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Showing results (531-540 of 545) with videos related to

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Journal of Medicinal Chemistry|October 24, 2014
Discovery of dual leucine zipper kinase (DLK, MAP3K12) inhibitors with activity in neurodegeneration modelsSnahel Patel, Frederick Cohen, Brian J Dean, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Discovery and Biological Profiling of Potent and Selective mTOR Inhibitor GDC-0349Zhonghua Pei, Elizabeth Blackwood, Lichuan Liu, et al.
Science Immunology|November 8, 2024
Macrophage LRRK2 hyperactivity impairs autophagy and induces Paneth cell dysfunctionShengxiang Sun, Miki Hodel, Xiang Wang, et al.
Journal of Medicinal Chemistry|March 30, 2018
Discovery of a Potent (4 R,5 S)-4-Fluoro-5-methylproline Sulfonamide Transient Receptor Potential Ankyrin 1 Antagonist and Its Methylene Phosphate Prodrug Guided by Molecular ModelingHuifen Chen, Matthew Volgraf, Steven Do, et al.
JRSM Cardiovascular Disease|June 22, 2023
Comparison of the use of blood pressure telemonitoring versus standard medical care in the achievement of short-term therapeutic goals in blood pressure in patients with uncontrolled hypertension: An open-label clinical trialM G Ramos-Zavala, F Grover-Páez, E G Cardona-Muñoz, et al.
Science Translational Medicine|February 6, 2015
Effect of selective LRRK2 kinase inhibition on nonhuman primate lungReina N Fuji, Michael Flagella, Miriam Baca, et al.
Molecular Neurodegeneration|August 7, 2025
LRRK2 kinase activity regulates Parkinson's disease-relevant lipids at the lysosomeMichael T Maloney, Xiang Wang, Rajarshi Ghosh, et al.
Journal of Medicinal Chemistry|December 21, 2013
Discovery of highly potent, selective, and brain-penetrant aminopyrazole leucine-rich repeat kinase 2 (LRRK2) small molecule inhibitorsAnthony A Estrada, Bryan K Chan, Charles Baker-Glenn, et al.
Science Translational Medicine|April 24, 2020
LRRK2 inhibitors induce reversible changes in nonhuman primate lungs without measurable pulmonary deficitsMarco A S Baptista, Kalpana Merchant, Ted Barrett, et al.
Elife|September 17, 2024
DNL343 is an investigational CNS penetrant eukaryotic initiation factor 2B activator that prevents and reverses the effects of neurodegeneration caused by the integrated stress responseErnie Yulyaningsih, Jung H Suh, Melania Fanok, et al.
Pageof 55

Showing results (531-540 of 545) with videos related to

Sort By:
Pageof 55
Journal of Medicinal Chemistry|October 24, 2014
Discovery of dual leucine zipper kinase (DLK, MAP3K12) inhibitors with activity in neurodegeneration modelsSnahel Patel, Frederick Cohen, Brian J Dean, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Discovery and Biological Profiling of Potent and Selective mTOR Inhibitor GDC-0349Zhonghua Pei, Elizabeth Blackwood, Lichuan Liu, et al.
Science Immunology|November 8, 2024
Macrophage LRRK2 hyperactivity impairs autophagy and induces Paneth cell dysfunctionShengxiang Sun, Miki Hodel, Xiang Wang, et al.
Journal of Medicinal Chemistry|March 30, 2018
Discovery of a Potent (4 R,5 S)-4-Fluoro-5-methylproline Sulfonamide Transient Receptor Potential Ankyrin 1 Antagonist and Its Methylene Phosphate Prodrug Guided by Molecular ModelingHuifen Chen, Matthew Volgraf, Steven Do, et al.
JRSM Cardiovascular Disease|June 22, 2023
Comparison of the use of blood pressure telemonitoring versus standard medical care in the achievement of short-term therapeutic goals in blood pressure in patients with uncontrolled hypertension: An open-label clinical trialM G Ramos-Zavala, F Grover-Páez, E G Cardona-Muñoz, et al.
Science Translational Medicine|February 6, 2015
Effect of selective LRRK2 kinase inhibition on nonhuman primate lungReina N Fuji, Michael Flagella, Miriam Baca, et al.
Molecular Neurodegeneration|August 7, 2025
LRRK2 kinase activity regulates Parkinson's disease-relevant lipids at the lysosomeMichael T Maloney, Xiang Wang, Rajarshi Ghosh, et al.
Journal of Medicinal Chemistry|December 21, 2013
Discovery of highly potent, selective, and brain-penetrant aminopyrazole leucine-rich repeat kinase 2 (LRRK2) small molecule inhibitorsAnthony A Estrada, Bryan K Chan, Charles Baker-Glenn, et al.
Science Translational Medicine|April 24, 2020
LRRK2 inhibitors induce reversible changes in nonhuman primate lungs without measurable pulmonary deficitsMarco A S Baptista, Kalpana Merchant, Ted Barrett, et al.
Elife|September 17, 2024
DNL343 is an investigational CNS penetrant eukaryotic initiation factor 2B activator that prevents and reverses the effects of neurodegeneration caused by the integrated stress responseErnie Yulyaningsih, Jung H Suh, Melania Fanok, et al.
Pageof 55