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0.3 keV carbon K ultrasoft X-rays are four times more effective than γ-rays inducing oncogenic cell transformation at low doses
0.3 keV carbon K ultrasoft X-rays are four times more effective than γ-rays inducing oncogenic cell transformation at low doses
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0.3 keV carbon K ultrasoft X-rays are four times more effective than γ-rays inducing oncogenic cell transformation at low doses

FRANKENBERG, D ; KÜHN, H ; FRANKENBERG-SCHWAGER, M ; LENHARD, W ; BECKONERT, S

International journal of radiation biology, 1995, Vol.68 (6), p.593-601 [Periódico revisado por pares]

London: Taylor & Francis

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2
0415 : CD28 deletion improves obesity-induced liver steatosis but increases adiposity in mice
0415 : CD28 deletion improves obesity-induced liver steatosis but increases adiposity in mice
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0415 : CD28 deletion improves obesity-induced liver steatosis but increases adiposity in mice

Poggi, Marjorie ; Morin, Stephanie O. ; Bastelica, Delphine ; Govers, Roland ; Canault, Matthias ; Bernot, Denis ; Verdier, Monique ; Burcelin, Rémy ; Nunès, Jacques ; Peiretti, Franck ; Alessi, Marie-Christine

Archives of cardiovascular diseases supplements, 2015-04, Vol.7 (2), p.140 [Periódico revisado por pares]

Elsevier/French Society of Cardiology

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3
0nduction of structural and numerical changes of chromosome, centrosome abnormality, multipolar spindles and multipolar division in cultured Chinese hamster V79 cells by exposure to a trivalent dimethylarsenic compound
0nduction of structural and numerical changes of chromosome, centrosome abnormality, multipolar spindles and multipolar division in cultured Chinese hamster V79 cells by exposure to a trivalent dimethylarsenic compound
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0nduction of structural and numerical changes of chromosome, centrosome abnormality, multipolar spindles and multipolar division in cultured Chinese hamster V79 cells by exposure to a trivalent dimethylarsenic compound

OCHI, Takafumi ; SUZUKI, Tosihide ; ISONO, Hideo ; SCHLAGENHAUFEN, Claudia ; GOESSLER, Walter ; TSUTSUI, Takeki

Mutation research. Fundamental and molecular mechanisms of mutagenesis, 2003, Vol.530 (1-2), p.59-71 [Periódico revisado por pares]

Amsterdam: Elsevier

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4
1,1-Diheterocyclic Ethylenes Derived from Quinaldine and Carbazole as New Tubulin-Polymerization Inhibitors: Synthesis, Metabolism, and Biological Evaluation
1,1-Diheterocyclic Ethylenes Derived from Quinaldine and Carbazole as New Tubulin-Polymerization Inhibitors: Synthesis, Metabolism, and Biological Evaluation
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1,1-Diheterocyclic Ethylenes Derived from Quinaldine and Carbazole as New Tubulin-Polymerization Inhibitors: Synthesis, Metabolism, and Biological Evaluation

Naret, Timothée ; Khelifi, Ilhem ; Provot, Olivier ; Bignon, Jérôme ; Levaique, Hélène ; Dubois, Joelle ; Souce, Martin ; Kasselouri, Athena ; Deroussent, Alain ; Paci, Angélo ; Varela, Paloma F ; Gigant, Benoît ; Alami, Mouad ; Hamze, Abdallah

Journal of medicinal chemistry, 2019-02, Vol.62 (4), p.1902-1916 [Periódico revisado por pares]

United States: American Chemical Society

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5
1,10-phenanthroline-copper, a footprinting reagent for single-stranded regions of RNAs
1,10-phenanthroline-copper, a footprinting reagent for single-stranded regions of RNAs
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1,10-phenanthroline-copper, a footprinting reagent for single-stranded regions of RNAs

Mazumder, Abhijit ; Chen, C.-h.B. ; Gaynor, Richard ; Sigman, David S.

Biochemical and biophysical research communications, 1992-09, Vol.187 (3), p.1503-1509 [Periódico revisado por pares]

SAN DIEGO: Elsevier Inc

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6
1,12-Substituted tetracyclines as antioxidant agents
1,12-Substituted tetracyclines as antioxidant agents
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1,12-Substituted tetracyclines as antioxidant agents

Lertvorachon, Jittiwud ; Kim, Jong-Pyung ; Soldatov, Dmitriy V. ; Boyd, Jason ; Roman, Gheorghe ; Cho, Sung Ju ; Popek, Tomasz ; Jung, Young-Sik ; Lau, Peter C.K. ; Konishi, Yasuo

Bioorganic & medicinal chemistry, 2005-08, Vol.13 (15), p.4627-4637 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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7
1,1,3 Tricyano-2-amino-1-propene (Triap) stimulates choline acetyltransferase activity in vitro and in vivo
1,1,3 Tricyano-2-amino-1-propene (Triap) stimulates choline acetyltransferase activity in vitro and in vivo
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1,1,3 Tricyano-2-amino-1-propene (Triap) stimulates choline acetyltransferase activity in vitro and in vivo

West Paul, J. ; DaVanzo, John P.

Brain research. Developmental brain research, 1992-06, Vol.67 (2), p.113-120 [Periódico revisado por pares]

Amsterdam: Elsevier B.V

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8
1,2-Benzothiazine 1,1-dioxide carboxylate derivatives as novel potent inhibitors of aldose reductase
1,2-Benzothiazine 1,1-dioxide carboxylate derivatives as novel potent inhibitors of aldose reductase
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1,2-Benzothiazine 1,1-dioxide carboxylate derivatives as novel potent inhibitors of aldose reductase

Chen, Xin ; Zhang, Shuzhen ; Yang, Yanchun ; Hussain, Saghir ; He, Minlan ; Gui, Dequan ; Ma, Bing ; Jing, Chaojun ; Qiao, Zhixin ; Zhu, Changjin ; Yu, Qun

Bioorganic & medicinal chemistry, 2011-12, Vol.19 (23), p.7262-7269 [Periódico revisado por pares]

Amsterdam: Elsevier Ltd

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9
1,2‐bis(2‐Aminophenoxy)ethane‐N,N,N′,N′‐tetraacetic acid induces caspase‐mediated apoptosis and reactive oxygen species‐mediated necrosis in cultured cortical neurons
1,2‐bis(2‐Aminophenoxy)ethane‐N,N,N′,N′‐tetraacetic acid induces caspase‐mediated apoptosis and reactive oxygen species‐mediated necrosis in cultured cortical neurons
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1,2‐bis(2‐Aminophenoxy)ethane‐N,N,N′,N′‐tetraacetic acid induces caspase‐mediated apoptosis and reactive oxygen species‐mediated necrosis in cultured cortical neurons

Han, Kong Sook ; Kang, Hyo Jung ; Kim, Eun Young ; Yoon, Won Joo ; Sohn, Seonghyang ; Kwon, Hyuk Jae ; Gwag, Byoung Joo

Journal of neurochemistry, 2001-07, Vol.78 (2), p.230-239 [Periódico revisado por pares]

Oxford, UK: Blackwell Science Ltd

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10
1,2-bis(4-hydroxyphenyl)-3,4-dihydro-6-hydroxynaphthalene, a photofluorogenic ligang for the estrogen receptor
1,2-bis(4-hydroxyphenyl)-3,4-dihydro-6-hydroxynaphthalene, a photofluorogenic ligang for the estrogen receptor
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1,2-bis(4-hydroxyphenyl)-3,4-dihydro-6-hydroxynaphthalene, a photofluorogenic ligang for the estrogen receptor

BINDAL, R. D ; KATZENELLENBOGEN, J. A

Photochemistry and photobiology, 1986, Vol.43 (2), p.121-126 [Periódico revisado por pares]

Malden, MA: Blackwell Publishing

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