نتایج جستجو برای: e polymorphisms

تعداد نتایج: 1081287  

Journal: :Hormones 2015
Genovefa D Kolovou Vana Kolovou Demosthenes B Panagiotakos Ioannis Vasiliadis Vassiliki Giannakopoulou Peggy M Kostakou Vassiliki Vartela Sophie Mavrogeni

OBJECTIVE In the present study, we evaluated the influence of lipoprotein lipase (LPL) and apolipoprotein (apo) E polymorphisms on lipid concentrations of 178 Greek men of similar age with coronary heart disease (CHD), but varying body mass index (BMI). DESIGN Patients were divided according to their BMI (in kg/m²) into three groups: lean (BMI = 20-24.9), overweight (BMI = 25-29.9), and obese...

Journal: :iranian biomedical journal 0
ایرج سعادت iraj saadat شاهپور امیدواری shahpour omidvari مصطفی سعادت mostafa saadat

glutathione s-transferases (gsts) are encoded by a superfamily of genes and play a role in the detoxification of potential carcinogens. the human gsts are divided into four classes: alpha, mu, pi and theta. previous studies indicated that the absence of the glutathione s-transferase m1 (gstm1) protein correlated with an increased risk of developing some types of cancers. association between spe...

Journal: :iranian red crescent medical journal 0
milad gholami department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, ir iran hossein darvish behavioral sciences research center, shahid beheshti university of medical sciences, tehran, ir iran habib ahmadi department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, ir iran simin rahimi-aliabadi department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, ir iran babak emamalizadeh department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, ir iran mohammad reza eslami amirabadi behavioral sciences research center, shahid beheshti university of medical sciences, tehran, ir iran

background multiple sclerosis (ms) is an autoimmune disease that affects the central nervous system (cns). ms is one of the most common cause of neurological impairment at a young age with a complex etiology. the forkhead/winged helix (foxp3) gene encodes a transcription factor that plays an important role in the working and progress of regulatory t cells. loss of the foxp3 function impairs the...

Journal: :anatomical sciences journal 0
hajar dahim falavarjan azad university kahin shahani falavarjan azad university ahmad sabanizadeh rafsanjan university of medical sciences mohsen mohsen mohsen سید مسعود ذوالحواریه

introduction: endometriosis is a prevalent gynecological disorder among women which is diagnosed by the growth of endometrial tissue outside of uterus and is mainly accompanied by severe pelvic pain and infertility. p53 also known as cellular tumor antigen p53 inside codons 11, 72 and 248 are contained with single nucleotide changes in which tends to be nearly rampant.this will probably be incr...

Journal: :hepatitis monthly 0
haiying zhang department of gastroenterology, the second affiliated hospital of qingdao university medical college, qingdao, china; department of gastroenterology, qingdao central hospital, qingdao, china; medical college of qingdao university, qingdao, china lizhen chen medical college of qingdao university, qingdao, china yongning xin department of gastroenterology, qingdao municipal hospital, qingdao, china; department of gastroenterology, qingdao municipal hospital, qingdao 266021, shandong province, china. tel: +86-53288905289, fax: +86-53288905293, e-mail:; shiying xuan, department of gastroenterology, qingdao municipal hospital, qingdao 266021, shandong province, china yuangui lou department of gastroenterology, the second affiliated hospital of qingdao university medical college, qingdao, china; department of gastroenterology, qingdao central hospital, qingdao, china yang liu medical college of qingdao university, qingdao, china shiying xuan department of gastroenterology, qingdao municipal hospital, qingdao, china; department of gastroenterology, qingdao municipal hospital, qingdao 266021, shandong province, china. tel: +86-53288905289, fax: +86-53288905293, e-mail:; shiying xuan, department of gastroenterology, qingdao municipal hospital, qingdao 266021, shandong province, china

conclusions our meta-analysis, while not ruling out possible publication bias, showed no association between gene polymorphisms of apoc3 and the risk of nafld development in different populations in the world. evidence acquisition we performed a meta-analysis of all relevant studies published in the literature. a total of 115 clinical trials or reports were identified, but only seven trials met...

2015
Xiao-guang Xiao Shu Xia Man Zou Qi Mei Lei Zhou Shu-jing Wang Yuan Chen

AIMS To analyze the distribution of uridine diphosphate glucuronosyltransferase (UGT)1A1 gene polymorphisms in Chinese patients with extensive-stage small-cell lung cancer (E-SCLC), and to evaluate correlations between the UGT1A1 gene polymorphisms and toxicity, and efficacy of irinotecan (CPT-11) based regimen in the patients with E-SCLC. METHODS The study analyzed the distribution of UGT1A1...

Journal: :journal of research in health sciences 0
khosro sardarian mohammad abasi ghasem solgi mehrdad hajilooi

background: previous studies revealed that selectins play key roles in homing of immune cells to inflamed tissues and lymphatic organs. l-selectins are expressed on immune cells and interact with p and e selectins to homing to the tissues, hence, the polymorphisms within the gene of l-selectins may are associated with alteration in its expression. thus, the current cross-sectional analytical st...

Journal: :Bioscience, biotechnology, and biochemistry 2010
Akemi Hosoda Takashi Inoue Chang C Mao Young-Hee Jeong Azumi Yamagishi Mingjuan Ye Tokuo Yamamoto Dong-Ho Kim Shigeru Saeki

Apolipoprotein E (apoE) polymorphism is associated with onset of Alzheimer's disease (AD). We found seven polymorphisms in apoE receptor 2 (ApoER2), an apoE-binding receptor, in Japanese sporadic AD patients, but no association of ApoER2 polymorphisms with AD. We consider that the functions of ApoER2 in the brain may be compensated for by those of other apoE-binding receptors such as VLDL recep...

2015
Piers Dawes Hazel Platt Michael Horan William Ollier Kevin Munro Neil Pendleton Antony Payton

OBJECTIVES/HYPOTHESIS Age-related hearing loss has a genetic component, but there have been limited genetic studies in this field. Both N-acetyltransferase 2 and apolipoprotein E genes have previously been associated. However, these studies have either used small sample sizes, examined a limited number of polymorphisms, or have produced conflicting results. Here we use a haplotype tagging appro...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید