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0.5 Gy Gamma Radiation Suppresses Production of TNF-α through Up-regulation of MKP-1 in Mouse Macrophage RAW264.7 Cells
0.5 Gy Gamma Radiation Suppresses Production of TNF-α through Up-regulation of MKP-1 in Mouse Macrophage RAW264.7 Cells
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0.5 Gy Gamma Radiation Suppresses Production of TNF-α through Up-regulation of MKP-1 in Mouse Macrophage RAW264.7 Cells

Tsukimoto, Mitsutoshi ; Homma, Takujiro ; Mutou, Yasuko ; Kojima, Shuji

Radiation research, 2009-02, Vol.171 (2), p.219-224 [Periódico revisado por pares]

United States: Radiation Research Society

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2
0507JS60 virus isolated in Xinjiang was identified as Liaoning virus
0507JS60 virus isolated in Xinjiang was identified as Liaoning virus
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0507JS60 virus isolated in Xinjiang was identified as Liaoning virus

Lv, Xin-Jun ; Lv, Zhi ; Sun, Xiao-Hong ; Fu, Shi-Hong ; Wang, Huan-Qin ; Tong, Su-Xiang ; Zhang, Song ; Attoui, H ; Liang, Guo-Dong

Bingdu xuebao, 2008-11, Vol.24 (6), p.438

China

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3
1-0-Hexadecyl-2-acetyl-sn-glycerol stimulates differentiation of HL-60 human promyelocytic leukemia cells to macrophage-like cells
1-0-Hexadecyl-2-acetyl-sn-glycerol stimulates differentiation of HL-60 human promyelocytic leukemia cells to macrophage-like cells
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1-0-Hexadecyl-2-acetyl-sn-glycerol stimulates differentiation of HL-60 human promyelocytic leukemia cells to macrophage-like cells

McNamara, M J ; Schmitt, J D ; Wykle, R L ; Daniel, L W

Biochemical and biophysical research communications, 1984-07, Vol.122 (2), p.824-830 [Periódico revisado por pares]

United States

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4
1-[(1-Methyl-1H-imidazol-2-yl)methyl]-4-phenylpiperidines as mGluR2 Positive Allosteric Modulators for the Treatment of Psychosis
1-[(1-Methyl-1H-imidazol-2-yl)methyl]-4-phenylpiperidines as mGluR2 Positive Allosteric Modulators for the Treatment of Psychosis
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1-[(1-Methyl-1H-imidazol-2-yl)methyl]-4-phenylpiperidines as mGluR2 Positive Allosteric Modulators for the Treatment of Psychosis

Zhang, Lei ; Brodney, Michael A ; Candler, John ; Doran, Angela C ; Duplantier, Allen J ; Efremov, Ivan V ; Evrard, Edel ; Kraus, Kenneth ; Ganong, Alan H ; Haas, Jessica A ; Hanks, Ashley N ; Jenza, Keith ; Lazzaro, John T ; Maklad, Noha ; McCarthy, Sheryl A ; Qian, Weimin ; Rogers, Bruce N ; Rottas, Melinda D ; Schmidt, Christopher J ; Siuciak, Judith A ; Tingley, F. David ; Zhang, Andy Q

Journal of medicinal chemistry, 2011-03, Vol.54 (6), p.1724-1739 [Periódico revisado por pares]

United States: American Chemical Society

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5
1-(1,2,5-Thiadiazol-4-yl)-4-azatricyclo[2.2.1.02,6]heptanes as New Potent Muscarinic M1 Agonists:  Structure−Activity Relationship for 3-Aryl-2-propyn-1-yloxy and 3-Aryl-2-propyn-1-ylthio Derivatives
1-(1,2,5-Thiadiazol-4-yl)-4-azatricyclo[2.2.1.02,6]heptanes as New Potent Muscarinic M1 Agonists:  Structure−Activity Relationship for 3-Aryl-2-propyn-1-yloxy and 3-Aryl-2-propyn-1-ylthio Derivatives
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1-(1,2,5-Thiadiazol-4-yl)-4-azatricyclo[2.2.1.02,6]heptanes as New Potent Muscarinic M1 Agonists:  Structure−Activity Relationship for 3-Aryl-2-propyn-1-yloxy and 3-Aryl-2-propyn-1-ylthio Derivatives

Jeppesen, Lone ; Olesen, Preben H ; Hansen, Lena ; Sheardown, Malcolm J ; Thomsen, Christian ; Rasmussen, Thøger ; Jensen, Anders Fink ; Christensen, Michael S ; Rimvall, Karin ; Ward, John S ; Whitesitt, Celia ; Calligaro, David O ; Bymaster, Frank P ; Delapp, Neil W ; Felder, Christian C ; Shannon, Harlan E ; Sauerberg, Per

Journal of medicinal chemistry, 1999-06, Vol.42 (11), p.1999-2006 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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6
1-(1H-Indol-3-yl)ethanamine Derivatives as Potent Staphylococcus aureus NorA Efflux Pump Inhibitors
1-(1H-Indol-3-yl)ethanamine Derivatives as Potent Staphylococcus aureus NorA Efflux Pump Inhibitors
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1-(1H-Indol-3-yl)ethanamine Derivatives as Potent Staphylococcus aureus NorA Efflux Pump Inhibitors

Hequet, Arnaud ; Burchak, Olga N. ; Jeanty, Matthieu ; Guinchard, Xavier ; Le Pihive, Emmanuelle ; Maigre, Laure ; Bouhours, Pascale ; Schneider, Dominique ; Maurin, Max ; Paris, Jean-Marc ; Denis, Jean-Noël ; Jolivalt, Claude

ChemMedChem, 2014-07, Vol.9 (7), p.1534-1545 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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7
1-[2-(2-Benzoyl- and 2-benzylphenoxy)ethyl]uracils as potent anti-HIV-1 agents
1-[2-(2-Benzoyl- and 2-benzylphenoxy)ethyl]uracils as potent anti-HIV-1 agents
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1-[2-(2-Benzoyl- and 2-benzylphenoxy)ethyl]uracils as potent anti-HIV-1 agents

Novikov, Mikhail S. ; Ivanova, Olga N. ; Ivanov, Alexander V. ; Ozerov, Alexander A. ; Valuev-Elliston, Vladimir T. ; Temburnikar, Kartik ; Gurskaya, Galina V. ; Kochetkov, Sergey N. ; Pannecouque, Christophe ; Balzarini, Jan ; Seley-Radtke, Katherine L.

Bioorganic & medicinal chemistry, 2011-10, Vol.19 (19), p.5794-5802 [Periódico revisado por pares]

England: Elsevier Ltd

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8
1-(2,4-Dihydroxyphenyl)-3-(2,4-dimethoxy-3-methylphenyl)propane, a Novel Tyrosinase Inhibitor with Strong Depigmenting Effects
1-(2,4-Dihydroxyphenyl)-3-(2,4-dimethoxy-3-methylphenyl)propane, a Novel Tyrosinase Inhibitor with Strong Depigmenting Effects
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1-(2,4-Dihydroxyphenyl)-3-(2,4-dimethoxy-3-methylphenyl)propane, a Novel Tyrosinase Inhibitor with Strong Depigmenting Effects

Nesterov, Alexandre ; Zhao, Jifu ; Minter, David ; Hertel, Carmen ; Ma, Wenwen ; Abeysinghe, Padmapriya ; Hong, Mei ; Jia, Qi

Chemical and Pharmaceutical Bulletin, 2008/09/01, Vol.56(9), pp.1292-1296 [Periódico revisado por pares]

Japan: The Pharmaceutical Society of Japan

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9
1,1-Dimethylallylcoumarins potently suppress both lipopolysaccharide- and interferon-gamma-induced nitric oxide generation in mouse macrophage RAW 264.7 cells
1,1-Dimethylallylcoumarins potently suppress both lipopolysaccharide- and interferon-gamma-induced nitric oxide generation in mouse macrophage RAW 264.7 cells
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1,1-Dimethylallylcoumarins potently suppress both lipopolysaccharide- and interferon-gamma-induced nitric oxide generation in mouse macrophage RAW 264.7 cells

Murakami, A ; Gao, G ; Omura, M ; Yano, M ; Ito, C ; Furukawa, H ; Takahashi, D ; Koshimizu, K ; Ohigashi, H

Bioorganic & medicinal chemistry letters, 2000-01, Vol.10 (1), p.59-62 [Periódico revisado por pares]

England

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10
1,10-Phenanthroline inhibition of lymphoblast cell cycle
1,10-Phenanthroline inhibition of lymphoblast cell cycle
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1,10-Phenanthroline inhibition of lymphoblast cell cycle

Falchuk, K H ; Krishan, A

Cancer research (Chicago, Ill.), 1977-07, Vol.37 (7 Pt 1), p.2050-2056 [Periódico revisado por pares]

United States

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Deste Autor:

  1. Battesti, D
  2. Franze, D
  3. Pinheiro, S
  4. Leite, K
  5. III, A

Neste Assunto:

  1. Cell Line
  2. Cell Line
  3. Science & Technology
  4. Life Sciences & Biomedicine
  5. Animals

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

Buscando em bases de dados remotas. Favor aguardar.