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Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 825 - 12
STIM1 and Orai1 are key components of the Ca2+-release activated Ca2+ (CRAC) current. Orai1, which represents the subunit forming the CRAC channel complex, is... 
CHANNEL FUNCTION | OPERATED CALCIUM-ENTRY | ORAI CHANNELS | MULTIDISCIPLINARY SCIENCES | MUTATION | CA2+ SENSOR | STORE | INTERACTION MOLECULE-1 STIM1 | PLASMA-MEMBRANE | SAM DOMAIN | CRAC CHANNEL | Calcium - metabolism | Dyslexia - metabolism | Humans | Dyslexia - pathology | Green Fluorescent Proteins - genetics | Calcium - chemistry | ORAI1 Protein - chemistry | Migraine Disorders - pathology | Stromal Interaction Molecule 1 - chemistry | Neoplasm Proteins - genetics | Binding Sites | Blood Platelet Disorders - genetics | ORAI1 Protein - metabolism | Amino Acid Sequence | Gene Expression | Models, Molecular | Recombinant Proteins - chemistry | Neoplasm Proteins - chemistry | Patch-Clamp Techniques | Migraine Disorders - genetics | Miosis - pathology | Luminescent Proteins - genetics | Muscle Fatigue - genetics | Miosis - metabolism | Blood Platelet Disorders - pathology | Ichthyosis - metabolism | Protein Multimerization | Erythrocytes, Abnormal - metabolism | Neoplasm Proteins - metabolism | Stromal Interaction Molecule 1 - genetics | Migraine Disorders - metabolism | Ichthyosis - pathology | Miosis - genetics | HEK293 Cells | Ichthyosis - genetics | Ion Transport | Protein Interaction Domains and Motifs | Spleen - pathology | Genes, Reporter | Recombinant Proteins - metabolism | Green Fluorescent Proteins - metabolism | Protein Conformation, alpha-Helical | ORAI1 Protein - genetics | Bacterial Proteins - genetics | Gene Expression Regulation | Recombinant Proteins - genetics | Spleen - abnormalities | Dyslexia - genetics | Point Mutation | Stromal Interaction Molecule 1 - metabolism | Erythrocytes, Abnormal - pathology | Spleen - metabolism | Protein Binding | Bacterial Proteins - metabolism | Blood Platelet Disorders - metabolism | Amino Acid Substitution | Luminescent Proteins - metabolism | Calcium channels | STIM1 protein | Activation | Exposure | Orai1 protein | Elongation | Calcium ions
Journal Article
The Journal of Physiology, ISSN 0022-3751, 11/2008, Volume 586, Issue 22, pp. 5383 - 5401
Ca2+ entry through store‐operated Ca2+ release‐activated Ca2+ (CRAC) channels initiates key functions such as gene expression and exocytosis of inflammatory... 
PHYSIOLOGY | 2-AMINOETHOXYDIPHENYL BORATE | STIM1 | STROMAL INTERACTION MOLECULE-1 | OPERATED CALCIUM-CHANNELS | ACTIVATED CA2+ CHANNELS | STORE DEPLETION | OLIGOMERIZATION | PLASMA-MEMBRANE | NEUROSCIENCES | CRAC CHANNEL | T-LYMPHOCYTES | Protein Subunits | Calcium Channels - metabolism | Humans | Multiprotein Complexes | Bacterial Proteins - chemistry | Endoplasmic Reticulum - metabolism | Green Fluorescent Proteins - genetics | Neoplasm Proteins - metabolism | Recombinant Fusion Proteins - metabolism | Protein Structure, Quaternary | Fluorescence Resonance Energy Transfer | Luminescent Proteins - chemistry | Severe Combined Immunodeficiency - metabolism | Membrane Proteins - metabolism | Protein Interaction Domains and Motifs | Green Fluorescent Proteins - chemistry | Neoplasm Proteins - genetics | Calcium Channels - genetics | Calcium Signaling | Stromal Interaction Molecule 1 | Cell Line | Green Fluorescent Proteins - metabolism | Mutagenesis, Site-Directed | Membrane Proteins - genetics | Bacterial Proteins - genetics | Neoplasm Proteins - chemistry | Recombinant Fusion Proteins - chemistry | ORAI1 Protein | Severe Combined Immunodeficiency - genetics | Membrane Proteins - chemistry | Calcium Channels - chemistry | Recombinant Fusion Proteins - genetics | Bacterial Proteins - metabolism | Luminescent Proteins - genetics | Protein Conformation | Ion Channel Gating | Luminescent Proteins - metabolism | Fluorescence | Physiological aspects | Gene expression | Index Medicus | Cellular
Journal Article
Annual Review of Biochemistry, ISSN 0066-4154, 6/2017, Volume 86, Issue 1, pp. 659 - 684
The endoplasmic reticulum (ER) has a broad localization throughout the cell and forms direct physical contacts with all other classes of membranous organelles,... 
stromal interaction molecule | PITP | extended synaptotagmins | STIM | phosphatidylinositol transfer protein | modulator | release-activated Ca | ORP | lipid transfer protein | oxysterol-binding protein (OSBP)-related protein | Orai | Stromal interaction molecule | Oxysterol-binding protein (OSBP)-related protein | Lipid transfer protein | Phosphatidylinositol transfer protein | Extended synaptotagmins | LIPID TRANSFER | OPERATED CA2+ ENTRY | OXYSTEROL-BINDING PROTEINS | BIOCHEMISTRY & MOLECULAR BIOLOGY | Ca2+ release-activated Ca2+ modulator | ER-PM | CALCIUM-ENTRY | PHOSPHATIDIC-ACID | PHOSPHOLIPID TRANSFER PROTEIN | INTERACTION MOLECULE-1 STIM1 | PHOSPHATIDYLINOSITOL-TRANSFER PROTEIN | Receptors, Steroid - metabolism | Calcium - metabolism | Humans | Endoplasmic Reticulum - metabolism | Homeostasis | Eukaryotic Cells - metabolism | Neoplasm Proteins - metabolism | Endoplasmic Reticulum - ultrastructure | Stromal Interaction Molecule 1 - genetics | Biological Transport | Eukaryotic Cells - ultrastructure | Cell Membrane - metabolism | Membrane Proteins - metabolism | Neoplasm Proteins - genetics | Calcium Signaling | ORAI1 Protein - metabolism | Gene Expression | ORAI1 Protein - genetics | Membrane Proteins - genetics | Cell Membrane - ultrastructure | Carrier Proteins - genetics | Stromal Interaction Molecule 1 - metabolism | Synaptotagmins - metabolism | Carrier Proteins - metabolism | Receptors, Steroid - genetics | Synaptotagmins - genetics | Physiological aspects | Cell membranes | Genetic aspects | Cellular signal transduction | Endoplasmic reticulum
Journal Article
Journal Article
Journal of Cellular Physiology, ISSN 0021-9541, 12/2017, Volume 232, Issue 12, pp. 3496 - 3509
An upregulation of Egr‐1 expression has been reported in models of atherosclerosis and intimal hyperplasia and, various vasoactive peptides and growth... 
Egr‐1 | Orai‐1 | CREB | STIM‐1 | angiotensin‐II | Egr-1 | angiotensin-II | Orai-1 | STIM-1 | CA2+ ENTRY | PHYSIOLOGY | ELEMENT-BINDING PROTEIN | NEOINTIMA FORMATION | KINASE-II | CELL BIOLOGY | SIGNAL-TRANSDUCTION | FIBROBLAST GROWTH FACTOR-2 | OPERATED CALCIUM-ENTRY | INOSITOL TRISPHOSPHATE RECEPTOR | INTERACTION MOLECULE-1 STIM1 | UP-REGULATION | Up-Regulation | Phosphorylation | Muscle, Smooth, Vascular - metabolism | Extracellular Signal-Regulated MAP Kinases - metabolism | Stromal Interaction Molecule 1 - genetics | Dose-Response Relationship, Drug | Transfection | RNA Interference | Time Factors | Inositol 1,4,5-Trisphosphate Receptors - metabolism | Early Growth Response Protein 1 - genetics | Inositol 1,4,5-Trisphosphate Receptors - antagonists & inhibitors | Myocytes, Smooth Muscle - drug effects | Myocytes, Smooth Muscle - metabolism | Calcium-Calmodulin-Dependent Protein Kinase Type 2 - metabolism | Muscle, Smooth, Vascular - drug effects | ORAI1 Protein - metabolism | Cell Line | Angiotensin II - pharmacology | Calmodulin - metabolism | ORAI1 Protein - genetics | Rats | Calcium Channel Blockers - pharmacology | Calcium-Calmodulin-Dependent Protein Kinase Type 2 - antagonists & inhibitors | Stromal Interaction Molecule 1 - metabolism | Animals | Calcium Signaling - drug effects | Cyclic AMP Response Element-Binding Protein - metabolism | Protein Kinase Inhibitors - pharmacology | Calmodulin - antagonists & inhibitors | Early Growth Response Protein 1 - metabolism | Calcium-binding proteins | Angiotensin | Phosphates | Calcium | Peptides | Pathogenesis | Hyperplasia | STIM1 protein | Smooth muscle | Activation | mRNA | Calcium signalling | Vascular diseases | Vasoactive agents | Calcium-binding protein | Atherosclerosis | Angiotensin II | Calmodulin | Inositol 1,4,5-trisphosphate receptors | Calcium (intracellular) | EGR-1 protein | RNA-mediated interference | Extracellular signal-regulated kinase | siRNA | Cyclic AMP response element-binding protein | Gene expression | Depletion | Ribonucleic acids | Arteriosclerosis | Ca2+/calmodulin-dependent protein kinase II | Index Medicus
Journal Article
Oncogene, ISSN 0950-9232, 01/2019, Volume 38, Issue 1, pp. 120 - 139
Glioblastomas (GBM) are the most aggressive brain cancers without effective therapeutics. The Hippo pathway transcriptional coactivators YAP/TAZ were... 
PROTEIN-KINASE-C | ACTIVATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | YAP | CELL-PROLIFERATION | TAZ | 2-AMINOETHYLDIPHENYL BORATE | CELL BIOLOGY | AMLODIPINE | STIM1 | ONCOLOGY | CA2 | GENETICS & HEREDITY | CHANNELS | Protein Kinases - metabolism | RNA, Small Interfering - genetics | Calcium - metabolism | Calcium Signaling - physiology | Humans | Neoplasm Proteins - physiology | Endoplasmic Reticulum - metabolism | Neoplasm Proteins - antagonists & inhibitors | Phosphoproteins - antagonists & inhibitors | Gene Knockdown Techniques | Protein Processing, Post-Translational - drug effects | Adaptor Proteins, Signal Transducing - antagonists & inhibitors | Endoplasmic Reticulum - drug effects | Female | Glioblastoma - metabolism | Phosphorylation - drug effects | Recombinant Proteins - metabolism | ORAI1 Protein - genetics | Protein-Serine-Threonine Kinases - physiology | Transcription Factors - antagonists & inhibitors | Phosphoproteins - genetics | Transcription Factors - genetics | Calcium Channel Blockers - pharmacology | Enzyme Activation - drug effects | ORAI1 Protein - physiology | Animals | Signal Transduction - drug effects | Calcium Signaling - drug effects | Mice, Nude | ORAI1 Protein - antagonists & inhibitors | Glioblastoma - pathology | Adaptor Proteins, Signal Transducing - genetics | Amlodipine - pharmacology | Cell Line, Tumor | Ionomycin - pharmacology | Thapsigargin - pharmacology | Signal Transduction - physiology | Mice | Protein Kinase C beta - physiology | Glioblastoma - drug therapy | Care and treatment | Transcription factors | Development and progression | Genetic aspects | Cellular signal transduction | Gene expression | Glioblastoma multiforme | Health aspects | Phosphorylation | Protein kinase C | Calcium (intracellular) | Cell survival | Transcription | Therapeutic applications | Glioblastoma | Kinases | Calcium influx |