Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Kristoff T. Homan"'
Publikováno v:
Molecules, Vol 19, Iss 10, Pp 16937-16949 (2014)
G protein-coupled receptor kinases (GRKs) have been implicated in human diseases ranging from heart failure to diabetes. Previous studies have identified several compounds that selectively inhibit GRK2, such as paroxetine and balanol. Far fewer selec
Externí odkaz:
https://doaj.org/article/2033a9864a144175bf8b70ccff2b629f
Autor:
Liang Zhang, Yuzhen Wang, Kristoff T. Homan, Stephanie M. Gaudette, Andrew J. McCluskey, Ying Chan, Joanne Murphy, Mary Abdalla, Christine M. Nelson, Victor Z. Sun, Jamie E. Erickson, Heather L. Knight, Anca Clabbers, Annette J. Schwartz Sterman, Soumya Mitra
Publikováno v:
Molecular Imaging and Biology.
Purpose To image colon-expressed alternatively spliced D domain of tenascin C in preclinical colitis models using near infrared (NIR)-labeled targeted molecular imaging agents. Procedures. A human IgG1 with nanomolar binding affinity specific to the
Autor:
Christine M. Nelson, Heather Knight, Jamie Erickson, Bradford L. McRae, Victor Sun, Annette J. Schwartz Sterman, Stephanie M. Gaudette, Grace Lynch, Kristoff T. Homan, Calvin S. Pohl, Sahana Bose, Liang Zhang, Soumya Mitra
Purpose To image colon-expressed alternatively spliced D domain of tenascin C in preclinical colitis models using near infrared (NIR) labeled targeted molecular imaging agents.Methods Human IgG and scFv fusion proteins specific to the alternatively s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7d2bc8d2a564fbddc2e3890916e5d33
https://doi.org/10.21203/rs.3.rs-984872/v1
https://doi.org/10.21203/rs.3.rs-984872/v1
Autor:
Anthony W Azevedo, Thuy Doan, Hormoz Moaven, Iza Sokal, Faiza Baameur, Sergey A Vishnivetskiy, Kristoff T Homan, John JG Tesmer, Vsevolod V Gurevich, Jeannie Chen, Fred Rieke
Publikováno v:
eLife, Vol 4 (2015)
Rod photoreceptors generate measurable responses to single-photon activation of individual molecules of the G protein-coupled receptor (GPCR), rhodopsin. Timely rhodopsin desensitization depends on phosphorylation and arrestin binding, which quenches
Externí odkaz:
https://doaj.org/article/4edccd85553d48d8a0ead6c6fbec1158
Publikováno v:
Biochemistry. 55:2841-2848
Interactions between proteins and cell membranes are critical for biological processes such as transmembrane signaling, and specific components of the membrane may play roles in helping to organize or mandate particular conformations of both integral
Autor:
Jessica Waninger-Saroni, Kelly M. Larimore, Paul D. Kirchhoff, Joseph Y. Cheung, Kristoff T. Homan, Osvaldo Cruz-Rodríguez, Helen V. Waldschmidt, John J.G. Tesmer, Marilyn C. Cato, Jianliang Song, Alessandro Cannavo, Scott D. Larsen, Walter J. Koch
Publikováno v:
Journal of Medicinal Chemistry. 59:3793-3807
G protein-coupled receptors (GPCRs) are central to many physiological processes. Regulation of this superfamily of receptors is controlled by GPCR kinases (GRKs), some of which have been implicated in heart failure. GSK180736A, developed as a Rho-ass
Autor:
Vsevolod V. Gurevich, Sergey A. Vishnivetskiy, Sayaka Inagaki, Kristoff T. Homan, John J.G. Tesmer, Jim White, Rodolfo Ghirlando, Reinhard Grisshammer
Publikováno v:
Biochemistry
G protein-coupled receptor kinases (GRKs) play an important role in the desensitization of G protein-mediated signaling of G protein-coupled receptors (GPCRs). The level of interest in mapping their phosphorylation sites has increased because recent
Autor:
Marilyn C. Cato, Osvaldo Cruz-Rodríguez, Alessandro Cannavo, Walter J. Koch, Joseph Y. Cheung, Kristoff T. Homan, Scott D. Larsen, Helen V. Waldschmidt, Jianliang Song, Michael W. Wilson, John J.G. Tesmer
In heart failure, the β-adrenergic receptors (βARs) become desensitized and uncoupled from heterotrimeric G proteins. This process is initiated by G protein-coupled receptor kinases (GRKs), some of which are upregulated in the failing heart, making
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bc95ad4ec5e668167ab16bfdd42fafb
http://hdl.handle.net/11588/732638
http://hdl.handle.net/11588/732638
Publikováno v:
Molecules (Basel, Switzerland)
Molecules, Vol 19, Iss 10, Pp 16937-16949 (2014)
Molecules
Volume 19
Issue 10
Pages 16937-16949
Molecules, Vol 19, Iss 10, Pp 16937-16949 (2014)
Molecules
Volume 19
Issue 10
Pages 16937-16949
G protein-coupled receptor kinases (GRKs) have been implicated in human diseases ranging from heart failure to diabetes. Previous studies have identified several compounds that selectively inhibit GRK2, such as paroxetine and balanol. Far fewer selec
Autor:
John J.G. Tesmer, Kristoff T. Homan
Publikováno v:
ACS Chemical Biology
Small molecules that inhibit the protein kinase A, G, and C (AGC) family of serine/threonine kinases can exert profound effects on cell homeostasis and thereby regulate fundamental processes such as heart rate, blood pressure, and metabolism, but the