Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Reena Chawla"'
Autor:
Rameez Ali, Sreenivasa Anugu, Reena Chawla, Violeta G. Demillo, Florian Goulinet-Mateo, Sagar Gyawali, Sunil Hamal, Dylan E. Jones, Katrin Lamprecht, Truc Le, Liezel A. Lumangtad, Nicholas C. Pflug, Alekhya Sama, Emily D. Scarbrough, Thomas W. Bell
Publikováno v:
ACS Omega, Vol 4, Iss 1, Pp 1254-1264 (2019)
Externí odkaz:
https://doaj.org/article/011f439bb7a647cc920377bf1d077276
Autor:
Marcel Patek, Zhiming Shan, Song Cai, May Khanna, Vijay Gokhale, Todd W. Vanderah, Reena Chawla, Shreya S. Bellampalli, Taylor Joel Woodward, David D. Scott, Angie Dorame, Yuan Zhou, Lindsey A. Chew, Aude Chefdeville, Kimberly Gomez, Cynthia L. Madura, Andrea G. Hohmann, Liberty François-Moutal, Jörg Isensee, Shizhen Luo, Jie Yu, Rajesh Khanna, Samantha Perez-Miller, Tim Hucho, Aubin Moutal
Publikováno v:
Science translational medicine. 13(619)
The voltage-gated sodium NaV1.7 channel, critical for sensing pain, has been actively targeted by drug developers; however, there are currently no effective and safe therapies targeting NaV1.7. Here, we tested whether a different approach, indirect N
Autor:
Melinda Fitzgerald, Amy L. Kretzmann, Haibo Jiang, Jeffrey A. Keelan, Tristan D. Clemons, Alaa M. Munshi, Laurence H. Hurley, Jean-Pierre Veder, Jessica A. Kretzmann, Charles S. Bond, Diwei Ho, Nicole M. Smith, Michael Archer, Priyanka Toshniwal, Michelle Nguyen, Amanda J. Blythe, Cameron W. Evans, Paul Guagliardo, Marck Norret, Reena Chawla, K. Swaminathan Iyer, Martin Saunders, Matt R. Kilburn
Publikováno v:
Nature Nanotechnology. 13:1148-1153
Gold nanorods are one of the most widely explored inorganic materials in nanomedicine for diagnostics, therapeutics and sensing1. It has been shown that gold nanorods are not cytotoxic and localize within cytoplasmic vesicles following endocytosis, w
Autor:
Prashansa Agrawal, Laurence H. Hurley, Reena Chawla, Natalie A. Van Ert, Christine E. Kaiser, Danzhou Yang
Publikováno v:
Journal of the American Chemical Society. 139:8522-8536
Activating KRAS mutations frequently occur in pancreatic, colorectal, and lung adenocarcinomas. While many attempts have been made to target oncogenic KRAS, no clinically useful therapies currently exist. Most efforts to target KRAS have focused on i
Autor:
Eddie T. Chiang, Venkateshwar Reddy Chappeta, Megan A. Turnidge, Reena Chawla, Danzhou Yang, Quinea R. Lassiter, Carmen Lee, Hector Quijada, Robert V. Brown, Shivani Phanse, Ping Zhao, Joe G.N. Garcia, Ting Wang, Laurence H. Hurley, Buket Onel, Sara M. Camp, Guanhui Wu, Vijay Gokhale
Publikováno v:
Journal of the American Chemical Society. 139:7456-7475
The platelet-derived growth factor receptor β (PDGFR-β) signaling pathway is a validated and important target for the treatment of certain malignant and nonmalignant pathologies. We previously identified a G-quadruplex-forming nuclease hypersensiti
Autor:
Thomas W. Bell, Nicholas C. Pflug, Sreenivasa Anugu, Florian Goulinet-Mateo, Katrin Lamprecht, Reena Chawla, Rameez Ali, Violeta G. Demillo, Emily D. Scarbrough, Sunil Hamal, Alekhya Sama, Sagar Gyawali, Truc D. T. Le, Liezel A. Lumangtad, Dylan E. Jones
Publikováno v:
ACS Omega, 4 (1)
ACS Omega, Vol 4, Iss 1, Pp 1254-1264 (2019)
ACS Omega
ACS Omega, Vol 4, Iss 1, Pp 1254-1264 (2019)
ACS Omega
Macrocyclic triamine disulfonamides can be synthesized by double Tsuji–Trost N-allylation reaction of open-chain disulfonamides with 2-alkylidene-1,3-propanediyl bis(carbonates). The previously used Atkins–Richman macrocyclization method generall
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::168293d30a812016f387b7d87a176d1c
https://hdl.handle.net/20.500.11850/322310
https://hdl.handle.net/20.500.11850/322310
Autor:
Reena Chawla, Nicholas C. Pflug, Dominique Schols, Victor Van Puyenbroeck, Thomas W. Bell, Kurt Vermeire, Alekhya Sama, Rameez Ali
Publikováno v:
Journal of Medicinal Chemistry. 59:2633-2647
Cyclotriazadisulfonamide prevents HIV entry into cells by down-modulating surface CD4 receptor expression through binding to the CD4 signal peptide. According to a two-site binding model, 28 new unsymmetrical analogues bearing a benzyl tail group and
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