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Journal of Neuroscience, ISSN 0270-6474, 10/2001, Volume 21, Issue 19, pp. 7691 - 7704
L-Serine is synthesized from glycolytic intermediate 3-phosphoglycerate and is an indispensable precursor for the synthesis of proteins, membrane lipids,... 
Immunohistochemistry | Brain | L-serine | Olfactory ensheathing glia | Mouse | Development | 3-Phosphoglycerate dehydrogenase | Astrocyte | In situ hybridization | development | 3-phosphoglycerate dehydrogenase | CEREBELLAR PURKINJE-CELLS | GLUCOSE DEPRIVATION | NEURON REGENERATION | brain | PRIMARY CULTURES | HIPPOCAMPAL-NEURONS | NEUROSCIENCES | FETAL MONKEY NEOCORTEX | mouse | olfactory ensheathing glia | AMINO-ACIDS | immunohistochemistry | RAT-BRAIN | BASIC-PROTEIN | astrocyte | DEVELOPMENTAL EXPRESSION | in situ hybridization | Antibody Specificity | Brain - embryology | Brain - enzymology | Serine - biosynthesis | Dendrites - ultrastructure | Stem Cells - cytology | Astrocytes - enzymology | Olfactory Bulb - embryology | Microscopy, Immunoelectron | RNA, Messenger - biosynthesis | Neuroglia - cytology | In Situ Hybridization | Organelles - ultrastructure | Stem Cells - enzymology | Gene Expression Regulation, Developmental | Organelles - enzymology | Cell Differentiation - physiology | Carbohydrate Dehydrogenases - genetics | Olfactory Bulb - cytology | Olfactory Bulb - enzymology | Astrocytes - cytology | Brain - cytology | Mice, Inbred C57BL | Neuroglia - enzymology | Synapses - enzymology | Synapses - ultrastructure | Phosphoglycerate Dehydrogenase | Cell Lineage - physiology | Animals | Dendrites - enzymology | Mice | Aging - metabolism | Carbohydrate Dehydrogenases - metabolism | Index Medicus
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 9/2009, Volume 186, Issue 6, pp. 805 - 816
The dynamin-related guanosine triphosphatase Drp1 mediates the division of mitochondria and peroxisomes. To understand the in vivo function of Drp1, complete... 
Cerebellum | Mitochondria | Peroxisomes | Neurons | Antibodies | Cytochromes | Reports | Mice | Giant cells | Embryos | Apoptosis | OUTER-MEMBRANE | APOPTOSIS | DOMINANT OPTIC ATROPHY | FUSION | MITOCHONDRIAL FISSION MACHINERY | SYNAPSE FORMATION | CYTOCHROME-C RELEASE | PROTEIN DLP1 | DIVISION | CELL-DEATH | CELL BIOLOGY | Mitochondria - enzymology | Trophoblasts - ultrastructure | Fibroblasts - enzymology | Giant Cells - enzymology | Microtubule-Associated Proteins - genetics | Microtubule-Associated Proteins - metabolism | Trophoblasts - enzymology | Cerebellum - enzymology | Fibroblasts - ultrastructure | Mitochondria - ultrastructure | Purkinje Cells - enzymology | Cerebellum - embryology | Myocytes, Cardiac - enzymology | Adenosine Triphosphate - metabolism | Ultrasonography | Microtubule-Associated Proteins - deficiency | Purkinje Cells - diagnostic imaging | Mice, Inbred C57BL | Cells, Cultured | Dynamins | Gestational Age | Mice, Knockout | Organogenesis | Animals | GTP Phosphohydrolases - metabolism | GTP Phosphohydrolases - genetics | GTP Phosphohydrolases - deficiency | Peroxisomes - enzymology | Cerebellum - ultrastructure | Mitochondrial Size | Myocytes, Cardiac - ultrastructure | Organelle Shape | Peroxisomes - ultrastructure | Giant Cells - ultrastructure | Physiological aspects | Brain | Embryonic development | Research | Guanosine triphosphatase | Embryology | Cellular biology | Rodents | Adenosine triphosphatase | Index Medicus
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 9/2006, Volume 103, Issue 39, pp. 14602 - 14607
Allopregnanolone (ALLO) and tetrahydrodeoxycorticosterone (THDOC) are potent positive allosteric modulators of GABA action at receptors. ALLO and THDOC are... 
Brain | Enzymes | Receptors | Messenger RNA | Neurons | Purkinje cells | Pyramidal cells | Neuroglia | Antibodies | Hippocampus | Glutamatergic neurons | 5α-reductase (type I) | GABAergic neurons | 3α-hydroxysteroid dehydrogenase | GABA(A) RECEPTOR FUNCTION | ALLOPREGNANOLONE SYNTHESIS | SOCIAL-ISOLATION | REELIN MESSENGER-RNA | MULTIDISCIPLINARY SCIENCES | IN-SITU HYBRIDIZATION | STEROID 5-ALPHA-REDUCTASE | glutamatergic neurons | 3 alpha-hydroxysteroid dehydrogenase | NEUROACTIVE STEROIDS | 5 alpha-reductase (type I) | GAMMA-AMINOBUTYRIC-ACID | RAT-BRAIN | 3-ALPHA-HYDROXYSTEROID DIHYDRODIOL DEHYDROGENASE | Brain - enzymology | Male | Neurons - cytology | Cerebellum - enzymology | RNA, Messenger - metabolism | Cerebral Cortex - cytology | Corpus Striatum - cytology | 3-alpha-Hydroxysteroid Dehydrogenase (B-Specific) - genetics | Amygdala - enzymology | 3-Oxo-5-alpha-Steroid 4-Dehydrogenase - metabolism | Hippocampus - enzymology | Corpus Striatum - enzymology | Olfactory Bulb - cytology | Olfactory Bulb - enzymology | Cerebral Cortex - enzymology | RNA, Messenger - genetics | Thalamus - enzymology | Rats | Amygdala - cytology | Hippocampus - cytology | Desoxycorticosterone - analogs & derivatives | Desoxycorticosterone - biosynthesis | Gene Expression Regulation, Enzymologic | Membrane Proteins | Animals | Pregnanolone - biosynthesis | 3-Oxo-5-alpha-Steroid 4-Dehydrogenase - genetics | 3-alpha-Hydroxysteroid Dehydrogenase (B-Specific) - metabolism | Neurons - enzymology | Cerebellum - cytology | Thalamus - cytology | Mice | GABA | Research | Progesterone | Oxidoreductases | Structure | Steroids | Proteins | Rodents | Cells | Index Medicus | Biological Sciences
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 02/2012, Volume 90, Issue 2, pp. 282 - 289
Genitopatellar syndrome (GPS) is a skeletal dysplasia with cerebral and genital anomalies for which the molecular basis has not yet been determined. By exome... 
STEM-CELLS | COACTIVATOR | PROTEIN | ANOMALIES | GENETICS & HEREDITY | PHENOTYPE | TUMOR | LMX1B | IDENTIFICATION | ABSENT PATELLAE | FEMALE | Blepharoptosis - genetics | Blepharophimosis - enzymology | Humans | Urogenital Abnormalities - enzymology | Histone Acetyltransferases - genetics | Male | Bone Diseases, Developmental - genetics | Cerebellum - abnormalities | Intellectual Disability - genetics | Exome | Blepharophimosis - genetics | Heart Defects, Congenital - genetics | Rubinstein-Taybi Syndrome - genetics | Epigenomics - methods | Blepharoptosis - enzymology | Heart Defects, Congenital - enzymology | Intellectual Disability - enzymology | Female | Rubinstein-Taybi Syndrome - enzymology | Musculoskeletal Abnormalities - enzymology | Abnormalities, Multiple - genetics | Mice, Inbred C57BL | Phenotype | Animals | Bone Diseases, Developmental - enzymology | Musculoskeletal Abnormalities - genetics | Abnormalities, Multiple - enzymology | Heterozygote | Mice | Mutation | Sequence Analysis, DNA - methods | Urogenital Abnormalities - genetics | Brain | Dysplasia | Usage | Genetic disorders | Gene mutations | Exome sequencing | Physiological aspects | Causes of | Genetic aspects | Research | Histones | Analysis | Genomics | Medical genetics | Proteins | Rodents | Epigenetics | Genetic research | Gene expression | Cells | Index Medicus | Report
Journal Article
Nature, ISSN 0028-0836, 2013, Volume 502, Issue 7471, pp. 372 - 376
Ca2+/calmodulin-dependent protein kinase II (CaMKII) is an enzyme with important regulatory functions in the heart and brain, and its chronic activation can be... 
N-ACETYLGLUCOSAMINE | MYOCYTES | MULTIDISCIPLINARY SCIENCES | HEART-FAILURE | CARDIAC-HYPERTROPHY | RECEPTOR | CYTOSOLIC PROTEINS | CARDIOMYOCYTES | MELLITUS | CA2+/CALMODULIN-DEPENDENT PROTEIN-KINASE | INSIGHT | Calcium - metabolism | Humans | Brain - enzymology | Hyperglycemia - complications | Glycosylation - drug effects | Acetylglucosamine - metabolism | Myocytes, Cardiac - enzymology | Diazooxonorleucine - pharmacology | Sarcoplasmic Reticulum - metabolism | Calcium-Calmodulin-Dependent Protein Kinase Type 2 - metabolism | Arrhythmias, Cardiac - metabolism | Diabetes Complications - metabolism | Rats | Glucose - pharmacology | Enzyme Activation - drug effects | Sulfonamides - pharmacology | Myocardium - cytology | Brain - drug effects | Hyperglycemia - metabolism | Myocardium - enzymology | Animals | Arrhythmias, Cardiac - enzymology | Glucose - metabolism | Hyperglycemia - enzymology | Myocytes, Cardiac - metabolism | Arrhythmias, Cardiac - complications | Diabetes Complications - enzymology | Mice | Benzylamines - pharmacology | Enzymes | Medical research | Arrhythmia | Protein biosynthesis | Glycosylation | Research | Risk factors | Complications and side effects | Hyperglycemia | Physiological aspects | Medicine, Experimental | Regulation | Protein kinases | Proteins | Brain | Phosphorylation | Rodents | Cardiomyocytes | Diabetes | Kinases | Index Medicus
Journal Article
Journal Article
Journal Article
Arthritis research & therapy, ISSN 1478-6354, 2004, Volume 6, Issue 6, pp. R551 - 556
Symptoms originating from the central nervous system (CNS) occur frequently in patients with systemic lupus erythematosus (SLE), and CNS involvement in lupus... 
matrix metalloproteinase-2 | PROTEIN | matrix metalloproteinase-9 | CEREBROSPINAL-FLUID INTERLEUKIN-6 | INVOLVEMENT | neuropsychiatric involvement in systemic lupus erythematosus | NECROSIS-FACTOR-ALPHA | RHEUMATOLOGY | MENINGITIS | MULTIPLE-SCLEROSIS | cerebrospinal fluid | NEUROPSYCHIATRIC LUPUS | magnetic resonance imaging of the brain | MATRIX-METALLOPROTEINASE-9 | EXPRESSION | BLOOD | Central Nervous System Diseases - pathology | Lupus Erythematosus, Systemic - complications | Humans | Meningitis, Aseptic - etiology | Middle Aged | Brain - enzymology | Interleukin-8 - cerebrospinal fluid | Male | Psychotic Disorders - cerebrospinal fluid | Myelitis, Transverse - enzymology | tau Proteins | Myelitis, Transverse - cerebrospinal fluid | Glial Fibrillary Acidic Protein - cerebrospinal fluid | Aged, 80 and over | Adult | Female | Interleukin-6 - cerebrospinal fluid | Psychotic Disorders - enzymology | Cerebrospinal Fluid Proteins - analysis | Lupus Erythematosus, Systemic - enzymology | Myelitis, Transverse - etiology | Seizures - enzymology | Central Nervous System Diseases - enzymology | Central Nervous System Diseases - cerebrospinal fluid | Matrix Metalloproteinase 2 - cerebrospinal fluid | Nerve Tissue Proteins - cerebrospinal fluid | Enzyme Induction | Lupus Erythematosus, Systemic - cerebrospinal fluid | Meningitis, Aseptic - cerebrospinal fluid | Leukocytosis - etiology | Magnetic Resonance Imaging | Central Nervous System Diseases - etiology | Adolescent | Seizures - etiology | Brain - pathology | Seizures - cerebrospinal fluid | Aged | Matrix Metalloproteinase 9 - cerebrospinal fluid | Lupus Erythematosus, Systemic - pathology | Meningitis, Aseptic - enzymology | Psychotic Disorders - etiology | Index Medicus | Myelitis | Brain/enzymology/pathology | Cerebrospinal Fluid Proteins/analysis | Interleukin-6/cerebrospinal fluid | Transverse/cerebrospinal fluid/enzymology/etiology | MEDICIN OCH HÄLSOVETENSKAP | Glial Fibrillary Acidic Protein/cerebrospinal fluid | Seizures/cerebrospinal fluid/enzymology/etiology | 80 and over | Psychotic Disorders/cerebrospinal fluid/enzymology/etiology | Aseptic/cerebrospinal fluid/enzymology/etiology | Lupus Erythematosus | Meningitis | fluid/enzymology/etiology/pathology | MEDICAL AND HEALTH SCIENCES | fluid/complications/enzymology/pathology | Leukocytosis/etiology | Nerve Tissue Proteins/cerebrospinal fluid | Matrix Metalloproteinase 9/cerebrospinal fluid | Interleukin-8/cerebrospinal fluid | Central Nervous System Diseases/cerebrospinal | Matrix Metalloproteinase 2/cerebrospinal fluid | Systemic/cerebrospinal
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 07/2005, Volume 25, Issue 28, pp. 6594 - 6600
Journal Article
Journal Article
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 11/2014, Volume 111, Issue 45, pp. E4878 - E4886
Inflammation is accompanied by the release of highly reactive oxygen and nitrogen species (RONS) that damage DNA, among other cellular molecules. Base excision... 
Aag/Mpg DNA glycosylase | DNA repair | Ischemia reperfusion | Liver | Base excision | GLYCOSYLASE | liver | MULTIDISCIPLINARY SCIENCES | DNA-DAMAGE | ischemia reperfusion | MECHANISMS | HMGB1 | CELL-DEATH | PROTECTS | PATHWAY | base excision | INFLAMMATION | POLY(ADP-RIBOSE) POLYMERASE-1 | STRESS | Inflammation - pathology | Liver - pathology | Liver - enzymology | Reactive Oxygen Species - metabolism | Kidney - pathology | Kidney - enzymology | Brain - enzymology | Brain Infarction - pathology | Hepatocytes - pathology | Acute Kidney Injury - genetics | HMGB1 Protein - genetics | HMGB1 Protein - metabolism | Cell Death | Reperfusion Injury - genetics | DNA Glycosylases - metabolism | Brain Infarction - enzymology | Reperfusion Injury - pathology | Acute Kidney Injury - pathology | Reactive Nitrogen Species - metabolism | Reperfusion Injury - enzymology | DNA Glycosylases - genetics | Acute Kidney Injury - enzymology | Mice, Knockout | Enzyme Induction - genetics | Poly(ADP-ribose) Polymerases - metabolism | Animals | Poly(ADP-ribose) Polymerases - genetics | DNA Repair | Brain - pathology | Inflammation - genetics | Mice | DNA Damage | Brain Infarction - genetics | Inflammation - enzymology | Hepatocytes - enzymology | Brain | Kidneys | DNA polymerase | Rodents | DNA damage | Index Medicus | Biological Sciences | PNAS Plus | Aag | Mpg DNA glycosylase
Journal Article