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The Journal of Physiology
|
April 19, 2003
Heteromeric HCN1-HCN4 channels: a comparison with native pacemaker channels from the rabbit sinoatrial node
Claudia Altomare, Benedetta Terragni, Chiara Brioschi, et al.
Phytomedicine : International Journal of Phytotherapy and Phytopharmacology
|
February 5, 2020
High content screening identifies licoisoflavone A as a bioactive compound of Tongmaiyangxin Pills to restrain cardiomyocyte hypertrophy via activating Sirt3
Rui Guo, Ningning Liu, Hao Liu, et al.
Vascular Pharmacology
|
July 10, 2024
NOD-1 activation increases the spontaneous activity and the I(f) current of murine sinoatrial node cells
Serena Canzolino, Giorgia Bertoli, Samira Bakhouba, et al.
Veterinary Journal (London, England : 1997)
|
September 9, 2010
Multinucleated giant cells with an osteoclast phenotype derived from caprine peripheral blood mononuclear cells
Giuliano Pisoni, Patrizia D'Amelio, Francesca Sassi, et al.
Vascular Pharmacology
|
July 10, 2024
A gain of function mutation in PITX2c gene linked to atrial fibrillation alters mitochondrial function and membrane excitability
Patrizia Benzoni, Lorenzo Da Dalt, Alessandro Cospito, et al.
European Heart Journal
|
February 10, 2017
A gain-of-function mutation in the cardiac pacemaker HCN4 channel increasing cAMP sensitivity is associated with familial Inappropriate Sinus Tachycardia
Mirko Baruscotti, Annalisa Bucchi, Raffaella Milanesi, et al.
Scientific Reports
|
April 16, 2016
INaP selective inhibition reverts precocious inter- and motorneurons hyperexcitability in the Sod1-G93R zebrafish ALS model
Lorena Benedetti, Anna Ghilardi, Elsa Rottoli, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
December 2, 2011
Recessive loss-of-function mutation in the pacemaker HCN2 channel causing increased neuronal excitability in a patient with idiopathic generalized epilepsy
Jacopo C DiFrancesco, Andrea Barbuti, Raffaella Milanesi, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 12, 2011
Deep bradycardia and heart block caused by inducible cardiac-specific knockout of the pacemaker channel gene Hcn4
Mirko Baruscotti, Annalisa Bucchi, Carlo Viscomi, et al.
Vascular Pharmacology
|
July 10, 2024
In-vitro studies of the NaV1.5 S805L Brugada mutation: The resting cell voltage is a critical element in determining the pathological or physiological phenotype of the current
David Molla, Anthony Frosio, Giorgia Bertoli, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 58) with videos related to
Sort By:
Page
of 6
The Journal of Physiology
|
April 19, 2003
Heteromeric HCN1-HCN4 channels: a comparison with native pacemaker channels from the rabbit sinoatrial node
Claudia Altomare, Benedetta Terragni, Chiara Brioschi, et al.
Phytomedicine : International Journal of Phytotherapy and Phytopharmacology
|
February 5, 2020
High content screening identifies licoisoflavone A as a bioactive compound of Tongmaiyangxin Pills to restrain cardiomyocyte hypertrophy via activating Sirt3
Rui Guo, Ningning Liu, Hao Liu, et al.
Vascular Pharmacology
|
July 10, 2024
NOD-1 activation increases the spontaneous activity and the I(f) current of murine sinoatrial node cells
Serena Canzolino, Giorgia Bertoli, Samira Bakhouba, et al.
Veterinary Journal (London, England : 1997)
|
September 9, 2010
Multinucleated giant cells with an osteoclast phenotype derived from caprine peripheral blood mononuclear cells
Giuliano Pisoni, Patrizia D'Amelio, Francesca Sassi, et al.
Vascular Pharmacology
|
July 10, 2024
A gain of function mutation in PITX2c gene linked to atrial fibrillation alters mitochondrial function and membrane excitability
Patrizia Benzoni, Lorenzo Da Dalt, Alessandro Cospito, et al.
European Heart Journal
|
February 10, 2017
A gain-of-function mutation in the cardiac pacemaker HCN4 channel increasing cAMP sensitivity is associated with familial Inappropriate Sinus Tachycardia
Mirko Baruscotti, Annalisa Bucchi, Raffaella Milanesi, et al.
Scientific Reports
|
April 16, 2016
INaP selective inhibition reverts precocious inter- and motorneurons hyperexcitability in the Sod1-G93R zebrafish ALS model
Lorena Benedetti, Anna Ghilardi, Elsa Rottoli, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
December 2, 2011
Recessive loss-of-function mutation in the pacemaker HCN2 channel causing increased neuronal excitability in a patient with idiopathic generalized epilepsy
Jacopo C DiFrancesco, Andrea Barbuti, Raffaella Milanesi, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 12, 2011
Deep bradycardia and heart block caused by inducible cardiac-specific knockout of the pacemaker channel gene Hcn4
Mirko Baruscotti, Annalisa Bucchi, Carlo Viscomi, et al.
Vascular Pharmacology
|
July 10, 2024
In-vitro studies of the NaV1.5 S805L Brugada mutation: The resting cell voltage is a critical element in determining the pathological or physiological phenotype of the current
David Molla, Anthony Frosio, Giorgia Bertoli, et al.
Page
of 6