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28篇 您的检索式:作者名="George CH"
    题名 作者 年代 出处 被引量
1Relation between common polymorphisms in genes related to inflammatory response and colorectal cancer显示文摘瞄准:在象 interleukin ( IL )那样的煽动性的反应相关的基因调查在普通单个核苷酸多型性( SNP )之间的协会-6, IL-8 ,肿瘤坏死因素高山哈( TNFalpha ), peroxisome 激活proliferators 的受体鲸鱼群妈( PPARgamma ),细胞间的粘附 molecule-1 ( ICAM-1 )和颜色的风险在一组希腊病人的表面的癌症( CRC )。方法:学习组由 222 个 CRC 病人和 200 健康控制组成了。Genotyping 用 PRC-RFLP 的等位基因特定的 PCR 被执行,结果被定序证实。我们在 IL-6 学习了 SNP 的协会(-174G>C), IL-8 (-251T>A), TNFalpha (-308G>A), ICAM-1 (R241G 和 K469E ) ,和 PPARgamma (Pro12Ala ) 基因和 CRC 的风险。结果:ICAM-1 的 IL-6 -174G, R241 和 K469 等位基因与 CRC 的增加的风险被联系(或 = 1.77, 95% CI:1.34-2.34;或 = 1.83, 95% CI:1.23-2.72;并且或 = 1.35, 95% CI:1.03-1.77 分别地) 。IL-8 和 TNFalpha 多型性没有效果。而 PPARgamma Pro12 遗传型与疾病的增加的风险被联系(或 = 1.78, 95% CI:1.25-2.49 ) 。结论:在在免疫逻辑的普通 SNP 之间的协会反应相关的基因和 CRC 在现在的学习被报导。除了使恶意开始和前进的机制清楚些, SNP 可以改进在风险的为亚人口的适当屏蔽。George Theodoropoulos Ioannis Papaconstantinou Evangelos Felekouras Nikolaos Nikiteas Petros Karakitsos Dimitris Panoussopoulos Andreas Ch Lazaris Efstratios Patsouris John Bramis Maria Gazouli 2006World Journal of Gastroenterology2006,12,31:16
2A branch and bound method for stochastic global optimization显示文摘Vladimir I Norkin Georg Ch Pfiug and Andrzej Ruszczynski 1998Math Prog1998,83,:2
3hnaging features of a heterogeneous group of disorders显示文摘Georg FE Jean CH Heinz T 1998Pediatr Radiol1998,28,:1
4Prevalence in the U- nited States of aac(6')-Ib-cr encoding a ciprofloxacin-modif- ying enzyme 显示文摘Park CH Robicsed A George J 2006Antimicrob Agents Chemother2006,50,39:1
5SCN1A splice variants exhibit divergent sensitivity to commonly used antiepileptic drugs 显示文摘Thompson CH Kahlig KM George AL 2011Epilepsia2011,52,5:1
6Kinase mutations and imatinib response in patients with metastatic gastrointestinal stromal tumor显示文摘Michael CH Christopher LC George DD 2003J Clin Oncol2003,21,:1
7BSA nanoparticle loaded atorvastatin ealcium-a new facet for an old drug 显示文摘Sripriyalakshmi S Anjali CH George PD 2014PLoS One2014,9,86:1
8Ryanodine re- ceptors and ventricular arrhythmias: emerging trends in mutations, mechanisms and therapies 显示文摘George CH Jundi H Thomas NL 2007J Mol Cell Car- diol2007,42,1:1
9Ryanodine receptor mutations associated with stress-induced ventricular tachycardia mediate increased calcium release in stimulated cardiomyo- cytes 显示文摘George CH Higgs GV Lai FA 2003Circulation Research2003,93,6:1
10Configurations of Series-Parallel Networks with Maximum Relia- bility 显示文摘Walter Gutiahr Georg Ch Pflug Andrzei Ruszczynski 1996Microelectronics and Reliability1996,36,2:1
11Diode-pumped Yb:GGG laser: comparison with Yb:YAG显示文摘S. Chénais F. Druon F. Balembois P. Georges A. Brenier G. Boulon 2002Optical Materials2002,,2:1
12Pnpt1 mediates NLRP3 inflammasome activation by MAVS and metabolic reprogramming in macrophages显示文摘Polyribonucleotide nucleotidyltransferase 1(Pnpt1)plays critical roles in mitochondrial homeostasis by controlling mitochondrial RNA(mt-RNA)processing,trafficking and degradation.Pnpt1 deficiency results in mitochondrial dysfunction that triggers a type I interferon response,suggesting a role in inflammation.However,the role of Pnpt1 in inflammasome activation remains largely unknown.In this study,we generated myeloid-specific Pnpt1-knockout mice and demonstrated that Pnpt1 depletion enhanced interleukin-1 beta(IL-1β)and interleukin-18(IL-18)secretion in a mouse sepsis model.Using cultured peritoneal and bone marrow-derived macrophages,we demonstrated that Pnpt1 regulated NLRP3 inflammasome-dependent IL-1βrelease in response to lipopolysaccharide(LPS),followed by nigericin,ATP or poly(I:C)treatment.Pnpt1 deficiency in macrophages increased glycolysis after LPS administration and mt-reactive oxygen species(mt-ROS)after NLRP3 inflammasome activation.Pnpt1 activation of the inflammasome was dependent on increased glycolysis and the expression of mitochondrial antiviral-signaling protein(MAVS)but not NF-κB signaling.Collectively,these data suggest that Pnpt1 is an important mediator of inflammation,as shown by activation of the NLRP3 inflammasome in murine sepsis and cultured macrophages.Chia George Hsu Wenjia Li Mark Sowden Camila Lage Chávez Bradford C.Berk 2023Cellular & Molecular Immunology2023,20,2:1
13Developing new anti-arrhythmics:clues from the molecular basis of cardiac ryanodine receptor(RyR2) Ca2+-release channel dysfunction显示文摘George CH Lai FA 2007Curr Pharm Des2007,13,31:1
14Ryanodine receptor mutations associated with stress-induced ventricular tachycardia mediate increased calcium release in stimulated cardiomyocytes显示文摘George CH Higgs GV Lai FA 2003Circ Res2003,93,6:1
15Arrhythmogenic mutation-linked defects in ryandine receptor autoregulation reveal a novel mechanism of Ca^2+ release channel dysfunction显示文摘George CH Jundi H Waiters N et ai 2006Circ Res2006,98,:1
16INSPIRE – Co-Simulation von Energie- und IKT-Systemen zur Evaluation von Smart-Grid-Applikationen显示文摘Sven Christian Müller Hanno Georg Markus Küch Christian Wietfeld 2014at - Automatisierungstechnik2014,,5:1
17BSA nanoparticle loaded atorvastatin calcium-a new facet for an old drug显示文摘Sripriyalakshmi S Anjali CH George PDC 2014Plos One2014,9,86:1
18Interaction of the plasmid-encoded quinolone resistance protein QnrA with Escherichia coil Topoisomerase Ⅳ 显示文摘John HT George A J David CH 2005Antimicrob Agents Chemother2005,49,7:1
19Vancomycin-resistant enterococci显示文摘Uttley AH Collins CH Naidoo J George RC 1988Lancet1988,1,:1
20Variation in red cell transfusion practice in the intensive care unit:a multicentre cohort study显示文摘PAUL CH GEORGE W CLAUDIO M 1999Critical Care1999,3,:1
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