نتایج جستجو برای: بیان ژن hnf 4α

تعداد نتایج: 68902  

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2012
Nobumichi Ohoka Keiichiro Okuhira Hongyan Cui Weijia Wu Ryuichiro Sato Mikihiko Naito Tomoko Nishimaki-Mogami

OBJECTIVE Hepatic ATP-binding cassette transporter A1 (ABCA1) plays the major role in maintaining plasma high-density lipoprotein levels by producing cholesterol-accepting nascent high-density lipoprotein, whereas peripheral ABCA1 is responsible for releasing cellular cholesterol. We previously reported that in rodents, cholesterol depletion reduces ABCA1 expression in peripheral but not hepati...

2014
Anna Algamas-Dimantov Einav Yehuda-Shnaidman Rachel Hertz Irena Peri Jacob Bar-Tana Betty Schwartz

The global obesity / diabetes epidemic has resulted in robust increase in the incidence of colorectal cancer (CRC). Epidemiological, animal and human studies have indicated efficacy of (n-3) PUFA in chemoprevention of sporadic and genetic-driven CRC. However, diabetes-promoted CRC presents a treatment challenge that surpasses that of sporadic CRC. This report analyzes the efficacy of (n-3) PUFA...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه بوعلی سینا - دانشکده علوم کشاورزی 1391

شیرین بیان از گیاهان دارویی با ارزش و بومی ایران است. تریترپنوئیدها از جمله متابولیتهای ثانویه مهم موجود در این گیاه هستند. گلیسیریزین یک تریترپنوئید ساپونین بوده و به فراوانی در قسمت زیرزمینی گیاه شیرین بیان یافت می شود. در این تحقیق با اعمال تنش خشکی به این گیاه، تاثیر تنش بر روی بیان ژنهای مهم مسیر بیوسنتزی تریترپنوئیدها بررسی شد. ژنهای مورد بررسی سکوآلن سینتاز، بتا-آمیرین سینتاز، لوپئول سین...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2007
Toshiro Sugimoto Masayoshi Sakaguchi Nobuhiro Ogawa Naoko Deji Takashi Uzu Yoshihiko Nishio Yutaka Eguchi Atsunori Kashiwagi

HNF-1b mutations. Most importantly, patients with an HNF-1b mutation may also be at risk of developing renal cell carcinomas, since recent evidence suggests that HNF-1b is a tumour suppressor gene [5]. In conclusion, patients with unexplained nephropathy and/or renal cysts should be routinely screened for an HNF-1b mutation in order to differentiate the RCAD syndrome from diabetic nephropathy. ...

2014
Young-Sun Lee Eun-Kyu Lee Hyun-Hee Oh Cheol Soo Choi Sujong Kim Hee-Sook Jun

Sodium meta-arsenite (SA) is implicated in the regulation of hepatic gluconeogenesis-related genes in vitro; however, the effects in vivo have not been studied. We investigated whether SA has antidiabetic effects in a type 2 diabetic mouse model. Diabetic db/db mice were orally intubated with SA (10 mg kg(-1) body weight/day) for 8 weeks. We examined hemoglobin A1c (HbA1c), blood glucose levels...

Journal: :Mathematical and computational applications 2022

The focal interest in this article is to investigate the Stefan blowing and Dufour Soret effects on hybrid nanofluid (HNF) flow towards a stretching cylinder with thermal radiation. governing equations are converted into ODE by using suitable transformations. boundary value problem solver (bvp4c), which package MATLAB, used solve resulting equations. Results show that rise enhances velocity, te...

Journal: :Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research 1997
R S Peterson D E Clevidence H Ye R H Costa

The hepatocyte nuclear factor-3 alpha (HNF-3 alpha) and -3 beta proteins share homology in the winged helix/fork head DNA binding domain and regulate cell-specific transcription in hepatocytes and respiratory epithelium. In this study, we used transfection assays to demonstrate that the -520 nucleotides upstream of the rat HNF-3 alpha gene were sufficient for cell-specific expression. We identi...

2002
Pascal Boileau Christian Wolfrum David Q. Shih Tien-An Yang Allan W. Wolkoff Markus Stoffel

Diabetes in subjects with hepatocyte nuclear factor (HNF)-1 gene mutations (maturity-onset diabetes of the young [MODY]-3) is characterized by impaired insulin secretion. Surprisingly, MODY3 patients exhibit hypersensitivity to the hypoglycemic actions of sulfonylurea therapy. To study the pharmacogenetic mechanism(s), we have investigated glibenclamide-induced insulin secretion, glibenclamide ...

Journal: :Human molecular genetics 2011
Hailian Shen Devin M Barry Jeffrey M Dale Virginia B Garcia Nigel A Calcutt Michael L Garcia

Mutations in neurofilament light (NF-L) have been linked to Charcot-Marie-Tooth disease type 2E (CMT2E) in humans. To provide insight into disease pathogenesis, we developed a novel line of CMT2E mice that constitutively express human NF-L (hNF-L) with a glutamic acid to lysine mutation at position 397 (hNF-L(E397K)). This new line of mice developed signs consistent with CMT2E patients. Disease...

Journal: :Endocrinology 2008
H S Freitas G F Anhê K F S Melo M M Okamoto M Oliveira-Souza S Bordin U F Machado

Mutations in Na(+)-glucose transporters (SGLT)-2 and hepatocyte nuclear factor (HNF)-1alpha genes have been related to renal glycosuria and maturity-onset diabetes of the young 3, respectively. However, the expression of these genes have not been investigated in type 1 and type 2 diabetes. Here in kidney of diabetic rats, we tested the hypotheses that SGLT2 mRNA expression is altered; HNF-1alph...

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