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Journal of Membrane Science, ISSN 0376-7388, 2010, Volume 352, Issue 1-2, pp. 126 - 135
Polymer blending is a versatile tool to combine the beneficial properties of two or more components in one single material. Here, we present the preparation,... 
Gas separation | PEBAX | Poly(dimethyl siloxane) (PDMS) | Carbon dioxide | Blend membrane | PEBAX (R) | POLYMER SCIENCE | PERMEABILITY | SEGMENTED BLOCK-COPOLYMERS | POLYETHYLENEGLYCOL PEG | COMPOSITE MEMBRANES | ENGINEERING, CHEMICAL | CA BLEND MEMBRANES | SILICONE-RUBBER | POLYMERIC MEMBRANES | TRANSPORT PROPERTIES | MIXED GASES | PERMEATION PROPERTIES
Journal Article
Journal of Membrane Science, ISSN 0376-7388, 2011, Volume 378, Issue 1-2, pp. 479 - 484
The current work describes the synthesis and mass transport properties of a series of blend membranes based on a highly permeable polyether based segmented... 
Poly(ethylene oxide) | Poly(dimethyl siloxane) | Block copolymer | Carbon dioxide | Blend membrane | POLYMER SCIENCE | OXIDE | MONOMER | ENGINEERING, CHEMICAL | GAS-PERMEATION PROPERTIES | CARBON-DIOXIDE CAPTURE | POLY(ETHYLENE GLYCOL) | TRANSPORT PROPERTIES
Journal Article
Journal of Membrane Science, ISSN 0376-7388, 2010, Volume 359, Issue 1-2, pp. 54 - 63
Polyether and especially poly(ethylene oxide) (PEO) based segmented block copolymers are very well known for their high CO permeability combined with a high CO... 
Poly(ethylene oxide) | Poly(propylene oxide) | Gas separation membranes | Morphology | Carbon dioxide | Segmented block copolymer | POLYMER SCIENCE | GLYCOL DIACRYLATE | PERMEABILITY | SEGMENTED BLOCK-COPOLYMERS | ENGINEERING, CHEMICAL | GAS-PERMEATION PROPERTIES | POLYMERIC MEMBRANES | SEPARATION
Journal Article
Journal of neuroinflammation, ISSN 1742-2094, 2012, Volume 9, Issue 1, pp. 133 - 133
Journal Article
International Journal of Greenhouse Gas Control, ISSN 1750-5836, 2011, Volume 5, Issue 1, pp. 26 - 36
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 03/2018, Volume 115, Issue 13, pp. E2997 - E3006
Inherited retinal degeneration (RD) is a devastating and currently untreatable neurodegenerative condition that leads to loss of photoreceptor cells and... 
CNG channel | Calpain | PKG | Apoptosis | In vivo imaging | in vivo imaging | ROD | MULTIDISCIPLINARY SCIENCES | GLUTATHIONE PEGYLATED LIPOSOMES | apoptosis | DEPENDENT PROTEIN-KINASE | PHOTORECEPTOR CELL-DEATH | calpain | MUTANT MICE | CYCLIC-GMP | CONE PHOTORECEPTORS | MOUSE RETINA | RETINITIS-PIGMENTOSA | Retina - drug effects | Cyclic GMP - pharmacology | Retina - metabolism | Retinal Degeneration - drug therapy | Blood-Retinal Barrier - drug effects | Cyclic GMP-Dependent Protein Kinases - metabolism | Retinal Degeneration - metabolism | Cyclic GMP - administration & dosage | Drug Delivery Systems | Blood-Retinal Barrier - metabolism | Animals | Cyclic GMP - analogs & derivatives | Signal Transduction - drug effects | Photoreceptor Cells - metabolism | Mice | Liposomes | Disease Models, Animal | Prevention | Drugs | Drug delivery systems | Usage | Retinal degeneration | Cyclic guanylic acid | Health aspects | Methods | Vehicles | Medical treatment | Guanosine | Medical services | Retina | Pharmacology | Drug delivery | Analogs | Heterogeneity | Cell activation | Cell death | Neurodegeneration | Cyclic GMP | Blindness | Eye diseases | Degeneration | Index Medicus | Biological Sciences | Physical Sciences | PNAS Plus | Clinical Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Oftalmologi | Ophthalmology | Klinisk medicin
Journal Article
Glia, ISSN 0894-1491, 2014, Volume 62, Issue 7, pp. 1125 - 1141
To ensure efficient energy supply to the high demanding brain, nutrients are transported into brain cells via specific glucose (GLUT) and monocarboxylate... 
neurodegeneration | nutrient transporters | reactive astrocytes | proliferator‐activated receptor gamma co‐activator 1‐alpha | Nutrient transporters | Neurodegeneration | Proliferator-activated receptor gamma co-activator 1-alpha | Reactive astrocytes | MOUSE-BRAIN | ACTIVATED RECEPTOR-GAMMA | NEUROSCIENCES | MCT2 | SKELETAL-MUSCLE | proliferator-activated receptor gamma co-activator 1-alpha | MITOCHONDRIAL CHANGES | LACTATE | NEURONS | ENERGY-METABOLISM | NF-KAPPA-B | EXPRESSION | Glutamate Plasma Membrane Transport Proteins - metabolism | Leukocytes - pathology | Microglia - metabolism | White Matter - metabolism | Humans | Middle Aged | Astrocytes - pathology | Male | Glucose Transporter Type 3 - metabolism | Brain - metabolism | Brain - blood supply | Monocarboxylic Acid Transporters - metabolism | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Aged, 80 and over | Microglia - pathology | Adult | Female | White Matter - blood supply | Multiple Sclerosis - metabolism | Cell Line | Endothelial Cells - metabolism | Axons - metabolism | Multiple Sclerosis, Chronic Progressive - pathology | Multiple Sclerosis, Chronic Progressive - metabolism | White Matter - pathology | Transcription Factors - metabolism | Axons - pathology | Brain - pathology | Multiple Sclerosis - pathology | Aged | Endothelial Cells - pathology | Leukocytes - metabolism | Astrocytes - metabolism | Proteins | Glucose metabolism | Brain | Multiple sclerosis | Physiological aspects | Brain damage | Development and progression | Glucose | Dextrose | Index Medicus
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 2014, Volume 128, Issue 5, pp. 691 - 703
Journal Article
Acta neuropathologica, ISSN 0001-6322, 2012, Volume 124, Issue 3, pp. 397 - 410
Alterations in sphingolipid metabolism are described to contribute to various neurological disorders. We here determined the expression of enzymes involved in... 
Pathology | Neurosciences | Multiple sclerosis | Medicine & Public Health | Astrocytes | Acid sphingomyelinase | Ceramide | Blood–brain barrier | Blood-brain barrier | INDUCED APOPTOSIS | NECROSIS-FACTOR-ALPHA | 1-PHOSPHATE RECEPTOR 1 | PATHOLOGY | NEUROSCIENCES | CLINICAL NEUROLOGY | SPHINGOSINE 1-PHOSPHATE | IN-VITRO | FTY720 | ENDOTHELIAL-CELLS | UP-REGULATION | EXPRESSION | Humans | Middle Aged | Astrocytes - pathology | Blood-Brain Barrier - physiopathology | Male | Monocytes - metabolism | Multiple Sclerosis - physiopathology | Monocytes - pathology | Aged, 80 and over | Adult | Female | Immunosuppressive Agents - pharmacology | Multiple Sclerosis - metabolism | Propylene Glycols - pharmacology | Astrocytes - drug effects | Ceramides - metabolism | Sphingomyelins - metabolism | Endothelial Cells - metabolism | Cells, Cultured | Fingolimod Hydrochloride | Blood-Brain Barrier - drug effects | Monocytes - drug effects | Sphingosine - pharmacology | Blood-Brain Barrier - pathology | Cell Movement - drug effects | Sphingosine - analogs & derivatives | Multiple Sclerosis - pathology | Aged | Endothelial Cells - pathology | Astrocytes - metabolism | Endothelial Cells - drug effects | Enzymes | Biological products | RNA | Sphingosine | Physiological aspects | Lipids | Inflammation | Index Medicus | Brain | Leukocyte migration | Sphingolipids | Gene expression | Metabolism | Substantia alba | Sphingomyelin phosphodiesterase | Neurological diseases | Monocytes | sphingomyelin | Lipid metabolism | Tumor necrosis factor- alpha
Journal Article
Journal of Controlled Release, ISSN 0168-3659, 12/2012, Volume 164, Issue 3, pp. 364 - 369
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 2014, Volume 128, Issue 2, pp. 267 - 277
Journal Article
Journal Article