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Joseph D Ho

Showing results (1-10 of 22) with videos related to

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Journal of Molecular Biology|September 13, 2002
The crystal structure of human cathepsin F and its implications for the development of novel immunomodulatorsJohn R Somoza, James T Palmer, Joseph D Ho
Advances in Pharmacology (San Diego, Calif.)|May 18, 2020
Discovery and pharmacology of the covalent GLP-1 receptor (GLP-1R) allosteric modulator BETP: A novel tool to probe GLP-1R pharmacologyFrancis S Willard, Joseph D Ho, Kyle W Sloop
Journal of Molecular Biology|February 27, 2007
The crystal structure of E. coli rRNA pseudouridine synthase RluEHu Pan, Joseph D Ho, Robert M Stroud, et al.
American Journal of Physiology. Endocrinology and Metabolism|July 10, 2024
Class B1 GPCRs: insights into multireceptor pharmacology for the treatment of metabolic diseasePanjamaporn Sangwung, Joseph D Ho, Tessa Siddall, et al.
Genes & Development|March 18, 2006
Novel arylpyrazole compounds selectively modulate glucocorticoid receptor regulatory activityJen-Chywan Wang, Nilesh Shah, Carlos Pantoja, et al.
Biochemical and Biophysical Research Communications|August 24, 2020
Synthetic protease-activated class B GPCRsFrancis S Willard, Tamika D Meredith, Aaron D Showalter, et al.
Acta Crystallographica. Section D, Biological Crystallography|November 28, 2002
Expression, purification, crystallization and preliminary X-ray diffraction studies of human cathepsin F complexed with an irreversible vinyl sulfone inhibitorJoseph D Ho, Yana Meltser, Joseph J Buggy, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 12, 2010
Function of human Rh based on structure of RhCG at 2.1 AFranz Gruswitz, Sarika Chaudhary, Joseph D Ho, et al.
Bioorganic & Medicinal Chemistry Letters|February 7, 2018
Determination of L-AP4-bound human mGlu8 receptor amino terminal domain structure and the molecular basis for L-AP4's group III mGlu receptor functional potency and selectivityJeffery M Schkeryantz, Qi Chen, Joseph D Ho, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 23, 2009
Crystal structure of human aquaporin 4 at 1.8 A and its mechanism of conductanceJoseph D Ho, Ronald Yeh, Andrew Sandstrom, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Journal of Molecular Biology|September 13, 2002
The crystal structure of human cathepsin F and its implications for the development of novel immunomodulatorsJohn R Somoza, James T Palmer, Joseph D Ho
Advances in Pharmacology (San Diego, Calif.)|May 18, 2020
Discovery and pharmacology of the covalent GLP-1 receptor (GLP-1R) allosteric modulator BETP: A novel tool to probe GLP-1R pharmacologyFrancis S Willard, Joseph D Ho, Kyle W Sloop
Journal of Molecular Biology|February 27, 2007
The crystal structure of E. coli rRNA pseudouridine synthase RluEHu Pan, Joseph D Ho, Robert M Stroud, et al.
American Journal of Physiology. Endocrinology and Metabolism|July 10, 2024
Class B1 GPCRs: insights into multireceptor pharmacology for the treatment of metabolic diseasePanjamaporn Sangwung, Joseph D Ho, Tessa Siddall, et al.
Genes & Development|March 18, 2006
Novel arylpyrazole compounds selectively modulate glucocorticoid receptor regulatory activityJen-Chywan Wang, Nilesh Shah, Carlos Pantoja, et al.
Biochemical and Biophysical Research Communications|August 24, 2020
Synthetic protease-activated class B GPCRsFrancis S Willard, Tamika D Meredith, Aaron D Showalter, et al.
Acta Crystallographica. Section D, Biological Crystallography|November 28, 2002
Expression, purification, crystallization and preliminary X-ray diffraction studies of human cathepsin F complexed with an irreversible vinyl sulfone inhibitorJoseph D Ho, Yana Meltser, Joseph J Buggy, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 12, 2010
Function of human Rh based on structure of RhCG at 2.1 AFranz Gruswitz, Sarika Chaudhary, Joseph D Ho, et al.
Bioorganic & Medicinal Chemistry Letters|February 7, 2018
Determination of L-AP4-bound human mGlu8 receptor amino terminal domain structure and the molecular basis for L-AP4's group III mGlu receptor functional potency and selectivityJeffery M Schkeryantz, Qi Chen, Joseph D Ho, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 23, 2009
Crystal structure of human aquaporin 4 at 1.8 A and its mechanism of conductanceJoseph D Ho, Ronald Yeh, Andrew Sandstrom, et al.
Pageof 3