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Proceedings of the National Academy of Sciences of the United States of America
|
May 22, 2013
Phosphatidylinositol-4,5-biphosphate-dependent rearrangement of TRPV4 cytosolic tails enables channel activation by physiological stimuli
Anna Garcia-Elias, Sanela Mrkonjic, Carlos Pardo-Pastor, et al.
Nature Communications
|
December 5, 2022
Cannabinoid non-cannabidiol site modulation of TRPV2 structure and function
Liying Zhang, Charlotte Simonsen, Lucie Zimova, et al.
Neurology. Genetics
|
April 12, 2016
Novel mutations highlight the key role of the ankyrin repeat domain in TRPV4-mediated neuropathy
Jeremy M Sullivan, Christina M Zimanyi, William Aisenberg, et al.
Nature Chemical Biology
|
October 17, 2022
A small molecule inhibitor prevents gut bacterial genotoxin production
Matthew R Volpe, José A Velilla, Martin Daniel-Ivad, et al.
The Journal of Biological Chemistry
|
December 3, 2025
Profiling the TRPV4 ankyrin repeat domain interactome and its disruption by neuromuscular disease-causing mutations
Alexis K Loder, Gage P Kosmanopoulos, William H Aisenberg, et al.
Neurology. Genetics
|
May 2, 2019
Homozygous <i>TRPV4</i> mutation causes congenital distal spinal muscular atrophy and arthrogryposis
Jose Velilla, Michael Mario Marchetti, Agnes Toth-Petroczy, et al.
Journal of Medicinal Chemistry
|
October 8, 2019
High-Affinity Alkynyl Bisubstrate Inhibitors of Nicotinamide <i>N</i>-Methyltransferase (NNMT)
Rocco L Policarpo, Ludovic Decultot, Elizabeth May, et al.
Neurology
|
June 8, 2012
Exome sequencing identifies a novel TRPV4 mutation in a CMT2C family
Guida Landouré, Jeremy M Sullivan, Janel O Johnson, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
March 8, 2013
Noddy, a mouse harboring a missense mutation in protocadherin-15, reveals the impact of disrupting a critical interaction site between tip-link cadherins in inner ear hair cells
Ruishuang Geng, Marcos Sotomayor, Kimberly J Kinder, et al.
Computational and Structural Biotechnology Journal
|
January 23, 2024
Experimental and computational biophysics to identify vasodilator drugs targeted at TRPV2 using agonists based on the probenecid scaffold
Èric Catalina-Hernández, Mario López-Martín, David Masnou-Sánchez, et al.
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of 9
Search research articles
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Showing results (71-80 of 87) with videos related to
Sort By:
Page
of 9
Proceedings of the National Academy of Sciences of the United States of America
|
May 22, 2013
Phosphatidylinositol-4,5-biphosphate-dependent rearrangement of TRPV4 cytosolic tails enables channel activation by physiological stimuli
Anna Garcia-Elias, Sanela Mrkonjic, Carlos Pardo-Pastor, et al.
Nature Communications
|
December 5, 2022
Cannabinoid non-cannabidiol site modulation of TRPV2 structure and function
Liying Zhang, Charlotte Simonsen, Lucie Zimova, et al.
Neurology. Genetics
|
April 12, 2016
Novel mutations highlight the key role of the ankyrin repeat domain in TRPV4-mediated neuropathy
Jeremy M Sullivan, Christina M Zimanyi, William Aisenberg, et al.
Nature Chemical Biology
|
October 17, 2022
A small molecule inhibitor prevents gut bacterial genotoxin production
Matthew R Volpe, José A Velilla, Martin Daniel-Ivad, et al.
The Journal of Biological Chemistry
|
December 3, 2025
Profiling the TRPV4 ankyrin repeat domain interactome and its disruption by neuromuscular disease-causing mutations
Alexis K Loder, Gage P Kosmanopoulos, William H Aisenberg, et al.
Neurology. Genetics
|
May 2, 2019
Homozygous <i>TRPV4</i> mutation causes congenital distal spinal muscular atrophy and arthrogryposis
Jose Velilla, Michael Mario Marchetti, Agnes Toth-Petroczy, et al.
Journal of Medicinal Chemistry
|
October 8, 2019
High-Affinity Alkynyl Bisubstrate Inhibitors of Nicotinamide <i>N</i>-Methyltransferase (NNMT)
Rocco L Policarpo, Ludovic Decultot, Elizabeth May, et al.
Neurology
|
June 8, 2012
Exome sequencing identifies a novel TRPV4 mutation in a CMT2C family
Guida Landouré, Jeremy M Sullivan, Janel O Johnson, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
March 8, 2013
Noddy, a mouse harboring a missense mutation in protocadherin-15, reveals the impact of disrupting a critical interaction site between tip-link cadherins in inner ear hair cells
Ruishuang Geng, Marcos Sotomayor, Kimberly J Kinder, et al.
Computational and Structural Biotechnology Journal
|
January 23, 2024
Experimental and computational biophysics to identify vasodilator drugs targeted at TRPV2 using agonists based on the probenecid scaffold
Èric Catalina-Hernández, Mario López-Martín, David Masnou-Sánchez, et al.
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of 9