نتایج جستجو برای: 1 y238x gene polymorphism

تعداد نتایج: 3607400  

قلی زاده, محسن, نجفی, مجتبی,

This research was conducted to find association of genetic variation in exon 1 and 3 of the follicle stimulating hormone beta (FSHB) subunit gene and litter size in Baluchi sheep. DNA was extracted using modified salting out method and polymerase chain reaction was used to amplify a fragment of 220 bp of exon 1 and a fragment of 427 bp of exon 3 along with a part of intron 2. Two methods of PCR...

ژورنال: پژوهش در پزشکی 2015

Abstract: Background and Aim: The increasing incidence of infertility is alarming. About 10-30% of infertility are classified as Unexplained Infertility (UI) which is not an absolute clinical condition. TGF-b1 is multifunctional cytokine and produced mainly by T regulatory (Treg) lymphocytes. This cytokine plays important roles in physiology of normal pregnancy. The association of Single...

Journal: :jundishapur journal of microbiology 0
nadia ghasemian medical cellular & molecular research center, golestan university of medical sciences, gorgan, ir iran majid shahbazi medical cellular & molecular research center, golestan university of medical sciences, gorgan, ir iran; medical cellular & molecular research center, golestan university of medical sciences, gorgan, ir iran. tel/fax: +98-1732421657

results the frequencies of the aa, at, and tt genotypes were 31%, 51%, and 18% in the chronic hbv patient group, and 40%, 45%, and 15% in the healthy control group, respectively. however, a lack of association of the + 874 polymorphism in the ifn-γ gene of those with chronic hbv infection was found. evaluation of hbv association with this polymorphism was significant under the dominant genetic ...

Abbas Shirdel, Abdollah Banihashem, Amireh Nejat Shokouhi, Azam Khedri, Behnoush Miladpour, Habibollah Esmaeili, Javad Behravan, Reza Entezari Heravi,

Background: The frequency of the multi-drug resistance 1 (MDR1) gene C3435T polymorphism differs in various ethnical populations such as Asian, African, and Caucasians populations. A silent C3435T polymorphism in exon 26 of MDR1 has been reported to be associated with a decreased expression of P-gp in TT genotypes carriers compared with CC genotypes carriers. Materials and Methods: To evaluate ...

رستمی, سارا, فریدونی, فرشته, محمدیان پناه, محمد, کهن, لیلا,

Background: Leptin is an adipokine made by fat cells and plays a key role in proliferation, cell survival, migration and immune response. Several studies have suggested that individuals with high serum leptin concentrations would increase the risk of breast cancer. G -2548A polymorphism in the leptin gene is located in the promoter region and is associated with the change of leptin serum level....

M. Ahani Azari R. Khatami Nejhad S. Yousefi,

In this study the genetic polymorphism of growth hormone (GH) gene as a candidate gene in livestock was investigated. Blood samples were randomly collected from 34 Alpine and 42 Saanen goats. DNA was extracted from blood samples and a 365 bp region of exon 5 of the GH genewas amplified by polymerase chain reaction (PCR). PCR products were analyzed using single strand conformation polymorphism (...

A. Farhadi, G. Rahimi-Mianji V. ‌Hemati Doust

Mastitis is one of the most serious and costly diseases affecting dairy cattle production. In the present study, effects of a lactoferrin gene polymorphism (intron 6) on milk somatic cell count (SCC) and subclinical mastitis was investigated in 121 Holstein dairy cattle. Two alleles of A and B and two genotypes of AA and AB were found in an EcoRI recognized single nucleotide polymorphism in int...

Journal: :medical journal of islamic republic of iran 0
ali mohammad foroughmand dept of genetics, college of sciences, shahid chamran university, ahvaz,iranسازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university) maryam haidari dept of genetics, college of sciences, shahid chamran university, ahvaz,iran.سازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university) hamid galehdari dept of genetics, college of sciences, shahid chamran university, ahvaz-iranسازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university) atefeh pooryasin dept of genetics, college of sciences, shahid chamran university, ahvaz,iran.سازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university) seyed reza kazeminejad dept of genetics, college of sciences, shahid chamran university, ahvaz,iran.سازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university) shiva hosseini dept of genetics, college of sciences, shahid chamran university, ahvaz, iranسازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university)

abstract   background: the disrupted-in-schizophrenia 1 (disc1) gene, on the chromosome position 1q42, was initially identified at the breakpoint of a balanced translocation, t(1,11)(q42.1q14.3), which segregated with major mental disorders in a large scottish family.   methods: our samples included 200 unrelated patients diagnosed with schizophrenia on the basis of dsm-iv criteria and 200 norm...

صفرپور, مهرنوش, پورخواجه, عبدالحسین, کهن, لیلا,

Background and purpose: Non-alcoholic fatty liver disease (NAFLD) is the major reason for abnormal liver function and is associated with obesity. Omentin (ITLN1) gene is highly expressed in visceral adipose tissue. The plasma omentin level is inversely correlated with obesity and serum omentin is elevated in patients with fatty liver diseases. This study investigated the association between Val...

Background and Aim: Coronary artery disease (CAD) is a multifactorial inherited disorder in which the arteries that blood to the heart muscle become hardened and narrowed. We aimed at investigating the role of rs5186 (A1166C) polymorphism the angiotensin II type 1 receptor (AGTR1) gene as risk factors in some Iranian CAD patients. Materials and Methods: In this case-control study 137 samples...

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