Výsledky vyhledávání - "Evelyne Muller"

Akademický článek

Preparation of Modified RNA Sequences for Biological Research

Autor: Stefan Pitsch, Philipp Wenter, Alfred Stutz, Luc Reymond, Sébastien Porcher, Andreas Peer, Evelyne Muller, Muthulaniappan Meyyappan, Frédéric Meylan, Cyrille Denarie, Damian Ackermann, Xiaolin Wu

Publikováno v: CHIMIA, Vol 59, Iss 11 (2005)

Our group is working on the development of reliable access to biologically relevant, long, and modified RNA sequences. Here, we briefly present the chemical synthesis of such sequences with 2?-O-triisopropylsilyloxymethyl (= 2?-O-tom) protected ribon

Externí odkaz: https://doaj.org/article/40fa4024082f40dcaf6a93389e43a849

Zobrazit plný text záznamu

A yeast-based screen reveals that sulfasalazine inhibits tetrahydrobiopterin biosynthesis

Autor: Hirohito Haruki, Evelyne Muller, Kai Johnsson, Miriam Grønlund Pedersen, Christopher Chidley

Publikováno v: Nature Chemica Biology

We introduce an approach for detection of drug-protein interactions that combines a new yeast three-hybrid screening for identification of interactions with affinity chromatography for their unambiguous validation. We applied the methodology to the p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a64c69ad120a6bd826be8af84feba71

Zobrazit plný text záznamu

Radiation-Induced DNA Damage: Formation, Measurement, and Biochemical Features

Autor: Sylvie Sauvaigo, Jean Cadet, Thierry Douki, Didier Gasparutto, Evelyne Muller, Jean-Pierre Pouget, Anthony Romieu, Sophie Bellon, Jean-Luc Ravanat, Sandrine Frelon

Publikováno v: Journal of Environmental Pathology, Toxicology and Oncology. 23:33-44

Most of the reactions induced by *OH radicals (indirect effects) and by one-electron oxidation (direct effects) as the result of exposure to ionizing radiation may be described for the four main DNA nucleobases. Relevant information is now available

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::604c7824f231055a22d7e65c8afdb354
https://doi.org/10.1615/jenvpathtoxoncol.v23.i1.30

Zobrazit plný text záznamu

Site-Specific Insertion of the (5R*) and (5S*) Diastereoisomers of 1-[2-Deoxy-β-D-erythro-pentofuranosyl]-5-hydroxyhydantoin into Oligodeoxyribonucleotides

Autor: Colette Lebrun, Didier Gasparutto, Jean Cadet, Evelyne Muller

Publikováno v: European Journal of Organic Chemistry. 2001:2091-2099

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::89fdc6b0c8ac4d9c2aeedd33767624dd
https://doi.org/10.1002/1099-0690(200106)2001:11<2091::aid-ejoc2091>3.0.co

Zobrazit plný text záznamu

Chemical and Biochemical Properties of Oligonucleotides that Contain (5′S,6S)-Cyclo-5,6-dihydro-2′-deoxyuridine and (5′S,6S)-Cyclo-5,6-dihydrothymidine, Two Main Radiation-Induced Degradation Products of Pyrimidine 2′-Deoxyribonucleosides

Autor: Evelyne Muller, Jean Cadet, Didier Gasparutto, Anthony Romieu, Michel Jaquinod

Publikováno v: Tetrahedron. 56:8689-8701

The first chemical synthesis of (5′S,6S)-cyclo-5,6-dihydro-2′-deoxyuridine [(5′S,6S)-CyclodHdUrd], a major product of gamma irradiation of oxygen free aqueous solution of 2′-deoxycytidine is reported. Subsequently, the latter cyclonucleoside

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::cc864bcb64191f354714c133281415d6
https://doi.org/10.1016/s0040-4020(00)00809-7

Zobrazit plný text záznamu

ChemInform Abstract: Convergent Synthesis of Potent Peptide Inhibitors of the Grb2-SH2 Domain by Palladium Catalyzed Coupling of a Terminal Alkyne

Autor: Joseph Schoepfer, Brigitte Gay, Nicole End, Evelyne Muller, Gisela Scheffel, Giorgio Caravatti, Pascal Furet

Publikováno v: ChemInform. 32

A new strategy was developed to prepare in a very efficient and convergent manner C-terminal modified tripeptides with high affinities for the Grb2-SH2 domain. Using Pd(PPh3)2Cl2 as catalyst, selected naphthyl iodides and triflates were coupled to Ac

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c448381f60a72cefd3fc238ca3b10e1c
https://doi.org/10.1002/chin.200133227

Zobrazit plný text záznamu

ChemInform Abstract: Site-Specific Insertion of the (5R*) and (5S*) Diastereoisomers of 1-[2-Deoxy-β-D-erythro-pentofuranosyl]-5-hydroxyhydantoin into Oligodeoxyribonucleotides

Autor: Jean Cadet, Didier Gasparutto, Evelyne Muller, Colette Lebrun

Publikováno v: ChemInform. 33

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::769dbff177379b8d382d00d1425c37cc
https://doi.org/10.1002/chin.200206257

Zobrazit plný text záznamu

Excision of the oxidatively formed 5-hydroxyhydantoin and 5-hydroxy-5-methylhydantoin pyrimidine lesions by Escherichia coli and Saccharomyces cerevisiae DNA N-glycosylases

Autor: Didier Gasparutto, Jean Cadet, Evelyne Muller, Serge Boiteux

Publikováno v: Biochimica et Biophysica Acta (BBA)-General Subjects
Biochimica et Biophysica Acta (BBA)-General Subjects, Elsevier, 2009, 1790 (1), pp.16-24. ⟨10.1016/j.bbagen.2008.10.001⟩
Biochimica et Biophysica Acta (BBA)-General Subjects, 2009, 1790 (1), pp.16-24. ⟨10.1016/j.bbagen.2008.10.001⟩

Background (5R⁎) and (5S⁎) diastereomers of 1-[2-deoxy-β- d -erythro-pentofuranosyl]-5-hydroxyhydantoin (5-OH-dHyd) and 1-[2-deoxy-β- d -erythro-pentofuranosyl]-5-hydroxy-5-methylhydantoin (5-OH-5-Me-dHyd) are major oxidation products of 2′-d

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83a225630ff02e19caaa250d78b1097e
https://pubmed.ncbi.nlm.nih.gov/18983898

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání