Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Fengmei Hua"'
Publikováno v:
Journal of International Medical Research, Vol 52 (2024)
Objective This study aimed to assess the reliability of the spot urine protein/creatinine (sP/Cr) ratio for evaluating proteinuria across different ranges and renal functions. Methods In this retrospective study, we analyzed 24-hour urine protein exc
Externí odkaz:
https://doaj.org/article/20d1a78772014c9a8fefef1baefbd623
Publikováno v:
Journal of International Medical Research, Vol 52 (2024)
The penetration of a peritoneal dialysis catheter into the intestinal cavity is a clinically rare complication. In the present retrospective clinical case series, 11 patients with uraemia who received continuous ambulatory peritoneal dialysis and att
Externí odkaz:
https://doaj.org/article/516e82d36e054e9195fb031d408a5735
Autor:
Barbara A. Schweitzer, Atli Thorarensen, Michael S. Davies, Steve R. Turner, Matthew James Pelc, James R. Kiefer, Brenda L. Case, Christie L. Funckes-Shippy, Jacqueline E. Day, Fengmei Hua, Dice Tom, William M. Abraham, Bradley E. Neal, John I. Trujillo, Joseph B. Moon, Blake Tanisha Danielle Rowe, Wei Huang, Craig D. Wegner, Dean Welsch, Chris P. Carron, Anup Zutshi, Bruce C. Hamper, Chad J. Warren, Rhonda S. Woerndle, Christine M. Kornmeier, Vickie M. Dilworth, Melanie L. Williams, Martin E. Dowty, Olson Kirk Lang, Melissa R. Radabaugh, Becky L. Hood, Jerry Z. Yang, Douglas C. Rohrer, Gina M. Jerome, Christine P. Bono
Publikováno v:
ACS Medicinal Chemistry Letters. 1:59-63
Hematopoietic prostaglandin D synthase (HPGDS) is primarly expressed in mast cells, antigen-presenting cells, and Th-2 cells. HPGDS converts PGH2 into PGD2, a mediator thought to play a pivotal role in airway allergy and inflammatory processes. In th
Autor:
Yurong Lai, Meng Li, Fengmei Hua, Yi Zheng, Na Li, Haodan Yuan, Archie Thurston, Joanne Wang, Mike Baratta, Guotao Song
Publikováno v:
European Journal of Pharmaceutical Sciences. 35:114-126
The large interspecies differences of hepatobiliary transport present a challenge for the allometric prediction of human biliary excretion for drug candidates primarily cleared via hepatobiliary secretion. In the present study, we determined the meta
Autor:
Leslie Z. Benet, Fengmei Hua, Charles G. Knutson, Mark P. Grillo, Kristi L. March, Joseph A. Ware
Publikováno v:
Chemical Research in Toxicology. 21:1933-1938
Diclofenac, a nonsteroidal antiinflammatory drug, is known to be metabolized to chemically reactive intermediates that transacylate GSH forming diclofenac-S-acyl-glutathione (D-SG) in vivo in rat and in vitro in rat and human hepatocytes. Recently, i
Autor:
Fengmei Hua, Mark P. Grillo
Publikováno v:
Chemical Research in Toxicology. 21:1749-1759
Ibuprofen is metabolized to chemically reactive ibuprofen-1- O-acyl-glucuronide (I-1- O-G) and ibuprofen- S-acyl-CoA (I-CoA) derivatives, which are proposed to mediate the formation of drug-protein adducts via the transacylation of protein nucleophil
Autor:
Daniel J. Waldon, P E Sanders, Fengmei Hua, Joseph A. Ware, Charles G. Knutson, Mark P. Grillo
Publikováno v:
Drug Metabolism and Disposition. 31:1327-1336
Diclofenac, a nonsteroidal anti-inflammatory drug, is metabolized to a reactive acyl glucuronide that has been proposed to mediate toxic adverse drug reactions associated with its use. In the present study, we examined the ability of diclofenac acyl
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 37(1)
We previously reported that hepatobiliary transporter multidrug resistance-associated protein (MRP2/Mrp2) is considered to be the major cause of the interspecies differences detected by efflux of fluorescent substrates in isolated hepatocytes. In the
Publikováno v:
Chemical research in toxicology. 16(11)
Diclofenac, a nonsteroidal anti-inflammatory drug, is metabolized to diclofenac-1-O-acyl glucuronide (D-1-O-G), a chemically reactive conjugate that has been implicated as playing a role in the idiosyncratic hepatoxicity associated with its use. The
Autor:
Mark P. Grillo, Fengmei Hua
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 31(11)
Zomepirac (ZP), a nonsteroidal anti-inflammatory drug that was withdrawn from use, is metabolized to zomepirac-1-O-acyl-glucuronide (ZP-1-O-G), a chemically reactive conjugate that has been implicated in the toxicity of the drug. In the present studi