نتایج جستجو برای: c yp3a4 and cyp3a5 gene polymorphisms

تعداد نتایج: 17103364  

Journal: :iranian journal of basic medical sciences 0
maryam fazelzadeh haghighi cancer immunology group, shiraz institute for cancer research, school of medicine, shiraz university of medical sciences, shiraz, iran mohammad ali ghayumi department of internal medicine, school of medicine, shiraz university of medical sciences, shiraz, iran farzane behzadnia cancer immunology group, shiraz institute for cancer research, school of medicine, shiraz university of medical sciences, shiraz, iran nasrollah erfani molecular medicine group, graduate school of advanced medical sciences and technologies, shiraz university of medical sciences, shiraz, iran

objective(s): foxp3 gene is an x-linked gene that encodes foxp3 protein, an essential transcription factor in cd4+cd25+foxp3+ regulatory t (treg) cells.  we aimed, in the present study, to investigate the association of two foxp3 polymorphisms, -2383 c/t (rs3761549) and ivs9+459 t/c (rs2280883), with lung cancer. materials and methods:  in a case-control study we analyzed genotypes and alleles ...

Journal: :gastroenterology and hepatology from bed to bench 0
seyed dawood mousavi nasab department of microbiology, faculty of medicine, kashan university of medical sciences, kashan, i.r. iran. rasoul baharlou department of microbiology, jahrom university of medical sciences, jahrom, iran ahmad piroozmand department of microbiology, faculty of medicine, kashan university of medical sciences, kashan, i.r. iran.autoimmune diseases research center, school of medicine, kashan university of medical sciences, kashan, iran. hadi toghyani department of virology, school of public health, tehran university of medical sciences, tehran, iran enayatollah shadmand department of microbiology, jahrom university of medical sciences, jahrom, iran hadi fazel department of virology, school of public health, tehran university of medical sciences, tehran, iran

aim : the purpose of this study was to compare the distribution of interleukin (il)-28b genotypes between iranian healthy individuals and patients with chronic hepatitis c based on the genotype. background : polymorphisms in the region of il-28b gene have been identified as the strongest genetic pretreatment predictor of sustained virological response (svr) in hepatitis c infection. patients an...

Journal: :The Canadian journal of hospital pharmacy 2013
Heather Naylor Jenna Robichaud

The calcineurin inhibitor tacrolimus is used to prevent organ rejection following renal transplant. This drug is metabolized through the hepatic cytochrome P450 (CYP450) 3A enzymes, in particular, CYP3A4 and CYP3A5. A strong relationship between CYP3A5 genetic polymorphisms and the pharmacokinetics of tacrolimus has been demonstrated in kidney, heart, and liver graft recipients. Previous studie...

Gharesi-Fard B Negahban L, Pahlavani B Zolghadri J

Background: Hypertension during pregnancy period along with the presence of protein in the urine, after the 20th weeks of gestation is called preeclampsia (PE). About five percent of all pregnancies are manifested with PE and its exact etiology has still remained unknown. The renin-angiotensin system (RAS) has an important role in the regulation of blood pressure during pregnancy and so pathoph...

Naeimi, Mahsa, Zahmatkesh Roudsari, Rasoul,

Background: Ulcerative colitis is a multifactorial disease in which the environmental and genetics factor are being involved together. Interleukins are a group of cytokine which are produced through T cells, monocytes, macrophages, and endothelial cells. Interleukin-10 is an important multitasking cytokine that has a key role in inflammatory responses. The promoter of interlekin-10 is highly po...

2016
Daiki Tsuji Midori Ikeda Keisuke Yamamoto Harumi Nakamori Yong-Il Kim Yohei Kawasaki Aki Otake Mari Yokoi Kazuyuki Inoue Keita Hirai Hidenori Nakamichi Umi Tokou Mitsuru Shiokawa Kunihiko Itoh

Chemotherapy-induced neutropenia (CIN) is one of the major adverse events that necessitate chemotherapy dose reduction. This study aimed to evaluate the association between grade 4 neutropenia and genetic polymorphisms in breast cancer patients. In this genetic polymorphism association study, peripheral blood samples from 100 consecutive breast cancer outpatients, between August 2012 and Septem...

ژورنال: پژوهش در پزشکی 2012
بردبار, مریم , رضایی, حلیمه , متولی باشی, مجید,

Abstract Background: Several single nucleotide polymorphisms have been found in CYP1A1 gene and it was reported that C allele in T/C gene polymorphism is associated with lung cancer. Current study investigates interaction between cigarette factor and C/T polymorphism in the m1 locus. Methods: Present study is a case-control and retrospective study. T/C polymorphism in 112 patients with lung...

Journal: :iranian journal of cancer prevention 0
f khatami b noorinayer s ghiasi r mohebi m hashemi mr zali

abstract background: gastric cancer is one of the most common malignant tumors in iran. hypomethylation and/or hypermethylation of dna have been described in gastric cancer and is presumed to be an early event in this process. objective: we hypothesized that single nucleotide polymorphisms of dnmt1 gene may be associated with the genetic susceptibility to gastric cancer. methods: 200 patients a...

Journal: :iranian red crescent medical journal 0
alireza parand iranian hospital, dubai, uae jale zolghadri infertility research center, gynecology and obstetrics department, shiraz university of medical sciences, shiraz, ir iran mozhgan nezam infertility research center, gynecology and obstetrics department, shiraz university of medical sciences, shiraz, ir iran abdolreza afrasiabi hematology research center, shiraz university of medical sciences, shiraz, ir iran sezaneh haghpanah hematology research center, shiraz university of medical sciences, shiraz, ir iran mehran karimi hematology research center, shiraz university of medical sciences, shiraz, ir iran; hematology research center, shiraz university of medical sciences, nemazee hospital, shiraz, ir iran. tel/fax: +98-7116473239; +98-9171123975

conclusions: we determined a significant higher frequency of protein s deficiency in patients with rpl compared with controls. but the frequency of protein c deficiency and the frequency of two common thrombophilic mutations (factor v leiden and prothrombin g20210a), were not significantly different between patients with recurrent miscarriage and healthy women. results: the mean functional acti...

Journal: :Blood 2004
Shinji Kishi Wenjian Yang Benoit Boureau Stanislas Morand Soma Das Peixian Chen Edwin H Cook Gary L Rosner Erin Schuetz Ching-Hon Pui Mary V Relling

Etoposide is a substrate for P-glycoprotein, CYP3A4, CYP3A5, and UGT1A1. Glucocorticoids modulate CYP3A and P-glycoprotein in preclinical models, but their effect on clinical etoposide disposition is unknown. We studied the pharmacokinetics of etoposide and its catechol metabolite in children with acute lymphoblastic leukemia, along with polymorphisms in CYP3A4, CYP3A5, MDR1, GSTP1, UGT1A1, and...

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