Zobrazeno 1 - 10
of 269
pro vyhledávání: '"John E. Scott"'
Autor:
Seoyeon Bok, Dong Yeon Shin, Alisha R. Yallowitz, Mark Eiseman, Michelle Cung, Ren Xu, Na Li, Jun Sun, Alfred L. Williams, John E. Scott, Bing Su, Jae-Hyuck Shim, Matthew B. Greenblatt
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-10 (2020)
Neurofibromatosis type I (NF1) is characterized by prominent skeletal abnormalities mediated in part by aberrant ERK pathway activation due to NF1 loss-of-function. Here, the authors report the MEKK2 is a key mediator of this aberrant ERK activation
Externí odkaz:
https://doaj.org/article/1bdc5e8883dd407b82aab19c4cfb975b
Publikováno v:
MethodsX, Vol 9, Iss , Pp 101927- (2022)
PTEN is a well-known tumor suppressor that is inactivated or suppressed at a high frequency in cancer. We sought an assay to screen compounds for ones that differentially inhibited proliferation or induced cytotoxicity in PTEN mutated cancer cells. W
Externí odkaz:
https://doaj.org/article/d4ebe48383f1404f8517558a0620731e
Autor:
Ladislas Robert
Publikováno v:
Pathologie Biologie. 60:334-335
Akademický článek
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Autor:
Stephen T.C. Wong, Li-An Yeh, John E. Scott, Hong Zhao, Alexandria T. Phan, Alfred L. Williams, Syed Ahmad, Xiaoping Zhu, Timothy Liu, Ren Kong
PDF file - 506KB, Supp. Fig. S1 2D structures of Amoxapine, Amoxapine's metabolites, Loxapine, and the previous reported potent GUS inhibitors - Inhibitor 1 and 2. Suppl. Fig. S2 The initial structures (left panel, Before MD) and the last snapshots (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49a225afd9a133bef2e1e79e54383b80
https://doi.org/10.1158/1078-0432.22454507
https://doi.org/10.1158/1078-0432.22454507
Autor:
Stephen T.C. Wong, Li-An Yeh, John E. Scott, Hong Zhao, Alexandria T. Phan, Alfred L. Williams, Syed Ahmad, Xiaoping Zhu, Timothy Liu, Ren Kong
Purpose: Irinotecan (CPT-11) induced diarrhea occurs frequently in patients with cancer and limits its usage. Bacteria β-glucuronidase (GUS) enzymes in intestines convert the nontoxic metabolite of CPT-11, SN-38G, to toxic SN-38, and finally lead to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92418d4a91128658e5adf62c7b2a8f9a
https://doi.org/10.1158/1078-0432.c.6522764.v1
https://doi.org/10.1158/1078-0432.c.6522764.v1
Publikováno v:
Trends in Applied Sciences Research. 15:242-252
Autor:
Mark Eiseman, Matthew B. Greenblatt, Jae-Hyuck Shim, Jun Sun, Alisha R. Yallowitz, Dong Yeon Shin, Na Li, Michelle Cung, Bing Su, Seoyeon Bok, Ren Xu, Alfred L. Williams, John E. Scott
Publikováno v:
Nature Communications
Nature Communications, Vol 11, Iss 1, Pp 1-10 (2020)
Nature Communications, Vol 11, Iss 1, Pp 1-10 (2020)
Neurofibromatosis type I (NF1) is characterized by prominent skeletal manifestations caused by NF1 loss. While inhibitors of the ERK activating kinases MEK1/2 are promising as a means to treat NF1, the broad blockade of the ERK pathway produced by th
Autor:
John E. Scott, Hamzah Kharabsheh
Publikováno v:
Biochem Biophys Res Commun
Triple-negative breast cancer (TNBC) remains the most challenging breast cancer subtype to treat. CoA synthase (CoAsy) is a bifunctional enzyme, encoded by the COASY gene, which catalyzes the last two steps of CoA biosynthesis. COASY has been reporte
Publikováno v:
SLAS Discov
Triple-negative breast cancer (TNBC) is a very aggressive form of breast cancer with few molecularly targeted therapies. We used a novel unbiased approach to identify higher-order synergistic or enhancer combinations of marketed kinase inhibitor drug