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Wyszukujesz frazę ""Sivarao DV"" wg kryterium: Autor


Wyświetlanie 1-10 z 10
Tytuł:
Test-retest reliability of tone- and 40 Hz train-evoked gamma oscillations in female rats and their sensitivity to low-dose NMDA channel blockade.
Autorzy:
Raza MU; Department of Pharmaceutical Sciences, Bill Gatton College of Pharmacy, East Tennessee State University, VA Building 7, Room 324, Maple Ave, Johnson City, TN, 37604, USA.
Sivarao DV; Department of Pharmaceutical Sciences, Bill Gatton College of Pharmacy, East Tennessee State University, VA Building 7, Room 324, Maple Ave, Johnson City, TN, 37604, USA. .
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Źródło:
Psychopharmacology [Psychopharmacology (Berl)] 2021 Aug; Vol. 238 (8), pp. 2325-2334. Date of Electronic Publication: 2021 May 04.
Typ publikacji:
Journal Article
MeSH Terms:
Excitatory Amino Acid Antagonists/*pharmacology
Gamma Rhythm/*drug effects
Gamma Rhythm/*physiology
Receptors, N-Methyl-D-Aspartate/*antagonists & inhibitors
Receptors, N-Methyl-D-Aspartate/*physiology
Acoustic Stimulation/methods ; Acoustic Stimulation/standards ; Animals ; Dizocilpine Maleate/pharmacology ; Dose-Response Relationship, Drug ; Evoked Potentials, Auditory/drug effects ; Evoked Potentials, Auditory/physiology ; Excitatory Amino Acid Agonists/pharmacology ; Female ; Rats ; Rats, Sprague-Dawley ; Receptors, N-Methyl-D-Aspartate/agonists ; Reproducibility of Results
Czasopismo naukowe
Tytuł:
The Novel, Nicotinic Alpha7 Receptor Partial Agonist, BMS-933043, Improves Cognition and Sensory Processing in Preclinical Models of Schizophrenia.
Autorzy:
Bristow LJ; Discovery Biology, Bristol-Myers Squibb Company, Wallingford, Connecticut, United States of America.
Easton AE; Discovery Biology, Bristol-Myers Squibb Company, Wallingford, Connecticut, United States of America.
Li YW; Discovery Biology, Bristol-Myers Squibb Company, Wallingford, Connecticut, United States of America.
Sivarao DV; Discovery Biology, Bristol-Myers Squibb Company, Wallingford, Connecticut, United States of America.
Lidge R; Discovery Biology, Bristol-Myers Squibb Company, Wallingford, Connecticut, United States of America.
Jones KM; Discovery Biology, Bristol-Myers Squibb Company, Wallingford, Connecticut, United States of America.
Post-Munson D; Discovery Biology, Bristol-Myers Squibb Company, Wallingford, Connecticut, United States of America.
Daly C; Discovery Biology, Bristol-Myers Squibb Company, Wallingford, Connecticut, United States of America.
Lodge NJ; Discovery Biology, Bristol-Myers Squibb Company, Wallingford, Connecticut, United States of America.
Gallagher L; Lead Discovery and Optimization, Bristol-Myers Squibb Company, Wallingford, Connecticut, United States of America.
Molski T; Discovery Biology, Bristol-Myers Squibb Company, Wallingford, Connecticut, United States of America.
Pieschl R; Discovery Biology, Bristol-Myers Squibb Company, Wallingford, Connecticut, United States of America.
Chen P; Discovery Biology, Bristol-Myers Squibb Company, Wallingford, Connecticut, United States of America.
Hendricson A; Lead Discovery and Optimization, Bristol-Myers Squibb Company, Wallingford, Connecticut, United States of America.
Westphal R; Discovery Biology, Bristol-Myers Squibb Company, Wallingford, Connecticut, United States of America.
Cook J; Discovery Chemistry, Bristol-Myers Squibb Company, Wallingford, Connecticut, United States of America.
Iwuagwu C; Discovery Chemistry, Bristol-Myers Squibb Company, Wallingford, Connecticut, United States of America.
Morgan D; Pharmaceutical Candidate Optimization, Bristol-Myers Squibb Company, Wallingford, Connecticut, United States of America.
Benitex Y; Pharmaceutical Candidate Optimization, Bristol-Myers Squibb Company, Wallingford, Connecticut, United States of America.
King D; Discovery Chemistry, Bristol-Myers Squibb Company, Wallingford, Connecticut, United States of America.
Macor JE; Discovery Chemistry, Bristol-Myers Squibb Company, Wallingford, Connecticut, United States of America.
Zaczek R; Discovery Biology, Bristol-Myers Squibb Company, Wallingford, Connecticut, United States of America.
Olson R; Discovery Chemistry, Bristol-Myers Squibb Company, Wallingford, Connecticut, United States of America.
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Źródło:
PloS one [PLoS One] 2016 Jul 28; Vol. 11 (7), pp. e0159996. Date of Electronic Publication: 2016 Jul 28 (Print Publication: 2016).
Typ publikacji:
Journal Article
MeSH Terms:
Cognition Disorders/*drug therapy
Quinuclidines/*therapeutic use
Schizophrenia/*drug therapy
Spiro Compounds/*therapeutic use
alpha7 Nicotinic Acetylcholine Receptor/*agonists
Animals ; Cognition Disorders/physiopathology ; Drug Evaluation, Preclinical ; HEK293 Cells ; Humans ; Male ; Mice ; Patch-Clamp Techniques ; Quinuclidines/pharmacology ; Radioligand Assay ; Rats ; Schizophrenia/physiopathology ; Spiro Compounds/pharmacology
Czasopismo naukowe
Tytuł:
The qEEG Signature of Selective NMDA NR2B Negative Allosteric Modulators; A Potential Translational Biomarker for Drug Development.
Autorzy:
Keavy D; Genetically Defined Diseases and Genomics, Bristol-Myers Squibb Company, Wallingford, CT, United States of America.
Bristow LJ; Genetically Defined Diseases and Genomics, Bristol-Myers Squibb Company, Wallingford, CT, United States of America.
Sivarao DV; Genetically Defined Diseases and Genomics, Bristol-Myers Squibb Company, Wallingford, CT, United States of America.
Batchelder M; Department of Veterinary Sciences, Bristol-Myers Squibb Company, Wallingford, CT, United States of America.
King D; Discovery Chemistry, Bristol-Myers Squibb Company, Wallingford, CT, United States of America.
Thangathirupathy S; Discovery Chemistry, Bristol-Myers Squibb Company, Wallingford, CT, United States of America.
Macor JE; Discovery Chemistry, Bristol-Myers Squibb Company, Wallingford, CT, United States of America.
Weed MR; Genetically Defined Diseases and Genomics, Bristol-Myers Squibb Company, Wallingford, CT, United States of America.
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Źródło:
PloS one [PLoS One] 2016 Apr 01; Vol. 11 (4), pp. e0152729. Date of Electronic Publication: 2016 Apr 01 (Print Publication: 2016).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Drug Design*
Biomarkers/*metabolism
Electroencephalography/*methods
Receptors, N-Methyl-D-Aspartate/*metabolism
Allosteric Regulation ; Animals ; Macaca fascicularis ; Receptors, N-Methyl-D-Aspartate/drug effects
Czasopismo naukowe
Tytuł:
The 40-Hz auditory steady-state response: a selective biomarker for cortical NMDA function.
Autorzy:
Sivarao DV; Genetically Defined Diseases, Bristol-Myers Squibb Co, Wallingford, Connecticut.
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Źródło:
Annals of the New York Academy of Sciences [Ann N Y Acad Sci] 2015 May; Vol. 1344, pp. 27-36. Date of Electronic Publication: 2015 Mar 21.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Cerebral Cortex*/metabolism
Cerebral Cortex*/physiopathology
Electroencephalography*
Evoked Potentials, Auditory*
Hallucinations*/metabolism
Hallucinations*/physiopathology
Schizophrenia*/metabolism
Schizophrenia*/physiopathology
Synaptic Transmission*
N-Methylaspartate/*metabolism
Animals ; Biomarkers/metabolism ; Humans
Czasopismo naukowe
    Wyświetlanie 1-10 z 10

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