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Association study of miR-100, miR-124-1, miR-218-2, miR-301b, miR-605, and miR-4293 polymorphisms and the risk of breast cancer in a sample of Iranian population.
TLDR
The finding showed that miR-218-2 rs11134527 and miR -301b rs384262 variant might contribute to increase the risk of BC in a sample of Iranian population and further studies are necessary to confirm the finding.
Pri-miR-34b/c rs4938723 polymorphism increased the risk of prostate cancer.
TLDR
It is proposed that Pri-miR-34 b/c rs4938723 variant may be a risk factor for the development of PCa in a sample of Iranian population.
Association between genetic variants in CD1A and CD1D genes and pulmonary tuberculosis in an Iranian population.
TLDR
The results of the present study suggest that CD1A rs411089 and CD1D rs859009 but not CD1 A rs366316, CD1 D rs973742 and CD859010 polymorphisms are associated with PTB in a sample of the Iranian population.
Detection of a 4-bp Insertion/deletion Polymorphism within the Promoter of EGLN2 Using Mismatch PCR-RFLP and Its Association with Susceptibility to Breast Cancer
TLDR
The findings did not support any association between the EGLN2 4-bp ins/del polymorphism and the risk of BC in the codominant, dominant, recessive and allele inheritance models tested.
Association between single nucleotide polymorphisms in the PI3K/AKT/mTOR pathway and bladder cancer risk in a sample of Iranian population
TLDR
It is suggested that PIK3CA rs6443624, AKT1 rs2498801, AKt1 rs1130233, as well mTOR rs2295080 polymorphism may be related to bladder cancer development in a sample of Iranian population.
Evaluation of 4‐bp insertion/deletion polymorphism within the 3′UTR of SGSM3 in bladder cancer using mismatch PCR‐RFLP method: A preliminary report
TLDR
An association between 4‐bp ins/del polymorphism in the 3′UTR of SGSM3 and the risk of bladder cancer in an Iranian population is supported and additional studies with larger sample sizes and diverse ethnicities are warranted.
Association of single nucleotide polymorphisms in AXIN2, BMP4, and IRF6 with Non-Syndromic Cleft Lip with or without Cleft Palate in a sample of the southeast Iranian population
TLDR
The results indicate that the BMP4 rs17563 variant is likely to confer a protective effect against the occurrence of NSCL/P in a sample of the southeast Iranian population.
Evaluation of transcobalamin II rs1801198 and transcobalamin II receptor rs2336573 gene polymorphisms in recurrent spontaneous abortion
TLDR
The findings showed no significant association between the TCN2 rs1801198 andTCN2R rs2336573 polymorphisms and the risk/protection of RSA and may provide a basis for future studies with larger sample sizes and different ethnicities on the role of TCN 2 and TCN1R polymorphisms in the pathogenesis of RSA.
The -2549 insertion/deletion polymorphism in the promoter region of VEGF is associated with the risk of recurrent spontaneous abortion.
TLDR
There is a significant association between the VEGF 18-bp ins/del polymorphism and risk of RSA in a sample of the southeast Iranian population and further studies on larger sample sizes and different ethnicities are required to validate the present findings.
Macrophage Migration Inhibitory Factor -173 G>C Gene Polymorphism Is Associated with Increased Risk of Nephrotic Syndrome in Children.
TLDR
The findings revealed that MIF -137 G>C variant was associated with increased risk of NS in male and no correlation between the variant and response to treatment was found.
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