Annual Review of Pharmacology and Toxicology, ISSN 0362-1642, 2006, Volume 46, Issue 1, pp. 235 - 276
Nitric oxide (NO) is a small, diffusible, lipophilic free radical gas that mediates significant and diverse signaling functions in nearly every organ system in...
Oxidative stress | eNOS | Caveolae | Cyclic GMP | VEGF | S-nitrosylation | Sphingosine 1-phosphate | Vascular signaling | FLUID SHEAR-STRESS | MESSENGER-RNA EXPRESSION | LIGHT-CHAIN PHOSPHATASE | cyclic GMP | LOW-DENSITY-LIPOPROTEIN | GROWTH-FACTOR RECEPTORS | SUPEROXIDE ANION PRODUCTION | VASCULAR SMOOTH-MUSCLE | vascular signaling | sphingosine l-phosphate | PROTEIN-PROTEIN INTERACTIONS | TOXICOLOGY | caveolae | oxidative stress | CORONARY-ARTERY-DISEASE | NEURONAL NO SYNTHASE | Animals | Isoenzymes - metabolism | Humans | Enzyme Inhibitors - pharmacology | Nitric Oxide - physiology | Nitric Oxide Synthase Type III - metabolism | Nitric Oxide - metabolism | Isoenzymes - antagonists & inhibitors | Gene Expression Regulation, Developmental - physiology | Nitric Oxide Synthase Type III - antagonists & inhibitors
Oxidative stress | eNOS | Caveolae | Cyclic GMP | VEGF | S-nitrosylation | Sphingosine 1-phosphate | Vascular signaling | FLUID SHEAR-STRESS | MESSENGER-RNA EXPRESSION | LIGHT-CHAIN PHOSPHATASE | cyclic GMP | LOW-DENSITY-LIPOPROTEIN | GROWTH-FACTOR RECEPTORS | SUPEROXIDE ANION PRODUCTION | VASCULAR SMOOTH-MUSCLE | vascular signaling | sphingosine l-phosphate | PROTEIN-PROTEIN INTERACTIONS | TOXICOLOGY | caveolae | oxidative stress | CORONARY-ARTERY-DISEASE | NEURONAL NO SYNTHASE | Animals | Isoenzymes - metabolism | Humans | Enzyme Inhibitors - pharmacology | Nitric Oxide - physiology | Nitric Oxide Synthase Type III - metabolism | Nitric Oxide - metabolism | Isoenzymes - antagonists & inhibitors | Gene Expression Regulation, Developmental - physiology | Nitric Oxide Synthase Type III - antagonists & inhibitors
Journal Article
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, ISSN 0735-1097, 12/2011, Volume 58, Issue 25, pp. 2683 - 2691
Objectives This paper examined whether nebivolol protects the heart via nitric oxide (NO) synthase and NO-dependent signaling in an in vivo model of acute...
MOLECULAR CHARACTERIZATION | nitric oxide | CARDIAC & CARDIOVASCULAR SYSTEMS | RAT | CARDIOVASCULAR-SYSTEM | neuronal nitric oxide synthase | beta adrenergic receptor | NEBIVOLOL | MECHANISMS | DEFICIENT MICE | cardiac ischemia | HUMAN BETA-3-ADRENERGIC RECEPTOR | endothelial nitric oxide synthase | 3RD-GENERATION BETA-BLOCKER | HUMAN HEART | AGONIST
MOLECULAR CHARACTERIZATION | nitric oxide | CARDIAC & CARDIOVASCULAR SYSTEMS | RAT | CARDIOVASCULAR-SYSTEM | neuronal nitric oxide synthase | beta adrenergic receptor | NEBIVOLOL | MECHANISMS | DEFICIENT MICE | cardiac ischemia | HUMAN BETA-3-ADRENERGIC RECEPTOR | endothelial nitric oxide synthase | 3RD-GENERATION BETA-BLOCKER | HUMAN HEART | AGONIST
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 12/2011, Volume 58, Issue 25, pp. 2683 - 2691
Objectives: This paper examined whether nebivolol protects the heart via nitric oxide (NO) synthase and NO-dependent signaling in an in vivo model of acute...
nitric oxide | adrenergic receptor | endothelial nitric oxide synthase | neuronal nitric oxide synthase | cardiac ischemia | beta
nitric oxide | adrenergic receptor | endothelial nitric oxide synthase | neuronal nitric oxide synthase | cardiac ischemia | beta
Journal Article
Molecular Neurobiology, ISSN 0893-7648, 3/2018, Volume 55, Issue 3, pp. 2645 - 2652
Nitric oxide (NO), a free radical gas, acts as a neurotransmitter or neuromodulator in the central nervous system (CNS). It has been widely explored as a...
Neurology | Neurosciences | Biomedicine | Nitric oxide | Neurobiology | Nitric oxide synthase | Neural stem cells | Proliferation | Neurogenesis | Cell Biology | ADULT NEUROGENESIS | SUBVENTRICULAR ZONE | NEUROSCIENCES | NEURAL STEM-CELLS | GROWTH-FACTOR RECEPTOR | IN-VITRO | CENTRAL-NERVOUS-SYSTEM | DIFFERENTIATION | DENTATE GYRUS | BRAIN | Brain - cytology | Nitric Oxide Synthase - chemistry | Animals | Neurogenesis - physiology | Humans | Brain - enzymology | Nitric Oxide Synthase - physiology | Neural Stem Cells - enzymology | Isoenzymes - physiology | Enzymes | Medical colleges | Neurons | Stem cells | Brain | Neurodegeneration | Medical treatment | Central nervous system | Isoforms | Inflammation | Neuromodulation | Nitric-oxide synthase
Neurology | Neurosciences | Biomedicine | Nitric oxide | Neurobiology | Nitric oxide synthase | Neural stem cells | Proliferation | Neurogenesis | Cell Biology | ADULT NEUROGENESIS | SUBVENTRICULAR ZONE | NEUROSCIENCES | NEURAL STEM-CELLS | GROWTH-FACTOR RECEPTOR | IN-VITRO | CENTRAL-NERVOUS-SYSTEM | DIFFERENTIATION | DENTATE GYRUS | BRAIN | Brain - cytology | Nitric Oxide Synthase - chemistry | Animals | Neurogenesis - physiology | Humans | Brain - enzymology | Nitric Oxide Synthase - physiology | Neural Stem Cells - enzymology | Isoenzymes - physiology | Enzymes | Medical colleges | Neurons | Stem cells | Brain | Neurodegeneration | Medical treatment | Central nervous system | Isoforms | Inflammation | Neuromodulation | Nitric-oxide synthase
Journal Article
Frontiers in Physiology, ISSN 1664-042X, 06/2016, Volume 7, p. 206
The family of nitric oxide synthases (NOS) has significant importance in various physiological mechanisms and is also involved in many pathological processes....
Hypertension | Neuronal nitric oxide synthase | Hydrogen peroxide | Vascular function | Nitric oxide | Atherosclerosis | atherosclerosis | INTERDOMAIN ELECTRON-TRANSFER | vascular function | nitric oxide | PHYSIOLOGY | ENDOTHELIAL DYSFUNCTION | SPONTANEOUSLY HYPERTENSIVE-RATS | NULL MUTANT MICE | hydrogen peroxide | neuronal nitric oxide synthase | SKELETAL-MUSCLE | SMOOTH-MUSCLE | L-ARGININE | HYDROGEN-PEROXIDE | CEREBRAL-BLOOD-FLOW | hypertension | NOS KNOCKOUT MICE | Physiological aspects | Neurons | Nitric Oxide | Hydrogen Peroxide
Hypertension | Neuronal nitric oxide synthase | Hydrogen peroxide | Vascular function | Nitric oxide | Atherosclerosis | atherosclerosis | INTERDOMAIN ELECTRON-TRANSFER | vascular function | nitric oxide | PHYSIOLOGY | ENDOTHELIAL DYSFUNCTION | SPONTANEOUSLY HYPERTENSIVE-RATS | NULL MUTANT MICE | hydrogen peroxide | neuronal nitric oxide synthase | SKELETAL-MUSCLE | SMOOTH-MUSCLE | L-ARGININE | HYDROGEN-PEROXIDE | CEREBRAL-BLOOD-FLOW | hypertension | NOS KNOCKOUT MICE | Physiological aspects | Neurons | Nitric Oxide | Hydrogen Peroxide
Journal Article
Cochrane Database of Systematic Reviews, ISSN 1469-493X, 04/2017, Volume 2017, Issue 4, pp. CD000398 - CD000398
Background Nitric oxide (NO) has multiple effects that may be beneficial in acute stroke, including lowering blood pressure, and promoting reperfusion and...
MIDDLE CEREBRAL-ARTERY | Stroke [drug therapy] | MICE DEFICIENT | Humans | TRANSDERMAL GLYCERYL TRINITRATE | Nitric Oxide Donors [therapeutic use] | Brain Ischemia [drug therapy] | RAPID INTERVENTION | BLOOD-PRESSURE | MEDICINE, GENERAL & INTERNAL | NEURONAL ISOFORM | Enzyme Inhibitors [therapeutic use] | ACUTE ISCHEMIC-STROKE | INFARCTION VOLUME | Arginine [therapeutic use] | RAT-BRAIN | Nitric Oxide Synthase [ antagonists & inhibitors] | ULTRA-ACUTE STROKE | Acute Disease | Nitroglycerin - therapeutic use | Nitric Oxide Synthase - antagonists & inhibitors | Stroke - drug therapy | Enzyme Inhibitors - therapeutic use | Randomized Controlled Trials as Topic | Brain Ischemia - drug therapy | Quality of Life | Nitroglycerin - adverse effects | Nitric Oxide Donors - therapeutic use | Stroke - mortality | Arginine - therapeutic use | Headache - chemically induced | Nitric Oxide Donors - adverse effects | Index Medicus
MIDDLE CEREBRAL-ARTERY | Stroke [drug therapy] | MICE DEFICIENT | Humans | TRANSDERMAL GLYCERYL TRINITRATE | Nitric Oxide Donors [therapeutic use] | Brain Ischemia [drug therapy] | RAPID INTERVENTION | BLOOD-PRESSURE | MEDICINE, GENERAL & INTERNAL | NEURONAL ISOFORM | Enzyme Inhibitors [therapeutic use] | ACUTE ISCHEMIC-STROKE | INFARCTION VOLUME | Arginine [therapeutic use] | RAT-BRAIN | Nitric Oxide Synthase [ antagonists & inhibitors] | ULTRA-ACUTE STROKE | Acute Disease | Nitroglycerin - therapeutic use | Nitric Oxide Synthase - antagonists & inhibitors | Stroke - drug therapy | Enzyme Inhibitors - therapeutic use | Randomized Controlled Trials as Topic | Brain Ischemia - drug therapy | Quality of Life | Nitroglycerin - adverse effects | Nitric Oxide Donors - therapeutic use | Stroke - mortality | Arginine - therapeutic use | Headache - chemically induced | Nitric Oxide Donors - adverse effects | Index Medicus
Journal Article
06/2012
Mammals are well adapted to respond to changes in ambient oxygen concentration (O2) by activating homeostatic physiological and cellular responses which...
Neuronal nitric oxide synthase | Knockout mice | Anemia | Cardiovascular | S-nitrosylation | Hemoglobin | Hypoxia-inducible factor | Hypoxia | 0719
Neuronal nitric oxide synthase | Knockout mice | Anemia | Cardiovascular | S-nitrosylation | Hemoglobin | Hypoxia-inducible factor | Hypoxia | 0719
Dissertation
Reviews in the Neurosciences, ISSN 0334-1763, 02/2015, Volume 26, Issue 1, pp. 105 - 117
Hypoxic or ischemic stress causes many serious brain injuries, including stroke and neonatal hypoxia ischemia encephalopathy. During brain hypoxia ischemia...
hypoxia | brain injury | nitric oxide synthase | ischemia | Hypoxia | Nitric oxide synthase | Ischemia | Brain injury | INDUCIBLE FACTOR-1-ALPHA | DEVELOPING RAT-BRAIN | INOS EXPRESSION | REPERFUSION INJURY | NEUROSCIENCES | CELL-DEATH | S-NITROSYLATION | ATTENUATES NEURONAL APOPTOSIS | CEREBRAL-ARTERY OCCLUSION | SER847 PHOSPHORYLATION | NF-KAPPA-B | Brain Ischemia - enzymology | Animals | Hypoxia, Brain - enzymology | Humans | Brain Ischemia - pathology | Nitric Oxide Synthase - metabolism | Nitric Oxide Synthase Type III - metabolism | Hypoxia, Brain - pathology | Nitric Oxide Synthase Type II - metabolism | Physiological aspects | Cerebral ischemia | Health aspects | Nitric oxide
hypoxia | brain injury | nitric oxide synthase | ischemia | Hypoxia | Nitric oxide synthase | Ischemia | Brain injury | INDUCIBLE FACTOR-1-ALPHA | DEVELOPING RAT-BRAIN | INOS EXPRESSION | REPERFUSION INJURY | NEUROSCIENCES | CELL-DEATH | S-NITROSYLATION | ATTENUATES NEURONAL APOPTOSIS | CEREBRAL-ARTERY OCCLUSION | SER847 PHOSPHORYLATION | NF-KAPPA-B | Brain Ischemia - enzymology | Animals | Hypoxia, Brain - enzymology | Humans | Brain Ischemia - pathology | Nitric Oxide Synthase - metabolism | Nitric Oxide Synthase Type III - metabolism | Hypoxia, Brain - pathology | Nitric Oxide Synthase Type II - metabolism | Physiological aspects | Cerebral ischemia | Health aspects | Nitric oxide
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 10/2012, Volume 109, Issue 41, pp. 16624 - 16629
Nitric oxide (NO) generated by neuronal NO synthase (nNOS) initiates penile erection, but has not been thought to participate in the sustained erection...
Alternative splicing | Phosphorylation | Calcium | Penile erection | Electrical stimulation | Antibodies | Oxides | Smooth muscle | Physiology | Physiological regulation | Phosphoantibody | Smooth muscle relaxation | Gasotransmitter | Cyclic GMP | Endothelial NOS | NNOS | NERVOUS-SYSTEM | ACTIVATION | PROTEIN-KINASE | MULTIDISCIPLINARY SCIENCES | cyclic GMP | endothelial NOS | AKT | smooth muscle relaxation | phosphoantibody | IN-VITRO | CORPUS CAVERNOSUM | CA2 | gasotransmitter | GENE-EXPRESSION | MICE | Immunohistochemistry | Penis - physiology | Electric Stimulation | Male | Penis - innervation | Penile Erection - drug effects | Nitric Oxide Synthase Type I - antagonists & inhibitors | Cyclic AMP-Dependent Protein Kinases - antagonists & inhibitors | Phosphorylation - drug effects | Cyclic AMP - metabolism | Cyclic AMP-Dependent Protein Kinases - metabolism | NG-Nitroarginine Methyl Ester - pharmacology | Colforsin - pharmacology | Mice, Inbred C57BL | Enzyme Inhibitors - pharmacology | Rats | Rats, Sprague-Dawley | Serine - metabolism | Blotting, Western | Mice, Knockout | Animals | Penis - metabolism | Nitric Oxide Synthase Type I - metabolism | Mice | Nitric Oxide Synthase Type I - genetics | Penile Erection - physiology | Penis | Nitric oxide | Physiological aspects | Cyclic adenylic acid | Research | Health aspects | Biological Sciences
Alternative splicing | Phosphorylation | Calcium | Penile erection | Electrical stimulation | Antibodies | Oxides | Smooth muscle | Physiology | Physiological regulation | Phosphoantibody | Smooth muscle relaxation | Gasotransmitter | Cyclic GMP | Endothelial NOS | NNOS | NERVOUS-SYSTEM | ACTIVATION | PROTEIN-KINASE | MULTIDISCIPLINARY SCIENCES | cyclic GMP | endothelial NOS | AKT | smooth muscle relaxation | phosphoantibody | IN-VITRO | CORPUS CAVERNOSUM | CA2 | gasotransmitter | GENE-EXPRESSION | MICE | Immunohistochemistry | Penis - physiology | Electric Stimulation | Male | Penis - innervation | Penile Erection - drug effects | Nitric Oxide Synthase Type I - antagonists & inhibitors | Cyclic AMP-Dependent Protein Kinases - antagonists & inhibitors | Phosphorylation - drug effects | Cyclic AMP - metabolism | Cyclic AMP-Dependent Protein Kinases - metabolism | NG-Nitroarginine Methyl Ester - pharmacology | Colforsin - pharmacology | Mice, Inbred C57BL | Enzyme Inhibitors - pharmacology | Rats | Rats, Sprague-Dawley | Serine - metabolism | Blotting, Western | Mice, Knockout | Animals | Penis - metabolism | Nitric Oxide Synthase Type I - metabolism | Mice | Nitric Oxide Synthase Type I - genetics | Penile Erection - physiology | Penis | Nitric oxide | Physiological aspects | Cyclic adenylic acid | Research | Health aspects | Biological Sciences
Journal Article
Behavioural Pharmacology, ISSN 0955-8810, 04/2015, Volume 26, Issue 3, pp. 282 - 288
Tapentadol, a new analgesic drug with a dual mechanism of action (μ-opioid receptor agonism and norepinephrine reuptake inhibition), is indicated for the...
NOS | antinociception | l-NIO | rat | l-NIL | 7-NI | tapentadol | l-NOArg | RAT SPINAL-CORD | THERMAL HYPERALGESIA | L-NOArg | OPIOID RECEPTOR AGONIST | DORSAL-ROOT GANGLIA | INTRAVENOUS MORPHINE | NEUROSCIENCES | NEUROPATHIC PAIN | SPINOTHALAMIC TRACT NEURONS | L-NIL | INDUCED HYPERALGESIA | L-NIO | BEHAVIORAL SCIENCES | PHARMACOLOGY & PHARMACY | MORPHINE ANTINOCICEPTION | REUPTAKE INHIBITOR | Nitric Oxide Synthase - drug effects | Analgesics, Opioid - pharmacology | Rats | Male | Receptors, Opioid, mu - agonists | Dose-Response Relationship, Drug | Animals | Analgesics, Opioid - administration & dosage | Pain - drug therapy | Pain - physiopathology | Phenols - administration & dosage | Nitric Oxide Synthase - metabolism | Disease Models, Animal | Phenols - pharmacology
NOS | antinociception | l-NIO | rat | l-NIL | 7-NI | tapentadol | l-NOArg | RAT SPINAL-CORD | THERMAL HYPERALGESIA | L-NOArg | OPIOID RECEPTOR AGONIST | DORSAL-ROOT GANGLIA | INTRAVENOUS MORPHINE | NEUROSCIENCES | NEUROPATHIC PAIN | SPINOTHALAMIC TRACT NEURONS | L-NIL | INDUCED HYPERALGESIA | L-NIO | BEHAVIORAL SCIENCES | PHARMACOLOGY & PHARMACY | MORPHINE ANTINOCICEPTION | REUPTAKE INHIBITOR | Nitric Oxide Synthase - drug effects | Analgesics, Opioid - pharmacology | Rats | Male | Receptors, Opioid, mu - agonists | Dose-Response Relationship, Drug | Animals | Analgesics, Opioid - administration & dosage | Pain - drug therapy | Pain - physiopathology | Phenols - administration & dosage | Nitric Oxide Synthase - metabolism | Disease Models, Animal | Phenols - pharmacology
Journal Article
Journal of Neurochemistry, ISSN 0022-3042, 12/2007, Volume 103, Issue 5, pp. 1843 - 1854
Increasing evidence suggests that depression may be associated with a lack of hippocampal neurogenesis. It is well established that neuronal nitric oxide...
neurogenesis | stress | neuronal nitric oxide synthase | nitric oxide | hippocampal | depression | Depression | Hippocampal | Neuronal nitric oxide synthase | Neurogenesis | Nitric oxide | Stress | PROGENITOR CELLS | RAT PARAVENTRICULAR NUCLEUS | ANTIDEPRESSANT-LIKE | BIOCHEMISTRY & MOLECULAR BIOLOGY | ADULT DENTATE GYRUS | CHRONIC MILD STRESS | ELEMENT-BINDING PROTEIN | CELL-PROLIFERATION | NEUROSCIENCES | PREFRONTAL CORTEX | ISCHEMIA STIMULATES NEUROGENESIS | ANXIOLYTIC-LIKE | Cell Proliferation | Depression - pathology | Enzyme Inhibitors - pharmacology | Zidovudine - pharmacology | Bromodeoxyuridine | Male | Hippocampus - pathology | Hindlimb Suspension - methods | Mice, Knockout | Nitric Oxide Synthase Type I - deficiency | Behavior, Animal | Depression - etiology | Indazoles - pharmacology | Animals | Drug Interactions | Analysis of Variance | Time Factors | Neurons - physiology | Mice | Nitric Oxide Synthase Type I - physiology | Stress, Psychological - complications | Neurons | Depression, Mental | Brain | Neurosciences | Chemistry | Brain research | Rodents | Mental depression
neurogenesis | stress | neuronal nitric oxide synthase | nitric oxide | hippocampal | depression | Depression | Hippocampal | Neuronal nitric oxide synthase | Neurogenesis | Nitric oxide | Stress | PROGENITOR CELLS | RAT PARAVENTRICULAR NUCLEUS | ANTIDEPRESSANT-LIKE | BIOCHEMISTRY & MOLECULAR BIOLOGY | ADULT DENTATE GYRUS | CHRONIC MILD STRESS | ELEMENT-BINDING PROTEIN | CELL-PROLIFERATION | NEUROSCIENCES | PREFRONTAL CORTEX | ISCHEMIA STIMULATES NEUROGENESIS | ANXIOLYTIC-LIKE | Cell Proliferation | Depression - pathology | Enzyme Inhibitors - pharmacology | Zidovudine - pharmacology | Bromodeoxyuridine | Male | Hippocampus - pathology | Hindlimb Suspension - methods | Mice, Knockout | Nitric Oxide Synthase Type I - deficiency | Behavior, Animal | Depression - etiology | Indazoles - pharmacology | Animals | Drug Interactions | Analysis of Variance | Time Factors | Neurons - physiology | Mice | Nitric Oxide Synthase Type I - physiology | Stress, Psychological - complications | Neurons | Depression, Mental | Brain | Neurosciences | Chemistry | Brain research | Rodents | Mental depression
Journal Article
Nature Communications, ISSN 2041-1723, 07/2017, Volume 8, Issue 1, p. 15937
Enteric nervous system neuropathy causes a wide range of severe gut motility disorders. Cell replacement of lost neurons using enteric neural stem cells (ENSC)...
INHIBITORY NEUROTRANSMISSION | MULTIDISCIPLINARY SCIENCES | GASTROINTESTINAL-TRACT | NEURONS | SMALL-INTESTINE | CAJAL | HIRSCHSPRUNGS-DISEASE | REBOUND EXCITATION | KNOCKOUT MICE | SLOW-TRANSIT CONSTIPATION | INTERSTITIAL-CELLS | Colon - enzymology | Enteric Nervous System - cytology | Humans | Mice, Inbred C57BL | Male | Intestinal Pseudo-Obstruction - enzymology | Nitric Oxide Synthase - genetics | Intestinal Pseudo-Obstruction - genetics | Intestinal Pseudo-Obstruction - physiopathology | Gastrointestinal Motility | Enteric Nervous System - enzymology | Neurons - transplantation | Animals | Nitric Oxide Synthase - deficiency | Neural Stem Cells - transplantation | Colon - physiopathology | Female | Intestinal Pseudo-Obstruction - surgery | Mice | Therapy | Motility | Neurons | Disorders | Recovery of function | Stem cell transplantation | Interstitial cells | Nervous system | Transplantation | Neuropathy | Interstitial cells of Cajal | Transit | Nitric-oxide synthase | Enteric nervous system | Restoration | Nitric oxide | Stem cells | Neural stem cells | Colon | Digestive tract | Gastric motility
INHIBITORY NEUROTRANSMISSION | MULTIDISCIPLINARY SCIENCES | GASTROINTESTINAL-TRACT | NEURONS | SMALL-INTESTINE | CAJAL | HIRSCHSPRUNGS-DISEASE | REBOUND EXCITATION | KNOCKOUT MICE | SLOW-TRANSIT CONSTIPATION | INTERSTITIAL-CELLS | Colon - enzymology | Enteric Nervous System - cytology | Humans | Mice, Inbred C57BL | Male | Intestinal Pseudo-Obstruction - enzymology | Nitric Oxide Synthase - genetics | Intestinal Pseudo-Obstruction - genetics | Intestinal Pseudo-Obstruction - physiopathology | Gastrointestinal Motility | Enteric Nervous System - enzymology | Neurons - transplantation | Animals | Nitric Oxide Synthase - deficiency | Neural Stem Cells - transplantation | Colon - physiopathology | Female | Intestinal Pseudo-Obstruction - surgery | Mice | Therapy | Motility | Neurons | Disorders | Recovery of function | Stem cell transplantation | Interstitial cells | Nervous system | Transplantation | Neuropathy | Interstitial cells of Cajal | Transit | Nitric-oxide synthase | Enteric nervous system | Restoration | Nitric oxide | Stem cells | Neural stem cells | Colon | Digestive tract | Gastric motility
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 03/2005, Volume 25, Issue 9, pp. 2366 - 2375
Here, we investigate the effects of endothelial nitric oxide synthase (eNOS) on angiogenesis, neurogenesis, neurotrophic factor expression, and neurological...
Focal cerebral ischemia | Angiogenesis | Neural progenitor cells | eNOS | BDNF | Neurogenesis | PROGENITOR CELLS | angiogenesis | FOCAL CEREBRAL-ISCHEMIA | FIBROBLAST-GROWTH-FACTOR | SUBVENTRICULAR ZONE | neural progenitor cells | SYNAPTIC PLASTICITY | HIPPOCAMPAL-NEURONS | NEUROSCIENCES | NEURAL STEM-CELLS | TELOMERASE ACTIVITY | neurogenesis | focal cerebral ischemia | MARROW STROMAL CELLS | FACTOR-INDUCED ANGIOGENESIS | Enzyme-Linked Immunosorbent Assay - methods | Infarction, Middle Cerebral Artery - physiopathology | Nestin | Cell Proliferation | Gene Expression - drug effects | Neurites - physiology | Microtubule-Associated Proteins - metabolism | Ki-67 Antigen - metabolism | Male | Infarction, Middle Cerebral Artery - metabolism | Nitric Oxide Synthase Type III - deficiency | Psychomotor Performance - physiology | Cell Movement - genetics | Cell Movement - physiology | Corneal Neovascularization | Time Factors | Gene Expression - physiology | Nitric Oxide Synthase Type III - physiology | Telomerase - metabolism | Blood Pressure - physiology | Brain-Derived Neurotrophic Factor - metabolism | Bromodeoxyuridine - metabolism | Vascular Endothelial Growth Factor A - pharmacology | Endothelial Cells - physiology | Disease Models, Animal | Recovery of Function - genetics | Mice, Inbred C57BL | Neuropeptides - metabolism | Psychomotor Performance - drug effects | Mice, Knockout | Naphthalenes | Oxepins | Immunohistochemistry - methods | Nerve Tissue Proteins - metabolism | Animals | Cell Count - methods | Nitric Oxide Synthase Type III - pharmacology | Brain - pathology | Mice | Neurologic Examination - methods | Intermediate Filament Proteins - metabolism | Neurobiology of Disease
Focal cerebral ischemia | Angiogenesis | Neural progenitor cells | eNOS | BDNF | Neurogenesis | PROGENITOR CELLS | angiogenesis | FOCAL CEREBRAL-ISCHEMIA | FIBROBLAST-GROWTH-FACTOR | SUBVENTRICULAR ZONE | neural progenitor cells | SYNAPTIC PLASTICITY | HIPPOCAMPAL-NEURONS | NEUROSCIENCES | NEURAL STEM-CELLS | TELOMERASE ACTIVITY | neurogenesis | focal cerebral ischemia | MARROW STROMAL CELLS | FACTOR-INDUCED ANGIOGENESIS | Enzyme-Linked Immunosorbent Assay - methods | Infarction, Middle Cerebral Artery - physiopathology | Nestin | Cell Proliferation | Gene Expression - drug effects | Neurites - physiology | Microtubule-Associated Proteins - metabolism | Ki-67 Antigen - metabolism | Male | Infarction, Middle Cerebral Artery - metabolism | Nitric Oxide Synthase Type III - deficiency | Psychomotor Performance - physiology | Cell Movement - genetics | Cell Movement - physiology | Corneal Neovascularization | Time Factors | Gene Expression - physiology | Nitric Oxide Synthase Type III - physiology | Telomerase - metabolism | Blood Pressure - physiology | Brain-Derived Neurotrophic Factor - metabolism | Bromodeoxyuridine - metabolism | Vascular Endothelial Growth Factor A - pharmacology | Endothelial Cells - physiology | Disease Models, Animal | Recovery of Function - genetics | Mice, Inbred C57BL | Neuropeptides - metabolism | Psychomotor Performance - drug effects | Mice, Knockout | Naphthalenes | Oxepins | Immunohistochemistry - methods | Nerve Tissue Proteins - metabolism | Animals | Cell Count - methods | Nitric Oxide Synthase Type III - pharmacology | Brain - pathology | Mice | Neurologic Examination - methods | Intermediate Filament Proteins - metabolism | Neurobiology of Disease
Journal Article
Journal of Molecular Biology, ISSN 0022-2836, 06/2018, Volume 430, Issue 12, pp. 1773 - 1785
Store-operated Ca entry (SOCE) mediated by stromal interacting molecule-1 (STIM1) and Orai1 represents a major route of Ca entry in mammalian cells and is...
stromal interaction molecule-1 | neuronal nitric oxide synthase | nitric oxide | store-operated calcium entry | S-nitrosylation | CARDIAC-FUNCTION | CHEMICAL-SHIFTS | BIOCHEMISTRY & MOLECULAR BIOLOGY | DEPLETION | RELEASE | CARDIOMYOCYTES | PLASMA-MEMBRANE | CALCIUM-ENTRY | INITIATION MECHANISM | OLIGOMERIZATION
stromal interaction molecule-1 | neuronal nitric oxide synthase | nitric oxide | store-operated calcium entry | S-nitrosylation | CARDIAC-FUNCTION | CHEMICAL-SHIFTS | BIOCHEMISTRY & MOLECULAR BIOLOGY | DEPLETION | RELEASE | CARDIOMYOCYTES | PLASMA-MEMBRANE | CALCIUM-ENTRY | INITIATION MECHANISM | OLIGOMERIZATION
Journal Article