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T Gampe

Showing results (11-20 of 27) with videos related to

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Acta Crystallographica. Section F, Structural Biology Communications|April 6, 2019
BacMam production and crystal structure of nonglycosylated apo human furin at 1.89 Å resolutionKenneth H Pearce, Laurie K Overton, Robert T Gampe, et al.
Biochemistry|July 2, 1991
NMR studies of [U-13C]cyclosporin A bound to cyclophilin: bound conformation and portions of cyclosporin involved in bindingS W Fesik, R T Gampe, H L Eaton, et al.
Molecular Cell|November 5, 2004
Structural basis for androgen receptor interdomain and coactivator interactions suggests a transition in nuclear receptor activation function dominanceBin He, Robert T Gampe, Adam J Kole, et al.
Molecular Cell|July 6, 2000
Asymmetry in the PPARgamma/RXRalpha crystal structure reveals the molecular basis of heterodimerization among nuclear receptorsR T Gampe, V G Montana, M H Lambert, et al.
Biochemistry|November 21, 1995
Catalytic activity of the SH2 domain of human pp60c-src; evidence from NMR, mass spectrometry, site-directed mutagenesis and kinetic studies for an inherent phosphatase activityR J Boerner, T G Consler, R T Gampe, et al.
Nature Structural & Molecular Biology|June 29, 2010
Structure of Rev-erbalpha bound to N-CoR reveals a unique mechanism of nuclear receptor-co-repressor interactionCaroline A Phelan, Robert T Gampe, Millard H Lambert, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 8, 2001
Structural determinants of ligand binding selectivity between the peroxisome proliferator-activated receptorsH E Xu, M H Lambert, V G Montana, et al.
Journal of Medicinal Chemistry|April 2, 2004
Structure-based design of potent retinoid X receptor alpha agonistsCurt D Haffner, James M Lenhard, Aaron B Miller, et al.
Bioorganic & Medicinal Chemistry Letters|November 18, 2005
Semicarbazone-based inhibitors of cathepsin K, are they prodrugs for aldehyde inhibitors?Kim K Adkison, David G Barrett, David N Deaton, et al.
Bioorganic & Medicinal Chemistry Letters|January 1, 1999
The formation of a covalent complex between a dipeptide ligand and the src SH2 domainK J Alligood, P S Charifson, R Crosby, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Acta Crystallographica. Section F, Structural Biology Communications|April 6, 2019
BacMam production and crystal structure of nonglycosylated apo human furin at 1.89 Å resolutionKenneth H Pearce, Laurie K Overton, Robert T Gampe, et al.
Biochemistry|July 2, 1991
NMR studies of [U-13C]cyclosporin A bound to cyclophilin: bound conformation and portions of cyclosporin involved in bindingS W Fesik, R T Gampe, H L Eaton, et al.
Molecular Cell|November 5, 2004
Structural basis for androgen receptor interdomain and coactivator interactions suggests a transition in nuclear receptor activation function dominanceBin He, Robert T Gampe, Adam J Kole, et al.
Molecular Cell|July 6, 2000
Asymmetry in the PPARgamma/RXRalpha crystal structure reveals the molecular basis of heterodimerization among nuclear receptorsR T Gampe, V G Montana, M H Lambert, et al.
Biochemistry|November 21, 1995
Catalytic activity of the SH2 domain of human pp60c-src; evidence from NMR, mass spectrometry, site-directed mutagenesis and kinetic studies for an inherent phosphatase activityR J Boerner, T G Consler, R T Gampe, et al.
Nature Structural & Molecular Biology|June 29, 2010
Structure of Rev-erbalpha bound to N-CoR reveals a unique mechanism of nuclear receptor-co-repressor interactionCaroline A Phelan, Robert T Gampe, Millard H Lambert, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 8, 2001
Structural determinants of ligand binding selectivity between the peroxisome proliferator-activated receptorsH E Xu, M H Lambert, V G Montana, et al.
Journal of Medicinal Chemistry|April 2, 2004
Structure-based design of potent retinoid X receptor alpha agonistsCurt D Haffner, James M Lenhard, Aaron B Miller, et al.
Bioorganic & Medicinal Chemistry Letters|November 18, 2005
Semicarbazone-based inhibitors of cathepsin K, are they prodrugs for aldehyde inhibitors?Kim K Adkison, David G Barrett, David N Deaton, et al.
Bioorganic & Medicinal Chemistry Letters|January 1, 1999
The formation of a covalent complex between a dipeptide ligand and the src SH2 domainK J Alligood, P S Charifson, R Crosby, et al.
Pageof 3