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11篇 您的检索式:作者名="Leng CT"
    题名 作者 年代 出处 被引量
1Resuscitation after prolonged ventricular fibrillation with use of monophasic and biphasic waveform pulses for external defibrillation显示文摘Leng CT Paradis NA Calkins H et td 2000Circulation2000,101,:1
2Resuscitation after prolonged ventricular fibrillation with use of monophasic and biphasic waveform pulses for external defibrillation显示文摘Leng CT Paradis NA Calkins H 0,,25:1
3Humoral mechanism in pathogenesis of portal hypertension显示文摘Hung CT Du RY Leng XS 1982Chin Med Egnl1982,95,6:1
4CIM4 is the signaling component ff the macrophage migration inhibitory tactor-CD74 reeeptor complex 显示文摘Shi X Leng L Warren K ct al 2006hnmunity2006,25,4:1
5The 'Humoral Mechanism':A factor in the pathogenesis of portal hypertension显示文摘Huang CT Du RY Leng XS 1982Zhonghua Waike Zazhi1982,20,9:1
6Humoral mechanism in pathogensis of portal hypertension显示文摘Huang CT Du RY Leng XS 1982Chin Med J1982,95,:1
7Effect of cimetidine on wedged hepatic venous pressure in cirrhotic patients 显示文摘Leng XS Huang CT Wang XG 1991Chin Med J1991,104,:1
8Resuscitation after pro- longed ventricular ibriUation with use of monophasic and biphasic waveform pulses for external defibrillation显示文摘Leng CT Paradis NA Calkins H 2000Circulation2000,101,:1
9Multipleroles of HDAC inhibition in neurodegenerative conditions显示文摘CKuang DM Leng Y Marinova Z* Kim HJ Chiu CT 2009Trends Neurosci2009,32,11:1
10Humoral mechanisms in the pathogensis of portal hypertension显示文摘HUANG CT DU RY LENG XS 1982Chinese M J1982,95,:1
11Genome sequencing reveals the role of rare genomic variants in Chinese patients with symptomatic intracranial atherosclerotic disease显示文摘Objectives The predisposition of intracranial atherosclerotic disease(ICAD)to East Asians over Caucasians infers a genetic basis which,however,remains largely unknown.Higher prevalence of vascular risk factors(VRFs)in Chinese over Caucasian patients who had a stroke,and shared risk factors of ICAD with other stroke subtypes indicate genes related to VRFs and/or other stroke subtypes may also contribute to ICAD.Methods Unrelated symptomatic patients with ICAD were recruited for genome sequencing(GS,60-fold).Rare and potentially deleterious single-nucleotide variants(SNVs)and small insertions/deletions(InDels)were detected in genome-wide and correlated to genes related to VRFs and/or other stroke subtypes.Rare aneuploidies,copy number variants(CNVs)and chromosomal structural rearrangements were also investigated.Lastly,candidate genes were used for pathway and gene ontology enrichment analysis.Results Among 92 patients(mean age at stroke onset 61.0±9.3 years),GS identified likely ICAD-associated rare genomic variants in 54.3%(50/92)of patients.Forty-eight patients(52.2%,48/92)had 59 rare SNVs/InDels reported or predicted to be deleterious in genes related to VRFs and/or other stroke subtypes.None of the 59 rare variants were identified in local subjects without ICAD(n=126).31 SNVs/InDels were related to conventional VRFs,and 28 were discovered in genes related to other stroke subtypes.Our study also showed that rare CNVs(n=7)and structural rearrangement(a balanced translocation)were potentially related to ICAD in 8.7%(8/92)of patients.Lastly,candidate genes were significantly enriched in pathways related to lipoprotein metabolism and cellular lipid catabolic process.Conclusions Our GS study suggests a role of rare genomic variants with various variant types contributing to the development of ICAD in Chinese patients.Mengmeng Shi Xinyi Leng Ying Li Zihan Chen Ye Cao Tiffany Chung Bonaventure YM Ip Vincent HL Ip Yannie OY Soo Florence SY Fan Sze Ho Ma Karen Ma Anne Y Y Chan Lisa WC Au Howan Leung Alexander Y Lau Vincent CT Mok Kwong Wai Choy Zirui Dong Thomas W Leung 2022Stroke & Vascular Neurology2022,7,3:0
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