| P2093 | author name string | Sandip Patel | |
| | Christopher J Penny | |
| P2860 | cites work | The Structure of the Potassium Channel: Molecular Basis of K+ Conduction and Selectivity | Q22337058 |
| | Dysregulation of lysosomal morphology by pathogenic LRRK2 is corrected by TPC2 inhibition | Q24307004 |
| | Essential requirement for two-pore channel 1 in NAADP-mediated calcium signaling | Q24316454 |
| | NAADP mobilizes calcium from acidic organelles through two-pore channels | Q24318546 |
| | Two-pore channels form homo- and heterodimers | Q24337485 |
| | TPC2 is a novel NAADP-sensitive Ca2+ release channel, operating as a dual sensor of luminal pH and Ca2+ | Q24621022 |
| | Pharmacological properties of the Ca2+-release mechanism sensitive to NAADP in the sea urchin egg | Q24672945 |
| | The crystal structure of a voltage-gated sodium channel | Q27670752 |
| | Structure of a bacterial voltage-gated sodium channel pore reveals mechanisms of opening and closing | Q27674040 |
| | Crystal structure of an orthologue of the NaChBac voltage-gated sodium channel | Q27679539 |
| | Structure of a Prokaryotic Sodium Channel Pore Reveals Essential Gating Elements and an Outer Ion Binding Site Common to Eukaryotic Channels | Q27680241 |
| | Two alternative conformations of a voltage-gated sodium channel | Q27685182 |
| | Two-pore channels at the intersection of endolysosomal membrane traffic | Q28085768 |
| | Coordination of agonist-induced Ca2+-signalling patterns by NAADP in pancreatic acinar cells | Q28138792 |
| | NAADP mobilizes Ca(2+) from reserve granules, lysosome-related organelles, in sea urchin eggs | Q28216586 |
| | High susceptibility to fatty liver disease in two-pore channel 2-deficient mice | Q28246421 |
| | Domain assembly of NAADP-gated two-pore channels | Q28250269 |
| | Crystal structure of a mammalian voltage-dependent Shaker family K+ channel | Q28260421 |
| | Expression of Ca²⁺-permeable two-pore channels rescues NAADP signalling in TPC-deficient cells | Q28260464 |
| | Membrane potential regulates nicotinic acid adenine dinucleotide phosphate (NAADP) dependence of the pH- and Ca2+-sensitive organellar two-pore channel TPC1 | Q28264441 |
| | TPC proteins are phosphoinositide- activated sodium-selective ion channels in endosomes and lysosomes | Q28276964 |
| | Unique inactivation properties of NAADP-sensitive Ca2+ release | Q28281723 |
| | Characterization of two-pore channel 2 (TPCN2)-mediated Ca2+ currents in isolated lysosomes | Q28283147 |
| | An NAADP-gated two-pore channel targeted to the plasma membrane uncouples triggering from amplifying Ca2+ signals | Q28294394 |
| | Two-pore channels (TPCs): current controversies | Q28302766 |
| | Convergent regulation of the lysosomal two-pore channel-2 by Mg²⁺, NAADP, PI(3,5)P₂ and multiple protein kinases | Q28307378 |
| | The two-pore channel TPCN2 mediates NAADP-dependent Ca(2+)-release from lysosomal stores | Q28585336 |
| | The versatility and universality of calcium signalling | Q29547402 |
| | The voltage-gated sodium channel TPC1 confers endolysosomal excitability. | Q30810815 |
| | Purified TPC isoforms form NAADP receptors with distinct roles for Ca(2+) signaling and endolysosomal trafficking | Q33816664 |
| | Ebola virus. Two-pore channels control Ebola virus host cell entry and are drug targets for disease treatment | Q34464824 |
| | Overview of molecular relationships in the voltage-gated ion channel superfamily. | Q34480285 |
| | International Union of Pharmacology. L. Nomenclature and structure-function relationships of CatSper and two-pore channels. | Q34480298 |
| | The Two-pore channel (TPC) interactome unmasks isoform-specific roles for TPCs in endolysosomal morphology and cell pigmentation | Q34583526 |
| | Membrane topology of NAADP-sensitive two-pore channels and their regulation by N-linked glycosylation. | Q34685254 |
| | Transient receptor potential mucolipin 1 (TRPML1) and two-pore channels are functionally independent organellar ion channels | Q35067713 |
| | Two-pore channels provide insight into the evolution of voltage-gated Ca2+ and Na+ channels. | Q35082699 |
| | NAADP on target | Q37997679 |
| | A primer of NAADP-mediated Ca(2+) signalling: From sea urchin eggs to mammalian cells | Q38275522 |
| | Coupling acidic organelles with the ER through Ca²⁺ microdomains at membrane contact sites. | Q38417593 |
| | Questioning regulation of two-pore channels by NAADP | Q39515801 |
| | Outer pore architecture of a Ca2+-selective TRP channel | Q40596874 |
| | Control by asparagine residues of calcium permeability and magnesium blockade in the NMDA receptor | Q41603790 |
| | Two pore channel 2 (TPC2) inhibits autophagosomal-lysosomal fusion by alkalinizing lysosomal pH. | Q41820235 |
| | Nicotinic acid adenine dinucleotide phosphate (NAADP) regulates autophagy in cultured astrocytes | Q41891896 |
| | Direct mobilisation of lysosomal Ca2+ triggers complex Ca2+ signals | Q42959504 |
| | pH-dependent regulation of lysosomal calcium in macrophages | Q43893449 |
| | A computational model of lysosome-ER Ca2+ microdomains. | Q50672345 |
| | The N-terminal region of two-pore channel 1 regulates trafficking and activation by NAADP. | Q50746326 |
| | Calcium signaling: NAADP ascends as a new messenger | Q73086519 |
| | Acidic Ca(2+) stores come to the fore | Q83879499 |
| | Role of TRPML and two-pore channels in endolysosomal cation homeostasis | Q83938128 |
| | Degeneration of an intracellular ion channel in the primate lineage by relaxation of selective constraints | Q84209506 |
| P433 | issue | 1 | |
| P304 | page(s) | 46-52 | |
| P577 | publication date | 2015-06-01 | |
| P1433 | published in | Messenger (Los Angeles, Calif. : Print) | Q27724829 |
| P1476 | title | Poring over two-pore channel pore mutants | |
| P478 | volume | 4 | |