نتایج جستجو برای: genotype frequencies

تعداد نتایج: 180285  

2017
Gerard Marshall Raj Jayanthi Mathaiyan Mukta Wyawahare Katiboina Srinivasa Rao Rekha Priyadarshini

Introduction: Drug transporters are key determinants of pharmacokinetic and pharmacodynamic profiles of certain drugs. SLC47A1 (MATE1) and SLC47A2 (MATE2) are major efflux transporters involved in the hepatic and renal excretion of many cationic drugs including metformin. Our study was proposed to determine the normative frequencies of the single nucleotide polymorphisms (SNPs) rs2289669 and rs...

Journal: :Experimental and therapeutic medicine 2015
Yong Su Gui-Lian Kong Ya-Li Su Yan Zhou Li-Fang Lv Qiong Wang Bao-Ping Huang Rui-Zhi Zheng Quan-Zhong Li Hui-Juan Yuan Zhi-Gang Zhao

This study aimed to investigate whether single nucleotide polymorphisms (SNPs) located near the gene of the ABO blood group play an important role in the genetic aetiology of menstrual disorders (MDs). Polymerase chain reaction-ligase detection reaction technology was used to detect eight SNPs near the ABO gene location on the chromosomes in 250 cases of MD and 250 cases of normal menstruation....

Journal: :تحقیقات دامپزشکی 0
محمد مهدی رنجبر گروه میکروبیولوژی و ایمونولوژی، دانشکده دامپزشکی دانشگاه تهران، تهران-ایران غلامرضا نیکبخت بروجنی گروه میکروبیولوژی و ایمونولوژی، دانشکده دامپزشکی دانشگاه تهران، تهران-ایران علیرضا قدردان مشهدی دانشکده دامپزشکی، دانشگاه شهید چمران اهواز، اهواز، ایران مهران دباغیان دانش آموخته دوره دکترای تخصصی ایمنی شناسی، دانشکده دامپزشکی دانشگاه تهران، تهران-ایران

background: major histocompatibility complex (mhc) comprises a group of genes, which plays a central role in immune response. the exon 2 of bula-drb3 is part of the mhc class ii in buffalo that highly polymorphic, found to be associated with resistance/susceptibility to infections and also with production parameters. objectives: the purpose of the present study is to identify bula-drb3 polymorp...

Journal: :Journal of neurology, neurosurgery, and psychiatry 2002
M Riemenschneider J Diehl U Müller H Förstl A Kurz

OBJECTIVES The apolipoprotein E (apoE) polymorphism, designated as epsilon2, epsilon3, epsilon4, is a genetic risk factor associated with several forms of dementia. Inconclusive results have been reported in patients with frontotemporal degeneration which prompted this study of the apoE polymorphism in a German sample with frontotemporal degeneration. METHODS the frequencies of the epsilon2 a...

Journal: :Genetics and molecular research : GMR 2014
V Antonio-Véjar O Del Moral-Hernández L C Alarcón-Romero E Flores-Alfaro M A Leyva-Vázquez D Hernández-Sotelo B Illades-Aguiar

In this study, we examined the distribution of genotype and allele frequencies of the C677T and A1298C polymorphisms in the methylenetetrahydrofolate-reductase gene (MTHFR) in two ethnic groups in the State of Guerrero, Mexico, which were compared with those of the Mestizo population of the region. A comparative study was conducted on 455 women from two ethnic groups and a group of Mestizo wome...

2013
Hee Seon Lee Seung-Hyun Kim Kyung Won Kim Ji Young Baek Hae-Sim Park Kyung Eun Lee Jung Yeon Hong Mi Na Kim Won Il Heo Myung Hyun Sohn Kyu-Earn Kim

Involvement of human histamine N-methyltransferase gene polymorphisms in susceptibility to atopic dermatitis in Korean children. We found an error in our published article. We apologize for any inconvenience this may have caused. The correct table is as below: Table 3. Genotype and allele frequencies of histamine N-methyltransferase (HNMT) polymorphisms in children with atopy Locus Genotype Ato...

2015
Asghar Ebadifar Nazila Ameli Hamid Reza Khorramkhorshid Mehdi Salehi Zeinabadi4 Kourosh Kamali Tayyebeh Khoshbakht

Background and aims. The aim of the present study is to determine the incidence of MTHFR C677 T and A1298C muta-tions in Iranian patients with cleft lip and/or cleft palate. Materials and methods. We screened 61 Iranian patients with cleft lip and/or cleft palate for mutations in the two alleles of MTHFR gene associated with cleft lip and/or palate: A1298C and C677T, using Polymerase Chain Reac...

Journal: :iranian journal of basic medical sciences 0
seyyedeh raheleh hosseyni-talei immunogenetic research center, mazandaran university of medical sciences, sari, iran abdolkarim mahrooz immunogenetic research center, mazandaran university of medical sciences, sari, iran department of clinical biochemistry and genetics, faculty of medicine, mazandaran university of medical sciences, sari, iran mohammad bagher hashemi-soteh immunogenetic research center, mazandaran university of medical sciences, sari, iran maryam ghaffari-cherati immunogenetic research center, mazandaran university of medical sciences, sari, iran ahad alizadeh department of epidemiology and reproductive health, reproductive epidemiology research center, royan institute for reproductive biomedicine, acecr, tehran, iran

objective(s): organic cation transporter 3 (oct3) as a high-capacity transporter contribute to the metabolism of metformin. the present study was conducted to determine the genotype frequencies of the variant oct3-1233g>a (rs2292334) in patients with newly diagnosed type 2 diabetes (t2d) and its relationship with response to metformin. materials and methods: this study included 150 patients wit...

Journal: :The Kobe journal of medical sciences 2005
Teguh Haryo Sasongko Ahmad Hamim Sadewa Pungky Ardani Kusuma Martua Parlindungan Damanik Myeong Jin Lee Hitoshi Ayaki Kandai Nozu Akinobu Goto Masafumi Matsuo Hisahide Nishio

BACKGROUND The angiotensin converting enzyme (ACE) gene carries insertion (I) and deletion (D) polymorphism within its intron 16. The presence of D-allele in the ACE gene has been reported as a probable genetic risk factor for idiopathic nephrotic syndrome (INS), especially the subtype of focal segmental glomerulosclerosis (FSGS). The D-allele may be related to poor responsiveness to steroid th...

Journal: :Human heredity 2012
Daniel J Schaid Jason P Sinnwell Gregory D Jenkins

BACKGROUND/AIMS Tests for whether observed genotype proportions fit Hardy Weinberg Equilibrium (HWE) are widely used in population genetics analyses, as well as to evaluate quality of genotype data. To date, all methods testing for HWE require subjects to be classified into discrete categories, yet it is becoming clear that the distribution of allele frequencies tends to be smooth over geograph...

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