No 396 0 0 14 1)andtheNaturalScienceFoundationofZhejiangProvince (No 396 498
OBJECTIVE: To get insight on the regulatory mechanism of Ki-67 gene expression in malignant cell cycle. METHODS: Non-radioactive in situ hybridization (ISH) was undertaken, combined with immunohistochemistry to study ...
关键词：EXONS In Situ Hybridization DIGOXIGENIN Hela Cells Humans Immunohistochemistry Ki-67 Antigen RNA  Messenger Research Support  Non-U.S. Gov't 
Identification of a mutation hotspot in exon 8 of Wilson disease gene by cycle sequencing被引量：2
《Chinese Medical Journal》2000年第2期76-78,共3页范玉新 余龙 江萤 许月芳 杨任民 韩咏竹 崔映宇 任明山 赵寿元 
ThisworkwassupportedbyNationalScienceFoundationofChina(No 39740 0 1 7)
Objective To screen for mutation hotspot of Wilson disease (WD) gene in Chinese population Methods Cycle sequencing was used to detect mutation in exon 8 of WD gene in 30 patients with Wilson disease Results The ...
关键词：Wilson disease WD gene cycle sequencing mutation detection 
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