نتایج جستجو برای: iranian gene pool

تعداد نتایج: 1216090  

Journal: :International Journal of Medical Microbiology 2009

2011
Arash Akhlaghi Shahin Shirani Naghmeh Ziaie Omid Pirhaji Majid Yaran Golnoosh Shahverdi Nizal Sarrafzadegan Alireza Khosravi Elham Khosravi

BACKGROUND The polymorphisms of cytochrome P450 2C19 (CYP2C19) gene are major prognostic factors for the response to clopidogrel therapy in patients with coronary artery diseases (CAD). The CYP2C19*2 is the most important allele responsible for resistance to clopidogrel therapy. This study examined CYP2C19 gene polymorphism (CYP2C19*1 and *2) in Iranian patients. METHODS This cross-sectional ...

Journal: :American Journal of Potato Research 2020

2017
Zohreh Moradi Ehsan Nazifi Mohsen Mehrvar

Sugarcane mosaic virus (SCMV) is one of the most damaging viruses infecting sugarcane, maize and some other graminaceous species around the world. To investigate the genetic diversity of SCMV in Iran, the coat protein (CP) gene sequences of 23 SCMV isolates from different hosts were determined. The nucleotide sequence identity among Iranian isolates was more than 96%. They shared nucleotide ide...

2017
Mansour Shakiba Mohammad Hashemi Zahra Rahbari Salah Mahdar Hiva Danesh Fatemeh Bizhani Gholamreza Bahari

It has been proposed that genetic factors account for 30%–50% of the risk for cocaine and heroin addiction. The present study was aimed to find out the impact of μ-opioid receptor gene (OPRM1) rs1799971 A > G and rs9479757 polymorphisms on heroin dependence in a sample of southeast Iranian population. This case-control study was done on 123 heroin addicts and 140 non-addicts Iranian male. Genom...

Journal: :Journal of pediatric endocrinology & metabolism : JPEM 2016
Mahnaz Seifi-Alan Roshanak Shamsi Aria Setoodeh Fatemeh Sayarifard Parisa Aghasi Farzad Kompani Soudeh Ghafouri-Fard Farzaneh Abbasi

Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED), also named as autoimmune polyglandular syndrome (APS) type 1, is a rare autosomal recessive disorder caused by mutations in autoimmune regulator (AIRE) gene. It is distinguished by an immune-mediated damage of endocrine tissues, chronic candidiasis, and ectodermal disorder. APECED has been shown to be frequent in some popu...

2009
Mehdi Azad Saeid Kaviani Masoud Soleimani Mehrdad Noruzinia

Received: 22/Jul/2008, Accepted: 8/Mar/2009 Objective: Thiopurine S-methyltransferase (TPMT) catalyses the S-methylation of thiopurine drugs. Low activity phenotypes are correlated with several mutations in the TPMT gene and adverse drug reactions. The molecular basis for dissimilar enzymatic activity of TPMT has been established in Caucasians, African-Americans and Southwest Asians, but it rem...

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