Zobrazeno 1 - 9
of 9
pro vyhledávání: '"John C, Lainson"'
Autor:
Natalie Iannuzo, Yannik A. Haller, Michelle McBride, Sabrina Mehari, John C. Lainson, Chris W. Diehnelt, Shelley E. Haydel
Publikováno v:
ACS Omega. 7:23967-23977
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13c8c29e37ba584fb14e8bad047e9d5b
https://doi.org/10.1021/acsomega.2c02844
https://doi.org/10.1021/acsomega.2c02844
Autor:
Stephen Albert Johnston, John C. Lainson, Zhan Gong Zhao, Kathryn Sykes, Chris W. Diehnelt, Luhui Shen, Justin R. Brown
Publikováno v:
RSC Advances. 10:29675-29681
Parallel measurement of large numbers of antigen–antibody interactions are increasingly enabled by peptide microarray technologies. Our group has developed an in situ synthesized peptide microarray of >400 000 frameshift neoantigens using mask-base
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7bf86667492fb4c241f7a488a8aa612
https://doi.org/10.1039/d0ra05267a
https://doi.org/10.1039/d0ra05267a
Autor:
Stephen Albert Johnston, Paul E. Belcher, Luhui Shen, Chris W. Diehnelt, Nidhi Gupta, Hugh S. Mason, John C. Lainson
Publikováno v:
Analytical Chemistry. 89:7174-7181
Noroviruses are the most common cause of acute gastroenteritis in the developed world. Noroviruses are a diverse group of nonenveloped RNA viruses that are continuously evolving. This leads to the rise of immunologically distinct strains of the same
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e6258020ca2fcccfae77e7aa49e1908
https://doi.org/10.1021/acs.analchem.7b01337
https://doi.org/10.1021/acs.analchem.7b01337
Autor:
Zhan-Gong Zhao, Stephen Albert Johnston, John C. Lainson, Nidhi Gupta, Valeriy Domenyuk, Chris W. Diehnelt
Publikováno v:
Bioconjugate Chemistry. 27:2505-2512
There is an ongoing need for affinity agents for emerging viruses and new strains of current human viruses. We therefore developed a robust and modular system for engineering high-affinity synbody ligands for the influenza A/Puerto Rico/8/1934 H1N1 v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95d5de73c7e124fecab335f28ce6ba68
https://doi.org/10.1021/acs.bioconjchem.6b00447
https://doi.org/10.1021/acs.bioconjchem.6b00447
Autor:
Milene Tavares Batista, Stephen Albert Johnston, John C. Lainson, Sierra Nicole Murphy, Lui Shen
Publikováno v:
Cancer Immunology Research. 8:A28-A28
Development of cancer vaccines is currently focused on using neoantigens arising from mutations in the DNA of tumors. We have proposed, and demonstrated, that errors in RNA processing that create frameshift (FS) neoantigens are also a good source of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d49e9c061fb6dc89b0f9f818b69d032
https://doi.org/10.1158/2326-6074.tumimm19-a28
https://doi.org/10.1158/2326-6074.tumimm19-a28
Publikováno v:
Chemical communications (Cambridge, England). 54(12)
We demonstrate a platform to screen a virus pseudotyped with Ebola virus glycoprotein (GP) against a library of peptides that contain non-natural amino acids to develop GP affinity ligands. This system could be used for rapid development of peptide-b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0d7ce2b6cca43924cfd24ee941e0504
https://pubmed.ncbi.nlm.nih.gov/29297911
https://pubmed.ncbi.nlm.nih.gov/29297911
Publikováno v:
Bioconjugate Chemistry. 26:2125-2132
Synbodies show promise as a new class of synthetic antibiotics. Here, we explore improvements in their activity and production through conjugation chemistry. Maleimide conjugation is a widely used conjugation strategy due to its high yield, selectivi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac00f787e8df399a26ed7d68c7dc60f2
https://doi.org/10.1021/acs.bioconjchem.5b00420
https://doi.org/10.1021/acs.bioconjchem.5b00420
Autor:
John C. Lainson, Stephen Albert Johnston, Kathleen D. Triplett, Seth M. Daly, Pamela R. Hall, Chris W. Diehnelt
One proposed solution to the crisis of antimicrobial resistant (AMR) infections is the development of molecules that potentiate the activity of antibiotics for AMR bacteria, such as methicillin-resistant Staphylococcus aureus (MRSA). Rather than deve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2030b2d7567507805868465207c807b
https://europepmc.org/articles/PMC5554890/
https://europepmc.org/articles/PMC5554890/
Publikováno v:
Bioconjugate Chemistry; Oct2015, Vol. 26 Issue 10, p2125-2132, 8p