| P50 | author | Lucia Banci | Q21264278 |
| | Francesca Cantini | Q28316949 |
| | Andrea Saponaro | Q89164458 |
| | Bina Santoro | Q89164465 |
| | Matteo E. Mangoni | Q42439630 |
| | Anna Moroni | Q56436877 |
| | Vincenzo Maione | Q59682049 |
| | Pietro Mesirca | Q63928589 |
| P2093 | author name string | Alessandro Porro | |
| | Chiara Donadoni | |
| | Annalisa Bucchi | |
| | Dario DiFrancesco | |
| | Gerhard Thiel | |
| | Bianca Introini | |
| P2860 | cites work | Tetramerization dynamics of C-terminal domain underlies isoform-specific cAMP gating in hyperpolarization-activated cyclic nucleotide-gated channels | Q24293586 |
| | Applications and Challenges for Use of Cell-Penetrating Peptides as Delivery Vectors for Peptide and Protein Cargos | Q26769800 |
| | Fundamental molecular mechanism for the cellular uptake of guanidinium-rich molecules | Q27337839 |
| | Structural basis for modulation and agonist specificity of HCN pacemaker channels | Q27642009 |
| | HADDOCK: a protein-protein docking approach based on biochemical or biophysical information | Q27860814 |
| | Protein backbone angle restraints from searching a database for chemical shift and sequence homology | Q27861108 |
| | Muscarinic modulation of cardiac rate at low acetylcholine concentrations | Q69945253 |
| | Properties of hyperpolarization-activated pacemaker current defined by coassembly of HCN1 and HCN2 subunits and basal modulation by cyclic nucleotide | Q28364054 |
| | Association with the auxiliary subunit PEX5R/Trip8b controls responsiveness of HCN channels to cAMP and adrenergic stimulation | Q28576494 |
| | Structures of the Human HCN1 Hyperpolarization-Activated Channel | Q28975760 |
| | Combined automated NOE assignment and structure calculation with CYANA. | Q30372955 |
| | A reduced mechanical model for cAMP-modulated gating in HCN channels | Q30397292 |
| | Structural basis for the mutual antagonism of cAMP and TRIP8b in regulating HCN channel function | Q34407624 |
| | Direct activation of cardiac pacemaker channels by intracellular cyclic AMP. | Q34580492 |
| | Hyperpolarization-activated cation currents: from molecules to physiological function | Q35019781 |
| | Trafficking and gating of hyperpolarization-activated cyclic nucleotide-gated channels are regulated by interaction with tetratricopeptide repeat-containing Rab8b-interacting protein (TRIP8b) and cyclic AMP at distinct sites | Q35063427 |
| | Unfolded proteins and protein folding studied by NMR. | Q35860163 |
| | Gating of HCN channels by cyclic nucleotides: residue contacts that underlie ligand binding, selectivity, and efficacy | Q36016444 |
| | Cell-Penetrating Peptides: From Basic Research to Clinics | Q36283554 |
| | Voltage sensor movement and cAMP binding allosterically regulate an inherently voltage-independent closed-open transition in HCN channels | Q36299682 |
| | Salt bridges and gating in the COOH-terminal region of HCN2 and CNGA1 channels | Q36445761 |
| | A secondary structural transition in the C-helix promotes gating of cyclic nucleotide-regulated ion channels | Q36812460 |
| | TRIP8b splice variants form a family of auxiliary subunits that regulate gating and trafficking of HCN channels in the brain. | Q37288658 |
| | Binding of the auxiliary subunit TRIP8b to HCN channels shifts the mode of action of cAMP | Q37343871 |
| | HCN2 ion channels: an emerging role as the pacemakers of pain | Q38011927 |
| | Peptide therapeutics: current status and future directions | Q38275750 |
| | Mechanism for the inhibition of the cAMP dependence of HCN ion channels by the auxiliary subunit TRIP8b. | Q38597175 |
| | The Current State of Peptide Drug Discovery: Back to the Future? | Q38652744 |
| | Structural mechanism for the regulation of HCN ion channels by the accessory protein TRIP8b | Q39539572 |
| | Pacemaker mechanisms in cardiac tissue. | Q40486018 |
| | TRIP8b regulates HCN1 channel trafficking and gating through two distinct C-terminal interaction sites. | Q41894685 |
| | Allostery between two binding sites in the ion channel subunit TRIP8b confers binding specificity to HCN channels. | Q47773861 |
| | Protein kinase A regulates inflammatory pain sensitization by modulating HCN2 channel activity in nociceptive sensory neurons | Q48000237 |
| | Dual allosteric modulation of pacemaker (f) channels by cAMP and voltage in rabbit SA node. | Q52223109 |
| | Molecular mechanism of cAMP modulation of HCN pacemaker channels. | Q53889028 |
| | Identification by NMR of the binding surface for the histidine-containing phosphocarrier protein HPr on the N-terminal domain of enzyme I of the Escherichia coli phosphotransferase system. | Q54567671 |
| | Properties of the hyperpolarizing-activated current (if) in cells isolated from the rabbit sino-atrial node | Q57980198 |
| P407 | language of work or name | English | Q1860 |
| P577 | publication date | 2018-06-20 | |
| P1433 | published in | eLife | Q2000008 |
| P1476 | title | A synthetic peptide that prevents cAMP regulation in mammalian hyperpolarization-activated cyclic nucleotide-gated (HCN) channels | |
| P478 | volume | 7 | |