Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Irene Zegar"'
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
Abstract The aim of this research is twofold: 1) to shed light on zika’s binding and entry mechanism while 2) demonstrating the effectiveness of our magnetic relaxation platform to achieve this goal. Magnetic relaxation-sensitive nanoparticles (MRN
Externí odkaz:
https://doaj.org/article/2f50a8688b7244638129e5ef7c50007d
Publikováno v:
Scientific Reports
Scientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
Scientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
The aim of this research is twofold: 1) to shed light on zika’s binding and entry mechanism while 2) demonstrating the effectiveness of our magnetic relaxation platform to achieve this goal. Magnetic relaxation-sensitive nanoparticles (MRNPs) are u
Autor:
James Foresman, Adrian McAfee, Irene Zegar, Bill Lackamp, Keaton Wilbur, Marie Montague, Daniel Mungula
Publikováno v:
The FASEB Journal. 29
Publikováno v:
Biochemistry. 35(13)
The thermodynamics of the binding of the Sac7d protein of Sulfolobus acidocaldarius to double-stranded DNA has been characterized using spectroscopic signals arising from both the protein and the DNA. Ligand binding density function analysis has been
Autor:
Irene Zegar, Astrid Gräslund, Per-Olof Lycksell, Bengt Jernström, Magdalena Eriksson, Bengt Nordén
Publikováno v:
Carcinogenesis. 8:899-905
Poly d[(G-C)(G-C)] in B or Z conformation has been incubated with the anti-diastereomer of trans-7,8-dihydroxy-9,10-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene (anti-BPDE). Enzymatic hydrolysis, circular dichroism (CD) and light absorption were used to s
Publikováno v:
Chemico-Biological Interactions. 72:277-293
The non-covalent DNA interaction of the anticancer drug ellipticine (Scheme I, 1a) as well as an indolo[2,3-b]-quinoxaline derivative (Scheme I, 3b) with a dimethylaminoethyl side chain has been studied by light absorption, linear dichroism (LD) and
The B → Z Transition in Poly[d(G-C)·d(G-C)] After Covalent Binding of Anti-Benzo(a)Pyrenediolepoxide
Autor:
Astrid Gräslund, Irene Zegar, Magdalena Eriksson, Bengt Jernström, Per-Olof Lycksell, Bengt Nordén
Publikováno v:
Structure, Dynamics and Function of Biomolecules ISBN: 9783642717079
(+)-anti-7,8-dihydroxy-9,10-oxy-7,8,9,10-tetrahydrobenzo(a)pyrene (BPDE) is a highly carcinogenic metabolite of benzo(a)pyrene (BP), which binds covalently and with high specificity to the exocyclic amino group of guanine in DNA (1) (Fig. 1).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::140bbf7311fde990a2d1a3164fb47a84
https://doi.org/10.1007/978-3-642-71705-5_50
https://doi.org/10.1007/978-3-642-71705-5_50