Lack of association between paraoxonase-1 Q192R polymorphism and rheumatoid arthritis in southeast Iran.
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Association between interleukin-1 receptor associated kinase 1 rs3027898 A/C gene polymorphism and rheumatoid arthritis.First survey of the three gene polymorphisms (PON1 Q192R, eNOS E298D and eNOS C-786T) potentially associated with coronary artery spasm in African populations and comparison with worldwide data.A 40-bp insertion/deletion polymorphism of Murine Double Minute2 (MDM2) increased the risk of breast cancer in Zahedan, Southeast Iran.Functional polymorphisms of FAS and FASL gene and risk of breast cancer - pilot study of 134 cases.Anti-cyclic citrullinated peptide antibodies and paraoxonase-1 polymorphism in rheumatoid arthritis.Evaluation of rs3102735 and rs2073617 Osteoprotegerin Gene Polymorphisms and the Risk of Childhood Acute lymphoblastic Leukemia in Zahedan Southeast Iran.Lack of Association between miRNA-146a rs2910164 and miRNA-499 rs3746444 Gene Polymorphisms and Susceptibility to Pulmonary Tuberculosis.Addressing the link between paraoxonase-1 gene variants and the incidence of early onset myocardial infarction.Evaluation of haptoglobin genotypes in patients with metabolic syndrome: A preliminary report.Association between IFN-γ +874A/T and IFN-γR1 (-611A/G, +189T/G, and +95C/T) Gene Polymorphisms and Chronic Periodontitis in a Sample of Iranian PopulationMacrophage migration inhibitory factor -173 G/C polymorphism is associated with an increased risk of pulmonary tuberculosis in Zahedan, Southeast Iran.Aberrant promoter methylation profile of Niemann-pick type C1 gene in cardiovascular diseaseAssociation of Adiponectin rs1501299 and rs266729 Gene Polymorphisms With Nonalcoholic Fatty Liver Disease.CD226 rs763361 (Gly307Ser) polymorphism is associated with susceptibility to rheumatoid arthritis in Zahedan, southeast IranA 45-bp insertion/deletion polymorphism of UCP2 gene is associated with metabolic syndrome.Lectin, galactoside-binding, soluble, 3 rs4652 A/C gene variation and the risk for rheumatoid arthritis.Evaluation of paraoxonase activity in children with nephrotic syndrome.Lack of Association Between Dopamine Beta-Hydroxylase (DBH) 19-bp Insertion/Deletion Polymorphism and Risk of Schizophrenia.Association between the rs1805081 polymorphism of Niemann-Pick type C1 gene and cardiovascular disease in a sample of an Iranian population.Frequency of thiopurine S-methyltransferase (TPMT) alleles in southeast Iranian population.Association of PTPN22 rs2476601 and EGFR rs17337023 Gene polymorphisms and rheumatoid arthritis in Zahedan, Southeast Iran.Relationship between γ-interferon gene polymorphisms and susceptibility to brucellosis infection.Association between CDH1 and MSX1 gene polymorphisms and the risk of nonsyndromic cleft lip and/or cleft palate in a southeast Iranian population.A functional polymorphism in the miR-146a gene is associated with the risk of childhood acute lymphoblastic leukemia: a preliminary report.Genotyping of -374A/T, -429A/G, and 63 bp Ins/del polymorphisms of RAGE by rapid one-step hexaprimer amplification refractory mutation system polymerase chain reaction in breast cancer patients.Evaluation of UDP-glucuronosyltransferase 2B17 (UGT2B17) and dihydrofolate reductase (DHFR) genes deletion and the expression level of NGX6 mRNA in breast cancer.FHIT promoter DNA methylation and expression analysis in childhood acute lymphoblastic leukemia.Lack of relationship between PTEN 32-bp and TP53 16-bp Ins/Del polymorphisms and chronic hepatitis B virus infection.DROSHA rs642321 Polymorphism Influence Susceptibility to Childhood Acute Lymphoblastic Leukemia: A Preliminary Report.Relationship between phosphoinositide-3-kinase genetic polymorphism and schizophrenia.A tetra-primer amplification refractory mutation system-polymerase chain reaction for the detection of rs8099917 IL28B genotype.Association between paraoxonase-1 gene Q192R and L55M polymorphisms in systemic lupus erythematosus (SLE) and anti-phospholipid syndrome (APS) in a population from Cairo of Egypt.Association between paraoxonase-1 gene polymorphisms and risk of metabolic syndrome.Association of functional polymorphism at the miR-502-binding site in the 3' untranslated region of the SETD8 gene with risk of childhood acute lymphoblastic leukemia, a preliminary report.Investigation of aPON1gene polymorphism (rs662 polymorphism) as predictor of subclinical atherosclerosis in patients with rheumatoid arthritis: Table 1Association of IRGM polymorphisms and susceptibility to pulmonary tuberculosis in Zahedan, Southeast Iran
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P2860
Lack of association between paraoxonase-1 Q192R polymorphism and rheumatoid arthritis in southeast Iran.
description
2010 nî lūn-bûn
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2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
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2010年學術文章
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2010年學術文章
@zh-hant
name
Lack of association between pa ...... d arthritis in southeast Iran.
@en
Lack of association between pa ...... d arthritis in southeast Iran.
@nl
type
label
Lack of association between pa ...... d arthritis in southeast Iran.
@en
Lack of association between pa ...... d arthritis in southeast Iran.
@nl
prefLabel
Lack of association between pa ...... d arthritis in southeast Iran.
@en
Lack of association between pa ...... d arthritis in southeast Iran.
@nl
P2093
P356
P1476
Lack of association between pa ...... d arthritis in southeast Iran.
@en
P2093
A K Moazeni-Roodi
D M Kordi-Tamandani
G R Bardestani
P304
P356
10.4238/VOL9-1GMR728
P577
2010-02-23T00:00:00Z