Zobrazeno 1 - 10
of 140
pro vyhledávání: '"Stuart L, Warriner"'
Autor:
Kristian Hollingsworth, Antonio Di Maio, Sarah-Jane Richards, Jean-Baptiste Vendeville, David E. Wheatley, Claire E. Council, Tessa Keenan, Hélène Ledru, Harriet Chidwick, Kun Huang, Fabio Parmeggiani, Andrea Marchesi, Wengang Chai, Ryan McBerney, Tomasz P. Kamiński, Matthew R. Balmforth, Alexandra Tamasanu, James D. Finnigan, Carl Young, Stuart L. Warriner, Michael E. Webb, Martin A. Fascione, Sabine Flitsch, M. Carmen Galan, Ten Feizi, Matthew I. Gibson, Yan Liu, W. Bruce Turnbull, Bruno Linclau
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-14 (2024)
Abstract Glycan-mediated interactions play a crucial role in biology and medicine, influencing signalling, immune responses, and disease pathogenesis. However, the use of glycans in biosensing and diagnostics is limited by cross-reactivity, as certai
Externí odkaz:
https://doaj.org/article/45fc41374e2f4ce2b12a1822076a1c13
Publikováno v:
RSC Chemical Biology. 4:216-222
Through the incorporation of a diazirine photocrosslinking group and a fluorophore, we developed and validated a photoaffinity probe with good selectivity and potent binding to formyl peptide receptor 1 in living cells.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a8e893c2c3242f0224f17f2d834d2bc0
https://doi.org/10.1039/d2cb00199c
https://doi.org/10.1039/d2cb00199c
Publikováno v:
ACS Omega, Vol 3, Iss 12, Pp 18466-18474 (2018)
Externí odkaz:
https://doaj.org/article/0c28752bda844c83af243b23cbfa275b
Autor:
Laura L. Cross, Rupesh Paudyal, Yasuko Kamisugi, Alan Berry, Andrew C. Cuming, Alison Baker, Stuart L. Warriner
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-9 (2017)
Designer organelles could allow the isolation of synthetic biological pathways from endogenous components of the host cell. Here the authors engineer a peroxisomal protein import pathway orthogonal to the naturally occurring system.
Externí odkaz:
https://doaj.org/article/50a54e6e36e545d2ab227403bffde353
Autor:
Jacob R. Hauser, Hester A. Beard, Mary E. Bayana, Katherine E. Jolley, Stuart L. Warriner, Robin S. Bon
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 2019-2025 (2016)
2-Cyanobenzothiazoles (CBTs) are useful building blocks for: 1) luciferin derivatives for bioluminescent imaging; and 2) handles for bioorthogonal ligations. A particularly versatile CBT is 6-amino-2-cyanobenzothiazole (ACBT), which has an amine hand
Externí odkaz:
https://doaj.org/article/4dec427fbe5d4b99afdcb709f5fe3d60
Autor:
Rafal Kulmaczewski, Isaac T. Armstrong, Pip Catchpole, Emily S. J. Ratcliffe, Hari Babu Vasili, Stuart L. Warriner, Oscar Cespedes, Malcolm A. Halcrow
Publikováno v:
Chemistry – A European Journal. 29
Four bis[2-{pyrazol-1-yl}-6-{pyrazol-3-yl}pyridine] ligands have been synthesized, with butane-1,4-diyl (L
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12c51892cbc69135546426693490262b
https://doi.org/10.1002/chem.202202578
https://doi.org/10.1002/chem.202202578
Autor:
Izar Capel Berdiell, Stuart L. Warriner, Malcolm A. Halcrow, Oscar Cespedes, Rafal Kulmaczewski
Publikováno v:
European Journal of Inorganic Chemistry. 2020:4334-4340
Treatment of 2,4,6‐trifluoropyridine with sodium imidazolate, then 2 equiv. sodium pyrazolate, in two reaction steps yields the title ligand L in 40 % overall yield. Crystalline [FeL2][BF4]2 and [FeL2][ClO4]2 are isostructural high‐spin complexes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b8fd57682ca7bb62d91a0173f09b3b3
https://doi.org/10.1002/ejic.202000782
https://doi.org/10.1002/ejic.202000782
Autor:
Andrew J. Wilson, Fruzsina Hobor, Christopher P. Tinworth, Adam Nelson, Stuart L. Warriner, Adam I. Green
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
Protein–protein interactions (PPIs) provide a rich source of potential targets for drug discovery and biomedical science research. However, the identification of structural‐diverse starting points for discovery of PPI inhibitors remains a signifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2962f6455eadb81a18b3b9fdc54ed800
http://europepmc.org/articles/PMC7496268
http://europepmc.org/articles/PMC7496268
Autor:
null Sonja Srdanovic, null Madita Wolter, null Chi H. Trinh, null Christian Ottmann, null Stuart L. Warriner, null Andrew J. Wilson
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b18e8fd0b0adc9ea31f35fa6ef8b76b
https://doi.org/10.1111/febs.16433/v2/response1
https://doi.org/10.1111/febs.16433/v2/response1
Publikováno v:
RSC chemical biology. 3(5)
Using the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1498cb0be002e7bdc4600927c407dd1e
https://pubmed.ncbi.nlm.nih.gov/35656480
https://pubmed.ncbi.nlm.nih.gov/35656480