نتایج جستجو برای: polymorphism gene cat

تعداد نتایج: 1215418  

2012
Alexsandra Schneider Victor A. David Warren E. Johnson Stephen J. O'Brien Gregory S. Barsh Marilyn Menotti-Raymond Eduardo Eizirik

The occurrence of melanism (darkening of the background coloration) is documented in 13 felid species, in some cases reaching high frequencies at the population level. Recent analyses have indicated that it arose multiple times in the Felidae, with three different species exhibiting unique mutations associated with this trait. The causative mutations in the remaining species have so far not bee...

Journal: :Journal of advances in medical and biomedical research 2023

Single-Nucleotide Polymorphism of rs11061971 (+219 A>T) in Adiponectin Receptor 2 (AdipoR2) Gene and its Association with Risk Type Diabetes among Iranian Population

Fatemeh Hosseini Mohammadreza Bazrafshani Najmeh NezamabadiPour Saeedeh Parvaresh

Background & Aims: Vesicoureteral Reflux (VUR) is a congenital defect of the urinary tract which has been reported in approximately 1% of children. Several immunological and genetic factors are listed as major causes of this problem. The C825T polymorphism of the GNB3 gene is among the genetic factors that may be involved in the development or progression of the disease. Participatory role o...

بوالحسنی, اعظم, حبیب, اسدالله, نصیری, محبوبه, کهن, لیلا,

Introduction: Leptin, the obese (ob) gene product, is a cytokine-like hormone secreted mainly from adipose tissue acting on a receptor site in the hypothalamus to inhibit food intake and stimulate energy expenditure. A G-2548G polymorphism in the leptin gene promoter has a strong influence on leptin gene expression and adipose tissue secretion. The aim of this study was to examine the associati...

Background and purpose: Chronic lymphocytic leukemia (CLL) is the most common form of adult leukemia characterized by the accumulation of seemingly mature type B lymphocytes in peripheral blood and lymphatic organs. One of the main markers used in the diagnosis and prognosis of CLL is the CD38 gene. Polymorphism is considered to be a major genetic source of phenotypic change within a species an...

ژورنال: یافته 2018

Background: Alzheimer's disease is a multi-factorial disorder. The genes involved in Alzheimer's disease act as risk factors. The aim of this study was to investigate the APOE gene polymorphism in patients with Alzheimer's disease in Iran. Materials and Methods: In this analytical-descriptive study, 50 patients with Alzheimer's were investigated. Polymorphism of the APOE gene was investigated ...

Journal: :cell journal 0

objective: people are usually susceptible to carcinogenic aromatic amines, present in cigarrette smoke and polluted environment, which can cause dna damage. therefore, maintenance of genomic dna integrity is a direct result of proper function of dna repair enzymes. polymorphic diversity could affect the function of repair enzymes and thus augment the risk of different cancers. xeroderma pigment...

Journal: :iranian journal of medical sciences 0
s.h. jahadi-hossieni organ transplant rearch center, namazee hospital shiraz university of medical sciences shiraz iran. e. kamali department of immunology school of medicine namazee hospital shiraz university of medical sciences shiraz iran m. samani department of ophthalmology & namazee hospital shiraz university of medical sciences shiraz iran a. katbab department of ophthalmology & namazee hospital shiraz university of medical sciences shiraz iran h. khoshniat department of ophthalmology & namazee hospital shiraz university of medical sciences shiraz iran h. movahhedan department of ophthalmology & namazee hospital shiraz university of medical sciences shiraz iran

background: correlations between bone marrow, heart, kidney, liver, skin and lung transplant rejection or survival with human cytokine gene polymorphisms have been described. there are also reports about the role of cytokines and tumor necrosis factors-alpha (tnf-α) on corneal transplant in animal models. further studies are needed to clarify the role of cytokines in corneal allograft rejection...

The present study was carried out to investigate the association of C/T single nucleotide polymorphism(SNP)in exon 5 of stearoyl-CoA desaturase 1 (SCD1) gene and A/C SNP in the 3' untranslated region of oxidized low density lipoprotein receptor 1 (OLR1)gene with milk production traits in Iranian Holstein dairy Cattle. The blood samples of 153 (for OLR1) and 308 (for SCD1) dairy cattle from thre...

Journal: :Czech Journal of Animal Science 2021

Molecular cloning, functional characterization, tissue expression and polymorphism analysis of buffalo PRDX6 gene | Yongwang Miao, Lihua Qiu, Xinyang Fan, Xiaohong Teng, Pei Wang Agricultural Journals

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