scholarly article | Q13442814 |
P2093 | author name string | Saverio Gentile | |
P2860 | cites work | A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome | Q24316980 |
The protein kinase complement of the human genome | Q24324497 | ||
Rac GTPase signaling through the PP5 protein phosphatase | Q24546372 | ||
Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism | Q28117072 | ||
Rapid signaling at the plasma membrane by a nuclear receptor for thyroid hormone | Q28303035 | ||
Modulation of rat erg1, erg2, erg3 and HERG K+ currents by thyrotropin-releasing hormone in anterior pituitary cells via the native signal cascade | Q28361745 | ||
Peptide and protein library screening defines optimal substrate motifs for AKT/PKB. | Q30652695 | ||
Structural basis of protein kinase C isoform function | Q33973406 | ||
Ion Channel Voltage Sensors: Structure, Function, and Pathophysiology | Q34139997 | ||
Long QT syndrome: cellular basis and arrhythmia mechanism in LQT2. | Q34150435 | ||
Kinetic and catalytic mechanisms of protein kinases | Q34465987 | ||
Cyclosporin and Timothy syndrome increase mode 2 gating of CaV1.2 calcium channels through aberrant phosphorylation of S6 helices | Q34944217 | ||
Inherited neuronal ion channelopathies: new windows on complex neurological diseases | Q35226085 | ||
Realistic simulation of the activation of voltage-gated ion channels | Q35807726 | ||
The human ERG1 channel polymorphism, K897T, creates a phosphorylation site that inhibits channel activity | Q36936368 | ||
Channelopathies: a review | Q37060980 | ||
Potassium channel phosphorylation in excitable cells: providing dynamic functional variability to a diverse family of ion channels | Q37082375 | ||
The role of calmodulin kinase II in myocardial physiology and disease | Q37192039 | ||
Genetics and cardiac channelopathies. | Q37729709 | ||
Thyroid hormone receptor TRbeta1 mediates Akt activation by T3 in pancreatic beta cells. | Q40172304 | ||
Voltage-gated ion channels and electrical excitability | Q41737177 | ||
Common Genetic Variation in KCNH2 Is Associated With QT Interval Duration | Q57072945 | ||
P433 | issue | 10 | |
P304 | page(s) | 1757-1761 | |
P577 | publication date | 2012-08-24 | |
P1433 | published in | ChemMedChem | Q2962252 |
P1476 | title | Ion channel phosphorylopathy: a link between genomic variation and human disease | |
P478 | volume | 7 |
Q38465804 | Identification of drug targets related to the induction of ventricular tachyarrhythmia through a systems chemical biology approach |
Q40639170 | Isoform-specific dynamic translocation of PKC by α1-adrenoceptor stimulation in live cells |
Q51119613 | Roles of PKC Isoforms in PMA-Induced Modulation of the hERG Channel (Kv11.1). |
Search more.