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1. Tau molecular diversity contributes to clinical heterogeneity in Alzheimer’s disease

2. Author Correction: Tau molecular diversity contributes to clinical heterogeneity in Alzheimer’s disease

3. Enhanced Clearance of Aβ in Brain by Sustaining the Plasmin Proteolysis Cascade

4. Synthesis and structure–activity relationship of a novel series of heterocyclic sulfonamide γ-secretase inhibitors

5. Abstract 1909: Pan-TGF-β inhibition with PD-1 blockade as a combination treatment strategy to augment anti-tumor immune response in hepatocellular carcinoma

6. Abstract 4451: Combination of local mRNA immunotherapy with systemic immune checkpoint blockade demonstrates anti-tumor activity across a diverse range of preclinical syngeneic tumor models

9. Aminomethyl-Derived Beta Secretase (BACE1) Inhibitors: Engaging Gly230 without an Anilide Functionality

10. Chemoproteomic profiling reveals that cathepsin D off-target activity drives ocular toxicity of β-secretase inhibitors

11. Utilizing Structures of CYP2D6 and BACE1 Complexes To Reduce Risk of Drug–Drug Interactions with a Novel Series of Centrally Efficacious BACE1 Inhibitors

12. Discovery of a Series of Efficient, Centrally Efficacious BACE1 Inhibitors through Structure-Based Drug Design

13. Aminomethyl-Derived Beta Secretase (BACE1) Inhibitors: Engaging Gly230 without an Anilide Functionality.

14. ( S) -N-(5-Chlorothiophene-2-sulfonyl)-β,β-diethylalaninol a Notch-1-sparing γ-secretase inhibitor

15. P4-278: Clinical gamma-secretase inhibitors (GSIs) alter beta-amyloid 40/42 ratio in brain and show CSF beta-amyloid rebound in vivo

16. P4–291: Predicting in vivo BACE inhibitor efficacy: Are human iPS‐derived neurons superior?

21. P4-277: Evaluation of beta-amyloid-lowering efficacy of a novel BACE1 inhibitor in multiple species

24. Discovery of a novel series of Notch-sparing γ-secretase inhibitors

25. Application of the Bicyclo[1.1.1]pentane Motif as a Nonclassical Phenyl Ring Bioisostere in the Design of a Potent and Orally Active γ-Secretase Inhibitor

26. Pharmacological Assessment of <i>γ</i>-Secretase Activity from Rodent and Human Brain

27. Metabolism-Directed Design of Oxetane-Containing Arylsulfonamide Derivatives as γ-Secretase Inhibitors

28. Quantitative Pharmacokinetic/Pharmacodynamic Analyses Suggest That the 129/SVE Mouse Is a Suitable Preclinical Pharmacology Model for Identifying Small-Molecule γ-Secretase Inhibitors

29. P3-220: Age-dependent disruption in hippocampal theta oscillation in APP/PS1 mice

32. Begacestat (GSI-953): A Novel, Selective Thiophene Sulfonamide Inhibitor of Amyloid Precursor Protein γ-Secretase for the Treatment of Alzheimer's Disease

35. Discovery of Begacestat, a Notch-1-Sparing γ-Secretase Inhibitor for the Treatment of Alzheimer’s Disease

36. Impact of Apolipoprotein E (ApoE) Polymorphism on Brain ApoE Levels

37. P2-302: GSI-953 is a potent APP-selective gamma-secretase inhibitor for the treatment of Alzheimer's disease

38. P2-337: Characterization of the affinity of GSI-953 for binding to gamma-secretase and comparison to benchmark gamma-secretase inhibitors

39. Discovery of a Series of Efficient,Centrally EfficaciousBACE1 Inhibitors through Structure-Based Drug Design.

40. P4-244: Discovery of a novel series of notch-sparing γ-secretase inhibitors

42. Acute γ-Secretase Inhibition Improves Contextual Fear Conditioning in the Tg2576 Mouse Model of Alzheimer's Disease

43. In Vitro and In Vivo Activities of Syn2190, a Novel β-Lactamase Inhibitor

44. Studies on Penam Sulfones. II. Synthesis and .BETA.-Lactamase Inhibitory Activity of 2.BETA.-Carboxamide Penicillanic Acid Sulfones.

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