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James M Cook

Showing results (11-20 of 329) with videos related to

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Proceedings. Biological Sciences|March 30, 2022
Common endosymbionts affect host fitness and sex allocation via egg size provisioningAlihan Katlav, James M Cook, Markus Riegler
Oecologia|March 18, 2017
Brood sex ratio variance, developmental mortality and virginity in a gregarious parasitoid waspIan C W Hardy, James M Cook
Microbial Ecology|April 8, 2017
Relative Abundance and Strain Diversity in the Bacterial Endosymbiont Community of a Sap-Feeding Insect Across Its Native and Introduced Geographic RangeCaroline Fromont, Markus Riegler, James M Cook
FEMS Microbiology Ecology|October 6, 2016
Phylogeographic analyses of bacterial endosymbionts in fig homotomids (Hemiptera: Psylloidea) reveal codiversification of both primary and secondary endosymbiontsCaroline Fromont, Markus Riegler, James M Cook
Organic Letters|September 27, 2002
Regiospecific, enantiospecific total synthesis of the alkoxy-substituted indole bases, 16-epi-N(a)-methylgardneral, 11-methoxyaffinisine, and 11-methoxymacroline as well as the indole alkaloids alstophylline and macralstonineXiaoxiang Liu, Jeffrey R Deschamp, James M Cook
Organic Letters|March 10, 2006
Enantiospecific synthesis of (+)-N(a)-methylpericyclivine and (-)-N(a)-methylakuammidine as well as the ring-A oxygenated natural products, (+)-10-methoxy N(a)-methylpericyclivine and 10-hydroxy N(a)-methylpericyclivineP V V Srirama Sarma, James M Cook
BMC Evolutionary Biology|October 17, 2006
Deep mtDNA divergences indicate cryptic species in a fig-pollinating waspEleanor R Haine, Joanne Martin, James M Cook
Journal of the American Chemical Society|February 5, 2004
Stereocontrolled total synthesis of (-)-vincamajinine and (-)-11-methoxy-17-epivincamajineJianming Yu, Xiangyu Z Wearing, James M Cook
The Journal of Organic Chemistry|May 7, 2005
A general strategy for the synthesis of vincamajine-related indole alkaloids: stereocontrolled total synthesis of (+)-dehydrovoachalotine, (-)-vincamajinine, and (-)-11-methoxy-17-epivincamajine as well as the related quebrachidine diol, vincamajine diol, and vincarinolJianming Yu, Xiangyu Z Wearing, James M Cook
Molecular Ecology|February 16, 2016
One step ahead: a parasitoid disperses farther and forms a wider geographic population than its fig wasp hostTimothy L Sutton, Markus Riegler, James M Cook
Pageof 33

Showing results (11-20 of 329) with videos related to

Sort By:
Pageof 33
Proceedings. Biological Sciences|March 30, 2022
Common endosymbionts affect host fitness and sex allocation via egg size provisioningAlihan Katlav, James M Cook, Markus Riegler
Oecologia|March 18, 2017
Brood sex ratio variance, developmental mortality and virginity in a gregarious parasitoid waspIan C W Hardy, James M Cook
Microbial Ecology|April 8, 2017
Relative Abundance and Strain Diversity in the Bacterial Endosymbiont Community of a Sap-Feeding Insect Across Its Native and Introduced Geographic RangeCaroline Fromont, Markus Riegler, James M Cook
FEMS Microbiology Ecology|October 6, 2016
Phylogeographic analyses of bacterial endosymbionts in fig homotomids (Hemiptera: Psylloidea) reveal codiversification of both primary and secondary endosymbiontsCaroline Fromont, Markus Riegler, James M Cook
Organic Letters|September 27, 2002
Regiospecific, enantiospecific total synthesis of the alkoxy-substituted indole bases, 16-epi-N(a)-methylgardneral, 11-methoxyaffinisine, and 11-methoxymacroline as well as the indole alkaloids alstophylline and macralstonineXiaoxiang Liu, Jeffrey R Deschamp, James M Cook
Organic Letters|March 10, 2006
Enantiospecific synthesis of (+)-N(a)-methylpericyclivine and (-)-N(a)-methylakuammidine as well as the ring-A oxygenated natural products, (+)-10-methoxy N(a)-methylpericyclivine and 10-hydroxy N(a)-methylpericyclivineP V V Srirama Sarma, James M Cook
BMC Evolutionary Biology|October 17, 2006
Deep mtDNA divergences indicate cryptic species in a fig-pollinating waspEleanor R Haine, Joanne Martin, James M Cook
Journal of the American Chemical Society|February 5, 2004
Stereocontrolled total synthesis of (-)-vincamajinine and (-)-11-methoxy-17-epivincamajineJianming Yu, Xiangyu Z Wearing, James M Cook
The Journal of Organic Chemistry|May 7, 2005
A general strategy for the synthesis of vincamajine-related indole alkaloids: stereocontrolled total synthesis of (+)-dehydrovoachalotine, (-)-vincamajinine, and (-)-11-methoxy-17-epivincamajine as well as the related quebrachidine diol, vincamajine diol, and vincarinolJianming Yu, Xiangyu Z Wearing, James M Cook
Molecular Ecology|February 16, 2016
One step ahead: a parasitoid disperses farther and forms a wider geographic population than its fig wasp hostTimothy L Sutton, Markus Riegler, James M Cook
Pageof 33