Results 201 to 210 of about 38,087 (260)

Retraction: Metformin protects from rotenone-induced nigrostriatal neuronal death in adult mice by activating AMPK-FOXO3 signaling and mitigation of angiogenesis. [PDF]

Front Mol Neurosci
Frontiers Editorial Office.
europepmc   +1 more source

Nicotinamide counteracts Rotenone-induced mitochondrial and neuronal dysfunction in a translational early-life model. [PDF]

Sci Rep
Siena A, Souza E Silva LF, Araujo VC, Ribeiro MR, de Sá Lima L, Andreotti DZ, Orellana AM, Kawamoto EM, Silva Junior PI, Scavone C, Rosenstock TR.   +10 more
europepmc   +1 more source

A metabolism-specific drug-repurposing screen reveals itraconazole as a potent OXPHOS inhibitor in acute myeloid leukemia.

Blood
Himonas E, de Beauchamp L, Zerbst D, Desmares-Romain E, Sarnello D, Kalkman ER, Rattigan KM, James D, Shokry E, Copland M, Griessinger E, Récher C, De Mas V, Vergez F, Sumpton D, Schimmer AD, Minden MD, Gottlieb E, Shanks E, Sarry JE, Helgason GV.   +20 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

Rotenone

2000
Abstract Rotenone and rotenoids, which are found in several strains of the Derris (e.g., Derris elliptica) and Lonchocarpus (e.g., Lonchocarpus utilis, L. urucu, L. nicou) genera (9), have been used by native people as a fish poison. In recent times, rotenone has been employed extensively as an agricultural and household insecticide ...
openaire   +1 more source

Carcinogenesis with the insecticide rotenone

Life Sciences, 1983
Rotenone is an insecticide which has been used extensively for a long time, and is now widely used in the U.S.A. and other industrialized countries. Rotenone is used mainly as an agricultural insecticide, household garden insecticide and water plant pesticide. Through these uses, rotenone may now be reaching the human male and female in these countries
openaire   +2 more sources

Synthesis of (–)-Rotenone

Agricultural and Biological Chemistry, 1979
A new synthesis of (–)-rotenone (1) has been accomplished. Decarboxylation and Vilsmeier formylation of (–)-tubaic acid (3) afforded (–)-tubaaldehyde (2) which was the key intermediate of (–)-rotenone synthesis. Condensation of 2 and Grignard reagent of phenyl 2-propynyl ether (5) and subsequent oxidation afforded (–)-1-(2,3-dihydro-4-hydroxy-2 ...
Iku Sasaki, Kyohei Yamashita
openaire   +1 more source

Mechanism of the Physiological Action of Rotenone

Nature, 1960
ROTENONE has been widely used as a poison for the extinction of fish populations. Its action was earlier ascribed to a histolysis of the gills1 and a blocking of the circulation2 in the gills. Recently, one of us3 has demonstrated that these effects are secondary changes due to advanced stages of poisoning.
P E, LINDAHL, K E, OBERG
openaire   +2 more sources

The rotenone model of Parkinson's disease

Trends in Neurosciences, 2003
tetrodotoxin-insensitive [Ca]i elevations in astrocytes, subsequent a Ca2þ-dependent release of glutamate and, finally, activation of metabotropic glutamate receptors in otherastrocytes.However,wefullyagreewithAndersonand Nedergaard that there is an enormous amount of experimental and theoretical work yet to be done to characterize neurone-to-astrocyte
Céline, Perier, Jordi, Bové, Miquel, Vila, Serge, Przedborski   +3 more
openaire   +2 more sources

Rotenone

Journal of the Franklin Institute, 1932
  +4 more sources

Rotenone

Industrial & Engineering Chemistry, 1933
H. L. Haller, P. S. Schaffer
openaire   +2 more sources