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Neurology
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October 26, 1999
Bilateral thalamic stimulation for the treatment of essential tremor
R Pahwa, K L Lyons, S B Wilkinson, et al.
Journal of Medicinal Chemistry
|
February 14, 2008
Structures of the ligand-binding core of iGluR2 in complex with the agonists (R)- and (S)-2-amino-3-(4-hydroxy-1,2,5-thiadiazol-3-yl)propionic acid explain their unusual equipotency
Mads Beich-Frandsen, Darryl S Pickering, Osman Mirza, et al.
Neurochemical Research
|
August 23, 2017
Effects of Dimeric PSD-95 Inhibition on Excitotoxic Cell Death and Outcome After Controlled Cortical Impact in Rats
Jens Bak Sommer, Anders Bach, Hana Malá, et al.
ACS Chemical Neuroscience
|
January 9, 2019
N1-Substituted Quinoxaline-2,3-diones as Kainate Receptor Antagonists: X-ray Crystallography, Structure-Affinity Relationships, and in Vitro Pharmacology
Jakob Pallesen, Stine Møllerud, Karla Frydenvang, et al.
Journal of Neurochemistry
|
July 1, 1993
A comparison of two alternatively spliced forms of a metabotropic glutamate receptor coupled to phosphoinositide turnover
D S Pickering, C Thomsen, P D Suzdak, et al.
ACS Chemical Neuroscience
|
May 22, 2020
Ionotropic Glutamate Receptor GluA2 in Complex with Bicyclic Pyrimidinedione-Based Compounds: When Small Compound Modifications Have Distinct Effects on Binding Interactions
Karla Frydenvang, Darryl S Pickering, Giridhar U Kshirsagar, et al.
Molecular Pharmacology
|
December 14, 2004
Tyr702 is an important determinant of agonist binding and domain closure of the ligand-binding core of GluR2
Anne Frandsen, Darryl S Pickering, Bente Vestergaard, et al.
ACS Chemical Neuroscience
|
April 10, 2015
Binding mode of an α-amino acid-linked quinoxaline-2,3-dione analogue at glutamate receptor subtype GluK1
Charles S Demmer, Charlotte Møller, Patricia M G E Brown, et al.
Journal of Medicinal Chemistry
|
February 11, 2016
Tweaking Subtype Selectivity and Agonist Efficacy at (S)-2-Amino-3-(3-hydroxy-5-methyl-isoxazol-4-yl)propionic acid (AMPA) Receptors in a Small Series of BnTetAMPA Analogues
Shuang-Yan Wang, Younes Larsen, Cristina Vara Navarrete, et al.
Journal of Medicinal Chemistry
|
June 27, 2008
Chemo-enzymatic synthesis of (2S,4R)-2-amino-4-(3-(2,2-diphenylethylamino)-3-oxopropyl)pentanedioic acid: a novel selective inhibitor of human excitatory amino acid transporter subtype 2
Emanuelle Sagot, Anders A Jensen, Darryl S Pickering, et al.
Page
of 23
Search research articles
Search
Showing results (161-170 of 225) with videos related to
Sort By:
Page
of 23
Neurology
|
October 26, 1999
Bilateral thalamic stimulation for the treatment of essential tremor
R Pahwa, K L Lyons, S B Wilkinson, et al.
Journal of Medicinal Chemistry
|
February 14, 2008
Structures of the ligand-binding core of iGluR2 in complex with the agonists (R)- and (S)-2-amino-3-(4-hydroxy-1,2,5-thiadiazol-3-yl)propionic acid explain their unusual equipotency
Mads Beich-Frandsen, Darryl S Pickering, Osman Mirza, et al.
Neurochemical Research
|
August 23, 2017
Effects of Dimeric PSD-95 Inhibition on Excitotoxic Cell Death and Outcome After Controlled Cortical Impact in Rats
Jens Bak Sommer, Anders Bach, Hana Malá, et al.
ACS Chemical Neuroscience
|
January 9, 2019
N1-Substituted Quinoxaline-2,3-diones as Kainate Receptor Antagonists: X-ray Crystallography, Structure-Affinity Relationships, and in Vitro Pharmacology
Jakob Pallesen, Stine Møllerud, Karla Frydenvang, et al.
Journal of Neurochemistry
|
July 1, 1993
A comparison of two alternatively spliced forms of a metabotropic glutamate receptor coupled to phosphoinositide turnover
D S Pickering, C Thomsen, P D Suzdak, et al.
ACS Chemical Neuroscience
|
May 22, 2020
Ionotropic Glutamate Receptor GluA2 in Complex with Bicyclic Pyrimidinedione-Based Compounds: When Small Compound Modifications Have Distinct Effects on Binding Interactions
Karla Frydenvang, Darryl S Pickering, Giridhar U Kshirsagar, et al.
Molecular Pharmacology
|
December 14, 2004
Tyr702 is an important determinant of agonist binding and domain closure of the ligand-binding core of GluR2
Anne Frandsen, Darryl S Pickering, Bente Vestergaard, et al.
ACS Chemical Neuroscience
|
April 10, 2015
Binding mode of an α-amino acid-linked quinoxaline-2,3-dione analogue at glutamate receptor subtype GluK1
Charles S Demmer, Charlotte Møller, Patricia M G E Brown, et al.
Journal of Medicinal Chemistry
|
February 11, 2016
Tweaking Subtype Selectivity and Agonist Efficacy at (S)-2-Amino-3-(3-hydroxy-5-methyl-isoxazol-4-yl)propionic acid (AMPA) Receptors in a Small Series of BnTetAMPA Analogues
Shuang-Yan Wang, Younes Larsen, Cristina Vara Navarrete, et al.
Journal of Medicinal Chemistry
|
June 27, 2008
Chemo-enzymatic synthesis of (2S,4R)-2-amino-4-(3-(2,2-diphenylethylamino)-3-oxopropyl)pentanedioic acid: a novel selective inhibitor of human excitatory amino acid transporter subtype 2
Emanuelle Sagot, Anders A Jensen, Darryl S Pickering, et al.
Page
of 23