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The EMBO Journal
|
September 21, 2007
Requirement for O-linked N-acetylglucosaminyltransferase in lymphocytes activation
Alexander Golks, Thi-Thanh Thao Tran, Jean Francois Goetschy, et al.
Chemmedchem
|
November 15, 2007
Synthesis and immobilization of erythro-C14-omega-aminosphingosine-1-phosphate as a potential tool for affinity chromatography
Thomas Ullrich, Michael Ghobrial, Carsten Peters, et al.
The Journal of Biological Chemistry
|
April 30, 2003
A comparative functional analysis of plasma membrane Ca2+ pump isoforms in intact cells
Marisa Brini, Luisa Coletto, Nicola Pierobon, et al.
Nature Chemical Biology
|
May 12, 2009
Persistent signaling induced by FTY720-phosphate is mediated by internalized S1P1 receptors
Florian Mullershausen, Frédéric Zecri, Cihan Cetin, et al.
Bioorganic & Medicinal Chemistry Letters
|
October 21, 2005
NBD-labeled derivatives of the immunomodulatory drug FTY720 as tools for metabolism and mode of action studies
Peter Ettmayer, Thomas Baumruker, Danilo Guerini, et al.
European Journal of Biochemistry
|
March 5, 2002
Uncoupling of protein-3 induces an uncontrolled uncoupling of mitochondria after expression in muscle derived L6 cells
Danilo Guerini, Elisabetta Prati, Urvi Desai, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 4, 2009
Pyrazole derived from (+)-3-carene; a novel potent, selective scaffold for sphingosine-1-phosphate (S1P(1)) receptor agonists
Frédéric J Zécri, Rainer Albert, Gregory Landrum, et al.
Nature
|
September 5, 2003
Proton-sensing G-protein-coupled receptors
Marie-Gabrielle Ludwig, Miroslava Vanek, Danilo Guerini, et al.
SLAS Discovery : Advancing Life Sciences R & D
|
July 22, 2017
Identification of SPPL2a Inhibitors by Multiparametric Analysis of a High-Content Ultra-High-Throughput Screen
Xian Zhang, Marjo Götte, Yvonne Ibig-Rehm, et al.
Chemmedchem
|
September 4, 2010
Design and synthesis of selective and potent orally active S1P5 agonists
Henri Mattes, Kumlesh Kumar Dev, Rochdi Bouhelal, et al.
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of 4
Search research articles
Search
Showing results (11-20 of 33) with videos related to
Sort By:
Page
of 4
The EMBO Journal
|
September 21, 2007
Requirement for O-linked N-acetylglucosaminyltransferase in lymphocytes activation
Alexander Golks, Thi-Thanh Thao Tran, Jean Francois Goetschy, et al.
Chemmedchem
|
November 15, 2007
Synthesis and immobilization of erythro-C14-omega-aminosphingosine-1-phosphate as a potential tool for affinity chromatography
Thomas Ullrich, Michael Ghobrial, Carsten Peters, et al.
The Journal of Biological Chemistry
|
April 30, 2003
A comparative functional analysis of plasma membrane Ca2+ pump isoforms in intact cells
Marisa Brini, Luisa Coletto, Nicola Pierobon, et al.
Nature Chemical Biology
|
May 12, 2009
Persistent signaling induced by FTY720-phosphate is mediated by internalized S1P1 receptors
Florian Mullershausen, Frédéric Zecri, Cihan Cetin, et al.
Bioorganic & Medicinal Chemistry Letters
|
October 21, 2005
NBD-labeled derivatives of the immunomodulatory drug FTY720 as tools for metabolism and mode of action studies
Peter Ettmayer, Thomas Baumruker, Danilo Guerini, et al.
European Journal of Biochemistry
|
March 5, 2002
Uncoupling of protein-3 induces an uncontrolled uncoupling of mitochondria after expression in muscle derived L6 cells
Danilo Guerini, Elisabetta Prati, Urvi Desai, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 4, 2009
Pyrazole derived from (+)-3-carene; a novel potent, selective scaffold for sphingosine-1-phosphate (S1P(1)) receptor agonists
Frédéric J Zécri, Rainer Albert, Gregory Landrum, et al.
Nature
|
September 5, 2003
Proton-sensing G-protein-coupled receptors
Marie-Gabrielle Ludwig, Miroslava Vanek, Danilo Guerini, et al.
SLAS Discovery : Advancing Life Sciences R & D
|
July 22, 2017
Identification of SPPL2a Inhibitors by Multiparametric Analysis of a High-Content Ultra-High-Throughput Screen
Xian Zhang, Marjo Götte, Yvonne Ibig-Rehm, et al.
Chemmedchem
|
September 4, 2010
Design and synthesis of selective and potent orally active S1P5 agonists
Henri Mattes, Kumlesh Kumar Dev, Rochdi Bouhelal, et al.
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of 4