Следене
Matt Kennedy
Matt Kennedy
Потвърден имейл адрес: merck.com
Заглавие
Позовавания
Позовавания
Година
Human platelet/erythroleukemia cell prostaglandin G/H synthase: cDNA cloning, expression, and gene chromosomal assignment
CD Funk, LB Funk, ME Kennedy, AS Pong, GA Fitzgerald
The FASEB journal 5 (9), 2304-2312, 1991
8301991
The BACE1 inhibitor verubecestat (MK-8931) reduces CNS β-amyloid in animal models and in Alzheimer’s disease patients
ME Kennedy, AW Stamford, X Chen, K Cox, JN Cumming, MF Dockendorf, ...
Science translational medicine 8 (363), 363ra150-363ra150, 2016
4532016
Function, therapeutic potential and cell biology of BACE proteases: current status and future prospects
R Vassar, PH Kuhn, C Haass, ME Kennedy, L Rajendran, PC Wong, ...
Journal of neurochemistry 130 (1), 4-28, 2014
4012014
Tau molecular diversity contributes to clinical heterogeneity in Alzheimer’s disease
S Dujardin, C Commins, A Lathuiliere, P Beerepoot, AR Fernandes, ...
Nature medicine 26 (8), 1256-1263, 2020
3102020
MLi-2, a potent, selective, and centrally active compound for exploring the therapeutic potential and safety of LRRK2 kinase inhibition
MJ Fell, C Mirescu, K Basu, B Cheewatrakoolpong, DE DeMong, JM Ellis, ...
Journal of Pharmacology and Experimental Therapeutics 355 (3), 397-409, 2015
2552015
The roles of inflammation and immune mechanisms in Alzheimer's disease
LJ Van Eldik, MC Carrillo, PE Cole, D Feuerbach, BD Greenberg, ...
Alzheimer's & Dementia: Translational Research & Clinical Interventions 2 (2 …, 2016
1972016
Nonselective and Gβγ-insensitive weaver K+ channels
B Navarro, ME Kennedy, B Velimirović, D Bhat, AS Peterson, ...
Science 272 (5270), 1950-1953, 1996
1921996
Mutations of the alpha 2A-adrenergic receptor that eliminate detectable palmitoylation do not perturb receptor-G-protein coupling.
ME Kennedy, LE Limbird
Journal of Biological Chemistry 268 (11), 8003-8011, 1993
1791993
Discovery of cyclic acylguanidines as highly potent and selective β-site amyloid cleaving enzyme (BACE) inhibitors: Part I Inhibitor design and validation
Z Zhu, ZY Sun, Y Ye, J Voigt, C Strickland, EM Smith, J Cumming, L Wang, ...
Journal of medicinal chemistry 53 (3), 951-965, 2010
1652010
Discovery of the 3-imino-1, 2, 4-thiadiazinane 1, 1-dioxide derivative verubecestat (MK-8931)–a β-site amyloid precursor protein cleaving enzyme 1 inhibitor for the treatment …
JD Scott, SW Li, APJ Brunskill, X Chen, K Cox, JN Cumming, M Forman, ...
Journal of medicinal chemistry 59 (23), 10435-10450, 2016
1562016
Application of fragment-based NMR screening, X-ray crystallography, structure-based design, and focused chemical library design to identify novel μM leads for the development …
YS Wang, C Strickland, JH Voigt, ME Kennedy, BM Beyer, MM Senior, ...
Journal of medicinal chemistry 53 (3), 942-950, 2010
1562010
Structure based design of iminohydantoin BACE1 inhibitors: identification of an orally available, centrally active BACE1 inhibitor
JN Cumming, EM Smith, L Wang, J Misiaszek, J Durkin, J Pan, U Iserloh, ...
Bioorganic & medicinal chemistry letters 22 (7), 2444-2449, 2012
1492012
Functional and biochemical evidence for G-protein-gated inwardly rectifying K+ (GIRK) channels composed of GIRK2 and GIRK3
TM Jelacic, ME Kennedy, K Wickman, DE Clapham
Journal of Biological Chemistry 275 (46), 36211-36216, 2000
1372000
Discovery of a 3-(4-pyrimidinyl) indazole (MLi-2), an orally available and selective leucine-rich repeat kinase 2 (LRRK2) inhibitor that reduces brain kinase activity
JD Scott, DE DeMong, TJ Greshock, K Basu, X Dai, J Harris, A Hruza, ...
Journal of medicinal chemistry 60 (7), 2983-2992, 2017
1222017
GIRK4 confers appropriate processing and cell surface localization to G-protein-gated potassium channels
ME Kennedy, J Nemec, S Corey, K Wickman, DE Clapham
Journal of Biological Chemistry 274 (4), 2571-2582, 1999
1071999
Discovery of an orally available, brain penetrant BACE1 inhibitor that affords robust CNS Aβ reduction
AW Stamford, JD Scott, SW Li, S Babu, D Tadesse, R Hunter, Y Wu, ...
ACS medicinal chemistry letters 3 (11), 897-902, 2012
1042012
Potent pyrrolidine-and piperidine-based BACE-1 inhibitors
U Iserloh, Y Wu, JN Cumming, J Pan, LY Wang, AW Stamford, ...
Bioorganic & Medicinal Chemistry Letters 18 (1), 414-417, 2008
1022008
Gβγ binding to GIRK4 subunit is critical for G protein-gated K+ channel activation
G Krapivinsky, ME Kennedy, J Nemec, I Medina, L Krapivinsky, ...
Journal of Biological Chemistry 273 (27), 16946-16952, 1998
1011998
LRRK2 inhibitors induce reversible changes in nonhuman primate lungs without measurable pulmonary deficits
MAS Baptista, K Merchant, T Barrett, S Bhargava, DK Bryce, JM Ellis, ...
Science translational medicine 12 (540), eaav0820, 2020
932020
Discovery of an orally efficaceous 4-phenoxypyrrolidine-based BACE-1 inhibitor
U Iserloh, J Pan, AW Stamford, ME Kennedy, Q Zhang, L Zhang, ...
Bioorganic & medicinal chemistry letters 18 (1), 418-422, 2008
892008
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