نتایج جستجو برای: genotype frequency

تعداد نتایج: 565280  

Journal: :Asian Pacific journal of cancer prevention : APJCP 2014
Sukhpreet Kaur Vasudha Sambyal Kamlesh Guleria Mridu Manjari Meena Sudan Manjit Singh Uppal Neeti Rajan Singh Gursimran Singh Harpreet Singh

BACKGROUND To investigate the relationship of five TP53 polymorphisms (p.P47S, p.R72P, PIN3 ins16bp, p.R213R and r.13494g>a) with the esophageal cancer (EC) risk in North Indians. MATERIALS AND METHODS Genotyping of p.P47S, p.R72P, PIN3 ins16bp, p.R213R and r.13494g>a polymorphisms of TP53 in 136 sporadic EC patients and 136 controls using polymerase chain reaction and PCR-RFLP. RESULTS The...

Journal: :Genetics 1993
B P Kinghorn B W Kennedy C Smith

This paper describes a method for screening animal populations on an index of calculated probabilities of genotype status at an unknown single locus. Animals selected by such a method might then be candidates in test matings and genetic marker analyses for major gene detection. The method relies on phenotypic measures for a continuous trait plus identification of sire and dam. Some missing phen...

2016
Chad M Hunter Matthew C Robinson David L Aylor Nadia D Singh

Meiotic recombination is a genetic process that is critical for proper chromosome segregation in many organisms. Despite being fundamental for organismal fitness, rates of crossing over vary greatly between taxa. Both genetic and environmental factors contribute to phenotypic variation in crossover frequency, as do genotype-environment interactions. Here, we test the hypothesis that maternal ag...

2013
Mohammad Mehdi Heidari Seyed Khalil Foruzannia Mehri Khatami Mehdi Hadadzadeh Mahmoud Emami Meybodi

UNLABELLED Objective(s) : Apolipoprotein E genotype (APOE) polymorphism affects lipid levels and coronary artery disease (CAD) risk. The aim of this study was to study the association of the Apolipoprotein E genotypes with coronary artery disease in the Iranian population. MATERIALS AND METHODS The Apolipoprotein E genotype in DNA samples extracted from 66 CAD+ patients and 61 control subject...

Journal: :iranian journal of public health 0
k ghatreh samani dept. of biochemistry, school of medicine, shahrekord university of medical sciences, shahrekord, i m noori drug applied research center and biotechnology research canter, tabriz university of medical scienc m rohbani nobar drug applied research center and biotechnology research canter, tabriz university of medical scienc m hashemzadeh chaleshtory cellular and molecular research center, shahrekord university of medical sciences, shahrekord, iran e farrokhi cellular and molecular research center, shahrekord university of medical sciences, shahrekord, iran m darabi amin drug applied research center and biotechnology research canter, tabriz university of medical scienc

background: the t allele of the hepatic lipase (hl) c-514t polymorphism was previously found to be associated with lower plasma hl activity. here, we examined the association between this polymorphism and plasma hdl-cholesterol concentrations in patients with coronary arteries stenosis. methods: we studied 342 subjects undergoing coronary angiography in two groups of non cad (n=146) and cad (n=...

Journal: :hepatitis monthly 0
seyed hossein aalaei-andabili molecular immunology research center, department of immunology, school of medicine, tehran university of medical sciences, tehran, ir iran bita behnava middle east liver disease center, tehran, ir iran; baqiyatallah research center for gastroenterology and liver disease (brcgl), baqiyatallah university of medical sciences, tehran, ir iran shima salimi middle east liver disease center, tehran, ir iran; baqiyatallah research center for gastroenterology and liver disease (brcgl), baqiyatallah university of medical sciences, tehran, ir iran heidar sharafi middle east liver disease center, tehran, ir iran; baqiyatallah research center for gastroenterology and liver disease (brcgl), baqiyatallah university of medical sciences, tehran, ir iran seyed moayed alavian middle east liver disease center, tehran, ir iran; iran hepatitis network (ihn), tehran, ir iran; middle east liver disease center, tehran, ir iran. tel: +98-2188067114, fax: +98-2188067114

conclusions there were significant linkages between hcv genotypes and il28b genotypes/alleles. patients with a favorable il28b and genotypes 1 and 4 hcv infection stand a better chance to clear hcv in the acute phase. objectives this meta-analysis was designed to determine the world-wide distribution patterns of il28b genotypes and alleles, and to find possible linkages between il28b and hcv ge...

Journal: :Diabetes 2007
Masaaki Ochi Haruhiko Osawa Yushi Hirota Kazuo Hara Yasuharu Tabara Yoshiharu Tokuyama Ikki Shimizu Azuma Kanatsuka Yasuhisa Fujii Jun Ohashi Tetsuro Miki Naoto Nakamura Takashi Kadowaki Mitsuo Itakura Masato Kasuga Hideichi Makino

OBJECTIVE Resistin is an adipocyte-secreted cytokine associated with insulin resistance in mice. We previously reported that the G/G genotype of a resistin single nucleotide polymorphism (SNP) at -420 increases type 2 diabetes susceptibility by enhancing its promoter activity. The aim of the present study was to determine the relevance of SNP -120 in a large number of subjects. RESEARCH DESIG...

2005
T. K. Biswas T. K. Bhattacharya A. D. Narayan S. Badola Pushpendra Kumar Arjava Sharma

The study was carried out in Sahiwal, Holstein Friesian, Jersey and crossbred cattle and Murrah, Bhadwari, Jaffarabadi, Nagpuri and Surti buffaloes maintained at different organized herds to work out the polymorphism at growth hormone locus and study its effect on birth weight. A 223 bp fragment of the gene was amplified and digested with Alu I restriction enzyme. Two alleles, L and V with thre...

2017
Bo Zhang Lin Lu Zhaolin Lu

Objective The spectrum of molecular defects in Chinese patients with 21-hydroxylase deficiency (21-OHD), and genotype-phenotype relationships are unknown. Methods We screened eight patients with non-classical (NC) 21-OHD and 35 with classical 21-OHD, and detected nine known mutations. Results The most frequent mutation among the 43 21-OHD cases was p.Ile172Asn (allele frequency, 36.0%), followe...

Journal: :iranian journal of biotechnology 2007
payam pour mohammadi ahmad moieni mokhtar jalali-javaran

this study involves in vitro androgenesis of zea maysl. via anther culture. combination of two embryoinduction media (imss & ypm) in presence of different colchicine concentrations (0, 100, 200, 250, 300and 400 mg/l ) in the pretreatment medium (iml) andpretreatment duration (0, 3, 6 and 9 days) in twogenotypes (dh5×dh7 and eth-m82) were tested.after colchicine pretreatment, anthers were tr...

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