skip to main content
Idioma:
Refinado por: assunto: Natural Sciences remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
large-scale chemical modification screen identifies design rules to generate siRNAs with high activity, high stability and low toxicity
large-scale chemical modification screen identifies design rules to generate siRNAs with high activity, high stability and low toxicity
Material Type:
Artigo 		Adicionar ao Meu Espaço

large-scale chemical modification screen identifies design rules to generate siRNAs with high activity, high stability and low toxicity

Bramsen, Jesper B ; Laursen, Maria B ; Nielsen, Anne F ; Hansen, Thomas B ; Bus, Claus ; Langkjær, Niels ; Babu, B. Ravindra ; Højland, Torben ; Abramov, Mikhail ; Van Aerschot, Arthur ; Odadzic, Dalibor ; Smicius, Romualdas ; Haas, Jens ; Andree, Cordula ; Barman, Jharna ; Wenska, Malgorzata ; Srivastava, Puneet ; Zhou, Chuanzheng ; Honcharenko, Dmytro ; Hess, Simone ; Müller, Elke ; Bobkov, Georgii V ; Mikhailov, Sergey N ; Fava, Eugenio ; Meyer, Thomas F ; Chattopadhyaya, Jyoti ; Zerial, Marino ; Engels, Joachim W ; Herdewijn, Piet ; Wengel, Jesper ; Kjems, Jørgen

Nucleic acids research, 2009-05, Vol.37 (9), p.2867-2881 [Periódico revisado por pares]

England: Oxford University Press

Texto completo disponível

Citações Citado por
2
Comparison of the RNase H Cleavage Kinetics and Blood Serum Stability of the North-Conformationally Constrained and 2‘-Alkoxy Modified Oligonucleotides
Comparison of the RNase H Cleavage Kinetics and Blood Serum Stability of the North-Conformationally Constrained and 2‘-Alkoxy Modified Oligonucleotides
Material Type:
Artigo 		Adicionar ao Meu Espaço

Comparison of the RNase H Cleavage Kinetics and Blood Serum Stability of the North-Conformationally Constrained and 2‘-Alkoxy Modified Oligonucleotides

Honcharenko, Dmytro ; Barman, Jharna ; Varghese, Oommen P

Biochemistry (Easton), 2007-05, Vol.46 (19), p.5635-5646 [Periódico revisado por pares]

United States: American Chemical Society

Texto completo disponível

Citações Citado por
3
Conformationally-constrained indeno[2,1-c]quinolines--a new class of anti-mycobacterial agents
Conformationally-constrained indeno[2,1-c]quinolines--a new class of anti-mycobacterial agents
Material Type:
Artigo 		Adicionar ao Meu Espaço

Conformationally-constrained indeno[2,1-c]quinolines--a new class of anti-mycobacterial agents

Upadhayaya, Ram Shankar ; Lahore, Santosh V ; Sayyed, Aftab Y ; Dixit, Shailesh S ; Shinde, Popat D ; Chattopadhyaya, Jyoti

Organic & biomolecular chemistry, 2010-01, Vol.8 (9), p.2180-2197 [Periódico revisado por pares]

England

Texto completo disponível

Citações Citado por
4
Conformationally Constrained 2‘-N,4‘-C-Ethylene-Bridged Thymidine (Aza-ENA-T):  Synthesis, Structure, Physical, and Biochemical Studies of Aza-ENA-T-Modified Oligonucleotides
Conformationally Constrained 2‘-N,4‘-C-Ethylene-Bridged Thymidine (Aza-ENA-T):  Synthesis, Structure, Physical, and Biochemical Studies of Aza-ENA-T-Modified Oligonucleotides
Material Type:
Artigo 		Adicionar ao Meu Espaço

Conformationally Constrained 2‘-N,4‘-C-Ethylene-Bridged Thymidine (Aza-ENA-T):  Synthesis, Structure, Physical, and Biochemical Studies of Aza-ENA-T-Modified Oligonucleotides

Varghese, Oommen P ; Barman, Jharna ; Pathmasiri, Wimal ; Plashkevych, Oleksandr ; Honcharenko, Dmytro ; Chattopadhyaya, Jyoti

Journal of the American Chemical Society, 2006-11, Vol.128 (47), p.15173-15187 [Periódico revisado por pares]

Washington, DC: American Chemical Society

Texto completo disponível

Citações Citado por
5
Synthesis and antimycobacterial activity of prodrugs of indeno[2,1- c]quinoline derivatives
Synthesis and antimycobacterial activity of prodrugs of indeno[2,1- c]quinoline derivatives
Material Type:
Artigo 		Adicionar ao Meu Espaço

Synthesis and antimycobacterial activity of prodrugs of indeno[2,1- c]quinoline derivatives

Upadhayaya, Ram Shankar ; Shinde, Popat D. ; Kadam, Sandip A. ; Bawane, Amit N. ; Sayyed, Aftab Y. ; Kardile, Ramakant A. ; Gitay, Pallavi N. ; Lahore, Santosh V. ; Dixit, Shailesh S. ; Földesi, András ; Chattopadhyaya, Jyoti

European journal of medicinal chemistry, 2011-04, Vol.46 (4), p.1306-1324 [Periódico revisado por pares]

Kidlington: Elsevier Masson SAS

Texto completo disponível

Citações Citado por
6
Novel quinoline and naphthalene derivatives as potent antimycobacterial agents
Novel quinoline and naphthalene derivatives as potent antimycobacterial agents
Material Type:
Artigo 		Adicionar ao Meu Espaço

Novel quinoline and naphthalene derivatives as potent antimycobacterial agents

Upadhayaya, Ram Shankar ; Vandavasi, Jaya Kishore ; Kardile, Ramakant A. ; Lahore, Santosh V. ; Dixit, Shailesh S. ; Deokar, Hemantkumar S. ; Shinde, Popat D. ; Sarmah, Manash P. ; Chattopadhyaya, Jyoti

European journal of medicinal chemistry, 2010-05, Vol.45 (5), p.1854-1867 [Periódico revisado por pares]

Kidlington: Elsevier Masson SAS

Texto completo disponível

Citações Citado por
7
Synthesis and structure of azole-fused indeno[2,1-c]quinolines and their anti-mycobacterial properties
Synthesis and structure of azole-fused indeno[2,1-c]quinolines and their anti-mycobacterial properties
Material Type:
Artigo 		Adicionar ao Meu Espaço

Synthesis and structure of azole-fused indeno[2,1-c]quinolines and their anti-mycobacterial properties

Upadhayaya, Ram Shankar ; Shinde, Popat D ; Sayyed, Aftab Y ; Kadam, Sandip A ; Bawane, Amit N ; Poddar, Avijit ; Plashkevych, Oleksandr ; Földesi, Andras ; Chattopadhyaya, Jyoti

Organic & biomolecular chemistry, 2010-01, Vol.8 (24), p.5661-5673 [Periódico revisado por pares]

England

Texto completo disponível

Citações Citado por
8
High-quality oligo-RNA synthesis using the new 2′-O-TEM protecting group by selectively quenching the addition of p-tolyl vinyl sulphone to exocyclic amino functions
High-quality oligo-RNA synthesis using the new 2′-O-TEM protecting group by selectively quenching the addition of p-tolyl vinyl sulphone to exocyclic amino functions
Material Type:
Artigo 		Adicionar ao Meu Espaço

High-quality oligo-RNA synthesis using the new 2′-O-TEM protecting group by selectively quenching the addition of p-tolyl vinyl sulphone to exocyclic amino functions

Zhou, Chuanzheng ; Pathmasiri, Wimal ; Honcharenko, Dmytro ; Chatterjee, Subhrangsu ; Barman, Jharna ; Chattopadhyaya, Jyoti

Canadian journal of chemistry, 2007-04, Vol.85 (4), p.293-301 [Periódico revisado por pares]

Ottawa, Canada: NRC Research Press

Texto completo disponível

Citações Citado por

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Data de Publicação 

De até
Refinar
  1. Antes de2006  (1)
  2. 2006Até2006  (1)
  3. 2007Até2008  (2)
  4. 2009Até2010  (4)
  5. Após 2010  (1)
  6. Mais opções open sub menu

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.