نتایج جستجو برای: glucuronosyltransferase gene

تعداد نتایج: 1142424  

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تربیت مدرس - دانشکده علوم پزشکی 1391

مطالعات انجام شده روی مکانیسمهای تکوینی و تکاملی گلبولهای قرمز منجر به دستیابی بشر به مفاهیم پایه و مهمی در ارتباط با مکانیسمهای عمومی تنظیم بیان ژن وشکل گیری بافتها شده است. تمایز اختصاصی به رده ارتیروئید و هر رده دیگری، شدیداً وابسته به تنظیم در سطح بیان ژن و فاکتورهای کنترلی خاص نظیر سیتوکین ها، فاکتورهای نسخه برداری ویژه، عناصر کنترل کننده چرخه سلولی، تکثیر،آپوپتوز و عناصر سیگنالینگ داخل سلو...

Journal: :Biopharmaceutics & drug disposition 2009
Ho-Chul Shin Hye-Ryoung Kim Hee-Jung Cho Hee Yi Soo-Min Cho Dong-Goo Lee A M Abd El-Aty Jin-Suk Kim Duxin Sun Gordon L Amidon

The purpose of this study was to compare the expression profiles of drug-metabolizing enzymes in the intestine of mouse, rat and human. Total RNA was isolated from the duodenum and the mRNA expression was measured using Affymetrix GeneChip oligonucleotide arrays. Detected genes from the intestine of mouse, rat and human were ca. 60% of 22690 sequences, 40% of 8739 and 47% of 12559, respectively...

Journal: :Cancer research 2009
Andrea S Blevins-Primeau Dongxiao Sun Gang Chen Arun K Sharma Carla J Gallagher Shantu Amin Philip Lazarus

Tamoxifen (TAM) is a selective estrogen receptor modulator widely used in the prevention and treatment of breast cancer. A major mode of metabolism of the major active metabolites of TAM, 4-OH-TAM and endoxifen, is by glucuronidation via the UDP-glucuronosyltransferase (UGT) family of enzymes. To examine whether polymorphisms in the UGT enzymes responsible for the glucuronidation of active TAM ...

2013
Xiangyu CAO Baomin LI Sheng LI Jun WANG Xinfeng LIU Weiping LI

Intestinal bacteria play a key role to change the properties of drugs or herbal components, including therapeutic role, toxicity and pharmacokinetic behaviour. The present study aims to investigate the role of intestinal bacteria in changing the inhibitory potential of herbal components towards drug-metabolizing enzymes (DMEs) through comparing the inhibition of UDP-glucuronosyltransferase (UGT...

Journal: :Angewandte Chemie 2021

UDP-glucuronosyltransferase 1A1 (UGT1A1) is a vital metabolic enzyme responsible for the clearance of endogenous substances and drugs. Hitherto, development fluorescent probes UGTs was severely restricted due to poor isoform selectivity on–off or blue-shifted fluorescence response. Herein, we established novel “molecular-splicing” strategy construct highly selective near-infrared (NIR) probe, H...

2014
Marianna Tziotou Vassiliki Kalotychou Anna Ntokou Revekka Tzanetea Iakovos Armenis Marianna Varsou Konstantinos Konstantopoulos Nicolas Tsavaris Yannis Rombos

Uridine glucuronosyltransferase (UGT) gene polymorphisms have been linked to irinotecan toxicity. Our purpose was to study the association between UGT1A1*28, UGT1A7*2, and UGT1A7*3 polymorphisms and irinotecan toxicity in Greek patients receiving low-dose weekly irinotecan. Blood samples were collected for 46 patients. DNA was extracted and UGT1A1 promoter and UGT1A7 exon 1 genotyping was carri...

Journal: :Biological & pharmaceutical bulletin 2014
Yukiko Sakakibara Miki Katoh Masaya Suzuki Ryoko Kawabe Keisuke Iwase Masayuki Nadai

Uridine 5'-diphosphate (UDP)-glucuronosyltransferase 1A (UGT1A), which catalyzes major phase II reactions, is regulated by endogenous and exogenous factors via nuclear receptors such as the aryl hydrocarbon receptor (AhR). Glucocorticoid, one of the adrenocortical hormones, regulates AhR and UGT1A expression. We examined the effects of adrenalectomy on the expression and induction of UGT1A via ...

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