Search research articles
Contact Us
Filters
Showing results (51-60 of 67) with videos related to
Page
of 7
Sort By:
International Journal of Molecular Sciences
|
May 5, 2021
Novel <i>SCN5A</i> p.Val1667Asp Missense Variant Segregation and Characterization in a Family with Severe Brugada Syndrome and Multiple Sudden Deaths
Michelle M Monasky, Emanuele Micaglio, Giuseppe Ciconte, et al.
International Journal of Molecular Sciences
|
November 11, 2022
Alterations of the Sialylation Machinery in Brugada Syndrome
Andrea Ghiroldi, Giuseppe Ciconte, Pasquale Creo, et al.
Journal of Cellular Biochemistry
|
July 19, 2008
Hypoxia-induced modifications in plasma membranes and lipid microdomains in A549 cells and primary human alveolar cells
Laura Botto, Botto Laura, Egidio Beretta, et al.
Cardiovascular Research
|
September 14, 2017
The expression of the rare caveolin-3 variant T78M alters cardiac ion channels function and membrane excitability
Giulia Campostrini, Mattia Bonzanni, Alessio Lissoni, et al.
Frontiers in Pharmacology
|
April 21, 2017
Pharmacological and Biochemical Characterization of TLQP-21 Activation of a Binding Site on CHO Cells
Laura Molteni, Laura Rizzi, Elena Bresciani, et al.
International Journal of Molecular Sciences
|
October 28, 2023
Unravelling Novel <i>SCN5A</i> Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights
Anthony Frosio, Emanuele Micaglio, Ivan Polsinelli, et al.
Pharmacological Research
|
September 17, 2020
Gabapentin treatment in a patient with KCNQ2 developmental epileptic encephalopathy
Maria Virginia Soldovieri, Elena Freri, Paolo Ambrosino, et al.
Free Radical Biology & Medicine
|
April 9, 2017
Simultaneous overexpression of human E5NT and ENTPD1 protects porcine endothelial cells against H<sub>2</sub>O<sub>2</sub>-induced oxidative stress and cytotoxicity in vitro
Elisa Chisci, Marco De Giorgi, Elisa Zanfrini, et al.
Neurobiology of Disease
|
June 25, 2018
A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability
Mattia Bonzanni, Jacopo C DiFrancesco, Raffaella Milanesi, et al.
Journal of Molecular and Cellular Cardiology
|
August 13, 2015
Acetylation mediates Cx43 reduction caused by electrical stimulation
Viviana Meraviglia, Valerio Azzimato, Claudia Colussi, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 67) with videos related to
Sort By:
Page
of 7
International Journal of Molecular Sciences
|
May 5, 2021
Novel <i>SCN5A</i> p.Val1667Asp Missense Variant Segregation and Characterization in a Family with Severe Brugada Syndrome and Multiple Sudden Deaths
Michelle M Monasky, Emanuele Micaglio, Giuseppe Ciconte, et al.
International Journal of Molecular Sciences
|
November 11, 2022
Alterations of the Sialylation Machinery in Brugada Syndrome
Andrea Ghiroldi, Giuseppe Ciconte, Pasquale Creo, et al.
Journal of Cellular Biochemistry
|
July 19, 2008
Hypoxia-induced modifications in plasma membranes and lipid microdomains in A549 cells and primary human alveolar cells
Laura Botto, Botto Laura, Egidio Beretta, et al.
Cardiovascular Research
|
September 14, 2017
The expression of the rare caveolin-3 variant T78M alters cardiac ion channels function and membrane excitability
Giulia Campostrini, Mattia Bonzanni, Alessio Lissoni, et al.
Frontiers in Pharmacology
|
April 21, 2017
Pharmacological and Biochemical Characterization of TLQP-21 Activation of a Binding Site on CHO Cells
Laura Molteni, Laura Rizzi, Elena Bresciani, et al.
International Journal of Molecular Sciences
|
October 28, 2023
Unravelling Novel <i>SCN5A</i> Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights
Anthony Frosio, Emanuele Micaglio, Ivan Polsinelli, et al.
Pharmacological Research
|
September 17, 2020
Gabapentin treatment in a patient with KCNQ2 developmental epileptic encephalopathy
Maria Virginia Soldovieri, Elena Freri, Paolo Ambrosino, et al.
Free Radical Biology & Medicine
|
April 9, 2017
Simultaneous overexpression of human E5NT and ENTPD1 protects porcine endothelial cells against H<sub>2</sub>O<sub>2</sub>-induced oxidative stress and cytotoxicity in vitro
Elisa Chisci, Marco De Giorgi, Elisa Zanfrini, et al.
Neurobiology of Disease
|
June 25, 2018
A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability
Mattia Bonzanni, Jacopo C DiFrancesco, Raffaella Milanesi, et al.
Journal of Molecular and Cellular Cardiology
|
August 13, 2015
Acetylation mediates Cx43 reduction caused by electrical stimulation
Viviana Meraviglia, Valerio Azzimato, Claudia Colussi, et al.
Page
of 7