Désinfection des mains < Désoxyadénosine < Désoxycytidine

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List of bibliographic references indexed by Désoxyadénosine

Number of relevant bibliographic references: 8.

Ident.	Authors (with country if any)	Title
000617 (2019)	Annalisa Masi ; Arianna Sabbia ; Carla Ferreri ; Francesco Manoli ; Yanhao Lai ; Eduardo Laverde ; Yuan Liu [États-Unis] ; Marios G. Krokidis ; Chryssostomos Chatgilialoglu ; Maria Rosaria Faraone Mennella	Diastereomeric Recognition of 5’,8-cyclo-2’-Deoxyadenosine Lesions by Human Poly(ADP-ribose) Polymerase 1 in a Biomimetic Model
001346 (2016)	Haozhe Yang [Allemagne] ; Frank Seela [Allemagne]	Circular DNA by "Bis-Click" Ligation: Template-Independent Intramolecular Circularization of Oligonucleotides with Terminal Alkynyl Groups Utilizing Bifunctional Azides.
002B28 (2007)	Mariko Aso [Japon] ; John Walter Mirc ; Manami Kurita ; Noboru Koga ; Hiroshi Suemune	Studies on DNA dynamics using 2-N-tert-butylaminoxylpurines.
002B33 (2007)	Sergey Antsypovich [États-Unis] ; Danaè Quirk-Dorr ; Crystal Pitts ; Natalia Tretyakova	Site specific N6-(2-hydroxy-3,4-epoxybut-1-yl)adenine oligodeoxynucleotide adducts of 1,2,3,4-diepoxybutane: synthesis and stability at physiological pH.
003049 (2004)	Akihiro Ohkubo [Japon] ; Yusuke Ezawa ; Kohji Seio ; Mitsuo Sekine	O-selectivity and utility of phosphorylation mediated by phosphite triester intermediates in the N-unprotected phosphoramidite method.
003786 (1999)	I. Pontén [États-Unis] ; J M Sayer ; A S Pilcher ; H. Yagi ; S. Kumar ; D M Jerina ; A. Dipple	Sequence context effects on mutational properties of cis-opened benzo[c]phenanthrene diol epoxide-deoxyadenosine adducts in site-specific mutation studies.
003796 (1999)	J E Page [États-Unis] ; A S Pilcher ; H. Yagi ; J M Sayer ; D M Jerina ; A. Dipple	Mutational consequences of replication of M13mp7L2 constructs containing cis-opened benzo[a]pyrene 7,8-diol 9, 10-epoxide-deoxyadenosine adducts.
004255 (1994)	T H Broschard ; M. Wiessler ; C W Von Der Lieth ; H H Schmeiser	Translesional synthesis on DNA templates containing site-specifically placed deoxyadenosine and deoxyguanosine adducts formed by the plant carcinogen aristolochic acid.

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