| P50 | author | Sandip Patel | Q37379421 |
| P2093 | author name string | Jonathan S Marchant | |
| | Timothy F Walseth | |
| | Yaping Lin-Moshier | |
| P2860 | cites work | Leucine-rich repeat kinase 2 regulates autophagy through a calcium-dependent pathway involving NAADP | Q24293723 |
| | Inwardly rectifying potassium channels: their structure, function, and physiological roles | Q24296441 |
| | 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 |
| | Nicotinate-adenine dinucleotide phosphate-induced Ca(2+)-release does not behave as a Ca(2+)-induced Ca(2+)-release system | Q24534332 |
| | Photoaffinity labeling of high affinity nicotinic acid adenine dinucleotide phosphate (NAADP)-binding proteins in sea urchin egg | Q24600390 |
| | Photoaffinity labeling of nicotinic acid adenine dinucleotide phosphate (NAADP) targets in mammalian cells | Q24600457 |
| | TPC2 is a novel NAADP-sensitive Ca2+ release channel, operating as a dual sensor of luminal pH and Ca2+ | Q24621022 |
| | Nicotinic acid adenine dinucleotide phosphate regulates skeletal muscle differentiation via action at two-pore channels | Q24633669 |
| | Pharmacological disruption of calcium channel trafficking by the alpha2delta ligand gabapentin | Q24656027 |
| | Pharmacological properties of the Ca2+-release mechanism sensitive to NAADP in the sea urchin egg | Q24672945 |
| | Voltage-gated sodium channel-associated proteins and alternative mechanisms of inactivation and block | Q26991734 |
| | Coordination of agonist-induced Ca2+-signalling patterns by NAADP in pancreatic acinar cells | Q28138792 |
| | Spatial control of Ca2+ signaling by nicotinic acid adenine dinucleotide phosphate diffusion and gradients | Q28139670 |
| | Molecular cloning of a novel form (two-repeat) protein related to voltage-gated sodium and calcium channels | Q28141035 |
| | Sperm deliver a new second messenger: NAADP | Q28204936 |
| | NAADP mobilizes Ca(2+) from reserve granules, lysosome-related organelles, in sea urchin eggs | Q28216586 |
| | Voltage-gated potassium channels: regulation by accessory subunits | Q28239190 |
| | Primary sequence and immunological characterization of beta-subunit of high conductance Ca(2+)-activated K+ channel from smooth muscle | Q28243668 |
| | Domain assembly of NAADP-gated two-pore channels | Q28250269 |
| | Membrane potential regulates nicotinic acid adenine dinucleotide phosphate (NAADP) dependence of the pH- and Ca2+-sensitive organellar two-pore channel TPC1 | Q28264441 |
| | Linking NAADP to ion channel activity: a unifying hypothesis | Q28265293 |
| | An ancestral deuterostome family of two-pore channels mediates nicotinic acid adenine dinucleotide phosphate-dependent calcium release from acidic organelles | Q28265825 |
| | Acidic calcium stores open for business: expanding the potential for intracellular Ca2+ signaling | Q28277133 |
| | Activation and inactivation of Ca2+ release by NAADP+ | Q28277642 |
| | Unique inactivation properties of NAADP-sensitive Ca2+ release | Q28281723 |
| | Characterization of two-pore channel 2 (TPCN2)-mediated Ca2+ currents in isolated lysosomes | Q28283147 |
| | Structural determination of a cyclic metabolite of NAD+ with intracellular Ca2+-mobilizing activity | Q28284283 |
| | An NAADP-gated two-pore channel targeted to the plasma membrane uncouples triggering from amplifying Ca2+ signals | Q28294394 |
| | Nicotinic Acid Adenine Dinucleotide Phosphate Analogues Containing Substituted Nicotinic Acid: Effect of Modification on Ca2+ Release | Q42700042 |
| | NAADP binding to its target protein in sea urchin eggs requires phospholipids | Q42815147 |
| | NAADP mobilizes Ca2+ from a thapsigargin-sensitive store in the nuclear envelope by activating ryanodine receptors | Q42917771 |
| | Nicotinic acid adenine dinucleotide phosphate (NAADP(+)) is an essential regulator of T-lymphocyte Ca(2+)-signaling | Q42920018 |
| | Nicotinic acid-adenine dinucleotide phosphate activates the skeletal muscle ryanodine receptor | Q43002260 |
| | Modulation of NAADP (nicotinic acid-adenine dinucleotide phosphate) receptors by K+ ions: evidence for multiple NAADP receptor conformations | Q43003228 |
| | Ca(2+) release induced by cADP-ribose is mediated by FKBP12.6 proteins in mouse bladder smooth muscle | Q43069759 |
| | Prolonged inactivation of nicotinic acid adenine dinucleotide phosphate-induced Ca2+ release mediates a spatiotemporal Ca2+ memory | Q43515742 |
| | NAADP receptors are present and functional in the heart | Q43670733 |
| | A putative two pore channel AtTPC1 mediates Ca(2+) flux in Arabidopsis leaf cells | Q43751036 |
| | Lack of effect of cADP-ribose and NAADP on the activity of skeletal muscle and heart ryanodine receptors | Q43757027 |
| | Role of FKBP12.6 in cADPR-induced activation of reconstituted ryanodine receptors from arterial smooth muscle | Q43917329 |
| | Nicotinic acid adenine dinucleotide phosphate mediates Ca2+ signals and contraction in arterial smooth muscle via a two-pool mechanism | Q44248159 |
| | Ryanodine receptor type I and nicotinic acid adenine dinucleotide phosphate receptors mediate Ca2+ release from insulin-containing vesicles in living pancreatic beta-cells (MIN6). | Q44285317 |
| | Nicotinic acid adenine dinucleotide phosphate potentiates neurite outgrowth | Q45140500 |
| | Calcium-Activated K+ Channels and Calcium-Induced Calcium Release by Slow Vacuolar Ion Channels in Guard Cell Vacuoles Implicated in the Control of Stomatal Closure | Q46244932 |
| | Role of cyclic ADP-ribose in Ca2+-induced Ca2+ release and vasoconstriction in small renal arteries | Q46646165 |
| | The vacuolar Ca2+-activated channel TPC1 regulates germination and stomatal movement | Q48146660 |
| | Characterization of NAADP(+) binding in sea urchin eggs | Q48562730 |
| | Treatment of stroke with a PSD-95 inhibitor in the gyrencephalic primate brain | Q48629603 |
| | The fluorescence protease protection (FPP) assay to determine protein localization and membrane topology. | Q50690888 |
| | NAADP mobilizes calcium from the endoplasmic reticular Ca(2+) store in T-lymphocytes. | Q50698075 |
| | NAADP controls cross-talk between distinct Ca2+ stores in the heart. | Q50700993 |
| | Planar patch clamp approach to characterize ionic currents from intact lysosomes. | Q51552498 |
| | Triggering of Ca2+ signals by NAADP-gated two-pore channels: a role for membrane contact sites? | Q51823379 |
| | Identification of the gene causing mucolipidosis type IV. | Q52165526 |
| | Direct Photoaffinity Labeling of the Kir6.2 Subunit of the ATP-sensitive K+Channel by 8-Azido-ATP | Q58449729 |
| | Inositol trisphosphate induces calcium release from nonmitochondrial stores i sea urchin egg homogenates | Q68945438 |
| | Nicotinate adenine dinucleotide phosphate (NAADP) triggers a specific calcium release system in sea urchin eggs | Q72536435 |
| | Widespread distribution of binding sites for the novel Ca2+-mobilizing messenger, nicotinic acid adenine dinucleotide phosphate, in the brain | Q73019132 |
| | Functional visualization of the separate but interacting calcium stores sensitive to NAADP and cyclic ADP-ribose | Q73198872 |
| | Structural determinants of nicotinic acid adenine dinucleotide phosphate important for its calcium-mobilizing activity | Q73575349 |
| | Identification of a calcium channel modulator using a high throughput yeast two-hybrid screen | Q77463629 |
| | Generation of specific Ca(2+) signals from Ca(2+) stores and endocytosis by differential coupling to messengers | Q79207730 |
| | NAADP as an intracellular messenger regulating lysosomal calcium-release channels | Q82669208 |
| | Nicotinic acid adenine dinucleotide phosphate and cyclic ADP-ribose regulate TRPM2 channels in T lymphocytes | Q83056883 |
| | Acidic Ca(2+) stores come to the fore | Q83879499 |
| | Degeneration of an intracellular ion channel in the primate lineage by relaxation of selective constraints | Q84209506 |
| | Pyridine nucleotide metabolites stimulate calcium release from sea urchin egg microsomes desensitized to inositol trisphosphate | Q28299232 |
| | Cyclic ADP-ribose binds to FK506-binding protein 12.6 to release Ca2+ from islet microsomes | Q28302379 |
| | KATP channels as molecular sensors of cellular metabolism | Q28303315 |
| | Messenger-specific role for nicotinic acid adenine dinucleotide phosphate in neuronal differentiation | Q28305783 |
| | A derivative of NADP mobilizes calcium stores insensitive to inositol trisphosphate and cyclic ADP-ribose | Q28306365 |
| | NAADP induces Ca2+ oscillations via a two-pool mechanism by priming IP3- and cADPR-sensitive Ca2+ stores | Q28366121 |
| | The potassium channel subunit Kvbeta3 interacts with pannexin 1 and attenuates its sensitivity to changes in redox potentials | Q28510336 |
| | NAADP-induced Ca(2+ signaling in response to endothelin is via the receptor subtype B and requires the integrity of lipid rafts/caveolae | Q28572693 |
| | The two-pore channel TPCN2 mediates NAADP-dependent Ca(2+)-release from lysosomal stores | Q28585336 |
| | TPC2 proteins mediate nicotinic acid adenine dinucleotide phosphate (NAADP)- and agonist-evoked contractions of smooth muscle | Q28588920 |
| | Transient receptor potential family members PKD1L3 and PKD2L1 form a candidate sour taste receptor | Q28592962 |
| | The versatility and universality of calcium signalling | Q29547402 |
| | Signals for sorting of transmembrane proteins to endosomes and lysosomes | Q29547469 |
| | Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents | Q29615755 |
| | Reconstitution of lysosomal NAADP-TRP-ML1 signaling pathway and its function in TRP-ML1(-/-) cells | Q30503399 |
| | Molecular properties of inositol 1,4,5-trisphosphate receptors | Q33666650 |
| | Purified TPC isoforms form NAADP receptors with distinct roles for Ca(2+) signaling and endolysosomal trafficking | Q33816664 |
| | TPCs: Endolysosomal channels for Ca2+ mobilization from acidic organelles triggered by NAADP | Q33840138 |
| | Inositol trisphosphate receptor Ca2+ release channels. | Q33983069 |
| | Two-pore channels: Regulation by NAADP and customized roles in triggering calcium signals | Q34065665 |
| | Quantitative proteomics of the Cav2 channel nano-environments in the mammalian brain. | Q34093833 |
| | Release of Ca2+ from a nonmitochondrial intracellular store in pancreatic acinar cells by inositol-1,4,5-trisphosphate | Q34264314 |
| | Acidic NAADP-sensitive calcium stores in the endothelium: agonist-specific recruitment and role in regulating blood pressure | Q34333480 |
| | Coordination of Ca2+ signalling by NAADP. | Q34336886 |
| | Overview of molecular relationships in the voltage-gated ion channel superfamily. | Q34480285 |
| | A transport mechanism for NAADP in a rat basophilic cell line | Q34483087 |
| | Functional biology of the alpha(2)delta subunits of voltage-gated calcium channels | Q34614867 |
| | Cyclic adenosine diphosphate ribose activates ryanodine receptors, whereas NAADP activates two-pore domain channels. | Q34684877 |
| | Membrane topology of NAADP-sensitive two-pore channels and their regulation by N-linked glycosylation. | Q34685254 |
| | Ryanodine receptor calcium release channels | Q34882627 |
| | Triazine dyes are agonists of the NAADP receptor. | Q35047514 |
| | The endoplasmic reticulum: a multifunctional signaling organelle | Q35051249 |
| | Transient receptor potential mucolipin 1 (TRPML1) and two-pore channels are functionally independent organellar ion channels | Q35067713 |
| | Lipid transfer and signaling at organelle contact sites: the tip of the iceberg | Q35141334 |
| | Suppression of inflammatory and neuropathic pain by uncoupling CRMP-2 from the presynaptic Ca²⁺ channel complex | Q35561043 |
| | NAADP-induced Ca2+ release -- a new signalling pathway. | Q35749148 |
| | Regulation of a proteinaceous elicitor-induced Ca2+ influx and production of phytoalexins by a putative voltage-gated cation channel, OsTPC1, in cultured rice cells. | Q35879911 |
| | The sodium channel accessory subunit Navβ1 regulates neuronal excitability through modulation of repolarizing voltage-gated K⁺ channels. | Q35944812 |
| | Emerging role of cyclic ADP-ribose (cADPR) in smooth muscle | Q36020152 |
| | Nicotinic acid adenine dinucleotide phosphate (NAADP)-mediated calcium signaling | Q36217193 |
| | GABA(A) receptor diversity and pharmacology | Q36579576 |
| | ADP-ribosyl cyclase: an enzyme that cyclizes NAD+ into a calcium-mobilizing metabolite | Q36743019 |
| | Multiplicity of protein interactions and functions of the voltage-gated calcium channel beta-subunit. | Q36880873 |
| | NAADP-mediated Ca2+ signaling via type 1 ryanodine receptor in T cells revealed by a synthetic NAADP antagonist | Q37229250 |
| | Investigating cADPR and NAADP in intact and broken cell preparations | Q37292810 |
| | Ryanodine receptor structure: progress and challenges | Q37300766 |
| | Localization and socialization: experimental insights into the functional architecture of IP3 receptors | Q37605803 |
| | Intracellular Ca2+ storage in health and disease: a dynamic equilibrium. | Q37699891 |
| | Associated proteins: The universal toolbox controlling ligand gated ion channel function | Q37719959 |
| | TPC1-SV channels gain shape | Q37860753 |
| | The endo-lysosomal system as an NAADP-sensitive acidic Ca(2+) store: role for the two-pore channels. | Q37870269 |
| | Cyclic ADP-ribose and NAADP: fraternal twin messengers for calcium signaling | Q37904885 |
| | GluN3 subunit-containing NMDA receptors: not just one-trick ponies | Q37975344 |
| | Solubilization of receptors for the novel Ca2+-mobilizing messenger, nicotinic acid adenine dinucleotide phosphate | Q38363072 |
| | Defining nicotinic agonist binding surfaces through photoaffinity labeling | Q38779796 |
| | An N-terminal dileucine motif directs two-pore channels to the tonoplast of plant cells | Q39366914 |
| | Acidic NAADP-releasable Ca(2+) compartments in the megakaryoblastic cell line MEG01. | Q39538658 |
| | NAADP links histamine H1 receptors to secretion of von Willebrand factor in human endothelial cells | Q39583631 |
| | Second messenger signaling: multiple receptors for NAADP. | Q39825378 |
| | Organelle selection determines agonist-specific Ca2+ signals in pancreatic acinar and beta cells | Q40609889 |
| | NAADP: a new second messenger for glucose-induced Ca2+ responses in clonal pancreatic beta cells | Q40672258 |
| | Time sensing by NAADP receptors. | Q41819567 |
| | Nicotinic acid-adenine dinucleotide phosphate mobilizes Ca2+ from a thapsigargin-insensitive pool | Q41865560 |
| | Nicotinic acid adenine dinucleotide phosphate (NAADP) regulates autophagy in cultured astrocytes | Q41891896 |
| | Unique kinetics of nicotinic acid-adenine dinucleotide phosphate (NAADP) binding enhance the sensitivity of NAADP receptors for their ligand | Q42254591 |
| | Regulation by FK506 and rapamycin of Ca2+ release from the sarcoplasmic reticulum in vascular smooth muscle: the role of FK506 binding proteins and mTOR. | Q42681982 |
| | Analogues of the nicotinic acid adenine dinucleotide phosphate (NAADP) antagonist Ned-19 indicate two binding sites on the NAADP receptor | Q42693432 |
| P433 | issue | 1 | |
| P304 | page(s) | 63-76 | |
| P577 | publication date | 2012-06-01 | |
| P1433 | published in | Messenger (Los Angeles, Calif. : Print) | Q27724829 |
| P1476 | title | The Molecular Basis for Ca2+ Signalling by NAADP: Two-Pore Channels in a Complex? | |
| P478 | volume | 1 | |