Chemical Reviews, ISSN 0009-2665, 11/2007, Volume 107, Issue 11, pp. 5318 - 5365
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2012, Volume 7, Issue 10, p. e48250
The recent discovery of hepcidin, the key iron regulatory hormone, has changed our view of iron metabolism, which in turn is long known to be linked with...
TRANSFERRIN SATURATION | INSULIN-RESISTANCE | MULTIDISCIPLINARY SCIENCES | FATTY LIVER | ATHEROSCLEROSIS | IRON OVERLOAD SYNDROME | BODY IRON | PREVALENCE | FERRITIN | EXPRESSION | ASSOCIATION | Predictive Value of Tests | Prognosis | Hemochromatosis Protein | Membrane Proteins - genetics | Humans | Middle Aged | Hepcidins - blood | Linear Models | Male | Histocompatibility Antigens Class I - genetics | Metabolic Syndrome - blood | C-Reactive Protein - metabolism | Analysis of Variance | Ferritins - blood | Metabolic Syndrome - diagnosis | Adult | Female | Aged | Mutation | Population Surveillance - methods | Iron - blood | Type 2 diabetes | Medical research | C-reactive protein | Analysis | Ferritin | Physiological aspects | Medicine, Experimental | Insulin resistance | Substance abuse treatment | Homeostasis | Population studies | Iron | Biology | Males | Metabolic syndrome | Rodents | Population | Blood pressure | Obesity | Liver diseases | Cytokines | Complications | Diabetes mellitus | Mass spectroscopy | Triglycerides | Metabolism | Insulin | Variance analysis | Medicine | Studies | Womens health | Diabetes | Females | Mass spectrometry | Hepcidin | Metabolic disorders
TRANSFERRIN SATURATION | INSULIN-RESISTANCE | MULTIDISCIPLINARY SCIENCES | FATTY LIVER | ATHEROSCLEROSIS | IRON OVERLOAD SYNDROME | BODY IRON | PREVALENCE | FERRITIN | EXPRESSION | ASSOCIATION | Predictive Value of Tests | Prognosis | Hemochromatosis Protein | Membrane Proteins - genetics | Humans | Middle Aged | Hepcidins - blood | Linear Models | Male | Histocompatibility Antigens Class I - genetics | Metabolic Syndrome - blood | C-Reactive Protein - metabolism | Analysis of Variance | Ferritins - blood | Metabolic Syndrome - diagnosis | Adult | Female | Aged | Mutation | Population Surveillance - methods | Iron - blood | Type 2 diabetes | Medical research | C-reactive protein | Analysis | Ferritin | Physiological aspects | Medicine, Experimental | Insulin resistance | Substance abuse treatment | Homeostasis | Population studies | Iron | Biology | Males | Metabolic syndrome | Rodents | Population | Blood pressure | Obesity | Liver diseases | Cytokines | Complications | Diabetes mellitus | Mass spectroscopy | Triglycerides | Metabolism | Insulin | Variance analysis | Medicine | Studies | Womens health | Diabetes | Females | Mass spectrometry | Hepcidin | Metabolic disorders
Journal Article
International Journal of Hydrogen Energy, ISSN 0360-3199, 09/2019
Journal Article
The Journal of Headache and Pain, ISSN 1129-2369, 12/2015, Volume 16, Issue S1, pp. 1 - 2
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2013, Volume 8, Issue 6
[This corrects the article on p. e48250 in vol. 7.].
Population studies | Metabolic syndrome | Hepcidin | Metabolic disorders
Population studies | Metabolic syndrome | Hepcidin | Metabolic disorders
Journal Article
Annals of Neurology, ISSN 0364-5134, 10/2012, Volume 72, Issue 4, pp. 610 - 624
Objective: Microvesicles (MVs) have been indicated as important mediators of intercellular communication and are emerging as new biomarkers of tissue damage....
SYSTEM | ACTIVATION | SPHINGOMYELINASE-DEFICIENT MICE | MEMBRANE-VESICLES | MICROGLIA | EXOSOMES | RELEASE | MEDIATORS | NEUROSCIENCES | OLIGODENDROCYTES | CLINICAL NEUROLOGY | CELL-DEATH | Nervous System Autoimmune Disease, Experimental - drug therapy | Sphingomyelin Phosphodiesterase - genetics | Spinal Cord - metabolism | Calcium Signaling - physiology | Nervous System Autoimmune Disease, Experimental - cerebrospinal fluid | Rats, Inbred Lew | Flow Cytometry | Inflammation - drug therapy | Lentivirus - genetics | Sphingomyelin Phosphodiesterase - physiology | Real-Time Polymerase Chain Reaction | Central Nervous System Diseases - cerebrospinal fluid | Mice, Inbred C57BL | Cells, Cultured | Inflammation - cerebrospinal fluid | Neuroglia - physiology | Cell Communication | Encephalitis - pathology | Rats | Microscopy, Electron | Rats, Sprague-Dawley | Blotting, Western | Mice, Knockout | Animals | Central Nervous System Diseases - drug therapy | Encephalitis - cerebrospinal fluid | Multiple Sclerosis - pathology | Neuroglia - metabolism | Mice | Biomarkers - cerebrospinal fluid | Microscopy, Fluorescence | Medical research | Multiple sclerosis | Rodents
SYSTEM | ACTIVATION | SPHINGOMYELINASE-DEFICIENT MICE | MEMBRANE-VESICLES | MICROGLIA | EXOSOMES | RELEASE | MEDIATORS | NEUROSCIENCES | OLIGODENDROCYTES | CLINICAL NEUROLOGY | CELL-DEATH | Nervous System Autoimmune Disease, Experimental - drug therapy | Sphingomyelin Phosphodiesterase - genetics | Spinal Cord - metabolism | Calcium Signaling - physiology | Nervous System Autoimmune Disease, Experimental - cerebrospinal fluid | Rats, Inbred Lew | Flow Cytometry | Inflammation - drug therapy | Lentivirus - genetics | Sphingomyelin Phosphodiesterase - physiology | Real-Time Polymerase Chain Reaction | Central Nervous System Diseases - cerebrospinal fluid | Mice, Inbred C57BL | Cells, Cultured | Inflammation - cerebrospinal fluid | Neuroglia - physiology | Cell Communication | Encephalitis - pathology | Rats | Microscopy, Electron | Rats, Sprague-Dawley | Blotting, Western | Mice, Knockout | Animals | Central Nervous System Diseases - drug therapy | Encephalitis - cerebrospinal fluid | Multiple Sclerosis - pathology | Neuroglia - metabolism | Mice | Biomarkers - cerebrospinal fluid | Microscopy, Fluorescence | Medical research | Multiple sclerosis | Rodents
Journal Article
Journal of Neurology, ISSN 0340-5354, 1/2017, Volume 264, Issue 1, pp. 102 - 111
Defects of the Fe/S cluster biosynthesis represent a subgroup of diseases affecting the mitochondrial energy metabolism. In the last years, mutations in four...
Neurology | Mitochondrial disorders | Neurosciences | Medicine & Public Health | Leukodystrophy | IBA57 | MMDS | Neuroradiology | RIBOFLAVIN | PROTEIN | BRAIN-STEM | NFU1 DEFICIENCY | CAVITATING LEUKOENCEPHALOPATHY | CLINICAL NEUROLOGY | ENCEPHALOPATHY | ENZYMES | MITOCHONDRIAL DYSFUNCTION | HYPERGLYCINEMIA | SPINAL-CORD INVOLVEMENT | Brain - diagnostic imaging | Follow-Up Studies | Brain Diseases - diagnosis | Humans | Brain Diseases - genetics | Neurodegenerative Diseases - diagnosis | Infant | Male | Neurodegenerative Diseases - genetics | Mitochondria - metabolism | Blotting, Western | Brain Diseases - physiopathology | Carrier Proteins - genetics | Magnetic Resonance Imaging | Phenotype | Carrier Proteins - metabolism | Neurodegenerative Diseases - physiopathology | Female | Mutation | Protein Stability | Cohort Studies | Fibroblasts - metabolism | Genetic aspects | Research | Gene mutations | Analysis | Risk factors | Globoid cell leukodystrophy
Neurology | Mitochondrial disorders | Neurosciences | Medicine & Public Health | Leukodystrophy | IBA57 | MMDS | Neuroradiology | RIBOFLAVIN | PROTEIN | BRAIN-STEM | NFU1 DEFICIENCY | CAVITATING LEUKOENCEPHALOPATHY | CLINICAL NEUROLOGY | ENCEPHALOPATHY | ENZYMES | MITOCHONDRIAL DYSFUNCTION | HYPERGLYCINEMIA | SPINAL-CORD INVOLVEMENT | Brain - diagnostic imaging | Follow-Up Studies | Brain Diseases - diagnosis | Humans | Brain Diseases - genetics | Neurodegenerative Diseases - diagnosis | Infant | Male | Neurodegenerative Diseases - genetics | Mitochondria - metabolism | Blotting, Western | Brain Diseases - physiopathology | Carrier Proteins - genetics | Magnetic Resonance Imaging | Phenotype | Carrier Proteins - metabolism | Neurodegenerative Diseases - physiopathology | Female | Mutation | Protein Stability | Cohort Studies | Fibroblasts - metabolism | Genetic aspects | Research | Gene mutations | Analysis | Risk factors | Globoid cell leukodystrophy
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PLoS Genetics, ISSN 1553-7390, 11/2012, Volume 8, Issue 11, p. e1003021
Fusion and fission of mitochondria maintain the functional integrity of mitochondria and protect against neurodegeneration, but how mitochondrial dysfunctions...
PROTEOLYTIC CLEAVAGE | DOMINANT OPTIC ATROPHY | FUSION | OPA1 | PHOSPHORYLATION | ALZHEIMERS-DISEASE | SPFH DOMAIN | GENETICS & HEREDITY | AXONAL-TRANSPORT | FISSION | M-AAA PROTEASE | Neurons - pathology | Phosphorylation | Neurodegenerative Diseases - pathology | Membrane Fusion | Optic Atrophy, Autosomal Dominant - metabolism | Repressor Proteins - genetics | tau Proteins - metabolism | Neurodegenerative Diseases - genetics | Mitochondria - metabolism | Mitochondria - pathology | Neurodegenerative Diseases - metabolism | Mitochondrial Membranes - metabolism | Morphogenesis | Animals | tau Proteins - genetics | Mitochondria - genetics | Optic Atrophy, Autosomal Dominant - genetics | Mice | Neurons - metabolism | Genome, Mitochondrial | Repressor Proteins - metabolism | Apoptosis | Mitochondria | Physiological aspects | Nervous system | Development and progression | Degeneration | Genetic aspects | Research | Health aspects | Membrane proteins | Proteins | Mitochondrial DNA | Neurodegeneration | Neurons | Rodents
PROTEOLYTIC CLEAVAGE | DOMINANT OPTIC ATROPHY | FUSION | OPA1 | PHOSPHORYLATION | ALZHEIMERS-DISEASE | SPFH DOMAIN | GENETICS & HEREDITY | AXONAL-TRANSPORT | FISSION | M-AAA PROTEASE | Neurons - pathology | Phosphorylation | Neurodegenerative Diseases - pathology | Membrane Fusion | Optic Atrophy, Autosomal Dominant - metabolism | Repressor Proteins - genetics | tau Proteins - metabolism | Neurodegenerative Diseases - genetics | Mitochondria - metabolism | Mitochondria - pathology | Neurodegenerative Diseases - metabolism | Mitochondrial Membranes - metabolism | Morphogenesis | Animals | tau Proteins - genetics | Mitochondria - genetics | Optic Atrophy, Autosomal Dominant - genetics | Mice | Neurons - metabolism | Genome, Mitochondrial | Repressor Proteins - metabolism | Apoptosis | Mitochondria | Physiological aspects | Nervous system | Development and progression | Degeneration | Genetic aspects | Research | Health aspects | Membrane proteins | Proteins | Mitochondrial DNA | Neurodegeneration | Neurons | Rodents
Journal Article
Catalysis Today, ISSN 0920-5861, 08/2017, Volume 291, pp. 29 - 35
In previous work, Na-doping of Pt/YSZ was found to facilitate the low temperature water gas shift reaction (LT-WGS), and the promoting effect was ascribed to...
Kinetic isotope effect (KIE) | Na doping | Methanol steam reforming | Yttrium stabilized zirconia (YSZ) | Water-gas-shift | Formic acid | Organic acids | Methanol
Kinetic isotope effect (KIE) | Na doping | Methanol steam reforming | Yttrium stabilized zirconia (YSZ) | Water-gas-shift | Formic acid | Organic acids | Methanol
Journal Article
10.
Full Text
Fischer-Tropsch synthesis: Direct cobalt nitrate reduction of promoted Co/TiO2 catalysts
Fuel, ISSN 0016-2361, 06/2019, Volume 245, Issue C, pp. 488 - 504
The effect of the direct reduction of cobalt nitrate versus the more conventional calcination/reduction treatment has been investigated. Porosity properties of...
Direct cobalt nitrate reduction | Fischer-Tropsch synthesis | TPR-EXAFS | Platinum | TPR-MS | Titania | Cobalt | Promoters | TPR-XANES | OXIDATION | WATER-GAS SHIFT | ENERGY & FUELS | STABILITY | X-RAY-ABSORPTION | RUTHENIUM | ALUMINA | REDUCIBILITY | ENGINEERING, CHEMICAL | CO/SIO2 | TITANIA-SUPPORTED COBALT | SELECTIVITY | Ruthenium | Deactivation | Catalysts | Cobalt oxides | Nitrates | Decomposition | Catalytic activity | Conversion | Nitrate reduction | Fischer-Tropsch process | Silver | Direct reduction | Roasting | Catalysis | Porosity | Surface area | Titanium dioxide | platinum | titania | direct cobalt nitrate reduction | cobalt | promoters
Direct cobalt nitrate reduction | Fischer-Tropsch synthesis | TPR-EXAFS | Platinum | TPR-MS | Titania | Cobalt | Promoters | TPR-XANES | OXIDATION | WATER-GAS SHIFT | ENERGY & FUELS | STABILITY | X-RAY-ABSORPTION | RUTHENIUM | ALUMINA | REDUCIBILITY | ENGINEERING, CHEMICAL | CO/SIO2 | TITANIA-SUPPORTED COBALT | SELECTIVITY | Ruthenium | Deactivation | Catalysts | Cobalt oxides | Nitrates | Decomposition | Catalytic activity | Conversion | Nitrate reduction | Fischer-Tropsch process | Silver | Direct reduction | Roasting | Catalysis | Porosity | Surface area | Titanium dioxide | platinum | titania | direct cobalt nitrate reduction | cobalt | promoters
Journal Article
11.
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Recuperation of nitrogen cycling in Amazonian forests following agricultural abandonment
Nature, ISSN 0028-0836, 06/2007, Volume 447, Issue 7147, pp. 995 - 998
Phosphorus ( P) is generally considered the most common limiting nutrient for productivity of mature tropical lowland forests growing on highly weathered...
COSTA-RICA | LAND-USE CHANGE | GLOBAL PATTERNS | REGROWTH | BRAZILIAN AMAZON | OXIDE EMISSIONS | MULTIDISCIPLINARY SCIENCES | EASTERN AMAZONIA | SOIL | ECOSYSTEMS | ISOTOPIC COMPOSITION | Trees - metabolism | Nitrogen - metabolism | Time Factors | Phosphorus - metabolism | Ecosystem | Brazil | Agriculture | Soil - analysis | Nitrous Oxide - metabolism | Phosphorus in the body | Nitrogen cycle | Research | Nitrification | Forest ecology | Soil sciences | Rainforests | Phosphorus | Nitrogen | Forestry | Cycles | Soils | Forests | Nitrous oxides | Lowlands | Tropical forests | Abandonment | Age
COSTA-RICA | LAND-USE CHANGE | GLOBAL PATTERNS | REGROWTH | BRAZILIAN AMAZON | OXIDE EMISSIONS | MULTIDISCIPLINARY SCIENCES | EASTERN AMAZONIA | SOIL | ECOSYSTEMS | ISOTOPIC COMPOSITION | Trees - metabolism | Nitrogen - metabolism | Time Factors | Phosphorus - metabolism | Ecosystem | Brazil | Agriculture | Soil - analysis | Nitrous Oxide - metabolism | Phosphorus in the body | Nitrogen cycle | Research | Nitrification | Forest ecology | Soil sciences | Rainforests | Phosphorus | Nitrogen | Forestry | Cycles | Soils | Forests | Nitrous oxides | Lowlands | Tropical forests | Abandonment | Age
Journal Article
Internal and Emergency Medicine, ISSN 1828-0447, 12/2018, Volume 13, Issue 8, pp. 1191 - 1200
As a consequence of population aging, we have witnessed in internal medicine hospital wards a progressive shift from a population of in-patients relatively...
Polypharmacy | Medicine & Public Health | Medication reconciliation | Inappropriate prescription | Internal Medicine | Deprescribing | Multimorbidity | Chronic diseases | Neurosciences | Aged | Medicine | Aging | Internal medicine | Elderly | Patients
Polypharmacy | Medicine & Public Health | Medication reconciliation | Inappropriate prescription | Internal Medicine | Deprescribing | Multimorbidity | Chronic diseases | Neurosciences | Aged | Medicine | Aging | Internal medicine | Elderly | Patients
Journal Article
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 1, p. e16406
Orexins are neuro-modulatory peptides involved in the control of diverse physiological functions through interaction with two receptors, orexin-1 (OX1R) and...
CEREBRAL BLOOD-VOLUME | SLEEP | ACTIVATION | PHARMACOLOGICAL MRI | CONDITIONED PLACE PREFERENCE | MULTIDISCIPLINARY SCIENCES | DRUG DISCOVERY | NEURONS | RAT-BRAIN | KNOCKOUT MICE | REWARD | Amphetamine - pharmacology | Receptors, Neuropeptide - antagonists & inhibitors | Rats | Orexin Receptors | Behavior, Animal | Activity Cycles - physiology | Magnetic Resonance Imaging | Animals | Motivation - physiology | Piperidines - pharmacology | Aminopyridines - pharmacology | Receptors, G-Protein-Coupled - antagonists & inhibitors | Brain Mapping | Dioxanes - pharmacology | Phenylurea Compounds - pharmacology | Reward | Physiological aspects | Cocaine | Sleep | Magnetic resonance imaging | Neuroimaging | Cluster analysis | Ecstasy | Drugs | Brain | Drug abuse | Animal models | Nuclear magnetic resonance--NMR | Peptides | Selectivity | Blood | Receptors | Rodents | Arousal | Neostriatum | Functional magnetic resonance imaging | Reinforcement | Physiology | Conditioning | Drug dosages | Sleep and wakefulness | Brain architecture | Statistical analysis | Orexins | Research & development--R&D | Cortex | Brain mapping | Metabolism | Anatomy | Substrates | Studies | Contrast agents | Brain research | Amphetamine | Psychopharmacology | Resonance | Nanotechnology | Research & development | Nuclear magnetic resonance | R&D | NMR
CEREBRAL BLOOD-VOLUME | SLEEP | ACTIVATION | PHARMACOLOGICAL MRI | CONDITIONED PLACE PREFERENCE | MULTIDISCIPLINARY SCIENCES | DRUG DISCOVERY | NEURONS | RAT-BRAIN | KNOCKOUT MICE | REWARD | Amphetamine - pharmacology | Receptors, Neuropeptide - antagonists & inhibitors | Rats | Orexin Receptors | Behavior, Animal | Activity Cycles - physiology | Magnetic Resonance Imaging | Animals | Motivation - physiology | Piperidines - pharmacology | Aminopyridines - pharmacology | Receptors, G-Protein-Coupled - antagonists & inhibitors | Brain Mapping | Dioxanes - pharmacology | Phenylurea Compounds - pharmacology | Reward | Physiological aspects | Cocaine | Sleep | Magnetic resonance imaging | Neuroimaging | Cluster analysis | Ecstasy | Drugs | Brain | Drug abuse | Animal models | Nuclear magnetic resonance--NMR | Peptides | Selectivity | Blood | Receptors | Rodents | Arousal | Neostriatum | Functional magnetic resonance imaging | Reinforcement | Physiology | Conditioning | Drug dosages | Sleep and wakefulness | Brain architecture | Statistical analysis | Orexins | Research & development--R&D | Cortex | Brain mapping | Metabolism | Anatomy | Substrates | Studies | Contrast agents | Brain research | Amphetamine | Psychopharmacology | Resonance | Nanotechnology | Research & development | Nuclear magnetic resonance | R&D | NMR
Journal Article