نتایج جستجو برای: respectively three different genotypic variants including aa

تعداد نتایج: 3886708  

2013
Seungbok Lee Seung Hwan Paik Hyun-Jin Kim Hyeong Ho Ryu Soeun Cha Seong Jin Jo Hee Chul Eun Jeong-Sun Seo Jong-Il Kim Oh Sang Kwon

Alopecia areata (AA) is a common autoimmune disorder mostly presented as round patches of hair loss and subclassified into alopecia totalis/alopecia universalis (AT/AU) based on the area of alopecia. Although AA is relatively common, only 5% of AA patients progress to AT/AU, which affect the whole scalp and whole body respectively. To determine genetic determinants of this orphan disease, we un...

Journal: :The Journal of general virology 2004
Rosa M Ordóñez Ana María Espinosa Dolores Javier Sánchez-González Juan Armendáriz-Borunda Jaime Berumen

Asian-American (AA) variants of human papillomavirus 16 (HPV-16) are linked to a high incidence of cervical cancer in Mexico, with some evidence strongly suggesting that they are more oncogenic than European (E) variants, including their association with younger women and their higher associated risk of cervical cancer. Differences in the regulation of viral E6/E7 oncogene transcription by the ...

2012
Minzhong Tang James A. Lautenberger Xiaojiang Gao Efe Sezgin Sher L. Hendrickson Jennifer L. Troyer Victor A. David Li Guan Carl E. Mcintosh Xiuchan Guo Yuming Zheng Jian Liao Hong Deng Michael Malasky Bailey Kessing Cheryl A. Winkler Mary Carrington Guy dé The Yi Zeng Stephen J. O'Brien

Nasopharyngeal carcinoma (NPC) is an epithelial malignancy facilitated by Epstein-Barr Virus infection. Here we resolve the major genetic influences for NPC incidence using a genome-wide association study (GWAS), independent cohort replication, and high-resolution molecular HLA class I gene typing including 4,055 study participants from the Guangxi Zhuang Autonomous Region and Guangdong provinc...

2014
Zhangyong Hu Jun Yang Guolian Xiong Han Shi Yuan Yuan Lin Fan Yali Wang

BACKGROUND Previous studies have shown that genetic variants in HLA-DP genes affect disease progression in hepatitis B virus (HBV) infection. OBJECTIVES We aimed to evaluate possible association between HLA-DPB1 rs9277534 polymorphism and different clinical complications of hepatitis B virus (HBV) infection. MATERIALS AND METHODS Snapshot assay was used to investigate the association of rs9...

2017
You Li Yongquan Huang Xue Liang Bingshuang Long Shiyi Chen Jiahao Lian Yi Wei Zhiyong Zhang Jian Qin

This study aims to determine the association between the apolipoprotein C-I polymorphism and the longevity and genetic variants in ApoC-I that can influence the serum lipid levels in Bama. ApoC-I genotypes were determined by Taqman single nucleotide polymorphism (SNP) genotyping assays in 178 long-lived inhabitants (longevity group aged from 90 to 110 years), 147 healthy controls (Control 1 gro...

2013
Ulrike Peters Kari E. North Praveen Sethupathy Steve Buyske Jeff Haessler Shuo Jiao Megan D. Fesinmeyer Rebecca D. Jackson Lew H. Kuller Aleksandar Rajkovic Unhee Lim Iona Cheng Fred Schumacher Lynne Wilkens Rongling Li Keri Monda Georg Ehret Khanh-Dung H. Nguyen Richard Cooper Cora E. Lewis Mark Leppert Marguerite R. Irvin C. Charles Gu Denise Houston Petra Buzkova Marylyn Ritchie Tara C. Matise Loic Le Marchand Lucia A. Hindorff Dana C. Crawford Christopher A. Haiman Charles Kooperberg

Genetic variants in intron 1 of the fat mass- and obesity-associated (FTO) gene have been consistently associated with body mass index (BMI) in Europeans. However, follow-up studies in African Americans (AA) have shown no support for some of the most consistently BMI-associated FTO index single nucleotide polymorphisms (SNPs). This is most likely explained by different race-specific linkage dis...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه رازی - دانشکده علوم 1389

fluorescence chemical sensors for the highly sensitive and selective determination of pb2+ , hg2+, co2+ and fe3+ ions in aqueous solutions are described. the ion sensing system was prepared by incorporating lipophilic ligand (l) as a neutral ion-selective fluoroionophore in the plasticized pvc membrane containing sodium tetraphenylborate or potasium tetrakis (p-chlorophenyl) borate as a liphoph...

Journal: :Inflammatory bowel diseases 2012
Oloruntosin Adeyanju David T Okou Clifton Huang Archana Kumar Cary Sauer Courtney Galloway Mahadev Prasad Jon Waters David J Cutler Michael E Zwick Tanvi Dhere Subra Kugathasan

BACKGROUND Crohn's disease (CD) is highly heritable. NOD2 has emerged as the main susceptibility gene among individuals of European ancestry; however, NOD2 does not appear to contribute to CD susceptibility among many non-European populations. Today's African American (AA) population represents an admixture of West African (80%) and European (20%) ancestry. Since genotype-based tools are becomi...

2017
Edwin J. Anaya-Pava Jesús Nares-Cisneros Rubén I. Cárdenas-Hernández Yolanda Jaramillo-Rodríguez Graciela Zambrano-Galván

PURPOSE To determine the frequency and association of polymorphisms in the TP53 and RB1 genes with clinical characteristics in a group of children with retinoblastoma (RB) in northern Mexico. METHODS A prospective, longitudinal, and analytical study of 11 patients diagnosed with RB was conducted. Endpoint PCR and high-resolution real-time PCR were performed. Chi-square and Student t tests wer...

Journal: :Journal of evolutionary biology 2015
M A Wenzel S B Piertney

The extent to which genotypic variation at a priori identified candidate genes can explain variation in complex phenotypes is a major debate in evolutionary biology. Whereas some high-profile genes such as the MHC or MC1R clearly do account for variation in ecologically relevant characters, many complex phenotypes such as response to parasite infection may well be underpinned by a large number ...

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