Search research articles
Contact Us
Filters
Showing results (1-10 of 31) with videos related to
Page
of 4
Sort By:
Journal of Experimental Botany
|
April 17, 2016
RhVI1 is a membrane-anchored vacuolar invertase highly expressed in Rosa hybrida L. petals
Domenica Farci, Gabriella Collu, Joanna Kirkpatrick, et al.
Plasmid
|
November 1, 2019
Seamless insert-plasmid assembly at sub-terminal homologous sequences
Anna-Sophia Krebs, Tobias Bierig, Gabriella Collu, et al.
Frontiers in Bioengineering and Biotechnology
|
January 7, 2021
Design, Expression, Purification, and Characterization of a YFP-Tagged 2019-nCoV Spike Receptor-Binding Domain Construct
Tobias Bierig, Gabriella Collu, Alain Blanc, et al.
Plant Molecular Biology
|
March 12, 2017
New insights into the operative network of FaEO, an enone oxidoreductase from Fragaria x ananassa Duch
Gabriella Collu, Domenica Farci, Francesca Esposito, et al.
European Journal of Medicinal Chemistry
|
October 14, 2017
Inhibitors of Yellow Fever Virus replication based on 1,3,5-triphenyl-4,5-dihydropyrazole scaffold: Design, synthesis and antiviral evaluation
Rossella Fioravanti, Nicoletta Desideri, Antonio Carta, et al.
European Journal of Medicinal Chemistry
|
July 11, 2006
4-Substituted anilino imidazo[1,2-a] and triazolo[4,3-a]quinoxalines. Synthesis and evaluation of in vitro biological activity
Paola Corona, Gabriella Vitale, Mario Loriga, et al.
Bioorganic & Medicinal Chemistry
|
January 30, 2008
Thiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 1: Parallel synthesis, molecular modelling and structure-activity relationship studies on O-[2-(hetero)arylethyl]-N-phenylthiocarbamates
Sara Cesarini, Andrea Spallarossa, Angelo Ranise, et al.
Medicinal Chemistry (Shariqah (United Arab Emirates))
|
June 22, 2006
Synthesis of variously substituted 3-phenoxymethyl quinoxalin-2-ones and quinoxalines capable to potentiate in vitro the antiproliferative activity of anticancer drugs in multi-drug resistant cell lines
Antonio Carta, Mario Loriga, Sandra Piras, et al.
Bioorganic & Medicinal Chemistry
|
January 30, 2008
Thiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 2: Parallel synthesis, molecular modelling and structure-activity relationship studies on analogues of O-(2-phenylethyl)-N-phenylthiocarbamate
Sara Cesarini, Andrea Spallarossa, Angelo Ranise, et al.
Journal of Medicinal Chemistry
|
May 9, 2014
Synthesis of novel fluoro analogues of MKC442 as microbicides
Yasser M Loksha, Erik B Pedersen, Roberta Loddo, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 31) with videos related to
Sort By:
Page
of 4
Journal of Experimental Botany
|
April 17, 2016
RhVI1 is a membrane-anchored vacuolar invertase highly expressed in Rosa hybrida L. petals
Domenica Farci, Gabriella Collu, Joanna Kirkpatrick, et al.
Plasmid
|
November 1, 2019
Seamless insert-plasmid assembly at sub-terminal homologous sequences
Anna-Sophia Krebs, Tobias Bierig, Gabriella Collu, et al.
Frontiers in Bioengineering and Biotechnology
|
January 7, 2021
Design, Expression, Purification, and Characterization of a YFP-Tagged 2019-nCoV Spike Receptor-Binding Domain Construct
Tobias Bierig, Gabriella Collu, Alain Blanc, et al.
Plant Molecular Biology
|
March 12, 2017
New insights into the operative network of FaEO, an enone oxidoreductase from Fragaria x ananassa Duch
Gabriella Collu, Domenica Farci, Francesca Esposito, et al.
European Journal of Medicinal Chemistry
|
October 14, 2017
Inhibitors of Yellow Fever Virus replication based on 1,3,5-triphenyl-4,5-dihydropyrazole scaffold: Design, synthesis and antiviral evaluation
Rossella Fioravanti, Nicoletta Desideri, Antonio Carta, et al.
European Journal of Medicinal Chemistry
|
July 11, 2006
4-Substituted anilino imidazo[1,2-a] and triazolo[4,3-a]quinoxalines. Synthesis and evaluation of in vitro biological activity
Paola Corona, Gabriella Vitale, Mario Loriga, et al.
Bioorganic & Medicinal Chemistry
|
January 30, 2008
Thiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 1: Parallel synthesis, molecular modelling and structure-activity relationship studies on O-[2-(hetero)arylethyl]-N-phenylthiocarbamates
Sara Cesarini, Andrea Spallarossa, Angelo Ranise, et al.
Medicinal Chemistry (Shariqah (United Arab Emirates))
|
June 22, 2006
Synthesis of variously substituted 3-phenoxymethyl quinoxalin-2-ones and quinoxalines capable to potentiate in vitro the antiproliferative activity of anticancer drugs in multi-drug resistant cell lines
Antonio Carta, Mario Loriga, Sandra Piras, et al.
Bioorganic & Medicinal Chemistry
|
January 30, 2008
Thiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 2: Parallel synthesis, molecular modelling and structure-activity relationship studies on analogues of O-(2-phenylethyl)-N-phenylthiocarbamate
Sara Cesarini, Andrea Spallarossa, Angelo Ranise, et al.
Journal of Medicinal Chemistry
|
May 9, 2014
Synthesis of novel fluoro analogues of MKC442 as microbicides
Yasser M Loksha, Erik B Pedersen, Roberta Loddo, et al.
Page
of 4