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Publication Listing for the MeSH term FIBROBLASTS. Found 3 abstracts

Narra K, Mullins SR, Lee HO, Strzemkowski-Brun B, Magalong K, Christiansen VJ, McKee PA, Egleston B, Cohen SJ, Weiner LM, Meropol NJ, Cheng JD. Phase II trial of single agent Val-boroPro (Talabostat) inhibiting fibroblast activation protein in patients with metastatic colorectal cancer. Cancer Biology & Therapy. 2007 Nov;6(11):1691-9.
Lin DI, Barbash O, Kumar KG, Weber JD, Harper JW, Klein-Szanto AJ, Rustgi A, Fuchs SY, Diehl JA, Zamek-Gliszczynski MJ, Nezasa KI, Tian XB, Bridges AS, Lee K, Belinsky MG, Kruh GD, Brouwer KL. Phosphorylation-dependent ubiquitination of cyclin D1 by the SCFFBX4-alpha B crystallin complex Evaluation of the role of multidrug resistance-associated protein (Mrp) 3 and Mrp4 in hepatic basolateral excretion of sulfate and glucuronide metabolites of acetaminophen, 4-methylumbelliferone, and harmol in Abcc3(-)/(-) and Abcc4(-)/(-) mice. Molecular cell. 2006 Dec;319(3):1485-91.
Cattani P, Hohaus S, Bellacosa A, Genuardi M, Cavallo S, Rovella V, Almadori G, Cadoni G, Galli J, Maurizi M, Fadda G, Neri G. Association between cyclin D1 (CCND1) gene amplification and human papillomavirus infection in human laryngeal squamous cell carcinoma. Clinical Cancer Research. 1998 Nov;4(11):2585-9.
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MeSH cloud from publications including the MeSH term FIBROBLASTS

FIBROBLASTS CELLULAR-TRANSFORMATION although additional basolateral excretion of sulfate conjugates serine protease -) and Abcc4(- respectively The basolateral excretory clearance of similar to 45% translocation of these hydrophilic metabolites have not been completely two basolateral efflux transporters Mrp3 and Mrp4-was evaluated by POLYMERASE CHAIN-REACTION HEAD KIDNEY DESTRUCTION BOX in Abcc3(- SERINE-PROTEASE MEDIATED DEGRADATION KNOCKOUT MICE 4-methylumbelliferyl glucuronide acetaminophen glucuronide-and harmol EXPRESSION RAT endogenous compounds undergo appreciable hepatic basolateral excretion -) mice using a cassette dosing approach In mediates the hepatic basolateral excretion of diverse glucuronide LIVER AB Although glucuronide and sulfate conjugates of many drugs and LONGITUDINAL DATA-ANALYSIS trial ALTERED HEPATOBILIARY DISPOSITION P53 fibroblast activation protein OBSTRUCTIVE CHOLESTASIS LACKING DOSE-ESCALATION ORGANIC ANION TRANSPORTER DNA NECK-CANCER 4-methylumbelliferone sulfate metabolites of acetaminophen-and harmol SMALL-MOLECULE phase II clinical basolateral excretory clearance of these glucuronide conjugates was P21(CIP1) direct evidence that Mrp3 and Mrp4 participate in the hepatic HPV tumor fibroblasts unaffected by the absence of Mrp4 These results provide the first similar to 85 glucuronide was reduced by similar to 96-and similar to conjugates PLUS FLUOROURACIL the involvement in this process of elucidated In the present study colorectal cancer they reveal that Mrp3 mechanism(s) are likely involved In addition Val-boroPro BILIARY-EXCRETION the mechanisms that govern basolateral into sinusoidal blood -) mice In contrast the basolateral excretory -) mice respectively 40%-in the livers of Abcc3(- BOX PROTEIN FBX4 LIGASE COMPLEX EPITHELIAL CANCERS NUCLEAR EXPORT LINKED-IMMUNOSORBENT-ASSAY TUMOR STROMAL VIRUS P27(KIP1) analyzing the hepatic basolateral excretion of the glucuronide and MUTATIONS tumor stroma CONJUGATED HYPERBILIRUBINEMIA PHASE the livers of Abcc3(- clearance of acetaminophen sulfate was reduced similar to 20 and 4-methylumbelliferyl sulfate was reduced similar to 50 similar to 20% and harmol sulfate was decreased similar to 30 and and similar to 65% COATED TUBES MONOCLONAL-ANTIBODY
Last updated on Friday, June 05, 2020