全部文献期刊学位论文会议报纸专利标准年鉴图书|学者科研项目
中外文文献  中文文献  外文文献
作者:Stanney K , Salvendy G , Deisinger J ...
来源:[J].International Journal of Human-Computer Interaction(IF 1.131), 2001, Vol.10 (2), pp.135-87PubMed
摘要:This report represents a committee summary of the current state of knowledge regarding aftereffects and sense of presence in virtual environments (VEs). The work presented in this article, and the proposed research agenda, are the result of a special session that was set up in th...
作者:Dhivya , Anand , Srilakshmiprabha ...
来源:[J].International Journal of Human Genetics(IF 0.187), 2016, Vol.16 (3-4), pp.128-131Taylor & Francis
摘要:Abstract(#br)Inflammatory bowel disease (IBD) is a group of disorders distinguished as Crohn’s Disease (CD) and Ulcerative colitis (UC). The etiology is multi-factorial and numerous genes are involved in the pathogenesis of IBD; hence the genetic cause is only moderately und...
作者:Vipin Gupta , Gagandeep Kaur Walia
来源:[J].International Journal of Human Genetics(IF 0.187), 2017, Vol.17 (3), pp.140-144Taylor & Francis
摘要:ABSTRACT(#br)The increased burden of type 2 diabetes mellitus (T2DM) has accelerated the number of genetic studies in different human populations for detecting at least predictive biomarkers related to T2DM. Genome-wide association designs have successfully identified number of p...
作者:Kar , Sivamani , Sivakumar
来源:[J].International Journal of Human Genetics(IF 0.187), 2015, Vol.15 (2), pp.51-54Taylor & Francis
摘要:Abstract(#br)Williams syndrome (OMIM 194050) is a rare multisystem genetic disorder with an incidence of 1/ 75000 which usually occurs sporadically caused by the deletion of 26 contiguous genes, including elastin (ELN) (OMIM 130160) on chromosome 7q11.23. The researchers present ...
作者:Lerttham , Fucharoen , Yamsri ...
来源:[J].International Journal of Human Genetics(IF 0.187), 2015, Vol.15 (4), pp.191-198Taylor & Francis
摘要:Abstract(#br)Haplotype associated with the -31 (A-G) β+ -thalassemia gene in seven Thai individuals were examined and compared with that described originally in Japanese. Seven polymorphic restriction sites within β-globin gene cluster were determined using allele...
作者:Temurhan , Tamay , Gurkan ...
来源:[J].International Journal of Human Genetics(IF 0.187), 2016, Vol.16 (1-2), pp.40-47Taylor & Francis
摘要:Abstract(#br)Significant effects of several modifying genes on the clinical features of cystic fibrosis (CF) have been reported. In the present study, the researchers investigated the effects of transforming growth factor beta 1 (TGFB1) and cluster of differentiation 14 (CD14) po...
作者:Vijayashree Priyadharsini Jayaseelan , Karthikeyan Muthusamy , Shridevi Venkatramani ...
来源:[J].International Journal of Human Genetics(IF 0.187), 2017, Vol.17 (4), pp.169-176Taylor & Francis
摘要:ABSTRACT(#br)Essential hypertension (EH) makes up ∼ 95 percent of all hypertensive cases and has no clear identifiable cause. Although EH has a strong genetic basis, identification of genes associated with it has been difficult because of the complexity of regulation of bloo...
作者:Balachandar , Ramkumar , Maheswari ...
来源:[J].International Journal of Human Genetics(IF 0.187), 2016, Vol.16 (3-4), pp.132-134Taylor & Francis
摘要:Abstract(#br)Duchenne muscular dystrophy (DMD) is an X-linked neuromuscular degenerative disorder initiated by mutation in the dystrophin gene that is located on chromosome Xp21.The present case is a novel report of DMD with co-occurrence of Autism associated disorder, which has ...
作者:Karkucak , Solak , Turan ...
来源:[J].International Journal of Human Genetics(IF 0.187), 2015, Vol.15 (3), pp.93-96Taylor & Francis
摘要:Abstract(#br)Mannose-Binding Lectin (MBL) plays an important role in innate immunity. MBL2 gene polymorphisms affect MBL serum levels. Therefore, this increases the risk of infection and may result in predisposition to autoimmune diseases. The aim of this study was to investigate...
作者:Yesilkaya , Karkucak , Coban ...
来源:[J].International Journal of Human Genetics(IF 0.187), 2015, Vol.15 (4), pp.183-189Taylor & Francis
摘要:Abstract(#br)The aim of the present study is to investigate the relationship between angiotensin-converting enzyme (ACE) gene polymorphism and pulmonary embolism by comparing the frequency of ACE gene polymorphism between cases diagnosed with pulmonary embolism with that of the c...

我们正在为您处理中,这可能需要一些时间,请稍等。

资源合作:cnki.scholar@cnki.net, +86-10-82896619   意见反馈:scholar@cnki.net

×