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Journal of Neuroinflammation, ISSN 1742-2094, 05/2014, Volume 11, Issue 1, p. 95
Complement activation at the C3 convertase level has been associated with acute neuroinflammation and secondary brain injury after severe head trauma. The... 
Cr2-/-mice | Complement receptor | Neuroinflammation | Secondary brain injury | Closed head injury | SYSTEM | AUTOANTIBODIES | TISSUE-INJURY | IMMUNITY | ACTIVATION | NATURAL ANTIBODIES | IMMUNOLOGY | NEUROSCIENCES | NEUROPROTECTION | C3 | COMPLEMENT-RECEPTOR-2 | Cr2(-/-) mice | ACCUMULATION | Microglia - metabolism | Neurons - pathology | Craniocerebral Trauma - blood | Homeodomain Proteins - metabolism | Receptors, Complement 3d - immunology | Male | fas Receptor - metabolism | Brain - metabolism | Proto-Oncogene Proteins c-bcl-2 - metabolism | Phosphopyruvate Hydratase - blood | Receptors, Complement 3d - genetics | Female | Neurons - metabolism | Disease Models, Animal | Complement C3 - metabolism | Mice, Inbred C57BL | Receptors, Complement 3b - deficiency | Receptors, Complement 3d - deficiency | Homeodomain Proteins - genetics | Mice, Knockout | Immunoglobulin M - therapeutic use | Animals | Craniocerebral Trauma - drug therapy | Brain - pathology | Mice | Craniocerebral Trauma - pathology | Astrocytes - metabolism | Immunoglobulin M | B cells | Neurons | Cell death | Cytokines | Neuropathology | Colleges & universities | Nervous system | Experiments | Bone surgery | Polymerase chain reaction | Signal transduction | Scholarships & fellowships | Head injuries | Brain research | Blood-brain barrier | Rodents | Brain damage | Laboratory animals
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2017, Volume 12, Issue 5, p. e0176363
Mitochondrial respiratory chain dysfunction has been identified in a number of neurodegenerative disorders. Infantile cerebellar-retinal degeneration... 
ACID | RAT | MALONYL-COA | MULTIDISCIPLINARY SCIENCES | CITRATE | IRON | DYSFUNCTION | ENERGY-METABOLISM | PROTEINS | HUNTINGTONS-DISEASE | CYCLE | Aconitic Acid - blood | Humans | Ketoglutaric Acids - blood | Child, Preschool | Heredodegenerative Disorders, Nervous System - diagnosis | Male | Aconitate Hydratase - deficiency | Biomarkers - blood | Hydroxybutyrates - blood | Heredodegenerative Disorders, Nervous System - blood | Metabolomics - methods | Isocitrates - blood | Phosphoenolpyruvate - blood | Adolescent | Female | Aconitate Hydratase - genetics | Child | Metabolomics | Mitochondria | Analysis | Research | Aconitase | Health aspects | Blood plasma | Cerebellum | Brain | Pediatrics | Dehydrogenases | 4-Hydroxynonenal | Liver | Carbon dioxide | Retina | Mitochondrial DNA | Assaying | Dehydrogenase | Inactivation | Genetic screening | Proteins | Antioxidants | Enzymatic activity | Neurodegeneration | Aging | Genetics | Biocompatibility | Ataxia | Bioindicators | Diagnosis | Catalysis | Alzheimer's disease | Movement disorders | Deoxyribonucleic acid--DNA | Carbohydrates | Enzymes | AMP | Neurodegenerative diseases | Abnormalities | Cultures | Metabolism | Gene expression | Fatty acids | Children & youth | Diseases | Neurology | Hospitals | Insects | Biomarkers | Guardians | Poisoning | Mutation | Acetic acid | Kidney transplantation | Huntingtons disease | Oxidative stress | Families & family life | Iron | Biosynthesis | Infections | Kinases | AMP-activated protein kinase | Control | Missense mutation | Metabolites | Children | Paralysis | Adenosine triphosphate | Urine | Alanine | Kidneys | Aging (artificial) | Adenine | Pharmacology | Standards | Computer programs | Lobes | Medicine | Brain research | Proteomics | Acidosis | Respiration | Alzheimers disease | ATP | Plasmas (physics) | Cancer | Deoxyribonucleic acid | DNA
Journal Article
Nature Cell Biology, ISSN 1465-7392, 07/2017, Volume 19, Issue 7, pp. 833 - 843
Journal Article
Tree Physiology, ISSN 0829-318X, 03/2013, Volume 33, Issue 3, pp. 320 - 329
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 11/2013, Volume 22, Issue 22, pp. 4460 - 4473
Journal Article
Virchows Archiv, ISSN 0945-6317, 5/2018, Volume 472, Issue 5, pp. 789 - 796
Hereditary leiomyomatosis and renal cell carcinoma (HLRCC) syndrome is a rare autosomal dominant disease caused by germline mutations in the fumarate hydratase... 
HLRCC syndrome | Leiomyoma | Immunohistochemistry | Pathology | Fumarate hydratase | Medicine & Public Health | Uterus | Uterine | Smooth muscle tumor | Hospitals | Gene mutations | Resveratrol | Feature recognition | Muscles | Smooth muscle | Fibroids | Nuclei | Patients | Nodules | DNA microarrays | Morphology | Consultation | Genetics | Mutation | Clear cell-type renal cell carcinoma | Tumors
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