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Showing results (331-340 of 344) with videos related to

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Cancer Immunology, Immunotherapy : CII|January 27, 2024
Activation of cytotoxic lymphocytes through CD6 enhances killing of cancer cellsMikel Gurrea-Rubio, Qi Wu, M Asif Amin, et al.
Research Square|October 27, 2023
Activation of Cytotoxic Lymphocytes Through CD6 Enhances Killing of Cancer CellsMikel Gurrea-Rubio, Qi Wu, M Asif Amin, et al.
Cardiology in the Young|November 21, 2022
A novel algorithm for classification of interatrial communications within the oval fossa in the newbornSofie Dannesbo, Elisabeth Blixenkrone-Moeller, Christian A Pihl, et al.
JCI Insight|January 26, 2021
CD6 is a target for cancer immunotherapyJeffrey H Ruth, Mikel Gurrea-Rubio, Kalana S Athukorala, et al.
ACS Medicinal Chemistry Letters|May 26, 2015
Discovery of a Potent Class of PI3Kα Inhibitors with Unique Binding Mode via Encoded Library Technology (ELT)Hongfang Yang, Patricia F Medeiros, Kaushik Raha, et al.
Biochemistry|March 17, 2009
Fragment-based discovery of nonpeptidic BACE-1 inhibitors using tetheringWenjin Yang, Raymond V Fucini, Bruce T Fahr, et al.
Nature Reviews. Gastroenterology & Hepatology|April 21, 2016
Expert consensus document: Cholangiocarcinoma: current knowledge and future perspectives consensus statement from the European Network for the Study of Cholangiocarcinoma (ENS-CCA)Jesus M Banales, Vincenzo Cardinale, Guido Carpino, et al.
BMJ Open|August 26, 2021
Co-designing a dashboard of predictive analytics and decision support to drive care quality and client outcomes in aged care: a mixed-method study protocolKristiana Ludlow, Johanna Westbrook, Mikaela Jorgensen, et al.
Bioorganic & Medicinal Chemistry Letters|April 5, 2011
Discovery of a potent and highly selective PDK1 inhibitor via fragment-based drug discoveryDaniel A Erlanson, Joseph W Arndt, Mark T Cancilla, et al.
Journal of Medicinal Chemistry|August 16, 2012
Discovery of highly potent and selective small molecule ADAMTS-5 inhibitors that inhibit human cartilage degradation via encoded library technology (ELT)Hongfeng Deng, Heather O'Keefe, Christopher P Davie, et al.
Pageof 35

Showing results (331-340 of 344) with videos related to

Sort By:
Pageof 35
Cancer Immunology, Immunotherapy : CII|January 27, 2024
Activation of cytotoxic lymphocytes through CD6 enhances killing of cancer cellsMikel Gurrea-Rubio, Qi Wu, M Asif Amin, et al.
Research Square|October 27, 2023
Activation of Cytotoxic Lymphocytes Through CD6 Enhances Killing of Cancer CellsMikel Gurrea-Rubio, Qi Wu, M Asif Amin, et al.
Cardiology in the Young|November 21, 2022
A novel algorithm for classification of interatrial communications within the oval fossa in the newbornSofie Dannesbo, Elisabeth Blixenkrone-Moeller, Christian A Pihl, et al.
JCI Insight|January 26, 2021
CD6 is a target for cancer immunotherapyJeffrey H Ruth, Mikel Gurrea-Rubio, Kalana S Athukorala, et al.
ACS Medicinal Chemistry Letters|May 26, 2015
Discovery of a Potent Class of PI3Kα Inhibitors with Unique Binding Mode via Encoded Library Technology (ELT)Hongfang Yang, Patricia F Medeiros, Kaushik Raha, et al.
Biochemistry|March 17, 2009
Fragment-based discovery of nonpeptidic BACE-1 inhibitors using tetheringWenjin Yang, Raymond V Fucini, Bruce T Fahr, et al.
Nature Reviews. Gastroenterology & Hepatology|April 21, 2016
Expert consensus document: Cholangiocarcinoma: current knowledge and future perspectives consensus statement from the European Network for the Study of Cholangiocarcinoma (ENS-CCA)Jesus M Banales, Vincenzo Cardinale, Guido Carpino, et al.
BMJ Open|August 26, 2021
Co-designing a dashboard of predictive analytics and decision support to drive care quality and client outcomes in aged care: a mixed-method study protocolKristiana Ludlow, Johanna Westbrook, Mikaela Jorgensen, et al.
Bioorganic & Medicinal Chemistry Letters|April 5, 2011
Discovery of a potent and highly selective PDK1 inhibitor via fragment-based drug discoveryDaniel A Erlanson, Joseph W Arndt, Mark T Cancilla, et al.
Journal of Medicinal Chemistry|August 16, 2012
Discovery of highly potent and selective small molecule ADAMTS-5 inhibitors that inhibit human cartilage degradation via encoded library technology (ELT)Hongfeng Deng, Heather O'Keefe, Christopher P Davie, et al.
Pageof 35