| P50 | author | Bertil Hille | Q202480 |
| | Liangyi Chen | Q55641102 |
| | Joseph G Duman | Q74428312 |
| P2093 | author name string | Eamonn J Dickson | |
| | Mark W Moody | |
| P2860 | cites work | Orai1 is an essential pore subunit of the CRAC channel | Q24300383 |
| | STIM1 clusters and activates CRAC channels via direct binding of a cytosolic domain to Orai1 | Q24315782 |
| | A mutation in Orai1 causes immune deficiency by abrogating CRAC channel function | Q28305026 |
| | Application of Improved Wavelet Transform in Biological Particle Detection* | Q58207995 |
| | Contributions of Intracellular Compartments to Calcium Dynamics: Implicating an Acidic Store | Q58208016 |
| | Role of Ca2+/K+ ion exchange in intracellular storage and release of Ca2+ | Q59095257 |
| | The molecular organization of adrenal chromaffin granules | Q71374039 |
| | Signal flows from two phospholipase C-linked receptors are independent in PC12 cells | Q72557655 |
| | Mouse mast cell secretory granules can function as intracellular ionic oscillators | Q28363682 |
| | A model for receptor-regulated calcium entry | Q29620427 |
| | STIMulating store-operated Ca(2+) entry | Q30489311 |
| | Cytosolic Ca2+ prevents the subplasmalemmal clustering of STIM1: an intrinsic mechanism to avoid Ca2+ overload | Q30581095 |
| | Molecular spectroscopy and dynamics of intrinsically fluorescent proteins: coral red (dsRed) and yellow (Citrine). | Q30950919 |
| | Kinetics of PIP2 metabolism and KCNQ2/3 channel regulation studied with a voltage-sensitive phosphatase in living cells | Q33615029 |
| | Molecular basis of calcium signaling in lymphocytes: STIM and ORAI | Q33819323 |
| | Essential role for the CRAC activation domain in store-dependent oligomerization of STIM1. | Q33881690 |
| | ATP-independent luminal oscillations and release of Ca2+ and H+ from mast cell secretory granules: implications for signal transduction | Q34182292 |
| | Acidocalcisomes - conserved from bacteria to man. | Q34398973 |
| | Imaging direct, dynamin-dependent recapture of fusing secretory granules on plasma membrane lawns from PC12 cells | Q34430018 |
| | Orai1 contributes to the establishment of an apoptosis-resistant phenotype in prostate cancer cells. | Q34545497 |
| | STIM1 and STIM2 are located in the acidic Ca2+ stores and associates with Orai1 upon depletion of the acidic stores in human platelets | Q34752168 |
| | Secretory granules are recaptured largely intact after stimulated exocytosis in cultured endocrine cells. | Q34763388 |
| | Molecular physiology of the SERCA and SPCA pumps | Q35051259 |
| | Orai1-mediated I (CRAC) is essential for neointima formation after vascular injury. | Q35188746 |
| | Local cytosolic Ca2+ elevations are required for stromal interaction molecule 1 (STIM1) de-oligomerization and termination of store-operated Ca2+ entry | Q35378683 |
| | Local Ca2+ signals in cellular signalling | Q35752804 |
| | Dense core secretory vesicles revealed as a dynamic Ca(2+) store in neuroendocrine cells with a vesicle-associated membrane protein aequorin chimaera. | Q36293994 |
| | Rapid inactivation of depletion-activated calcium current (ICRAC) due to local calcium feedback | Q36411634 |
| | Calcium transport mechanisms of PC12 cells. | Q36517762 |
| | Short pulses of acetylcholine stimulation induce cytosolic Ca2+ signals that are excluded from the nuclear region in pancreatic acinar cells | Q36816532 |
| | Evidence that zymogen granules are not a physiologically relevant calcium pool. Defining the distribution of inositol 1,4,5-trisphosphate receptors in pancreatic acinar cells | Q36851752 |
| | Bcl-2-mediated alterations in endoplasmic reticulum Ca2+ analyzed with an improved genetically encoded fluorescent sensor | Q37700695 |
| | Role of secretory granules in inositol 1,4,5-trisphosphate-dependent Ca(2+) signaling: from phytoplankton to mammals | Q37822967 |
| | Goblet cells secretion and mucogenesis | Q37918864 |
| | Orai1 and STIM1 are critical for breast tumor cell migration and metastasis | Q39888627 |
| | Inositol 1,4,5-trisphosphate receptors, secretory granules and secretion in endocrine and neuroendocrine cells | Q40542905 |
| | The AP-1 adaptor complex binds to immature secretory granules from PC12 cells, and is regulated by ADP-ribosylation factor | Q41233302 |
| | Low-molecular-weight constituents of isolated insulin-secretory granules. Bivalent cations, adenine nucleotides and inorganic phosphate | Q41791223 |
| | Inositol 1,4,5-trisphosphate-triggered Ca2+ release from bovine adrenal medullary secretory vesicles. | Q41904431 |
| | Ca2+ dynamics in the secretory vesicles of neurosecretory PC12 and INS1 cells | Q42800047 |
| | Mechanisms of pH regulation in the regulated secretory pathway | Q43636961 |
| | pH-dependent regulation of lysosomal calcium in macrophages | Q43893449 |
| | 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 |
| | Calcium requirements for exocytosis do not delimit the releasable neuropeptide pool | Q44346131 |
| | Melanin has a role in Ca2+ homeostasis in human melanocytes. | Q44352751 |
| | Potent inhibition of Ca2+ release-activated Ca2+ channels and T-lymphocyte activation by the pyrazole derivative BTP2. | Q44725330 |
| | Calcium dynamics in catecholamine-containing secretory vesicles | Q46464274 |
| | Recapture after exocytosis causes differential retention of protein in granules of bovine chromaffin cells. | Q50796308 |
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 51 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | E3539-48 | |
| P577 | publication date | 2012-11-26 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Orai-STIM-mediated Ca2+ release from secretory granules revealed by a targeted Ca2+ and pH probe | |
| P478 | volume | 109 | |