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Biochimica Et Biophysica Acta. Biomembranes
|
September 16, 2017
Importance of the REM (Ras exchange) domain for membrane interactions by RasGRP3
Agnes Czikora, Noemi Kedei, Heather Kalish, et al.
Molecular Pharmacology
|
January 27, 2004
Design of a high-affinity competitive antagonist of the vanilloid receptor selective for the calcium entry-linked receptor population
Attila Tóth, Peter M Blumberg, Zili Chen, et al.
Biomolecules & Therapeutics
|
July 15, 2019
Combination of a Rapidly Penetrating Agonist and a Slowly Penetrating Antagonist Affords Agonist Action of Limited Duration at the Cellular Level
Larry V Pearce, Jihyae Ann, Peter M Blumberg, et al.
The Journal of Biological Chemistry
|
November 13, 2008
Characterization of the differential roles of the twin C1a and C1b domains of protein kinase C-delta
Yongmei Pu, Susan H Garfield, Noemi Kedei, et al.
Molecular and Cellular Biology
|
December 12, 2001
Tyrosine phosphorylation of protein kinase Cdelta is essential for its apoptotic effect in response to etoposide
Michal Blass, Ilana Kronfeld, Gila Kazimirsky, et al.
Biochemical and Biophysical Research Communications
|
June 11, 2002
Thapsigargin binds to and inhibits the cloned vanilloid receptor-1
Attila Tóth, Noémi Kedei, Tamás Szabó, et al.
Cellular Signalling
|
September 21, 2017
The C1 domain of Vav3, a novel potential therapeutic target
Jessica S Kelsey, Tamás Géczy, Christopher J Kaler, et al.
The Journal of Biological Chemistry
|
October 9, 2003
RasGRP1 represents a novel non-protein kinase C phorbol ester signaling pathway in mouse epidermal keratinocytes
Reshmi A Rambaratsingh, James C Stone, Peter M Blumberg, et al.
Journal of Medicinal Chemistry
|
August 19, 2008
Conformationally constrained analogues of diacylglycerol. 30. An investigation of diacylglycerol-lactones containing heteroaryl groups reveals compounds with high selectivity for Ras guanyl nucleotide-releasing proteins
Saïd El Kazzouli, Nancy E Lewin, Peter M Blumberg, et al.
Chemmedchem
|
August 8, 2006
Synthesis and pharmacological evaluation of 8- and 9-substituted benzolactam-v8 derivatives as potent ligands for protein kinase C, a therapeutic target for Alzheimer's disease
Ulrich R Mach, Nancy E Lewin, Peter M Blumberg, et al.
Page
of 19
Search research articles
Search
Showing results (11-20 of 183) with videos related to
Sort By:
Page
of 19
Biochimica Et Biophysica Acta. Biomembranes
|
September 16, 2017
Importance of the REM (Ras exchange) domain for membrane interactions by RasGRP3
Agnes Czikora, Noemi Kedei, Heather Kalish, et al.
Molecular Pharmacology
|
January 27, 2004
Design of a high-affinity competitive antagonist of the vanilloid receptor selective for the calcium entry-linked receptor population
Attila Tóth, Peter M Blumberg, Zili Chen, et al.
Biomolecules & Therapeutics
|
July 15, 2019
Combination of a Rapidly Penetrating Agonist and a Slowly Penetrating Antagonist Affords Agonist Action of Limited Duration at the Cellular Level
Larry V Pearce, Jihyae Ann, Peter M Blumberg, et al.
The Journal of Biological Chemistry
|
November 13, 2008
Characterization of the differential roles of the twin C1a and C1b domains of protein kinase C-delta
Yongmei Pu, Susan H Garfield, Noemi Kedei, et al.
Molecular and Cellular Biology
|
December 12, 2001
Tyrosine phosphorylation of protein kinase Cdelta is essential for its apoptotic effect in response to etoposide
Michal Blass, Ilana Kronfeld, Gila Kazimirsky, et al.
Biochemical and Biophysical Research Communications
|
June 11, 2002
Thapsigargin binds to and inhibits the cloned vanilloid receptor-1
Attila Tóth, Noémi Kedei, Tamás Szabó, et al.
Cellular Signalling
|
September 21, 2017
The C1 domain of Vav3, a novel potential therapeutic target
Jessica S Kelsey, Tamás Géczy, Christopher J Kaler, et al.
The Journal of Biological Chemistry
|
October 9, 2003
RasGRP1 represents a novel non-protein kinase C phorbol ester signaling pathway in mouse epidermal keratinocytes
Reshmi A Rambaratsingh, James C Stone, Peter M Blumberg, et al.
Journal of Medicinal Chemistry
|
August 19, 2008
Conformationally constrained analogues of diacylglycerol. 30. An investigation of diacylglycerol-lactones containing heteroaryl groups reveals compounds with high selectivity for Ras guanyl nucleotide-releasing proteins
Saïd El Kazzouli, Nancy E Lewin, Peter M Blumberg, et al.
Chemmedchem
|
August 8, 2006
Synthesis and pharmacological evaluation of 8- and 9-substituted benzolactam-v8 derivatives as potent ligands for protein kinase C, a therapeutic target for Alzheimer's disease
Ulrich R Mach, Nancy E Lewin, Peter M Blumberg, et al.
Page
of 19