Zobrazeno 1 - 10
of 619
pro vyhledávání: '"S. Thayumanavan"'
Exogenous Introduction of Initiator and Executioner Caspases Results in Different Apoptotic Outcomes
Publikováno v:
JACS Au, Vol 1, Iss 8, Pp 1240-1256 (2021)
Externí odkaz:
https://doaj.org/article/72d8e511927844128801c27706b55122
Autor:
Kingshuk Dutta, Ritam Das, Jing Ling, Rafael Mayoral Monibas, Ester Carballo-Jane, Ahmet Kekec, Danqing Dennis Feng, Songnian Lin, James Mu, Robert Saklatvala, S. Thayumanavan, Yingkai Liang
Publikováno v:
ACS Omega, Vol 5, Iss 28, Pp 17531-17542 (2020)
Externí odkaz:
https://doaj.org/article/e07bb7861fcc44ce9fd240665f45f633
Publikováno v:
Langmuir. 39:1793-1803
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9034c019f6414cdc69177470d9dc92f6
https://doi.org/10.1021/acs.langmuir.2c02622
https://doi.org/10.1021/acs.langmuir.2c02622
Autor:
Uyen Huynh, Peidong Wu, Jingyi Qiu, Theeraphop Prachyathipsakul, Khushboo Singh, D. Joseph Jerry, Jingjing Gao, S. Thayumanavan
Publikováno v:
Biomacromolecules. 24:849-857
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5ff057585cb9594156df962c8df9e38
https://doi.org/10.1021/acs.biomac.2c01269
https://doi.org/10.1021/acs.biomac.2c01269
Publikováno v:
Chemistry Central Journal, Vol 12, Iss 1, Pp 1-9 (2018)
Abstract A series of D–A dyads and D–A–D triads molecular systems based on triphenylamine and 9-ethyl-carbarzole as donor (D) and BODIPY as acceptor (A) has been designed and synthesized. The optoelectronic properties including optical, electro
Externí odkaz:
https://doaj.org/article/8a2f2272dd5546d49e97ed968c1638c1
Autor:
Ranit Dutta, Sparsh Makhaik, Peiyao Zhao, Kristalle G. Cruz, Kwang-Won Park, Hongxu Liu, Trisha L. Andrew, Jeanne A. Hardy, S. Thayumanavan
Publikováno v:
Analytical Chemistry. 94:12699-12705
Reporting the activity of a specific viral protease remains an acute need for rapid point-of-care detection strategies that can distinguish active infection from a resolved infection. In this work, we present a simple colorimetric approach for report
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dadaaba415ae93ec29fbd771646f47c3
https://doi.org/10.1021/acs.analchem.2c02033
https://doi.org/10.1021/acs.analchem.2c02033
Multisite Labeling of Proteins Using the Ligand-Directed Reactivity of Triggerable Michael Acceptors
Autor:
Myrat Kurbanov, Zachary J. Kirsch, Jithu Krishna, Ranit Dutta, Richard W. Vachet, S. Thayumanavan
Publikováno v:
Bioconjugate Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c440fafa7336b0122ff12adfe4f96a9
https://doi.org/10.1021/acs.bioconjchem.3c00155
https://doi.org/10.1021/acs.bioconjchem.3c00155
Publikováno v:
Bioconjugate Chemistry. 33:1996-2007
Recent success of mRNA-based COVID-19 vaccines have bolstered the strength of nucleic acids as a therapeutic platform. The number of new clinical trial candidates is skyrocketing with the potential to address many unmet clinical needs. Despite advanc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39acb284e2dc84998e9b88532f853894
https://doi.org/10.1021/acs.bioconjchem.2c00058
https://doi.org/10.1021/acs.bioconjchem.2c00058
Autor:
Khushboo Singh, Mine Canakci, Pintu Kanjilal, Natalie Williams, Sudarvili Shanthalingam, Barbara A. Osborne, S. Thayumanavan
Publikováno v:
Bioconjug Chem
Targeted delivery of chemotherapeutic drugs can improve their therapeutic efficiency by localizing their toxic effects at the diseased site. This is often achieved either by direct conjugation of drugs to antibodies targeting overexpressed receptors
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05d6ae8952fbf978253d9622178f6b98
https://doi.org/10.1021/acs.bioconjchem.2c00024
https://doi.org/10.1021/acs.bioconjchem.2c00024
Publikováno v:
Polymer International. 71:562-568
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90d6a5bad9cd130355b3a35607dff73c
https://doi.org/10.1002/pi.6352
https://doi.org/10.1002/pi.6352