154 results on '"Holladay, M."'
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2. Agonists and Antagonists of Nicotinic Acetylcholine Receptors
3. ABT — 418, a Novel Nicotinic Agonist
4. Effects of activating NK cell receptor expression and NK cell reconstitution on the outcomes of unrelated donor hematopoietic cell transplantation for hematologic malignancies
5. Large-scale isolation of CD133+ progenitor cells from G-CSF mobilized peripheral blood stem cells
6. Effect of extended immunosuppressive drug treatment on B cell vs T cell reconstitution in pediatric bone marrow transplant recipients
7. Taking Care of Supply
8. Enterprise Modelling the Telecommunications Industry
9. A one-step large-scale method for T- and B-cell depletion of mobilized PBSC for allogeneic transplantation
10. OSS responsibilities
11. Structure-activity and computer modeling studies on potent and selective CCK-A agonist tetrapeptides containing (N-Me)Asp or (N-Me)Asp-(N-Me)Phe
12. Design of cholecystokinin analogs with high affinity and selectivity for brain CCK receptors
13. 7. farmaco-resistenza e sinergia tra farmaci
14. ChemInform Abstract: Synthesis of α-Benzyl γ-Lactam, α-Benzyl δ- Lactam, and α-Benzylproline Derivatives as Conformationally Restricted Analogues of Phenylalaninamide.
15. ChemInform Abstract: Structure-Activity Studies on 2-Methyl-3-(2(S)-pyrrolidinylmethoxy) pyridine (ABT-089): An Orally Bioavailable 3-Pyridyl Ether Nicotinic Acetylcholine Receptor Ligand with Cognition-Enhancing Properties.
16. ChemInform Abstract: Efficient Asymmetric Synthesis of ABT-594; a Potent, Orally Effective Analgesic.
17. The New Spirituality: An Introduction to Progressive Belief in the Twenty-First Century. By Gordon Lynch. London: I. B. Tauris & Co Ltd. 2007. 218 pp. $74.95
18. Editorial: Church, State, and the Presidential Campaign of 2008
19. Inhibitory KIR–HLA receptor–ligand mismatch in autologous haematopoietic stem cell transplantation for solid tumour and lymphoma
20. ChemInform Abstract: Structure—Activity Studies Related to ABT‐594, a Potent Nonopioid Analgesic Agent: Effect of Pyridine and Azetidine Ring Substitutions on Nicotinic Acetylcholine Receptor Binding Affinity and Analgesic Activity in Mice.
21. Design of Cholecystokinin Analogs with High Affinity and Selectivity for Brain CCK Receptors
22. ChemInform Abstract: Novel 2‐(2′‐Furo[3,2‐b]pyridinyl) Pyrrolidines: Potent Neuronal Nicotinic Acetylcholine Receptor Ligands.
23. ChemInform Abstract: Novel 3‐Pyridyl Ethers with Subnanomolar Affinity for Central Neuronal Nicotinic Acetylcholine Receptors (nAChR′s).
24. Effects of selective CCK receptor agonists on food intake after central or peripheral administration in rats
25. ChemInform Abstract: trans‐3‐n‐Propyl‐L‐proline is a Highly Favorable, Conformationally Restricted Replacement for Methionine in the C‐Terminal Tetrapeptide of Cholecystokinin. Stereoselective Synthesis of 3‐Allyl‐ and 3‐n‐ Propyl‐L‐proline Derivatives from 4‐Hydroxy‐L‐proline.
26. ChemInform Abstract: Conformationally Constrained Amino Acids. Synthesis and Optical Resolution of 3-Substituted Proline Derivatives.
27. A71378: a CCK agonist with high potency and selectivity for CCK-A receptors
28. Purification of human natural killer cells using a clinical-scale immunomagnetic method.
29. Large-scale isolation of CD133+progenitor cells from G-CSF mobilized peripheral blood stem cells.
30. A large-scale method for T cell depletion: towards graft engineering of mobilized peripheral blood stem cells.
31. Effect of extended immunosuppressive drug treatment on B cell vs T cell reconstitution in pediatric bone marrow transplant recipients.
32. Synthesis and Structure−Activity Studies on N-[5-(1H-Imidazol-4-yl)-5,6,7,8-tetrahydro-1-naphthalenyl]methanesulfonamide, an Imidazole-Containing α<INF>1A</INF>-Adrenoceptor Agonist<SUP>1</SUP>
33. Synthesis and Structure−Activity Relationships of a Novel Series of 2,3,5,6,7,9-Hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-Dioxide K<INF>ATP</INF> Channel Openers: Discovery of (−)-(9S)-9-(3-Bromo-4-fluorophenyl)-2,3,5,6,7,9- hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-Dioxide (A-278637), a Potent K<INF>ATP</INF> Opener That Selectively Inhibits Spontaneous Bladder Contractions
34. ABT-594 [(R)-5-(2-azetidinylmethoxy)-2-chloropyridine]: a novel, orally effective antinociceptive agent acting via neuronal nicotinic acetylcholine receptors: II. In vivo characterization.
35. ABT-594 [(R)-5-(2-azetidinylmethoxy)-2-chloropyridine]: a novel, orally effective analgesic acting via neuronal nicotinic acetylcholine receptors: I. In vitro characterization.
36. ABT-089 [2-methyl-3-(2-(S)-pyrrolidinylmethoxy)pyridine dihydrochloride]: II. A novel cholinergic channel modulator with effects on cognitive performance in rats and monkeys.
37. ABT-089 [2-methyl-3-(2-(S)-pyrrolidinylmethoxy)pyridine]: I. A potent and selective cholinergic channel modulator with neuroprotective properties.
38. Structure-activity studies related to ABT-594, a potent nonopioid analgesic agent: Effect of pyridine and azetidine ring substitutions on nicotinic acetylcholine receptor binding affinity and analgesic activity in mice
39. Amino acid-derived piperidides as novel CCK~B ligands with anxiolytic-like properties
40. The role of neuronal nicotinic acetylcholine receptors in antinociception: Effects of ABT-594
41. Distinct requirements for activation at CCK-A and CCK-B/gastrin receptors: studies with a C-terminal hydrazide analogue of cholecystokinin tetrapeptide (30-33).
42. Identification and Initial Structure−Activity Relationships of (R)-5-(2-Azetidinylmethoxy)-2-chloropyridine (ABT-594), a Potent, Orally Active, Non-Opiate Analgesic Agent Acting via Neuronal Nicotinic Acetylcholine Receptors
43. Neuronal Nicotinic Acetylcholine Receptors as Targets for Drug Discovery
44. Structure−Activity Studies on 2-Methyl-3-(2(S)-pyrrolidinylmethoxy)pyridine (ABT-089): An Orally Bioavailable 3-Pyridyl Ether Nicotinic Acetylcholine Receptor Ligand with Cognition-Enhancing Properties
45. Novel 3-Pyridyl Ethers with Subnanomolar Affinity for Central Neuronal Nicotinic Acetylcholine Receptors
46. Antinociceptive effects of the novel neuronal nicotinic acetylcholine receptor agonist, ABT-594, in mice
47. Novel 2-(2'-furo[3,2-b]pyridinyl) pyrrolidines: potent neuronal nicotinic acetylcholine receptor ligands
48. N-[3-(1H-Imidazol-4-ylmethyl)phenyl]ethanesulfonamide (ABT-866, 1),<SUP>1</SUP> a Novel α<INF>1</INF>-Adrenoceptor Ligand with an Enhanced in Vitro and in Vivo Profile Relative to Phenylpropanolamine and Midodrine
49. Synthesis and structure-activity relationships of 5-substituted pyridine analogues of 3-[2-((S)-pyrrolidinyl)methoxy]pyridine, A-84543
50. Convenient Preparation of O-Linked Polymer-Bound N-Substituted Hydroxylamines, Intermediates for Synthesis of N-Substituted Hydroxamic Acids
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