???pagination.result.count???
???pagination.result.page???
1
Similarity in gene-regulatory networks suggests that cancer cells share characteristics of embryonic neural cells. , Zhang Z ., J Biol Chem. August 4, 2017; 292 (31): 12842-12859.
Transdifferentiation from cornea to lens in Xenopus laevis depends on BMP signalling and involves upregulation of Wnt signalling. , Day RC., BMC Dev Biol. January 26, 2011; 11 54.
Purified E255L mutant SERCA1a and purified PfATP6 are sensitive to SERCA-type inhibitors but insensitive to artemisinins. , Cardi D., J Biol Chem. August 20, 2010; 285 (34): 26406-16.
The glutamate receptor GluR5 agonist (S)-2-amino-3-(3-hydroxy-7,8-dihydro-6H-cyclohepta[d]isoxazol-4-yl)propionic acid and the 8-methyl analogue: synthesis, molecular pharmacology, and biostructural characterization. , Clausen RP., J Med Chem. August 13, 2009; 52 (15): 4911-22.
Tetrazolyl isoxazole amino acids as ionotropic glutamate receptor antagonists: synthesis, modelling and molecular pharmacology. , Frølund B., Bioorg Med Chem. September 15, 2005; 13 (18): 5391-8.
Structural determinants of agonist-specific kinetics at the ionotropic glutamate receptor 2. , Holm MM., Proc Natl Acad Sci U S A. August 23, 2005; 102 (34): 12053-8.
(S)-2-Amino-3-(3-hydroxy-7,8-dihydro-6H-cyclohepta[d]isoxazol-4-yl)propionic acid, a potent and selective agonist at the GluR5 subtype of ionotropic glutamate receptors. Synthesis, modeling, and molecular pharmacology. , Brehm L., J Med Chem. April 10, 2003; 46 (8): 1350-8.
Stereochemistry and molecular pharmacology of (S)-thio-ATPA, a new potent and selective GluR5 agonist. , Stensbøl TB., Eur J Pharmacol. January 12, 2001; 411 (3): 245-53.
Resolution, absolute stereochemistry and molecular pharmacology of the enantiomers of ATPA. , Stensbøl TB., Eur J Pharmacol. September 10, 1999; 380 (2-3): 153-62.
Resolution, absolute stereochemistry, and enantiopharmacology of the GluR1-4 and GluR5 antagonist 2-amino-3-[5- tert-butyl-3-(phosphonomethoxy)-4-isoxazolyl]propionic acid. , Møller EH., Chirality. January 1, 1999; 11 (10): 752-9.
Antagonist properties of a phosphono isoxazole amino acid at glutamate R1-4 (R,S)-2-amino-3-(3-hydroxy-5-methyl-4-isoxazolyl)propionic acid receptor subtypes. , Wahl P., Mol Pharmacol. March 1, 1998; 53 (3): 590-6.
Pharmacology and toxicology of ATOA, an AMPA receptor antagonist and a partial agonist at GluR5 receptors. , Wahl P., Neuropharmacology. January 1, 1998; 37 (10-11): 1205-10.