User profiles for Nathalie Rioux
Nathalie RiouxCertara Verified email at h3biomedicine.com Cited by 3258 |
A selective inhibitor of PRMT5 with in vivo and in vitro potency in MCL models
Protein arginine methyltransferase-5 (PRMT5) is reported to have a role in diverse cellular
processes, including tumorigenesis, and its overexpression is observed in cell lines and …
processes, including tumorigenesis, and its overexpression is observed in cell lines and …
[HTML][HTML] Epidemiologic data of primary glomerular diseases in western France
…, F Leonetti, G Cam, E Laruelle, V Autuly, N Rioux - Kidney international, 2004 - Elsevier
Epidemiologic data of primary glomerular diseases in western France. Between January 1,
1976, and December 31, 2002, histologic diagnosis of primary glomerular diseases (PGD) …
1976, and December 31, 2002, histologic diagnosis of primary glomerular diseases (PGD) …
[PDF][PDF] Anti-tumor activity of the type I PRMT inhibitor, GSK3368715, synergizes with PRMT5 inhibition through MTAP loss
…, SV Gerhart, LH Mitchell, ND Adams, N Rioux… - Cancer cell, 2019 - cell.com
Type I protein arginine methyltransferases (PRMTs) catalyze asymmetric dimethylation of
arginines on proteins. Type I PRMTs and their substrates have been implicated in human …
arginines on proteins. Type I PRMTs and their substrates have been implicated in human …
Inhibitors of lipoxygenase: a new class of cancer chemopreventive agents.
N Rioux, A Castonguay - Carcinogenesis, 1998 - academic.oup.com
5-Lipoxygenase is a key enzyme in the metabolism of arachidonic acid to leukotrienes. The
preventive efficacy of 5-lipoxygenase inhibitors against lung tumorigenesis was determined …
preventive efficacy of 5-lipoxygenase inhibitors against lung tumorigenesis was determined …
Prevention of NNK-induced lung tumorigenesis in A/J mice by acetylsalicylic acid and NS-398
N Rioux, A Castonguay - Cancer research, 1998 - AACR
Acetylsalicylic acid (ASA) is known to prevent cancer development, but its mechanism of
action remains unclear. In this study, we compared the efficacies of this nonspecific …
action remains unclear. In this study, we compared the efficacies of this nonspecific …
Structure and property guided design in the identification of PRMT5 tool compound EPZ015666
The recent publication of a potent and selective inhibitor of protein methyltransferase 5 (PRMT5)
provides the scientific community with in vivo-active tool compound EPZ015666 (…
provides the scientific community with in vivo-active tool compound EPZ015666 (…
EPZ011989, a potent, orally-available EZH2 inhibitor with robust in vivo activity
Inhibitors of the protein methyltransferase Enhancer of Zeste Homolog 2 (EZH2) may have
significant therapeutic potential for the treatment of B cell lymphomas and other cancer …
significant therapeutic potential for the treatment of B cell lymphomas and other cancer …
H3B-6527 is a potent and selective inhibitor of FGFR4 in FGF19-driven hepatocellular carcinoma
…, R Hurley, T Satoh, K Yu, E Park, N Rioux… - Cancer research, 2017 - AACR
Activation of the fibroblast growth factor receptor FGFR4 by FGF19 drives hepatocellular
carcinoma (HCC), a disease with few, if any, effective treatment options. While a number of pan-…
carcinoma (HCC), a disease with few, if any, effective treatment options. While a number of pan-…
Aryl pyrazoles as potent inhibitors of arginine methyltransferases: identification of the first PRMT6 tool compound
LH Mitchell, AE Drew, SA Ribich, N Rioux… - ACS medicinal …, 2015 - ACS Publications
A novel aryl pyrazole series of arginine methyltransferase inhibitors has been identified.
Synthesis of analogues within this series yielded the first potent, selective, small molecule …
Synthesis of analogues within this series yielded the first potent, selective, small molecule …
Preclinical profile of BI 224436, a novel HIV-1 non-catalytic-site integrase inhibitor
BI 224436 is an HIV-1 integrase inhibitor with effective antiviral activity that acts through a
mechanism that is distinct from that of integrase strand transfer inhibitors (INSTIs). This 3-…
mechanism that is distinct from that of integrase strand transfer inhibitors (INSTIs). This 3-…