نتایج جستجو برای: vntr

تعداد نتایج: 1669  

Journal: : 2021

For people working in dental prosthesis laboratories (DPL), metal alloys and methylmethacrylate-based monomers polymers used the laboratory can pose occupational risks. These risks cause health problems toxic effects on human health. This study purposes of researching exposure because manufacturing operations variable number tandem repeat (VNTR) polymorphisms IL-1Ra IL-4 genes. 29 DPL workers, ...

Golbahar Haghighi, Iraj Saadat, Maryam Kamkar, Mostafa Saadat,

Phenylketonuria (PKU) is one of the most common metabolic inborn diseases caused by mutations in the phenylalanine hydroxylase (PAH) gene. This gene is linked to a variable number of tandem repeats (VNTR) region which is a polymorphic marker that facilitates the implementation of prenatal diagnosis and carrier screening. In this study, VNTR with 13 repeats that has not been reported previously ...

Journal: :Clinical chemistry 1996
J H Wu M S Chern S K Lo M S Wen J T Kao

Apolipoprotein B gene 3' variable number tandem repeat (VNTR) and related regions were amplified by PCR and analyzed by agarose gel electrophoresis. Eighteen VNTR alleles (VNTR25, 26, 29, 31, 33, 35, 37, 39, 41, 43, 45, 47, 49, 51, 53, 55, 58, 60) and 45 genotypes were observed in 477 Taiwanese subjects. The VNTR35 allele and genotype VNTR35/35 were observed most frequently in this population. ...

2016
Hassan Ravansalar Keyvan Tadayon3 Kiarash Ghazvini

BACKGROUND AND OBJECTIVES Molecular typing methods are important and useful tools to assess the transmission, diversity of strains and differentiation between new infections and relapses which can effectively help in controlling infections. The aim of this study was to evaluate the molecular typing methods which have been used in Iran. By evaluating the results and discriminatory power of each ...

2012
Hui Li Jia-Xin Wang Dong-Dong Wu Hua-Wei Wang Nelson Leung-Sang Tang Ya-Ping Zhang

CLEC4M is a C-type lectin gene serving as cell adhesion receptor and pathogen recognition receptor. It recognizes several pathogens of important public health concern. In particular, a highly polymorphic variable number tandem repeat (VNTR) at the neck-region of CLEC4M had been associated with genetic predisposition to some infectious diseases. To gain insight into the origin and evolution of t...

Journal: :Endokrynologia Polska 2011
Wojciech Fendler Izabela Klich Agnieszka Cieślik-Heinrich Krystyna Wyka Agnieszka Szadkowska Wojciech Młynarski

BACKGROUND Human leukocyte antigens (HLA) complex and INS-IGF2 5'VNTR loci are principal determinants of the risk of type 1 diabetes mellitus (T1DM). Carriage of class III allele is protective, while class I/I homozygosity increases the risk of T1DM. MATERIAL AND METHODS HLA and 5'VNTR allele frequencies were summarised and multivariate logistic regression models with interaction evaluation w...

2012
Soma Ghosh M. Zulfiquer Hossain Michael Borges Michael G. Goggins Roxann G. Ingersoll James R. Eshleman Alison P. Klein Scott E. Kern

5-Fluorouracil (5FU), a widely used chemotherapeutic drug, inhibits the DNA replicative enzyme, thymidylate synthase (Tyms). Prior studies implicated a VNTR (variable numbers of tandem repeats) polymorphism in the 5'-untranslated region (5'-UTR) of the TYMS gene as a determinant of Tyms expression in tumors and normal tissues and proposed that these VNTR genotypes could help decide fluoropyrimi...

2014
Saeedeh Salimi Milad Mohammadoo-Khorasani Minoo Yaghmaei Mojgan Mokhtari Maryam Moossavi

Preeclampsia (PE) is a pregnancy-specific disorder that results in maternal mortality and morbidity. Growing evidence indicated that cytokines are involved in the pathogenesis of PE and interleukin-4 VNTR polymorphism could be implicated in altering the PE risk. The aim of this study was to evaluate the possible association between IL-4 VNTR polymorphism and susceptibility to PE in Iranian popu...

2010
Fabio Ricardo Pablos de Souza Pedro Alejandro Vozzi Reginaldo Aparecido Vila Arione Augusti Boligon Marli Aparecida Vani Galerani Raysildo Barbosa Lobo Lucia Regina Martelli

MUC1 is a heavily glycosylated mammalian transmembrane protein expressed by mucosal secretory tissues for both protection against microbial infection and lubrication. An important characteristic of MUC1 is its variable number of tandem repeats (VNTR) containing several sites for O-glycosylation. VNTR length has been associated with many human diseases and with certain economically important tra...

Hassan Mohabatkar, Iraj Saadat, Maryam Kamkar, Mostafa Saadat,

Dear Editor Analysis of the phenylalanine hydroxylase (PAH McKusick 261600) gene in different populations has revealed more than 320 different mutations associated with phenylketonuria (PKU). One of these mutations, IVS10nt546, results in severe PAH deficiency due to defective mRNA splicing. It accounts for about 40 percent of all mutant alleles in Turkish and between 10 to 20 percent of all mu...

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