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The Journal of Biological Chemistry
|
May 14, 2005
A variable residue in the pore of Kv1 channels is critical for the high affinity of blockers from sea anemones and scorpions
Bernard Gilquin, Sandrine Braud, Mats A L Eriksson, et al.
International Journal of Pharmaceutics
|
June 21, 2022
Customized cationic nanoemulsions loading triamcinolone acetonide for corneal neovascularization secondary to inflammatory processes
Ana R Fernandes, Lorena B Vidal, Elena Sánchez-López, et al.
American Journal of Respiratory and Critical Care Medicine
|
July 27, 2019
Systemic Amyloidosis Mimicking Lung Cancer
Adam S Fisch, Florian J Fintelmann, Maria L Garcia-Moliner, et al.
Journal of Magnetic Resonance Imaging : JMRI
|
August 30, 2014
Characteristic time courses of cortical and medullary sodium signals measured by noninvasive (23) Na-MRI in rat kidney induced by furosemide
Haiying Liu, Dan Zhou, Maria L Garcia, et al.
Pathogens (Basel, Switzerland)
|
August 4, 2019
Therapeutic Interventions for Countering Leishmaniasis and Chagas's Disease: From Traditional Sources to Nanotechnological Systems
Eliana B Souto, João Dias-Ferreira, Sara A Craveiro, et al.
Assay and Drug Development Technologies
|
December 17, 2010
A pharmacologically validated, high-capacity, functional thallium flux assay for the human Ether-à-go-go related gene potassium channel
William A Schmalhofer, Andrew M Swensen, Brande S Thomas, et al.
Trends in Molecular Medicine
|
December 23, 2015
The 'Omics' of Amyotrophic Lateral Sclerosis
Diana Caballero-Hernandez, Miguel G Toscano, Marta Cejudo-Guillen, et al.
International Journal of Pharmaceutics
|
February 28, 2016
Biopharmaceutical evaluation of epigallocatechin gallate-loaded cationic lipid nanoparticles (EGCG-LNs): In vivo, in vitro and ex vivo studies
Joana F Fangueiro, Ana C Calpena, Beatriz Clares, et al.
Assay and Drug Development Technologies
|
May 13, 2008
A high-capacity membrane potential FRET-based assay for the sodium-coupled glucose co-transporter SGLT1
Adam B Weinglass, Andrew M Swensen, Jessica Liu, et al.
Molecular Pharmacology
|
August 30, 2008
ProTx-II, a selective inhibitor of NaV1.7 sodium channels, blocks action potential propagation in nociceptors
William A Schmalhofer, Jeffrey Calhoun, Rachel Burrows, et al.
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of 13
Search research articles
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Showing results (51-60 of 122) with videos related to
Sort By:
Page
of 13
The Journal of Biological Chemistry
|
May 14, 2005
A variable residue in the pore of Kv1 channels is critical for the high affinity of blockers from sea anemones and scorpions
Bernard Gilquin, Sandrine Braud, Mats A L Eriksson, et al.
International Journal of Pharmaceutics
|
June 21, 2022
Customized cationic nanoemulsions loading triamcinolone acetonide for corneal neovascularization secondary to inflammatory processes
Ana R Fernandes, Lorena B Vidal, Elena Sánchez-López, et al.
American Journal of Respiratory and Critical Care Medicine
|
July 27, 2019
Systemic Amyloidosis Mimicking Lung Cancer
Adam S Fisch, Florian J Fintelmann, Maria L Garcia-Moliner, et al.
Journal of Magnetic Resonance Imaging : JMRI
|
August 30, 2014
Characteristic time courses of cortical and medullary sodium signals measured by noninvasive (23) Na-MRI in rat kidney induced by furosemide
Haiying Liu, Dan Zhou, Maria L Garcia, et al.
Pathogens (Basel, Switzerland)
|
August 4, 2019
Therapeutic Interventions for Countering Leishmaniasis and Chagas's Disease: From Traditional Sources to Nanotechnological Systems
Eliana B Souto, João Dias-Ferreira, Sara A Craveiro, et al.
Assay and Drug Development Technologies
|
December 17, 2010
A pharmacologically validated, high-capacity, functional thallium flux assay for the human Ether-à-go-go related gene potassium channel
William A Schmalhofer, Andrew M Swensen, Brande S Thomas, et al.
Trends in Molecular Medicine
|
December 23, 2015
The 'Omics' of Amyotrophic Lateral Sclerosis
Diana Caballero-Hernandez, Miguel G Toscano, Marta Cejudo-Guillen, et al.
International Journal of Pharmaceutics
|
February 28, 2016
Biopharmaceutical evaluation of epigallocatechin gallate-loaded cationic lipid nanoparticles (EGCG-LNs): In vivo, in vitro and ex vivo studies
Joana F Fangueiro, Ana C Calpena, Beatriz Clares, et al.
Assay and Drug Development Technologies
|
May 13, 2008
A high-capacity membrane potential FRET-based assay for the sodium-coupled glucose co-transporter SGLT1
Adam B Weinglass, Andrew M Swensen, Jessica Liu, et al.
Molecular Pharmacology
|
August 30, 2008
ProTx-II, a selective inhibitor of NaV1.7 sodium channels, blocks action potential propagation in nociceptors
William A Schmalhofer, Jeffrey Calhoun, Rachel Burrows, et al.
Page
of 13