Nature Reviews Cancer, ISSN 1474-175X, 10/2005, Volume 5, Issue 10, pp. 786 - 795
Recent research has highlighted the fundamental role of the tumour's extracellular metabolic microenvironment in malignant invasion. This microenvironment is...
BREAST-CANCER CELLS | CD44 INTERACTION | EXTRACELLULAR ACIDIFICATION | PERICELLULAR PROTEOLYSIS | RHOA ACTIVATION | ONCOLOGY | AEROBIC GLYCOLYSIS | TUMOR-CELL-MIGRATION | INTRACELLULAR PH | NA-H EXCHANGER | CATHEPSIN-B | Neoplasms - metabolism | Signal Transduction | Neoplasm Invasiveness | Sodium-Hydrogen Exchangers - physiology | Humans | Cation Transport Proteins - physiology | Sodium-Hydrogen Exchangers - chemistry | Neoplasm Metastasis | Animals | Membrane Proteins - chemistry | Membrane Proteins - physiology | Mice | Cation Transport Proteins - chemistry | Neoplasms - pathology | Sodium-Hydrogen Exchanger 1 | Hydrogen-Ion Concentration | Control | Physiological aspects | Genetic aspects | Metastasis | Research | Identification and classification | Risk factors | Oncogenes
BREAST-CANCER CELLS | CD44 INTERACTION | EXTRACELLULAR ACIDIFICATION | PERICELLULAR PROTEOLYSIS | RHOA ACTIVATION | ONCOLOGY | AEROBIC GLYCOLYSIS | TUMOR-CELL-MIGRATION | INTRACELLULAR PH | NA-H EXCHANGER | CATHEPSIN-B | Neoplasms - metabolism | Signal Transduction | Neoplasm Invasiveness | Sodium-Hydrogen Exchangers - physiology | Humans | Cation Transport Proteins - physiology | Sodium-Hydrogen Exchangers - chemistry | Neoplasm Metastasis | Animals | Membrane Proteins - chemistry | Membrane Proteins - physiology | Mice | Cation Transport Proteins - chemistry | Neoplasms - pathology | Sodium-Hydrogen Exchanger 1 | Hydrogen-Ion Concentration | Control | Physiological aspects | Genetic aspects | Metastasis | Research | Identification and classification | Risk factors | Oncogenes
Journal Article
Recent Patents on Anti-Cancer Drug Discovery, ISSN 1574-8928, 2013, Volume 8, Issue 1, pp. 85 - 99
Cancer cells and tissues, regardless of their origin and genetic background, have an aberrant regulation of hydrogen ion dynamics leading to a reversal of the...
HOE642 | NHE1 | pH and cancer | Tumor microenvironment | Cariporide | H | Proton transport in cancer | Invasion | Angiogenesis | Amiloride | Na | exchanger | MDR | Growth factors | proton transport in cancer | CELL STRUCTURES | TUMOR INVASION | Na+/H+ exchanger | growth factors | MYOCARDIAL-INFARCTION | INTRACELLULAR-PH | angiogenesis | ION TRANSLOCATION | MOLECULAR-ORIGINS | SODIUM-HYDROGEN EXCHANGER | invasion | ONCOLOGY | cariporide | PHARMACOLOGY & PHARMACY | EXTRACELLULAR-MATRIX | tumor microenvironment | MELANOMA-CELLS | CATHEPSIN-B
HOE642 | NHE1 | pH and cancer | Tumor microenvironment | Cariporide | H | Proton transport in cancer | Invasion | Angiogenesis | Amiloride | Na | exchanger | MDR | Growth factors | proton transport in cancer | CELL STRUCTURES | TUMOR INVASION | Na+/H+ exchanger | growth factors | MYOCARDIAL-INFARCTION | INTRACELLULAR-PH | angiogenesis | ION TRANSLOCATION | MOLECULAR-ORIGINS | SODIUM-HYDROGEN EXCHANGER | invasion | ONCOLOGY | cariporide | PHARMACOLOGY & PHARMACY | EXTRACELLULAR-MATRIX | tumor microenvironment | MELANOMA-CELLS | CATHEPSIN-B
Journal Article
Biochemical Journal, ISSN 0264-6021, 02/2007, Volume 401, Issue 3, pp. 623 - 633
The mammalian NHE (Na+/H+ exchanger) is a ubiquitously expressed integral membrane protein that regulates intracellular pH by removing a proton in exchange for...
Intracellular pH | exchanger (NHE) | Cation transport | Membrane protein | Structure-function analysis | NhaA | ACTIVATED PROTEIN-KINASE | MYOCARDIAL-INFARCTION | BIOCHEMISTRY & MOLECULAR BIOLOGY | CARBOXYL-TERMINAL REGION | X-RAY-STRUCTURE | ESCHERICHIA-COLI | CALCINEURIN HOMOLOGOUS PROTEIN | intracellular pH | Na+/H+ exchanger (NHE) | SODIUM-HYDROGEN EXCHANGER | structure-function analysis | membrane protein | NA-H EXCHANGE | MOLECULAR-CLONING | cation transport | TRANSMEMBRANE SEGMENT-IV | Sodium-Hydrogen Exchangers - chemistry | Animals | Sodium-Hydrogen Exchangers - metabolism | H+ exchanger (NHE) | CaM, calmodulin | pHi, intracellular pH | Review | CAII, carbonic anhydrase II | NHE, Na+ | ERK1 | H+ exchanger | IL, intracellular loop | structure–function analysis | TM, transmembrane | CHP, calcineurin homologous protein | EL, extracellular loop | ERM, ezrin, radixin and moesin | SERCA, sarcoplasmic | 2, extracellular-signal-regulated kinase 1 | endoplasmic reticulum Ca2+-ATPase | PIP2, phosphatidylinositol 4,5-bisphosphate | Na+ | HSP70, heat-shock protein 70 | MAPK, mitogen-activated protein kinase
Intracellular pH | exchanger (NHE) | Cation transport | Membrane protein | Structure-function analysis | NhaA | ACTIVATED PROTEIN-KINASE | MYOCARDIAL-INFARCTION | BIOCHEMISTRY & MOLECULAR BIOLOGY | CARBOXYL-TERMINAL REGION | X-RAY-STRUCTURE | ESCHERICHIA-COLI | CALCINEURIN HOMOLOGOUS PROTEIN | intracellular pH | Na+/H+ exchanger (NHE) | SODIUM-HYDROGEN EXCHANGER | structure-function analysis | membrane protein | NA-H EXCHANGE | MOLECULAR-CLONING | cation transport | TRANSMEMBRANE SEGMENT-IV | Sodium-Hydrogen Exchangers - chemistry | Animals | Sodium-Hydrogen Exchangers - metabolism | H+ exchanger (NHE) | CaM, calmodulin | pHi, intracellular pH | Review | CAII, carbonic anhydrase II | NHE, Na+ | ERK1 | H+ exchanger | IL, intracellular loop | structure–function analysis | TM, transmembrane | CHP, calcineurin homologous protein | EL, extracellular loop | ERM, ezrin, radixin and moesin | SERCA, sarcoplasmic | 2, extracellular-signal-regulated kinase 1 | endoplasmic reticulum Ca2+-ATPase | PIP2, phosphatidylinositol 4,5-bisphosphate | Na+ | HSP70, heat-shock protein 70 | MAPK, mitogen-activated protein kinase
Journal Article
Canadian Journal of Physiology and Pharmacology, ISSN 0008-4212, 11/2006, Volume 84, Issue 11, pp. 1081 - 1095
In mammalian eukaryotic cells, the Na+/H+ exchanger is a family of membrane proteins that regulates ions fluxes across membranes. Plasma membrane isoforms of...
Phosphorylation | Ischemia | pH regulation | Heart hypertrophy | exchanger | Membrane proteins | heart hypertrophy | HAMSTER LUNG FIBROBLASTS | PHYSIOLOGY | Na+/H+ exchanger | ACTIVATED PROTEIN-KINASE | CALCINEURIN HOMOLOGOUS PROTEIN | GROWTH-FACTOR ACTIVATION | II SIGNAL-TRANSDUCTION | ischemia | membrane proteins | AMILORIDE-SENSITIVE NA&/H | PHARMACOLOGY & PHARMACY | NA-H EXCHANGE | SMOOTH-MUSCLE-CELLS | MOLECULAR-CLONING | RAT VENTRICULAR MYOCYTES | phosphorylation
Phosphorylation | Ischemia | pH regulation | Heart hypertrophy | exchanger | Membrane proteins | heart hypertrophy | HAMSTER LUNG FIBROBLASTS | PHYSIOLOGY | Na+/H+ exchanger | ACTIVATED PROTEIN-KINASE | CALCINEURIN HOMOLOGOUS PROTEIN | GROWTH-FACTOR ACTIVATION | II SIGNAL-TRANSDUCTION | ischemia | membrane proteins | AMILORIDE-SENSITIVE NA&/H | PHARMACOLOGY & PHARMACY | NA-H EXCHANGE | SMOOTH-MUSCLE-CELLS | MOLECULAR-CLONING | RAT VENTRICULAR MYOCYTES | phosphorylation
Journal Article
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 11/2019, Volume 519, Issue 4, pp. 887 - 893
We investigated the effect of the modulation of Na/H exchanger 1 (NHE1) on apoptosis, differentiation, and chemoresistance in acute myeloid leukemia (AML)...
Cytarabine | Leukemia cells | Na/H exchanger 1 | PMA | Acute myeloid leukemia | HMA
Cytarabine | Leukemia cells | Na/H exchanger 1 | PMA | Acute myeloid leukemia | HMA
Journal Article
BBA - Biomembranes, ISSN 0005-2736, 10/2015, Volume 1848, Issue 10, pp. 2385 - 2393
The mammalian Na /H exchanger isoform 1 (NHE1) is a ubiquitously expressed integral membrane protein present in mammalian cells. It is made up of a hydrophobic...
Topology model | Membrane protein | Na+/H+ exchanger | pH regulation | Na + /H + exchanger | Na(+)/H(+) exchanger | MYOCARDIUM | MECHANISM | BIOCHEMISTRY & MOLECULAR BIOLOGY | MODEL | NHE1 ISOFORM | INHIBITION | BIOPHYSICS | AMINO-ACIDS | FUNCTIONAL-ANALYSIS | ANTIPORTER | TRANSMEMBRANE SEGMENT-IV | Amino Acid Sequence | Mutagenesis, Site-Directed | Cricetulus | Models, Chemical | Models, Molecular | Molecular Sequence Data | Sodium-Hydrogen Exchangers - metabolism | Sodium-Hydrogen Exchangers - chemistry | Sodium-Hydrogen Exchangers - ultrastructure | Animals | Protein Binding | Protein Conformation | Binding Sites | CHO Cells
Topology model | Membrane protein | Na+/H+ exchanger | pH regulation | Na + /H + exchanger | Na(+)/H(+) exchanger | MYOCARDIUM | MECHANISM | BIOCHEMISTRY & MOLECULAR BIOLOGY | MODEL | NHE1 ISOFORM | INHIBITION | BIOPHYSICS | AMINO-ACIDS | FUNCTIONAL-ANALYSIS | ANTIPORTER | TRANSMEMBRANE SEGMENT-IV | Amino Acid Sequence | Mutagenesis, Site-Directed | Cricetulus | Models, Chemical | Models, Molecular | Molecular Sequence Data | Sodium-Hydrogen Exchangers - metabolism | Sodium-Hydrogen Exchangers - chemistry | Sodium-Hydrogen Exchangers - ultrastructure | Animals | Protein Binding | Protein Conformation | Binding Sites | CHO Cells
Journal Article
Diabetologia, ISSN 0012-186X, 2018, Volume 61, Issue 3, pp. 722 - 726
Aims/hypothesis Sodium-glucose cotransporter 2 (SGLT2) inhibitors (SGLT2i) constitute a novel class of glucose-lowering (type 2) kidney-targeted agents. We...
Heart failure | Medicine & Public Health | Human Physiology | Sodium | Na + /H + exchanger | Cardiac | Metabolic Diseases | Internal Medicine | Diabetes | SGLT2i | Vasodilation | Na | exchanger | H | Na+/H+ exchanger | NHE-1 | MODEL | FAILURE | HYPERTROPHY | ENDOCRINOLOGY & METABOLISM | EMPAGLIFLOZIN | Glucosides - pharmacology | Sodium-Hydrogen Exchangers - drug effects | Canagliflozin - pharmacology | Sodium-Glucose Transporter 2 - metabolism | Male | Sodium-Glucose Transporter 2 Inhibitors | Sodium - metabolism | Sulfonamides - pharmacology | Sodium-Hydrogen Exchangers - metabolism | Animals | Myocytes, Cardiac - drug effects | Aminopyridines - pharmacology | Myocytes, Cardiac - metabolism | Cytosol - metabolism | Benzhydryl Compounds - pharmacology | Mice | Kidneys | Calcium | Hydrogen | Syngeneic grafts | Na+/H+-exchanging ATPase | Diabetes mellitus | Cardiomyocytes | Phosphocreatine | pH effects | Heart diseases | Binding sites | H+ exchanger | Na+ | Short Communication
Heart failure | Medicine & Public Health | Human Physiology | Sodium | Na + /H + exchanger | Cardiac | Metabolic Diseases | Internal Medicine | Diabetes | SGLT2i | Vasodilation | Na | exchanger | H | Na+/H+ exchanger | NHE-1 | MODEL | FAILURE | HYPERTROPHY | ENDOCRINOLOGY & METABOLISM | EMPAGLIFLOZIN | Glucosides - pharmacology | Sodium-Hydrogen Exchangers - drug effects | Canagliflozin - pharmacology | Sodium-Glucose Transporter 2 - metabolism | Male | Sodium-Glucose Transporter 2 Inhibitors | Sodium - metabolism | Sulfonamides - pharmacology | Sodium-Hydrogen Exchangers - metabolism | Animals | Myocytes, Cardiac - drug effects | Aminopyridines - pharmacology | Myocytes, Cardiac - metabolism | Cytosol - metabolism | Benzhydryl Compounds - pharmacology | Mice | Kidneys | Calcium | Hydrogen | Syngeneic grafts | Na+/H+-exchanging ATPase | Diabetes mellitus | Cardiomyocytes | Phosphocreatine | pH effects | Heart diseases | Binding sites | H+ exchanger | Na+ | Short Communication
Journal Article
Aging, ISSN 1945-4589, 07/2016, Volume 8, Issue 7, pp. 1291 - 1291
Na+/H+ exchanger | Metastasis | Triple-negative breast cancer | triple-negative breast cancer | Na plus /H plus exchanger | metastasis | NEGATIVE BREAST-CANCER | CELL BIOLOGY | GERIATRICS & GERONTOLOGY | Animals | Neoplasm Invasiveness | Triple Negative Breast Neoplasms - metabolism | Humans | Triple Negative Breast Neoplasms - pathology | Sodium-Hydrogen Exchangers - metabolism
Journal Article
International Journal of Molecular Sciences, ISSN 1661-6596, 05/2019, Volume 20, Issue 10, p. 2378
The human Na+/H+ exchanger isoform 1 (NHE1) is a plasma membrane transport protein that plays an important role in pH regulation in mammalian cells. Because of...
ERK (extracellular signal-regulated kinase) | Phosphorylation | Membrane transport | Scaffolding | exchanger | Intrinsically disordered protein | PH regulation | CHRONIC INHIBITION | AMINO-ACIDS SER | intrinsically disordered protein | scaffolding | BIOCHEMISTRY & MOLECULAR BIOLOGY | HEART-FAILURE | INTRACELLULAR PH | pH regulation | CHEMISTRY, MULTIDISCIPLINARY | SODIUM-HYDROGEN EXCHANGER | H+ exchanger | Na+ | membrane transport | MOLECULAR-CLONING | ACTIVATED PROTEIN-KINASES | phosphorylation | SIGNAL-REGULATED KINASE | DEPENDENT ACTIVATION | NA-H EXCHANGER | Na+/H+ exchanger
ERK (extracellular signal-regulated kinase) | Phosphorylation | Membrane transport | Scaffolding | exchanger | Intrinsically disordered protein | PH regulation | CHRONIC INHIBITION | AMINO-ACIDS SER | intrinsically disordered protein | scaffolding | BIOCHEMISTRY & MOLECULAR BIOLOGY | HEART-FAILURE | INTRACELLULAR PH | pH regulation | CHEMISTRY, MULTIDISCIPLINARY | SODIUM-HYDROGEN EXCHANGER | H+ exchanger | Na+ | membrane transport | MOLECULAR-CLONING | ACTIVATED PROTEIN-KINASES | phosphorylation | SIGNAL-REGULATED KINASE | DEPENDENT ACTIVATION | NA-H EXCHANGER | Na+/H+ exchanger
Journal Article
Canadian Journal of Physiology and Pharmacology, ISSN 0008-4212, 11/2006, Volume 84, Issue 11, pp. 1081 - 1095
In mammalian eukaryotic cells, the Na+/H+ exchanger is a family of membrane proteins that regulates ions fluxes across membranes. Plasma membrane isoforms of...
heart hypertrophy | membrane proteins | ischémie | exchanger | protéines membranaires | échangeur Na | pH regulation | phosphorylation | hypertrophie cardiaque | ischemia | régulation du pH | Neoplasms - metabolism | Heart Diseases - metabolism | Allosteric Regulation | Humans | Molecular Conformation | Cell Growth Processes - physiology | Sodium-Hydrogen Exchangers - metabolism | Intercellular Signaling Peptides and Proteins - metabolism | Sodium-Hydrogen Exchangers - chemistry | Animals | Hormones - metabolism | Cation Transport Proteins - metabolism | Isoenzymes - metabolism | Protein Binding | Cell Membrane - metabolism | Protein Processing, Post-Translational | Enzyme Activation | Cell Differentiation - physiology | Sodium-Hydrogen Exchanger 1 | Intracellular Fluid - metabolism | Hydrogen-Ion Concentration | Studies | Proteins | Membranes | Anatomy & physiology | Anemia
heart hypertrophy | membrane proteins | ischémie | exchanger | protéines membranaires | échangeur Na | pH regulation | phosphorylation | hypertrophie cardiaque | ischemia | régulation du pH | Neoplasms - metabolism | Heart Diseases - metabolism | Allosteric Regulation | Humans | Molecular Conformation | Cell Growth Processes - physiology | Sodium-Hydrogen Exchangers - metabolism | Intercellular Signaling Peptides and Proteins - metabolism | Sodium-Hydrogen Exchangers - chemistry | Animals | Hormones - metabolism | Cation Transport Proteins - metabolism | Isoenzymes - metabolism | Protein Binding | Cell Membrane - metabolism | Protein Processing, Post-Translational | Enzyme Activation | Cell Differentiation - physiology | Sodium-Hydrogen Exchanger 1 | Intracellular Fluid - metabolism | Hydrogen-Ion Concentration | Studies | Proteins | Membranes | Anatomy & physiology | Anemia
Journal Article
The Journal of Physiology, ISSN 0022-3751, 02/2019, Volume 597, Issue 3, pp. 849 - 867
Key points Exogenous Na+/H+ exchanger 1 (NHE1) expression stimulated the collective migration of epithelial cell sheets Stimulation with epidermal growth...
NHE1 | Na+/H+ exchanger | collective cell migration | MDCK cells | metastasis | EGF | Na | exchanger | H | ORTHOGONAL ARRAYS | CANCER-CELLS | PHYSIOLOGY | NEUROSCIENCES | INVASION | PDGFR-ALPHA | CHANNELS | EXPRESSION | POLARIZATION | Epidermal growth factor | Metastasis | Carrier proteins | Calcium-binding proteins | Cells | Fluorescence microscopy | Morphogenesis | Embryogenesis | Cysts | Hydrogen | Epithelial cells | Na+/H+-exchanging ATPase | Pseudopodia | Cell migration | Cell adhesion & migration | Cancer
NHE1 | Na+/H+ exchanger | collective cell migration | MDCK cells | metastasis | EGF | Na | exchanger | H | ORTHOGONAL ARRAYS | CANCER-CELLS | PHYSIOLOGY | NEUROSCIENCES | INVASION | PDGFR-ALPHA | CHANNELS | EXPRESSION | POLARIZATION | Epidermal growth factor | Metastasis | Carrier proteins | Calcium-binding proteins | Cells | Fluorescence microscopy | Morphogenesis | Embryogenesis | Cysts | Hydrogen | Epithelial cells | Na+/H+-exchanging ATPase | Pseudopodia | Cell migration | Cell adhesion & migration | Cancer
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 4/2009, Volume 185, Issue 1, pp. 163 - 176
We previously demonstrated that the primary cilium coordinates platelet-derived growth factor (PDGF) receptor (PDGFR)alpha-mediated migration in...
Up regulation | Cell growth | NIH 3T3 cells | Epithelial cells | Interphase | Cell cycle | Fibroblasts | Cell membranes | Cells | Cilia | SIGNAL-TRANSDUCTION | ACTIVATION | SERUM DEPRIVATION | ERM PROTEINS | CELL-MIGRATION | KINASE | INTRACELLULAR PH | GROWTH-FACTOR | MELANOMA-CELLS | NA-H EXCHANGER | CELL BIOLOGY | Cilia - physiology | Cell Line | NIH 3T3 Cells | Up-Regulation | Cation Transport Proteins - antagonists & inhibitors | Receptor, Platelet-Derived Growth Factor alpha - metabolism | Signal Transduction | Sodium-Hydrogen Exchangers - physiology | Amiloride - analogs & derivatives | Cation Transport Proteins - physiology | Platelet-Derived Growth Factor - pharmacology | RNA, Messenger - metabolism | Cell Movement - genetics | Cell Movement - physiology | Cilia - metabolism | Receptor, Platelet-Derived Growth Factor alpha - physiology | Cation Transport Proteins - analysis | Animals | Sodium-Hydrogen Exchangers - analysis | Amiloride - pharmacology | Mice | Sodium-Hydrogen Exchanger 1 | Sodium-Hydrogen Exchangers - antagonists & inhibitors
Up regulation | Cell growth | NIH 3T3 cells | Epithelial cells | Interphase | Cell cycle | Fibroblasts | Cell membranes | Cells | Cilia | SIGNAL-TRANSDUCTION | ACTIVATION | SERUM DEPRIVATION | ERM PROTEINS | CELL-MIGRATION | KINASE | INTRACELLULAR PH | GROWTH-FACTOR | MELANOMA-CELLS | NA-H EXCHANGER | CELL BIOLOGY | Cilia - physiology | Cell Line | NIH 3T3 Cells | Up-Regulation | Cation Transport Proteins - antagonists & inhibitors | Receptor, Platelet-Derived Growth Factor alpha - metabolism | Signal Transduction | Sodium-Hydrogen Exchangers - physiology | Amiloride - analogs & derivatives | Cation Transport Proteins - physiology | Platelet-Derived Growth Factor - pharmacology | RNA, Messenger - metabolism | Cell Movement - genetics | Cell Movement - physiology | Cilia - metabolism | Receptor, Platelet-Derived Growth Factor alpha - physiology | Cation Transport Proteins - analysis | Animals | Sodium-Hydrogen Exchangers - analysis | Amiloride - pharmacology | Mice | Sodium-Hydrogen Exchanger 1 | Sodium-Hydrogen Exchangers - antagonists & inhibitors
Journal Article
Journal of Molecular and Cellular Cardiology, ISSN 0022-2828, 2007, Volume 44, Issue 2, pp. 228 - 237
Abstract The mammalian Na+ /H+ exchanger is a pH regulatory membrane protein that uses the sodium gradient to translocate one intracellular proton in exchange...
Cardiovascular | Promoter | Sodium–hydrogen exchange | Sodium–lithium exchange | Cation binding | Gene splicing | Tissue distribution | pH regulation | Ischemia/reperfusion | Sodium-hydrogen exchange | Sodium-lithium exchange | PIG VENTRICULAR MYOCYTE | PROTEIN-KINASE-C | CARDIAC & CARDIOVASCULAR SYSTEMS | NEONATAL-RAT CARDIOMYOCYTES | SODIUM-LITHIUM COUNTERTRANSPORT | MESSENGER-RNA EXPRESSION | sodium-lithium exchange | H+ EXCHANGER | TRANSMEMBRANE SEGMENT-VII | tissue distribution | CELL BIOLOGY | ischemia/reperfusion | sodium-hydrogen exchange | gene splicing | GENE-EXPRESSION | promoter | HYDROGEN EXCHANGER | NA/H EXCHANGER | cation binding | Sodium-Hydrogen Exchangers - chemistry | Animals | Humans | Myocardium - metabolism | Cloning, Molecular | Sodium-Hydrogen Exchangers - genetics | Sodium-Hydrogen Exchangers - antagonists & inhibitors | Protein Transport | Sodium-Hydrogen Exchangers - metabolism
Cardiovascular | Promoter | Sodium–hydrogen exchange | Sodium–lithium exchange | Cation binding | Gene splicing | Tissue distribution | pH regulation | Ischemia/reperfusion | Sodium-hydrogen exchange | Sodium-lithium exchange | PIG VENTRICULAR MYOCYTE | PROTEIN-KINASE-C | CARDIAC & CARDIOVASCULAR SYSTEMS | NEONATAL-RAT CARDIOMYOCYTES | SODIUM-LITHIUM COUNTERTRANSPORT | MESSENGER-RNA EXPRESSION | sodium-lithium exchange | H+ EXCHANGER | TRANSMEMBRANE SEGMENT-VII | tissue distribution | CELL BIOLOGY | ischemia/reperfusion | sodium-hydrogen exchange | gene splicing | GENE-EXPRESSION | promoter | HYDROGEN EXCHANGER | NA/H EXCHANGER | cation binding | Sodium-Hydrogen Exchangers - chemistry | Animals | Humans | Myocardium - metabolism | Cloning, Molecular | Sodium-Hydrogen Exchangers - genetics | Sodium-Hydrogen Exchangers - antagonists & inhibitors | Protein Transport | Sodium-Hydrogen Exchangers - metabolism
Journal Article