نتایج جستجو برای: hek 293 cells

تعداد نتایج: 1389104  

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2010
Yong-Hae Han Dennis Busler Yang Hong Yuan Tian Cliff Chen A David Rodrigues

17alpha-Ethinylestradiol (EE2), a synthetic and potent estrogen receptor agonist, is extensively metabolized in both intestine and liver and is largely excreted in bile and urine as the 3-O-sulfate (EE2-Sul) and 3-O-glucuronide. In the present study, EE2-Sul was evaluated as a substrate of various transporters known to be expressed in the kidney. Uptake studies were performed with human epithel...

Journal: :The Journal of biological chemistry 1999
R A Hall R F Spurney R T Premont N Rahman J T Blitzer J A Pitcher R J Lefkowitz

The Na(+)/H(+) exchanger regulatory factor (NHERF) is constitutively phosphorylated in cells, but the site(s) of this phosphorylation and the kinase(s) responsible for it have not been identified. We show here that the primary site of constitutive NHERF phosphorylation in human embryonic kidney 293 (HEK-293) cells is Ser(289), and that the stoichiometry of phosphorylation is near 1 mol/mol. NHE...

Journal: :The Journal of biological chemistry 2013
Henry A Dunn Cornelia Walther Christina M Godin Randy A Hall Stephen S G Ferguson

The corticotropin-releasing factor (CRF) receptor 1 (CRFR1) is a target for the treatment of psychiatric diseases such as depression, schizophrenia, anxiety disorder, and bipolar disorder. The carboxyl-terminal tail of the CRFR1 terminates in a PDZ-binding motif that provides a potential site for the interaction of PSD-95/Discs Large/Zona Occludens 1 (PDZ) domain-containing proteins. In this st...

Journal: :Biopolymers 2008
Ge Jiang Kitae Park Jiseok Kim Ki Su Kim Eun Ju Oh Hyungu Kang Su-Eun Han Yu-Kyoung Oh Tae Gwan Park Sei Kwang Hahn

A novel target specific small interfering RNA (siRNA) delivery system was successfully developed using polyethyleneimine (PEI)-hyaluronic acid (HA) conjugate. Anti-PGL3-Luc siRNA was used as a model system suppressing the PGL3-Luc gene expression. The siRNA/PEI-HA complex with an average size of ca. 21 nm appeared to be formed by electrostatic interaction between the negatively charged siRNA an...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2001
T R Cummins F Aglieco M Renganathan R I Herzog S D Dib-Hajj S G Waxman

Although rat brain Nav1.3 voltage-gated sodium channels have been expressed and studied in Xenopus oocytes, these channels have not been studied after their expression in mammalian cells. We characterized the properties of the rat brain Nav1.3 sodium channels expressed in human embryonic kidney (HEK) 293 cells. Nav1.3 channels generated fast-activating and fast-inactivating currents. Recovery f...

Journal: :The American journal of physiology 1999
Isabelle Fernandes Richard Béliveau Gérard Friedlander Caroline Silve

The aim of the present study was to characterize the type(s) of NaPO4 cotransporter expressed in the human renal cell line HEK-293 and its regulation by parathyroid hormone (PTH) in wild-type cells and in cells transfected by the PTH/PTH-related protein (PTHrP) receptor. The results showed that human embryonic kidney HEK-293 cells expressed NaPO4 cotransporter type III (PiT1) mRNA and protein. ...

Journal: :Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2005
Marina Hermes Sandra von Hippel Hartmut Osswald Doris Kloor

BACKGROUND/AIMS The methylation potential (MP) is defined as the ratio of S-adenosylmethionine (AdoMet) to S-adenosylhomocysteine (AdoHcy). It was shown recently that hypoxia increases AdoMet/AdoHcy ratio in HepG2 cells (Hermes et al., Exp Cell Res 294: 325-334, 2004). In the present study, we compared AdoMet/AdoHcy ratio and energy metabolism in HepG2, HEK-293, HeLa, MCF-7 and SK-HEP-1 cell li...

2013
Byung Joo Kim

Ginsenoside, one of the active ingredients of Panax ginseng, has a variety of physiologic and pharmacologic effects. The purpose of this study was to explore the effects of ginsenoside Rd (G-Rd) on melastatin type transient receptor potential 7 (TRPM7) channels with respect to the proliferation and survival of AGS and MCF-7 cells (a gastric and a breast cancer cell line, respectively). AGS and ...

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