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0610009K11Rik, a testis-specific and germ cell nuclear receptor-interacting protein
0610009K11Rik, a testis-specific and germ cell nuclear receptor-interacting protein
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0610009K11Rik, a testis-specific and germ cell nuclear receptor-interacting protein

Zhang, Heng ; Denhard, Leslie A. ; Zhou, Huaxin ; Liu, Lan-Hsin ; Lan, Zi-Jian

Biochemical and biophysical research communications, 2008-02, Vol.366 (4), p.898-904 [Periódico revisado por pares]

United States: Elsevier Inc

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0.9% saline is neither normal nor physiological
0.9% saline is neither normal nor physiological
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0.9% saline is neither normal nor physiological

Li, Heng ; Sun, Shi-ren ; Yap, John Q. ; Chen, Jiang-hua ; Qian, Qi

Journal of Zhejiang University. B. Science, 2016-03, Vol.17 (3), p.181-187 [Periódico revisado por pares]

Hangzhou: Zhejiang University Press

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3
[1- 14C]Arachidonic acid incorporation into glycerolipids and prostaglandin synthesis in peritoneal macrophages: effect of chloramphenicol
[1- 14C]Arachidonic acid incorporation into glycerolipids and prostaglandin synthesis in peritoneal macrophages: effect of chloramphenicol
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[1- 14C]Arachidonic acid incorporation into glycerolipids and prostaglandin synthesis in peritoneal macrophages: effect of chloramphenicol

de Maroussem, Danielle ; Pipy, Bernard ; Beraud, Maryse ; Derache, Philippe ; Mathieu, Jean-René

Biochimica et biophysica acta. Lipids and lipid metabolism, 1985-03, Vol.834 (1), p.8-22 [Periódico revisado por pares]

Elsevier B.V

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4
1-[2-(2-Methoxyphenylamino)ethylamino]-3-(naphthalene-1- yloxy)propan-2-ol may be a promising anticancer drug
1-[2-(2-Methoxyphenylamino)ethylamino]-3-(naphthalene-1- yloxy)propan-2-ol may be a promising anticancer drug
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1-[2-(2-Methoxyphenylamino)ethylamino]-3-(naphthalene-1- yloxy)propan-2-ol may be a promising anticancer drug

Nishizaki, Tomoyuki ; Kanno, Takeshi ; Tsuchiya, Ayako ; Kaku, Yoshiko ; Shimizu, Tadashi ; Tanaka, Akito

Molecules, 2014-12, Vol.19 (12), p.21462-21472 [Periódico revisado por pares]

Switzerland: MDPI AG

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5
1,1-Diarylalkenes as anticancer agents: Dual inhibitors of tubulin polymerization and phosphodiesterase 4
1,1-Diarylalkenes as anticancer agents: Dual inhibitors of tubulin polymerization and phosphodiesterase 4
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1,1-Diarylalkenes as anticancer agents: Dual inhibitors of tubulin polymerization and phosphodiesterase 4

Ruchelman, Alexander L. ; Man, Hon-Wah ; Chen, Roger ; Liu, Wei ; Lu, Ling ; Cedzik, Dorota ; Zhang, Ling ; Leisten, Jim ; Collette, Alice ; Narla, Rama Krishna ; Raymon, Heather K. ; Muller, George W.

Bioorganic & medicinal chemistry, 2011-11, Vol.19 (21), p.6356-6374 [Periódico revisado por pares]

Amsterdam: Elsevier Ltd

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6
1,1-Dichloroethylene-Induced Clara Cell Damage Is Associated with In Situ Formation of the Reactive Epoxide . Immunohistochemical Detection of Its Glutathione Conjugate
1,1-Dichloroethylene-Induced Clara Cell Damage Is Associated with In Situ Formation of the Reactive Epoxide . Immunohistochemical Detection of Its Glutathione Conjugate
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1,1-Dichloroethylene-Induced Clara Cell Damage Is Associated with In Situ Formation of the Reactive Epoxide . Immunohistochemical Detection of Its Glutathione Conjugate

Forkert, Poh-Gek

American journal of respiratory cell and molecular biology, 1999-06, Vol.20 (6), p.1310-1318 [Periódico revisado por pares]

United States: Am Thoracic Soc

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7
1,1-Diphenyl-2-picrylhydrazyl radical-scavenging compounds from soybean miso and antiproliferative activity of isoflavones from soybean miso toward the cancer cell lines
1,1-Diphenyl-2-picrylhydrazyl radical-scavenging compounds from soybean miso and antiproliferative activity of isoflavones from soybean miso toward the cancer cell lines
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1,1-Diphenyl-2-picrylhydrazyl radical-scavenging compounds from soybean miso and antiproliferative activity of isoflavones from soybean miso toward the cancer cell lines

Hirota, A. (Shizuoka Univ. (Japan)) ; Taki, S ; Kawaii, S ; Yano, M ; Abe, N

Bioscience, biotechnology, and biochemistry, 2000-05, Vol.64 (5), p.1038-1040 [Periódico revisado por pares]

Tokyo: Japan Society for Bioscience, Biotechnology, and Agrochemistry

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8
1,10-Phenanthroline Inhibits Glycosylphosphatidylinositol Anchoring by Preventing Phosphoethanolamine Addition to Glycosylphosphatidylinositol Anchor Precursors
1,10-Phenanthroline Inhibits Glycosylphosphatidylinositol Anchoring by Preventing Phosphoethanolamine Addition to Glycosylphosphatidylinositol Anchor Precursors
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1,10-Phenanthroline Inhibits Glycosylphosphatidylinositol Anchoring by Preventing Phosphoethanolamine Addition to Glycosylphosphatidylinositol Anchor Precursors

Mann, Karl J ; Sevlever, Daniel

Biochemistry (Easton), 2001-02, Vol.40 (5), p.1205-1213 [Periódico revisado por pares]

United States: American Chemical Society

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9
1,10-Phenanthroline mediated hemolysis—evidence that 1,10-phenanthroline does not substitute specifically for C9
1,10-Phenanthroline mediated hemolysis—evidence that 1,10-phenanthroline does not substitute specifically for C9
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1,10-Phenanthroline mediated hemolysis—evidence that 1,10-phenanthroline does not substitute specifically for C9

Boyle, Michael D.P. ; Langone, John J. ; Borsos, Tibor

Molecular immunology, 1979-05, Vol.16 (5), p.307-312 [Periódico revisado por pares]

England: Elsevier Ltd

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10
1,10-Phenanthroline stimulates internucleosomal DNA fragmentation in isolated rat-liver nuclei by promoting the redox activity of endogenous copper ions
1,10-Phenanthroline stimulates internucleosomal DNA fragmentation in isolated rat-liver nuclei by promoting the redox activity of endogenous copper ions
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1,10-Phenanthroline stimulates internucleosomal DNA fragmentation in isolated rat-liver nuclei by promoting the redox activity of endogenous copper ions

Burkitt, M J ; Milne, L ; Nicotera, P ; Orrenius, S

Biochemical journal, 1996-01, Vol.313 ( Pt 1) (1), p.163-169 [Periódico revisado por pares]

England

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