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Sarah G Hymowitz

Showing results (31-40 of 54) with videos related to

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Structure (London, England : 1993)|August 11, 2011
Preparation of distinct ubiquitin chain reagents of high purity and yieldKen C Dong, Elizabeth Helgason, Christine Yu, et al.
Bioorganic & Medicinal Chemistry Letters|November 19, 2013
Structure-based design of substituted hexafluoroisopropanol-arylsulfonamides as modulators of RORcBenjamin P Fauber, Gladys de Leon Boenig, Brenda Burton, et al.
The Journal of Biological Chemistry|November 16, 2004
Structures of APRIL-receptor complexes: like BCMA, TACI employs only a single cysteine-rich domain for high affinity ligand bindingSarah G Hymowitz, Darshana R Patel, Heidi J A Wallweber, et al.
Nature Structural & Molecular Biology|January 29, 2020
Negative regulation of RAF kinase activity by ATP is overcome by 14-3-3-induced dimerizationNicholas P D Liau, Timothy J Wendorff, John G Quinn, et al.
Cancer Cell|August 27, 2014
Structure of the BRAF-MEK complex reveals a kinase activity independent role for BRAF in MAPK signalingJacob R Haling, Jawahar Sudhamsu, Ivana Yen, et al.
Blood|July 15, 2006
Synthetic anti-BR3 antibodies that mimic BAFF binding and target both human and murine B cellsChingwei V Lee, Sarah G Hymowitz, Heidi J Wallweber, et al.
ACS Chemical Biology|June 5, 2009
Antagonism of c-IAP and XIAP proteins is required for efficient induction of cell death by small-molecule IAP antagonistsChudi Ndubaku, Eugene Varfolomeev, Lan Wang, et al.
Science (New York, N.Y.)|October 25, 2011
Antagonists induce a conformational change in cIAP1 that promotes autoubiquitinationErin C Dueber, Allyn J Schoeffler, Andreas Lingel, et al.
Nature Medicine|September 4, 2007
Death-receptor O-glycosylation controls tumor-cell sensitivity to the proapoptotic ligand Apo2L/TRAILKlaus W Wagner, Elizabeth A Punnoose, Thomas Januario, et al.
Bioorganic & Medicinal Chemistry Letters|July 15, 2014
Reduction in lipophilicity improved the solubility, plasma-protein binding, and permeability of tertiary sulfonamide RORc inverse agonistsBenjamin P Fauber, Olivier René, Gladys de Leon Boenig, et al.
Pageof 6

Showing results (31-40 of 54) with videos related to

Sort By:
Pageof 6
Structure (London, England : 1993)|August 11, 2011
Preparation of distinct ubiquitin chain reagents of high purity and yieldKen C Dong, Elizabeth Helgason, Christine Yu, et al.
Bioorganic & Medicinal Chemistry Letters|November 19, 2013
Structure-based design of substituted hexafluoroisopropanol-arylsulfonamides as modulators of RORcBenjamin P Fauber, Gladys de Leon Boenig, Brenda Burton, et al.
The Journal of Biological Chemistry|November 16, 2004
Structures of APRIL-receptor complexes: like BCMA, TACI employs only a single cysteine-rich domain for high affinity ligand bindingSarah G Hymowitz, Darshana R Patel, Heidi J A Wallweber, et al.
Nature Structural & Molecular Biology|January 29, 2020
Negative regulation of RAF kinase activity by ATP is overcome by 14-3-3-induced dimerizationNicholas P D Liau, Timothy J Wendorff, John G Quinn, et al.
Cancer Cell|August 27, 2014
Structure of the BRAF-MEK complex reveals a kinase activity independent role for BRAF in MAPK signalingJacob R Haling, Jawahar Sudhamsu, Ivana Yen, et al.
Blood|July 15, 2006
Synthetic anti-BR3 antibodies that mimic BAFF binding and target both human and murine B cellsChingwei V Lee, Sarah G Hymowitz, Heidi J Wallweber, et al.
ACS Chemical Biology|June 5, 2009
Antagonism of c-IAP and XIAP proteins is required for efficient induction of cell death by small-molecule IAP antagonistsChudi Ndubaku, Eugene Varfolomeev, Lan Wang, et al.
Science (New York, N.Y.)|October 25, 2011
Antagonists induce a conformational change in cIAP1 that promotes autoubiquitinationErin C Dueber, Allyn J Schoeffler, Andreas Lingel, et al.
Nature Medicine|September 4, 2007
Death-receptor O-glycosylation controls tumor-cell sensitivity to the proapoptotic ligand Apo2L/TRAILKlaus W Wagner, Elizabeth A Punnoose, Thomas Januario, et al.
Bioorganic & Medicinal Chemistry Letters|July 15, 2014
Reduction in lipophilicity improved the solubility, plasma-protein binding, and permeability of tertiary sulfonamide RORc inverse agonistsBenjamin P Fauber, Olivier René, Gladys de Leon Boenig, et al.
Pageof 6