نتایج جستجو برای: snp polymorphism

تعداد نتایج: 116808  

2006
Junhua Xiao Xiujuan Xin Xiaohui Luan Dongzhi Wei Shengli Yang

We describe a modified single nucleotide polymorphism (SNP) typing method based on the restriction fragment length polymorphism polymerase chain reaction (RFLP-PCR). This is a simple, economical method without the need for special equipment. For most SNP loci, a common restriction endonuclease (Hind III, EcoR I or BamH I) recognizing site (RER) can be introduced into one allelic form, but not t...

2011
Yiping Li Xianli Li Li Shi Man Yang Ying Yang Wenyu Tao Lei Shi Yuxin Xiong Ying Zhang Yufeng Yao

Recently, many studies have reported that the SNP+45(T>G) and SNP+276(G>T) polymorphisms in the adiponectin gene are associated with type 2 diabetes (T2DM) in the Chinese Han population. However, the previous studies yielded many conflicting results. Thus, a meta-analysis of the association of the adiponectin gene with T2DM in the Chinese Han population is required. In the current study, we fir...

Journal: :Asian Pacific journal of cancer prevention : APJCP 2013
Hesham Mahmoud Saeed Mohammad Saud Alanazi Narasimha Reddy Parine Jilani Shaik Abdelhabib Semlali Othman Alharbi Nahla Azzam Abdulrahman Aljebreen Majid Almadi Manal Aly Shalaby

BACKGROUND Matrix metalloproteinase-2 (MMP-2) is an enzyme with proteolytic activity against matrix proteins, particularly basement membrane constituents. A single nucleotide polymorphism (SNP) at -1306, which disrupts a Sp1-type promoter site (CCACC box), results in strikingly lower promoter activity with the T allele. In the present study, we investigated whether this MMP-2 genetic polymorphi...

2015
Daisuke Nishizawa Shinya Kasai Junko Hasegawa Naomi Sato Fumihiko Tanioka Haruhiko Sugimura Kazutaka Ikeda Yoh Dobashi

To clarify the potential role of variability within and around the AKT1 gene in smoking behaviors, we performed a single-nucleotide polymorphism (SNP) analysis of the AKT1 gene in an elderly Japanese cohort. Genotypes of the rs2498794 SNP, which is located in the fifth intron region of the AKT1 gene, were marginally but significantly associated with smoking duration in the total 999 samples of ...

Journal: :Haematologica 2007
Atreyee Saha Saibal Mukherjee Mahua Maulik Giriraj Ratan Chandak Kunal Ray

Hemophilia A is an X-linked recessive bleeding disorder caused by defects in factor VIII gene (F8). Our study examines variations of single nucleotide polymorphism (SNP) in F8 in the Indian population and establishes the utility of a combination of SNP and microsatellite markers for the successful identification of carriers in the affected families.

Journal: :iranian journal of allergy, asthma and immunology 0
ali mosayebian department of immunology, school of medicine, isfahan university of medical sciences, isfahan, iran. mazdak ganjalikhani-hakemi cellular and molecular immunology research center, faculty of medicine, isfahan university of medical sciences, isfahan, iran. rezvan meshkat department of immunology, faculty of medicine, shahrekord university of medical sciences, shahrekord, iran. ramin ghasemi department of immunology, school of medicine, isfahan university of medical sciences, isfahan, iran. hossain khan-ahmad department of genetics and molecular biology, faculty of medicine, isfahan university of medical sciences, isfahan, iran. morteza samadi department of immunology, faculty of medicine, shahid sadoughi university of medical sciences, yazd, iran and reproductive immunology research center, shahid sadoughi university of medical sciences, yazd, iran.

the snp (rs11209026, arg381gln, r381q) in the il-23 receptor (il23r) confers protection against multiple inflammatory diseases, representing one of the most significant human genetic polymorphisms in inflammatory diseases. we, therefore, investigated the association between il-23 r r381q gene polymorphism and asthma.this case-control study was performed on 209 patients, and 200 healthy controls...

Journal: :Arquivos de gastroenterologia 2012
Evelyn Mendoza Torres Lourdes Luz Varela Prieto José Luis Villarreal Camacho Daniel Antonio Villanueva Torregroza

CONTEXT Genotyping of single nucleotide polymorphism (SNP C/T(-13910)) located upstream of the lactase gene is used to determine adult-type hypolactasia/lactase persistence in North-European Caucasian subjects. The applicability of this polymorphism has been studied by comparing it with the standard diagnostic methods in different populations. OBJECTIVE To compare the lactose hydrogen breath ...

Journal: :Carcinogenesis 2004
Jianhui Zhang Xia Jin Shumei Fang Yan Li Rui Wang Wei Guo Na Wang Yimin Wang Denggui Wen Lizhen Wei Gang Kuang Zhiming Dong

The matrix metalloproteinases (MMPs), a family of proteolytic enzymes that degrade different components of the extracellular matrix, play important roles in tumor development and invasion. A single adenine insertion/deletion polymorphism (6A/5A) in the MMP3 promoter region causes transcriptional elevation. The aim of this study was to assess the effects of this single nucleotide polymorphism (S...

Journal: :Bioinformatics 2003
Mark Harris Jeremy M. R. Martin John F. Peden Christopher J. Rawlings

UNLABELLED The high cost of genotyping single nucleotide polymorphisms (SNPs) generally prohibits the systematic mapping of entire genetic linkage regions in order to find the polymorphisms associated with increased risk of disease. In practice, SNPs are selected at approximately equal spacing across the linkage region to try to locate a SNP lying in the haplotype block of the disease SNP. The ...

2015
Ki-Hwan Kim Kang-Hyeon Ka Ji Hyoun Kang Sangil Kim Jung Won Lee Bong-Kyun Jeon Jung-Kuk Yun Sang Rul Park Hyuk Je Lee

We identified single nucleotide polymorphism (SNP) markers in the laccase gene to establish a line-diagnostic system for shiitake mushrooms. A total of 89 fungal isolates representing four lines, including Korean registered, Korean wild type, Chinese, and Japanese lines, were analyzed. The results suggest that SNP markers in the laccase gene can be useful for line typing in shiitake mushrooms.

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