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Monomeric type I and type III transforming growth factor-β receptors and their dimerization revealed by single-molecule imaging 被引量:10
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作者 Wei Zhang Jinghe Yuan +5 位作者 Yong Yang Li Xu Qiang Wang Wei Zuo Xiaohong Fang Ye-Guang Chen 《Cell Research》 SCIE CAS CSCD 2010年第11期1216-1223,共8页
Transforming growth factor-β (TGF-β) binds with two transmembrane serine/threonine kinase receptors, type Ⅱ (TβRII) and type Ⅰ receptors (TβRⅠ), and one accessory receptor, type Ⅲ receptor (TβRⅢ), to... Transforming growth factor-β (TGF-β) binds with two transmembrane serine/threonine kinase receptors, type Ⅱ (TβRII) and type Ⅰ receptors (TβRⅠ), and one accessory receptor, type Ⅲ receptor (TβRⅢ), to transduce signals across cell membranes. Previous biochemical studies suggested that TβRI and TβRIII are preexisted homo-dimers. Using single-molecule microscopy to image green fluorescent protein-labeled membrane proteins, for the first time we have demonstrated that TβRI and TβRⅢ could exist as monomers at a low expression level. Upon TGF-β1 stimu- lation, TβRI follows the general ligand-induced receptor dimerization model for activation, but this process is TβRⅡ- dependent. The monomeric status of the non-kinase receptor TβRⅢ is unchanged in the presence of TGF-β1. With the increase of receptor expression, both TβRI and TβRIII can be assembled into dimers on cell surfaces. 展开更多
关键词 single-molecule fluorescence TGF-β signaling Type I TGF-β receptor Type TGF-β receptor subunit stoi-chiometry
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Genetic Variants in EGFR/PLCE1 Pathway Are Associated with Prognosis of Esophageal Squamous Cell Carcinoma after Radical Resection 被引量:7
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作者 Yu-li WANG Ye YUAN +2 位作者 Xiao-xiao LUO Guang-yuan HU Ping G0NG 《Current Medical Science》 SCIE CAS 2019年第3期385-390,共6页
Esophageal cancer (EC) is one of the most deadly malignant diseases. Several studies revealed that variations of the phospholipase C epsilon 1 (PLCE1) gene were associated with EC susceptibility. PLCE1 is located down... Esophageal cancer (EC) is one of the most deadly malignant diseases. Several studies revealed that variations of the phospholipase C epsilon 1 (PLCE1) gene were associated with EC susceptibility. PLCE1 is located downstream of the epidermal growth factor receptor (EGFR) pathway. Presently, the single nucleotide polymorphisms (SNPs) of EGFR/PLCE1 genes and their associations with EC survival remain unclea匚 In this study, the associations between genetic variants in the EGFR/PLCE1 pathway and prognosis in 124 esophageal squamous cell carcinoma (ESCC) patients with radical resection were explored. The results showed that CC genotype of both PLCE1 rsl7109671 and EGFR rs2072454 was associated with ESCC prognosis. Multivariate analysis revealed that patients with the two unfavorable genotypes had the worst overall survival (OS) or disease-free survival (DFS)(HR=6.099, 95%CI=1.903-19.552;HR=3.994, 95%CI=1.49-10.702, respectively). Additionally, combination of SNPs and tumor stage could better predict OS (for AUC, 0.774 vs. 0.709) and PFS (for AUC, 0.773 vs. 0.704) than tumor stage alone.In conclusion, genetic variants of the EGFR/PLCE1 may be predictors of the prognosis of ESCC after surgery. The individuals with the CC genotype of PLCE1 rsl7109671 and EGFR rs2072454 should receive more aggressive treatments. 展开更多
关键词 ESOPHAGEAL SQUAMOUS cell carcinoma PROGNOSIS single NUCLEOTIDE polymorphism survival EPIDERMAL growth factor receptor
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Coupled single-cell and bulk RNA-seq analysis reveals the engulfment role of endothelial cells in atherosclerosis
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作者 Jianxiong Xu Jinxuan Wang +7 位作者 Hongping Zhang Yidan Chen Xiaojuan Zhang Ying Zhang Ming Xie Jun Xiao Juhui Qiu Guixue Wang 《Genes & Diseases》 SCIE CSCD 2024年第5期442-455,共14页
The clearance of apoptotic cell debris,containing professional phagocytosis and non-professional phagocytosis,is essential for maintaining the homeostasis of healthy tissues.Here,we discovered that endothelial cells c... The clearance of apoptotic cell debris,containing professional phagocytosis and non-professional phagocytosis,is essential for maintaining the homeostasis of healthy tissues.Here,we discovered that endothelial cells could engulf apoptotic cell debris in atherosclerotic plaque.Single-cell RNA sequencing(RNA-seq)has revealed a unique endothelial cell subpopulation in atherosclerosis,which was strongly associated with vascular injury-related pathways.Moreover,integrated analysis of three vascular injury-related RNA-seq datasets showed that the expression of scavenger receptor class B type 1(SR-B1)was up-regulated and specifically enriched in the phagocytosis pathway under vascular injury circumstances.Single-cell RNA-seq and bulk RNA-seq indicate that SR-B1 was highly expressed in a unique endothelial cell subpopulation of mouse aorta and strongly associated with the reorganization of cellular adherent junctions and cytoskeleton which were necessary for phagocytosis.Furthermore,SR-B1 was strongly required for endothelial cells to engulf apoptotic cell debris in atherosclerotic plaque of both mouse and human aorta.Overall,this study demonstrated that apoptotic cell debris could be engulfed by endothelial cells through SR-B1 and associated with the reorganization of cellular adherent junctions and cytoskeleton. 展开更多
关键词 Apoptotic cell debris ATHEROSCLEROSIS Endothelial engulfment single-cell RNA sequencing Scavenger receptor class B type 1
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CD14启动子-159位点基因多态性与糖尿病肾病的相关性研究 被引量:5
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作者 郑寿焕 金光明 柳明洙 《中华内分泌代谢杂志》 CAS CSCD 北大核心 2009年第4期409-411,共3页
目的研究2型糖尿病患者CD14启动子C-159T多态性分布,探讨该基因多态性与糖尿病肾病(ON)的相关性。方法应用聚合酶链反应-限制性片段长度多态性技术对308例2型糖尿病患者及145名正常对照者CD14基因启动子-159位点进行基因型分析。结果... 目的研究2型糖尿病患者CD14启动子C-159T多态性分布,探讨该基因多态性与糖尿病肾病(ON)的相关性。方法应用聚合酶链反应-限制性片段长度多态性技术对308例2型糖尿病患者及145名正常对照者CD14基因启动子-159位点进行基因型分析。结果(1)CD14启动子-159位点基因多态性在正常对照组和2型糖尿病组中的分布差异无统计学意义(P〉0.05);在未发生DN和发生DN的患者中,CD14启动子-159位点CC基因频率与CT+TT基因频率相比,差异有统计学意义(P〈0.05);(2)2型糖尿病患者在10年和20年时,发生DN的百分率分别为13.3%和23.4%;纯合子CC基因型2型糖尿病患者发生DN的风险高于CT+TT基因型患者。结论CD14启动子C-159T基因多态性与糖尿病的发病无关,但其中的CC纯合子基因是2型糖尿病患者进展为DN的遗传学风险因素。 展开更多
关键词 CD14启动子 糖尿病肾病 多态性 单核苷酸 脂多糖受体
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蓖麻蚕触角的结构和嗅觉感受细胞对化学气味物质的反应 被引量:3
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作者 孟联忠 赵新宇 徐小星 《北京大学学报(自然科学版)》 CSCD 北大核心 1994年第2期224-232,共9页
扫描电镜和透射电镜观察蓖麻蚕的触角和毛形感器。雄蛾触角上的毛形感器比雌蛾的长且多。雄蛾触角的每个毛形感器内有二个或三个树突。用41种人工合成化合物刺激蓖麻蚕触角,单细胞记录方法记录感受细胞的感受器电位和神经冲动发放发... 扫描电镜和透射电镜观察蓖麻蚕的触角和毛形感器。雄蛾触角上的毛形感器比雌蛾的长且多。雄蛾触角的每个毛形感器内有二个或三个树突。用41种人工合成化合物刺激蓖麻蚕触角,单细胞记录方法记录感受细胞的感受器电位和神经冲动发放发现,雄蛾对E6,Z11-十六碳二烯醛和E4,Z9-十四碳二烯醇,酯及醛反应明显。雌蛾触角对上述化合物无反应。 展开更多
关键词 蓖麻蚕 触角 化学气味 嗅觉
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New avenues for systematically inferring cellcell communication:through single-cell transcriptomics data 被引量:4
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作者 Xin Shao Xiaoyan Lu +2 位作者 Jie Liao Huajun Chen Xiaohui Fan 《Protein & Cell》 SCIE CAS CSCD 2020年第12期866-880,共15页
For multicellular organisms,cell-cell communication is essential to numerous biological processes.Drawing upon the latest development of single-cell RNA-sequencing(scRNA-seq),high-resolution transcriptomic data have d... For multicellular organisms,cell-cell communication is essential to numerous biological processes.Drawing upon the latest development of single-cell RNA-sequencing(scRNA-seq),high-resolution transcriptomic data have deepened our understanding of cellular phenotype heterogeneity and composition of complex tissues,which enables systematic cell-cell communication studies at a single-cell level.We first summarize a common workflow of cell-cell communication study using scRNA-seq data,which often includes data preparation,construction of communication networks,and result validation.Two common strategies taken to uncover cell-cell communications are reviewed,e.g.,physically vicinal structure-based and ligand-receptor interaction-based one.To conclude,challenges and current applications of cell-cell communication studies at a single-cell resolution are discussed in details and future perspectives are proposed. 展开更多
关键词 cell-cell communication single-cell RNA sequencing physical contact-dependent communication chemical signal-dependent communication ligand-receptor interaction network biology
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Predictors for partial suppression of spermatogenesis of hormonal male contraception 被引量:1
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作者 Jing-Wen Li Yi-Qun Gu 《Asian Journal of Andrology》 SCIE CAS CSCD 2008年第5期723-730,共8页
Aim: To analyze factors influencing the efficacy of hormonal suppression of spermatogenesis for male contraception. Methods: A nested case-control study was conducted, involving 43 subjects, who did not achieve azoo... Aim: To analyze factors influencing the efficacy of hormonal suppression of spermatogenesis for male contraception. Methods: A nested case-control study was conducted, involving 43 subjects, who did not achieve azoospermia or severe oligozoospermia when given monthly injections of 500 mg testosterone undecanoate (TU), defined as partial suppressors compared with 855 subjects who had suppressed spermatogenesis (complete suppressors). Sperm density, serum testosterone, luteinizing hormone (LH) and follicle stimulating hormone (FSH) concentrations at the baseline and the suppression phase were compared between partial and complete suppressors. Polymorphisms of androgen receptor (AR) and three single nucleotide variants and their haplotypes of FSH receptor (FSHR) genes determined by polymerase chain reaction (PCR) and DNA sequencing technique were compared between 29 partial and 34 complete suppressors. Results: Baseline serum LH level was higher and serum LH as well as FSH level during the suppression phase was less suppressed in partial suppressors. Additionally, in a logistic regression analysis larger testis volume, higher serum FSH concentrations alone, or interaction of serum LH, FSH, testosterone and sperm concentrations were associated with degree of suppression. The distribution of polymorphisms of AR or FSH receptor genes did not differ between partial and complete suppressors. In cases with incomplete FSH suppression (FSH 〉 0.2 IU/L), the chances of reaching azoospermia were 1.5 times higher in the subjects with more than 22 CAG triplet repeats. Conclusion: Partial suppression of spermatogenesis induced by 500 mg TU monthly injections is weakly influenced by hormonal and clinical features but not polymorphism in AR and FSHR genes. 展开更多
关键词 male contraception genetic polymorphism androgen receptor CAG repeats follicle stimulating hormone receptor single nucleotide polymorphism sperm concentration
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Super-resolution imaging and tracking of TGF-β receptor II on living cells 被引量:3
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作者 Zi Ye Nan Li +5 位作者 Libo Zhao Yahong Sun Hefei Ruan Mingliang Zhang Jinghe Yuan Xiaohong Fang 《Science Bulletin》 SCIE EI CAS CSCD 2016年第8期632-638,共7页
Single-particle tracking photoactivated local- ization microscopy (sptPALM) has recently emerged as a powerful tool for high-density imaging and tracking of individual molecules in living cells. In this work, we hav... Single-particle tracking photoactivated local- ization microscopy (sptPALM) has recently emerged as a powerful tool for high-density imaging and tracking of individual molecules in living cells. In this work, we have monitored and compared the diffusion dynamics of TGF-β type II receptor (TβRII) at high expression level using both traditional single-particle tracking (SPT) and sptPALM. The ligand-induced aggregation of TβRII oligomers was further indicated by sptPALM. Due to the capacity of distinguishing and tracking single molecules within diffraction limit, sptPALM outperforms traditional SPT by providing more accurate biophysical information, 展开更多
关键词 single-particle tracking Photoactivatedlocalization microscopy - single-moleculefluorescence imaging TGF-β receptor II Membranediffusion
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叶酸载体基因多态性与胎儿神经管缺陷 被引量:3
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作者 裴娇娇 谢江燕(审校) 伍小莉 《国际生殖健康/计划生育杂志》 CAS 2021年第6期519-523,共5页
叶酸是一组水溶性维生素(维生素B9)的天然存在形式,作为体内一碳单位转移酶系的辅酶,为体内甲基化反应和核酸合成提供重要原材料,其衍生物也是许多一碳单位转移反应的底物。叶酸的饮食来源包括绿叶蔬菜、豆类和强化谷物产品等。叶酸的... 叶酸是一组水溶性维生素(维生素B9)的天然存在形式,作为体内一碳单位转移酶系的辅酶,为体内甲基化反应和核酸合成提供重要原材料,其衍生物也是许多一碳单位转移反应的底物。叶酸的饮食来源包括绿叶蔬菜、豆类和强化谷物产品等。叶酸的生物利用度不仅取决于膳食摄入量,还取决于调节叶酸吸收和新陈代谢的细胞作用机制,以及叶酸代谢途径中关键载体的遗传多态性。鉴于相同饮食习惯的个体发生神经管缺陷(neural tube defect,NTD)的风险明显不同,相同叶酸浓度对红细胞的贡献也不同,因此,通过对叶酸吸收、转运的研究,从而认识并掌握NTD发生的机制变得越来越重要。叶酸载体基因是目前研究NTD发生机制的极佳候选基因,研究其多态性为科学地个体化补充易于吸收的叶酸提供依据。 展开更多
关键词 多态性 单核苷酸 叶酸 载体蛋白质类 叶酸受体 神经管缺损
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白细胞介素23受体的基因多态性与类风湿关节炎的相关性 被引量:3
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作者 谢庆云 魏萌 +2 位作者 符培亮 孙久一 钱齐荣 《临床荟萃》 CAS 2016年第1期40-44,共5页
目的探讨白细胞介素23受体(interleukin 23receptor,IL23R)基因的单核苷酸多态性(single nucleotide polymorphisms,SNPs)与类风湿关节炎(rheumatoid arthritis,RA)易感性之间的关系。方法采用病例对照研究,以228例RA患者和228例正常对... 目的探讨白细胞介素23受体(interleukin 23receptor,IL23R)基因的单核苷酸多态性(single nucleotide polymorphisms,SNPs)与类风湿关节炎(rheumatoid arthritis,RA)易感性之间的关系。方法采用病例对照研究,以228例RA患者和228例正常对照为研究对象,从Hapmap中国人群数据库中选取IL23R基因的标签SNPs(tag-SNPs)。用基质辅助激光解吸电离飞行时间质谱法(MALDI-TOF MS)对IL23R基因的14个tag-SNPs位点进行基因分型,分析其等位基因分布频率及位点间的交互情况。结果所检测的14个tag-SNPs中,共有3个位点rs10489628、rs10889675和rs10889677的基因型频率分布在RA组和对照组之间差异有统计学意义(P<0.05)。各类型的单倍体在两组间的分布差异均无统计意义(P>0.05)。结论IL23R基因的rs10489628、rs10889675和rs10889677与RA之间存在相关性。 展开更多
关键词 关节炎 类风湿 多态性 单核苷酸 受体 白细胞介素23 关联分析
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New insights on the pathogenesis of pyloric stenosis of infancy. A review with emphasis on the hyperacidity theory 被引量:1
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作者 Ian M. Rogers 《Open Journal of Pediatrics》 2012年第2期97-105,共9页
A review is presented on the theories concerning the cause of pyloric stenosis with emphasis on the primary position of inherited hyperacidity in pathogenesis. Existing theories are critically analysed and the hyperac... A review is presented on the theories concerning the cause of pyloric stenosis with emphasis on the primary position of inherited hyperacidity in pathogenesis. Existing theories are critically analysed and the hyperacidity theory is precisely defined in the light of recent physiological insights into the gastrointestinal hormone motilin. The progressive fixed fasting hypergastrinaemia within the first few weeks of life will, in the baby who inherits acid secretion at the top of the normal range, produce hyperacidity of sufficient severity to trigger the process of acid-induced work hypertrophy of the pylorus. The potential contribution of motilin is discussed. The baby who inherits a normal gastric acidity will not reach acid levels severe enough to trigger sphincter hypertrophy despite the early gastrin stimulus. The potential threat will cease when gastrin naturally declines with age and the pyloric canal becomes wider. Genetic factors clearly must also be involved and these are separately discussed. 展开更多
关键词 Infantile Hypertrophic Pyloric stenosis (IHPS) Immunohistochemistry Smooth Muscle CELLS Gastrin MOTILIN Gastrointestinal MOTILITY Erythromycin PYLOROMYOTOMY Acidification of the Stomach Pyloric SPHINCTER Function receptor Binding Pathogenesis Antral MOTILITY Gastric Outflow Obstruction Linkage Analysis single Nucleotide Polymorphism: Interstitial CELLS of Cahal Nitric Oxide Synthetase
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Modulation of firing activity by endogenous GABA_A receptors in the globus pallidus of MPTP-treated parkinsonian mice 被引量:1
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作者 Xin-Yi Chen Yan Xue +3 位作者 Hua Wang Su-Hong Zhu Xiao-Meng Hao Lei Chen 《Neuroscience Bulletin》 SCIE CAS CSCD 2013年第6期701-707,共7页
The globus pallidus in rodents,equivalent to the external segment of the globus pallidus in primates,plays an important role in movement regulation.Previous studies have shown abundant γ-aminobutyric acid(GABA)ergi... The globus pallidus in rodents,equivalent to the external segment of the globus pallidus in primates,plays an important role in movement regulation.Previous studies have shown abundant γ-aminobutyric acid(GABA)ergic innervation and GABAA receptors in the globus pallidus.In this study,we investigated the effects of endogenous GABAA receptors on the spontaneous firing activity of pallidal neurons in both normal and MPTP-treated mice using multi-barrel electrodes extracellular recordings in vivo.We found that in normal mice,pressure ejection of 0.1 mmol/L gabazine,a specific GABA A receptor antagonist,increased the spontaneous firing rate of globus pallidus neurons by 27.6 ± 5.6%.Furthermore,in MPTP mice(14 days after MPTP treatment),0.1 mmol/L gabazine increased the firing rates by 51.0 ± 7.9%,significantly greater than in normal mice.These results suggest that endogenous GABAA receptors modulate the activity of globus pallidus neurons.The present findings may provide a rationale for investigations into the potential role of GABAA receptors in Parkinson’s disease. 展开更多
关键词 globus pallidus GABA A receptor Parkinson’s disease single unit recording
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Erythropoietin Receptor Gene (EPOR) Polymorphisms are Associated with Sow Litter Sizes 被引量:1
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作者 ZHANG Long-chao WANG Li-gang LI Yong YAN Hua ZHAO Ke-bin WANG Li-xian 《Agricultural Sciences in China》 CAS CSCD 2011年第6期931-937,共7页
The erythropoietin receptor (EPOR) has shown to play an important role in fetal survival by promoting the maturation of red blood cells in many studies of uterine capacity and litter size in swine. In this study, we... The erythropoietin receptor (EPOR) has shown to play an important role in fetal survival by promoting the maturation of red blood cells in many studies of uterine capacity and litter size in swine. In this study, we screened the porcine EPOR gene for mutations and identified five single nucleotide polymorphisms (SNPs): g.705G〉T in intron 1, g.2 373C〉T in intron 4, and g.2 882C〉T, g.3 035A〉G, and g.3 132A〉T in intron 6. We then genotyped 247 Beijing Black (BB) sows and compared the polymorphism data with the litter sizes of 1 375 parities among the sows. At first parity, there was no association of g.2 882C〉T and g.3 132A〉T with litter sizes. However, the CT sows in g.2 882C〉T had 2.13 higher total number born (TNB) (P〈0.01) and 1.81 higher number born alive (NBA) (P〈0.01) than the CC sows and the heterozygous sows in g.3 132A〉T had the highest litter size when compared to the two homozygotes for the later parities (P〈0.05). In the g.3 035A〉G SNP, for the later parities, the TNB of the sows with the GG genotype was 3.81 higher (P〈0.01) and the NBA was 2.75 higher (P〈0.01) than that with the AA genotype but no difference at first parity. The G allele of the EPOR g.705G〉T SNP was associated with a greater litter size at both the first parity (P〈0.05) and later parities (P〈0.01). Furthermore, we determined the allele frequencies for this SNP among five Chinese indigenous pig breeds (Erhualian, Laiwu Black, Meishan, Min, and Rongchang) and three western commercial pig breeds (Duroc, Landrace, and Large White). The G allele of the EPOR g.705G〉T SNP was significantly more common in the more prolific Chinese breeds. These results indicated that the EPOR could be an important candidate gene for litter size and g.705G〉T can serve as a useful genetic marker for improving litter size in both first and later parities in swine. 展开更多
关键词 erythropoietin receptor litter size PIG single nucleotide polymorphism
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血管紧张素Ⅱ1型受体基因rs3772622位点多态性与非酒精性脂肪性肝病发病风险的相关性分析 被引量:2
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作者 刘洋 姜曼 +3 位作者 陈立震 杜水仙 辛永宁 宣世英 《临床肝胆病杂志》 CAS 2015年第7期1082-1087,共6页
目的探究血管紧张素Ⅱ1型受体(AGTR1)rs3772622位点多态性与非酒精性脂肪性肝病(NAFLD)的关系及该位点与patatin样磷酯酶域(PNPLA3)rs738409位点多态性的交互作用。方法选取2013年9月-2014年9月青岛市市立医院经临床B超诊断为NAFL... 目的探究血管紧张素Ⅱ1型受体(AGTR1)rs3772622位点多态性与非酒精性脂肪性肝病(NAFLD)的关系及该位点与patatin样磷酯酶域(PNPLA3)rs738409位点多态性的交互作用。方法选取2013年9月-2014年9月青岛市市立医院经临床B超诊断为NAFLD的患者241例及正常对照人群205例,采用PCR及基因型检测方法对AGTR1 rs3772622位点和PNPLA3 rs738409位点进行检测。运用统计学方法检测两位点等位基因频率、基因型频率及各项临床数据资料生化结果。计量资料行独立样本t检验,计数资料行χ2检验。通过二元Logistic回归分析AGTR1 rs3772622及PNPLA3 rs738409突变基因型罹患NAFLD的风险,使用广义多因子降维法(GMDR)研究两位点之间的交互作用。结果 AGTR1 rs3772622位点基因型及等位基因在NAFLD组与对照组中的分布频率差异无统计学意义(P〉0.05)。相对于野生型,AGTR1 rs3772622位点突变型并未增加NAFLD的发病风险(P〉0.05),PNPLA3 rs738409突变型人群患NAFLD的风险是野生型的2.09倍[OR=2.09,95%可信区间(95%CI):1.35~3.23,P=0.001]。AGTR1 rs3772622位点与PNPLA3 rs738409位点联合作用使NAFLD的发病风险明显增加(OR=3.60,95%CI:1.50~6.23,P〈0.001)。两突变基因双携带者与PNPLA3 rs738409单突变基因携带者生化指标的比较发现ALT、AST在两组间差异有统计学意义(P值均〈0.05)。结论中国人群中AGTR1 rs3772622位点多态性对NAFLD的发生发展无关。但其位点突变可增加PNPLA3rs738409位点突变患者罹患NAFLD的风险。 展开更多
关键词 脂肪肝 多态性 单核苷酸 受体 血管紧张素 1型 patatin样磷酯酶域
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诱骗受体和护骨素基因多态性与克罗恩病易感性和疾病表型的相关性 被引量:2
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作者 邵晓晓 林道泼 +3 位作者 孙良 林芊如 应时杰 余保平 《中华消化杂志》 CAS CSCD 北大核心 2019年第1期24-30,共7页
目的探讨浙江籍汉族人群中诱骗受体1、诱骗受体2和护骨素基因多态性与CD易感性的关系。方法纳入2008年4月至2017年7月于温州医科大学附属第二医院、温州医科大学附属第一医院、温州市中心医院和温州市人民医院消化内科确诊为CD的285例患... 目的探讨浙江籍汉族人群中诱骗受体1、诱骗受体2和护骨素基因多态性与CD易感性的关系。方法纳入2008年4月至2017年7月于温州医科大学附属第二医院、温州医科大学附属第一医院、温州市中心医院和温州市人民医院消化内科确诊为CD的285例患者,另外纳入同期在温州医科大学附属第二医院进行体检的572名健康对照者。采用SNaPshot技术检测研究对象诱骗受体1 (rs12549481)、诱骗受体2 (rs1133782)和护骨素(rs3102735) 3种单核苷酸多态性(SNP)。在CD组和健康对照组之间,采用非条件logistic回归分析各SNP的突变等位基因和基因型频率差异,评价其与CD临床病理特征、糖皮质激素和英夫利西单克隆抗体疗效的关系。结果 CD组诱骗受体2 (rs1133782)的突变等位基因A和基因型GA+AA频率分别为11.93%(68/570)和22.81%(65/285),分别高于健康对照组的8.22%(94/1 144)和15.91%(91/572),差异均有统计学意义(OR=1.513,95%CI 1.088~2.104,P=0.013;OR=1.562,95%CI 1.094~2.230,P=0.014);两组间诱骗受体1 (rs12549481)和护骨素(rs3102735)突变等位基因和基因型频率差异均无统计学意义(P均>0.05)。狭窄型CD患者诱骗受体1 (rs12549481)的突变等位基因C和基因型TC+CC频率分别为13.89%(25/180)和27.78%(25/90),分别低于非狭窄非穿透型CD患者的27.68%(62/224)和48.21%(54/112),差异均有统计学意义(OR=0.421,95%CI 0.252~0.705,P=0.001;OR=0.413,95%CI 0.229~0.747,P=0.003);穿透型CD患者诱骗受体2 (rs1133782)的突变等位基因A和基因型GA+AA频率分别为7.23%(12/166)和13.25%(11/83),分别低于非狭窄非穿透型CD患者的15.62%(35/224)和30.36%(34/112),差异均有统计学意义(OR=0.407,95%CI 0.205~0.809,P=0.009;OR=0.350,95%CI 0.165~0.743,P=0.005);CD不同疾病行为亚组之间,护骨素(rs3102735)的突变等位基因和基因型频率差异均无统计学意义(P均>0.012 5)。诱骗受体1 (rs12549481)、诱骗受体2 (rs1133782)和护骨素(rs3102735)基因多态性与糖皮质� 展开更多
关键词 CROHN病 多态性 单核苷酸 诱骗受体 护骨素
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Fusion protein of single-chain variable domain fragments for treatment of myasthenia gravis
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作者 Fangfang Li Fanping Meng +4 位作者 Quanxin Jin Changyuan Sun Yingxin Li Honghua Li Songzhu Jin 《Neural Regeneration Research》 SCIE CAS CSCD 2014年第8期851-856,共6页
Single-chain variable domain fragment (scFv) 637 is an antigen-specific scFv of myasthenia gravis. In this study, scFv and human serum albumin genes were conjugated and the fusion pro-tein was expressed in Pichia pa... Single-chain variable domain fragment (scFv) 637 is an antigen-specific scFv of myasthenia gravis. In this study, scFv and human serum albumin genes were conjugated and the fusion pro-tein was expressed in Pichia pastoris. The afifnity of scFv-human serum albumin fusion protein to bind to acetylcholine receptor at the neuromuscular junction of human intercostal muscles was detected by immunolfuorescence staining. The ability of the fusion protein to block myas-thenia gravis patient sera binding to acetylcholine receptors and its stability in healthy serum were measured by competitive ELISA. The results showed that the inhibition rate was 2.0-77.4%, and the stability of fusion protein in static healthy sera was about 3 days. This approach suggests the scFv-human serum albumin is a potential candidate for speciifc immunosuppressive therapy of myasthenia gravis. 展开更多
关键词 nerve regeneration myasthenia gravis acetylcholine receptor anti-acetylcholine re-ceptor antibody single-chain variable domain fragment human serum albumin fusion protein immunosuppressive therapy autoimmune disease NSFC grant neural regeneration
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THIRD OLFACTORY RECEPTOR CELL OF SHORT HAIRS OF SENSILLA TRICHODEA ON Antheraea polyphemus AND A. pernyi
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作者 吴才宏 H.J.BESTMANN 《Chinese Science Bulletin》 SCIE EI CAS 1989年第17期1475-1480,共6页
I.INTRODUCTION The sensilla trichodea has been accepted as the receiver of sex pheromone in Lepidotera moths. In Antheraea polyphemus and A. pemyi, there are at least two types of sensilla trichodea with different len... I.INTRODUCTION The sensilla trichodea has been accepted as the receiver of sex pheromone in Lepidotera moths. In Antheraea polyphemus and A. pemyi, there are at least two types of sensilla trichodea with different lengths which are called the long and short sensilla trichodea. Two pheromone components (E-6, Z-11-16 :Ac, E-6, Z-11-16:Al) are known of A. polyphemus. 展开更多
关键词 SENSILLA trichodea receptor CELL PHEROMONE single SENSILLUM recording Antheraea pernyi A polyphenus
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TGF-β、IL-4R基因单核苷酸多态性与中国人群经典霍奇金淋巴瘤发病关系的研究 被引量:1
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作者 王欣如 李丽珍 +4 位作者 黄涛 李颢 王鲁群 李湘新 李芳邻 《中华血液学杂志》 CAS CSCD 北大核心 2012年第12期1015-1019,共5页
目的研究转化生长因子-β1(TGF-β1)基因G-800A、C-509T及IL-4受体(IL-4R)基因V75I位点单核苷酸多态性与成人经典霍奇金淋巴瘤(CHL)易感性的关系。方法应用PCR-限制性片段长度多态性技术研究TGF-B1G-800A、C-509T,IL-4RV75I位点... 目的研究转化生长因子-β1(TGF-β1)基因G-800A、C-509T及IL-4受体(IL-4R)基因V75I位点单核苷酸多态性与成人经典霍奇金淋巴瘤(CHL)易感性的关系。方法应用PCR-限制性片段长度多态性技术研究TGF-B1G-800A、C-509T,IL-4RV75I位点多态性分布特点,并结合临床资料分析其与CHL发病风险的关系。结果TGF—B1C-509T、G-800A存在明显连锁不均衡性(D’0.879,r2=0.83,P=0.020);混合细胞型CHL组与对照组GT单倍体型的分布频数分别为53.1%和34.2%,差异有统计学意义(OR=2.35,P=0.000);突变型基因T/T在疾病组和对照组分布频数分别为38.8%和15.3%,差异有统计学意义(OR=3.654,P=0.000);结节硬化型CHL患者IL-4RV75I位点突变型基因A/A在疾病组和对照组分布频数分别为19.2%和41.75%,差异有统计学意义(OR=3.156,P=0.000)。结论TGF—B1G-800A、C-509T连锁单核苷酸多态性位点、IL-4RV75I位点多态性与中国人群CHL的发病风险存在相关性。 展开更多
关键词 淋巴瘤 霍奇金 多态性 单核苷酸 转化生长因子131 白细胞介素4 受体
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Probing Allosteric Modulation of Membrane Receptor in the Native State by Data Mining-Integrated Tracking Microscopy
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作者 Bin Xiong Jia Wu +4 位作者 Jinhui Shang Yancao Chen Yan He Xiao-Bing Zhang Weihong Tan 《CCS Chemistry》 CAS 2022年第9期3150-3161,共12页
As a general mechanism for governing the bioactivity of membrane receptors,allosteric modulation is critical in cell signaling and cell communication but remains difficult to measure in situ.Herein,we introduce a data... As a general mechanism for governing the bioactivity of membrane receptors,allosteric modulation is critical in cell signaling and cell communication but remains difficult to measure in situ.Herein,we introduce a data mining-integrated tracking microscopy(DMITM)to investigate allosteric modulation of membrane receptors in the native state in live cells.Using Kmeans clustering-based hidden Markov modeling to uncover the ligand binding and unbinding events with diffusivity variations of ligand-conjugated nanoprobes as observations. 展开更多
关键词 single-particle tracking allosteric modulation receptor activity binding kinetics free energy landscape
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SPECT脑血流灌注显像和受体显像对抑郁症的研究
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作者 原凌 刘建中 武志芳 《国际放射医学核医学杂志》 2007年第5期277-280,共4页
抑郁症的影像学检查有结构性脑成像和功能性脑成像,CT和MRI检查脑结构的异常既不显著又不具有特异性,而PET和SPECT提供了在活体内对抑郁症进行局部脑血流灌注和中枢神经递质与受体结构和功能的研究,为进一步探讨抑郁症的病因、发病... 抑郁症的影像学检查有结构性脑成像和功能性脑成像,CT和MRI检查脑结构的异常既不显著又不具有特异性,而PET和SPECT提供了在活体内对抑郁症进行局部脑血流灌注和中枢神经递质与受体结构和功能的研究,为进一步探讨抑郁症的病因、发病机制以及临床治疗提供客观依据。 展开更多
关键词 抑郁症 体层摄影术 发射型计算机 单光子 血液灌注 受体 5-羟色胺 受体 多巴胺
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