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Alessandro Grottesi

Showing results (41-50 of 46) with videos related to

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The Journal of Biological Chemistry|November 13, 2022
Role of the membrane anchor in the regulation of Lck activityNicla Porciello, Deborah Cipria, Giulia Masi, et al.
Plos One|May 20, 2016
A Calsequestrin-1 Mutation Associated with a Skeletal Muscle Disease Alters Sarcoplasmic Ca2+ ReleaseMaria Cristina D'Adamo, Luigi Sforna, Sergio Visentin, et al.
Frontiers in Physiology|February 3, 2015
Novel phenotype associated with a mutation in the KCNA1(Kv1.1) geneMaria C D'Adamo, Constanze Gallenmüller, Ilenio Servettini, et al.
Journal of Medicinal Chemistry|April 3, 2020
Insights into PPARγ Phosphorylation and Its Inhibition MechanismRoberta Montanari, Davide Capelli, Keiko Yamamoto, et al.
Scientific Reports|September 29, 2016
Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsyFederico Sicca, Elena Ambrosini, Maria Marchese, et al.
Human Molecular Genetics|May 6, 2014
Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotypeElena Ambrosini, Federico Sicca, Maria S Brignone, et al.
Pageof 5

Showing results (41-50 of 46) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 46 results.
The Journal of Biological Chemistry|November 13, 2022
Role of the membrane anchor in the regulation of Lck activityNicla Porciello, Deborah Cipria, Giulia Masi, et al.
Plos One|May 20, 2016
A Calsequestrin-1 Mutation Associated with a Skeletal Muscle Disease Alters Sarcoplasmic Ca2+ ReleaseMaria Cristina D'Adamo, Luigi Sforna, Sergio Visentin, et al.
Frontiers in Physiology|February 3, 2015
Novel phenotype associated with a mutation in the KCNA1(Kv1.1) geneMaria C D'Adamo, Constanze Gallenmüller, Ilenio Servettini, et al.
Journal of Medicinal Chemistry|April 3, 2020
Insights into PPARγ Phosphorylation and Its Inhibition MechanismRoberta Montanari, Davide Capelli, Keiko Yamamoto, et al.
Scientific Reports|September 29, 2016
Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsyFederico Sicca, Elena Ambrosini, Maria Marchese, et al.
Human Molecular Genetics|May 6, 2014
Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotypeElena Ambrosini, Federico Sicca, Maria S Brignone, et al.
Pageof 5