Genetic modifier genes for inherited heart and muscle disease 

Genetic mutations in single genes lead to inherited forms of cardiac and muscle disease. Cardiomyopathy from genetic mutations may develop in early or later ...
《岭南心血管病杂志》  2011年 第S1期 下载次数(21)| 被引次数(0)

Ehlers-Danlos syndrome type Ⅳ causing renovascular hypertension,diagnosed by clinical examination and genetic testing 

Ehlers-Danlos syndrome(EDS) type IV is a rare genetic condition characterized by thin,translucent skin and organ fragility.It may lead to organ rupture and carr...
2015年浙江省外科学学术年会暨国家级肝胆胰疾病诊治进展…  2015-12-10 下载次数(2)| 被引次数(0)

Role of genetic screening in a chinese woman of childbearing age with hypertrophic cardiomyopathy 

Objectives The objective of this study was to evaluate the role of genetic screening in a Chinese woman of childbearing age with hypertrophic cardiomyopathy....
《岭南心血管病杂志》  2011年 第S1期 下载次数(10)| 被引次数(0)

Genetic testing of inherited cardiomyopathy by next generation semiconductor sequencing technologies 

Objective Inherited cardiomyopathy(IC) is the most common genetic heterogeneity and clinical h eterogeneity cardiac disease. It also causes a significant propor...
中华医学会第十五次全国医学遗传学学术会议暨中国医师协…  2016-11-05 下载次数(1)| 被引次数()

The genetic study of ischemia induced arrhythmia and potassium channels 

Objectives Ischemia induced arrhythmia(ventricular tachycardia/ventricular fibrillation) is one of the major causes of death.Potassium channels change are li...
《岭南心血管病杂志》  2011年 第S1期 下载次数(21)| 被引次数(0)

CYP2C19 and PON1 genetic variants as potential predictors for the risk of bleeding in antiplatelet-treated patients 

AIM:Bleeding has emerged as an important outcome in antiplatelet treatment after percutaneous coronary intervention(PCI),but the study on the relationship be...
《中国病理生理杂志》  2012年 第11期 下载次数(18)| 被引次数(0)

Genetic and epigenetic predispositions underlying cardiovascular outcomes among patients treated with clopidogrel and aspirin 

Coronary artery disease(CAD) is a major cause of death and disability worldwide,and consumes a considerable amount of medical resources every year.Clopidogrel i...
《中国药理学与毒理学杂志》  2018年 第04期 下载次数(26)| 被引次数()

A genetic variation in NOSIAP is associated with idiopathic ventricular tachycardia(IVT) 

Objective Test the association between the variation rs 12143842 in NOS1AP and idiopathic ventric ular tachycardia(TVT). Methods A case control association s...
中华医学会心电生理和起搏分会第十次全国学术年会会议汇…  2012-09-13 下载次数(6)| 被引次数(0)

A novel genetic screen for leukemia stem cell immortalization genes 

Leukemia,like many other cancers,is thought to arise from a small population of stem cells that have the capacity to self-renewal extensively and to initiate...
《Journal of Nanjing Medical University》  2007年 第06期 下载次数(18)| 被引次数(0)

A comprehensive protocol for preimplantation genetic diagnosis(PGD) for patients with hemophilia B by Comparition of Karyomapping test and the conventional PCR methods including DNA direct suquecing and STRs analysis 

Objective Hemophilia B(HB) is the second most common form of hemophilia after hemophilia A. It is estimated that one in 30,000 live male births of all populatio...
中华医学会第十五次全国医学遗传学学术会议暨中国医师协…  2016-11-05 下载次数(7)| 被引次数()

Prevalence and Genetic analysis of α-and β-thalassemia in the Baise region of southern China 

Objective:Thalassemia is one of the most common hereditary blood disorders.Epidemiological data regarding the occurrence and distribution of thalassemia is impo...
第十四次全国医学遗传学学术会议论文汇编  2015-11-01 下载次数(7)| 被引次数(0)

Role of genetic screening in a Chinese woman of childbearing age with hypertrophic cardiomyopathy 

Objective The objective of this study was to evaluate the role of genetic screening in a Chinese woman of childbearing age with hypertrophic cardiomyopathy.M...
第十三次全国心血管病学术会议论文集  2011-06-23 下载次数(5)| 被引次数(0)

Genetics of coronary artery disease and myocardial infarction 

Atherosclerotic coronary artery disease(CAD) comprises a broad spectrum of clinical entities that include asymptomatic subclinical atherosclerosis and its clini...
《World Journal of Cardiology》  2016年 第01期 下载次数(44)| 被引次数(21)

Association of VEGF genetic polymorphisms with the clinical characteristics of non-Hodgkin's lymphoma 

PURPOSE:Vascular endothelial growth factor(VEGF) plays an important role in tumor angiogenesis and cancer progression The VEGF genetic polymorphisms were sho...
第五届全国中医药免疫学术研讨会——暨环境·免疫与肿瘤…  2009-10-01 下载次数(5)| 被引次数(0)

Genetic Diagnosis in a Big Chinese Family with Polycystic Kidney Disease and Thalassemia Minor 

Objective To identify genetic defects in a large family with polycystic kidney disease and thalasse mia minor. Method Whole genome next-generation sequencing wa...
中华医学会第十五次全国医学遗传学学术会议暨中国医师协…  2016-11-05 下载次数(2)| 被引次数()

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