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http://hub.abes.fr/acs/periodical/jmcmar/2003/volume_46/issue_8/101021jm0204441/authorship/4
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_4/101021jm050987l/authorship/5
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_7/101021jm701394a/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_9/101021jm050014l/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_17/101021jm070447j/authorship/5
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_14/101021jm800092x/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_20/101021jm0504499/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_14/101021jm800025e/authorship/8
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_24/101021jm801112u/authorship/3
http://hub.abes.fr/acs/periodical/jmcmar/1997/volume_40/issue_22/101021jm9703597/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/2003/volume_46/issue_11/101021jm020588f/authorship/5
http://hub.abes.fr/acs/periodical/jmcmar/1998/volume_41/issue_14/101021jm9801206/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_1/101021jm0508336/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_14/101021jm051288b/authorship/4
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_10/101021jm061439q/authorship/5
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_14/101021jm800091e/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/1999/volume_42/issue_11/101021jm990076/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2004/volume_47/issue_27/101021jm049409f/authorship/6
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Heteroaryl Analogues of AMPA. 2. Synthesis, Absolute Stereochemistry,Photochemistry, and Structure−Activity Relationships
Hydroxy-1,2,5-oxadiazolyl Moiety as Bioisoster of the Carboxy Function. Synthesis, IonizationConstants, and Pharmacological Characterization of γ-Aminobutyric Acid (GABA) RelatedCompounds
Chemo-Enzymatic Synthesis of a Series of 2,4-Syn-Functionalized (S)-Glutamate Analogues: New Insight into the Structure−Activity Relation of Ionotropic Glutamate Receptor Subtypes 5, 6, and 7
Synthesis and Pharmacological Characterization at Glutamate Receptors of the Four Enantiopure Isomers of Tricholomic Acid
Synthesis, Binding Affinity at Glutamic Acid Receptors, NeuroprotectiveEffects, and Molecular Modeling Investigation of Novel Dihydroisoxazole AminoAcids
Convergent Synthesis and Pharmacology of SubstitutedTetrazolyl-2-amino-3-(3-hydroxy-5-methyl-4-isoxazolyl)propionic acid Analogues
Novel High-Affinity and Selective Biaromatic 4-Substituted γ-Hydroxybutyric Acid (GHB) Analogues as GHB Ligands: Design, Synthesis, and Binding Studies
(S)-2-Amino-3-(3-hydroxy-7,8-dihydro-6H-cyclohepta[d]isoxazol-4-yl)propionicAcid, a Potent and Selective Agonist at the GluR5 Subtype of IonotropicGlutamate Receptors. Synthesis, Modeling, and Molecular Pharmacology
Potent 4-Arylalkyl-Substituted 3-Isothiazolol GABAA Competitive/Noncompetitive Antagonists: Synthesis and Pharmacology
Synthesis and Pharmacology of the Baclofen Homologues5-Amino-4-(4-chlorophenyl)pentanoic Acid and the R- and S-Enantiomers of5-Amino-3-(4-chlorophenyl)pentanoic Acid
Design, Synthesis, and Pharmacological Characterization of Novel, PotentNMDA Receptor Antagonists
Rational Design and Enantioselective Synthesis of(1R,4S,5R,6S)-3-Azabicyclo[3.3.0]octane-4,6-dicarboxylic Acid A Novel Inhibitor at HumanGlutamate Transporter Subtypes 1, 2, and 3
5-Substituted Imidazole-4-acetic Acid Analogues: Synthesis, Modeling, and PharmacologicalCharacterization of a Series of Novel γ-Aminobutyric AcidC Receptor Agonists
(S)-Homo-AMPA, a Specific Agonist at the mGlu6 Subtype of MetabotropicGlutamic Acid Receptors
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
Design, Synthesis, and Pharmacology of a Highly Subtype-Selective GluR1/2Agonist, (RS)-2-Amino-3-(4-chloro-3-hydroxy-5-isoxazolyl)propionic Acid(Cl-HIBO)
A Tetrazolyl-Substituted Subtype-Selective AMPA Receptor Agonist
N-Hydroxypyrazolyl Glycine Derivatives as Selective N-Methyl-d-aspartic Acid Receptor Ligands
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