Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Lucie J. Guetzoyan"'
Autor:
Lorenzo Frigerio, Markus Langhans, John Michael Lord, Guy J. Clarkson, Mathias Sorieul, Lynne M. Roberts, Stefan Hillmer, Lucie J. Guetzoyan, Robert A. Spooner, David Robinson
Publikováno v:
Traffic (Copenhagen, Denmark). 12(11)
We screened a panel of compounds derived from Exo2 - a drug that perturbs post-Golgi compartments and trafficking in mammalian cells - for their effect on the secretory pathway in Arabidopsis root epidermal cells. While Exo2 and most related compound
Autor:
Richard B. Sessions, Mahel Zeghouf, Lynne M. Roberts, Guy J. Clarkson, Robert A. Spooner, Jacqueline Cherfils, Frédéric Boal, David J. Stephens, Lucie J. Guetzoyan, J. Michael Lord
Publikováno v:
Traffic (Copenhagen, Denmark). 11(12)
Brefeldin A-mediated inhibition of ADP ribosylation factor (Arf) GTPases and their guanine nucleotide exchange factors, Arf-GEFs, has been a cornerstone of membrane trafficking research for many years. Brefeldin A (BFA) is relatively non-selective in
Publikováno v:
ChemInform. 41
The oxidative cyclisation of a range of benzothieno[2,3-d]pyrimidine hydrazones (7a–j) to the 1,2,4-triazolo[4,3-c]pyrimidines (8a–j) catalysed by lithium iodide or to the 1,2,4-triazolo[1,5-c]pyrimidines (10a–j) with sodium carbonate is presen
The oxidative cyclisation of a range of benzothieno[2,3-d]pyrimidine hydrazones (7a–j) to the 1,2,4-triazolo[4,3-c]pyrimidines (8a–j) catalysed by lithium iodide or to the 1,2,4-triazolo[1,5-c]pyrimidines (10a–j) with sodium carbonate is presen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c83d7d2e0b5d2bf760e77e638f7946f
http://wrap.warwick.ac.uk/3289/1/WRAP_Clarkson_EuroJMedChemClarkson2.pdf
http://wrap.warwick.ac.uk/3289/1/WRAP_Clarkson_EuroJMedChemClarkson2.pdf
Autor:
Lynne M. Roberts, J. Michael Lord, Robert A. Spooner, Frédéric Boal, Lucie J. Guetzoyan, Guy J. Clarkson, David J. Stephens
Publikováno v:
Molecular BioSystems. 6:2030
The small molecule 4-hydroxy-3-methoxybenzaldehyde (5,6,7,8-tetrahydro[1]benzothieno[2,3-\ud d]pyrimidin-4-yl)hydrazone (Exo2) stimulates morphological changes at the mammalian Golgi and\ud trans-Golgi network that are virtually indistinguishable fro