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2010, ISBN 9781405179546, xi, 297
Serving the needs of pigment cell biologists, cellular physiologists, developmental geneticists, researchers interested in melanoma and more, this new book... 
Genetics | Mice | Mice as laboratory animals | Color
Book
Acta Physiologica, ISSN 1748-1708, 02/2019, Volume 225, Issue 2, p. e13237
Journal Article
2008, 1. Aufl., Current topics in microbiology and immunology, ISBN 3540756477, Volume 324., xiii, 199
Book
Journal Article
2006, Practical approach series, ISBN 9780198550013, xxv, 334
The groundbreaking isolation of embryonic stem cells (or 'ES cells') of the mouse in the early 1980s triggered a sustained expansion of global research into... 
Stem Cells | physiology | Models, Animal | Embryo | Mice | Embryonic stem cells | Medicine: General Issues
Book
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 1/2011, Volume 108, Issue 2, pp. 751 - 756
Sphingosine 1-phosphate (S1P), a lysophospholipid, has gained relevance to multiple sclerosis through the discovery of FTY720 (fingolimod), recently approved... 
Receptors | Multiple sclerosis | Spinal cord | Astrocytes | Neurons | Lymphocytes | Central nervous system | Cell lines | Null condition | Mice | G protein-coupled receptor | Lysophospholipid | Neuroprotection | Knockout | knockout | EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | ACTIVATION | ORAL FINGOLIMOD | WHITE-MATTER | MULTIDISCIPLINARY SCIENCES | LYMPHOCYTE EGRESS | AGONISTS | neuroprotection | FIBRILLARY ACIDIC PROTEIN | SPHINGOSINE-1-PHOSPHATE | IMMUNOSUPPRESSANT FTY720 | CENTRAL-NERVOUS-SYSTEM | lysophospholipid | Studies | Prescription drugs | Phosphorylation | Immunology | Metabolites | Rodents | Lipids | Models | Gene expression | Animal models | Cell lineage | Data processing | Neuromodulation | Experimental allergic encephalomyelitis | sphingosine 1-phosphate receptors | Sphingosine 1-phosphate | Signal transduction | Gliosis | Demyelination | FTY720 | Glia | Protein transport | Astrocytes - cytology | Lymphocytes - metabolism | Propylene Glycols - pharmacology | Encephalomyelitis, Autoimmune, Experimental - metabolism | Receptors, G-Protein-Coupled - metabolism | Signal Transduction | Encephalomyelitis, Autoimmune, Experimental - drug therapy | Mice, Inbred C57BL | Gene Expression Regulation | Fingolimod Hydrochloride | Mice, Knockout | Sphingosine - pharmacology | Sphingosine - analogs & derivatives | Animals | Female | Receptors, Lysosphingolipid - metabolism | Immunosuppressive Agents - pharmacology | Disease Models, Animal | Multiple Sclerosis - drug therapy | Physiological aspects | Care and treatment | Index Medicus
Journal Article
Clinical & Experimental Immunology, ISSN 0009-9104, 11/2008, Volume 154, Issue 2, pp. 270 - 284
Journal Article
Nature Neuroscience, ISSN 1097-6256, 09/2011, Volume 14, Issue 9, pp. 1167 - 1173
Journal Article
Epilepsia, ISSN 0013-9580, 07/2018, Volume 59, Issue 7, pp. 1455 - 1468
ObjectiveNa(+)/K+-ATPase dysfunction, primary (mutation) or secondary (energy crisis, neurodegenerative disease) increases neuronal excitability in the brain.... 
epilepsy | D801N | 1A3 | alternating hemiplegia of childhood | ATP | parvalbumin | ATP1A3 | ALTERNATING HEMIPLEGIA | DYSTONIA-PARKINSONISM | STRATUM-ORIENS | SPREADING DEPRESSION | CLINICAL NEUROLOGY | DE-NOVO MUTATIONS | SODIUM-PUMP | CA1 REGION | RAT HIPPOCAMPUS | RAPID-ONSET | FOCAL EPILEPSY | Immunohistochemistry | Interneurons | Brain slice preparation | Epilepsy | Action potential | Depolarization | γ-Aminobutyric acid | Rodents | Hemiplegia | Children | Phenotypes | ATP 1A3 | EEG | Excitability | Na+/K+-exchanging ATPase | Parvalbumin | Electrical stimuli | Excitatory postsynaptic potentials | Pyramidal cells | Glutamatergic transmission | Mutation | Hippocampus | Bicuculline | Inhibitory postsynaptic potentials | Interneurons - physiology | Sodium-Potassium-Exchanging ATPase - genetics | Sodium-Potassium-Exchanging ATPase - physiology | Humans | Evoked Potentials | Electroencephalography | Epilepsy - physiopathology | Mice, Neurologic Mutants | gamma-Aminobutyric Acid - physiology | Patch-Clamp Techniques | Animals | DNA Mutational Analysis | Hemiplegia - genetics | Pyramidal Cells - physiology | Epilepsy - genetics | Mice | Hemiplegia - physiopathology | In Vitro Techniques | Child | Hippocampus - physiopathology | Genetic Carrier Screening | Disease Models, Animal | Nervous system diseases | Neurons | Analysis | GABA | Paralysis | Adenosine triphosphatase | Index Medicus
Journal Article
2014, ISBN 9781621820031, xiv, 521
"99% of mouse protein-coding genes have an equivalent homolog in the human genome, despite the striking differences in appearance between mouse and man. This... 
MEDICAL / Oncology | Animal models | SCIENCE / Life Sciences / Biology / Molecular Biology | Pathophysiology | Mice | Mice as laboratory animals | SCIENCE / Life Sciences / Biology / Developmental Biology | Cancer | Diseases
Book