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Plant Physiology, ISSN 0032-0889, 10/2013, Volume 163, Issue 2, pp. 914 - 928
Journal Article
PLoS Biol, ISSN 1544-9173, 05/2017, Volume 15, Issue 5, p. e1002605
In the vertebrate nervous system, myelination of axons for rapid impulse propagation requires the synthesis of large amounts of lipids and proteins by... 
Agricultural and Biological Sciences(all) | Immunology and Microbiology(all) | Biochemistry, Genetics and Molecular Biology(all) | Neuroscience(all) | Journal Article | CHOLESTEROL-METABOLISM | NERVOUS-SYSTEM | PROMOTE MYELINATION | IN-VITRO | ACID | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOLOGY | NEURONS | SCHWANN-CELLS | RAT-BRAIN | GLIAL-CELLS | MATURATION | Glial Fibrillary Acidic Protein - genetics | Oligodendroglia - metabolism | Humans | Astrocytes - pathology | Intracellular Signaling Peptides and Proteins - metabolism | Demyelinating Diseases - metabolism | Glial Fibrillary Acidic Protein - metabolism | Oligodendroglia - ultrastructure | Myelin Sheath - metabolism | Diet, High-Fat | Gene Deletion | Membrane Proteins - metabolism | Sterol Regulatory Element Binding Protein 2 - genetics | Sterol Regulatory Element Binding Protein 2 - metabolism | Demyelinating Diseases - pathology | Intracellular Signaling Peptides and Proteins - genetics | Biomarkers - metabolism | Microscopy, Electron, Transmission | Myelin Sheath - pathology | Membrane Proteins - genetics | Mice, Inbred C57BL | Lipid Metabolism | Mice, Transgenic | Demyelinating Diseases - prevention & control | Organ Specificity | Fatty Acid Synthase, Type I - metabolism | Nerve Tissue Proteins - genetics | Astrocytes - ultrastructure | Nerve Tissue Proteins - metabolism | Oligodendroglia - pathology | Animals | Myelin Sheath - ultrastructure | Protein Processing, Post-Translational | Mutation | Astrocytes - metabolism | Crosses, Genetic | Physiological aspects | Axons | Lipid metabolism | Observations | Astrocytes | Enrichment | Brain | Membranes | Propagation | Central nervous system | Neurobiology | Lipids | Nervous system | Biosynthesis | Glial cells | Gene deletion | Inactivation | Proteins | Clonal deletion | Oligodendrocytes | Sterol regulatory element-binding protein | Cleavage | Inhibition | Age | Fluctuations | Deactivation | Myelin | Neurons | Developmental biology | Schwann cells | Flux | Embryos | Mutants | Myelination | Brain research
Journal Article
Nature Communications, ISSN 2041-1723, 01/2019, Volume 10, Issue 1, p. 376
Journal Article
Neuron, ISSN 0896-6273, 04/2013, Volume 78, Issue 1, pp. 57 - 64
Valosin-containing protein (VCP) is a highly expressed member of the type II AAA+ ATPase family. VCP mutations are the cause of inclusion body myopathy,... 
LIPID-PEROXIDATION | SPINAL-CORD PATHOLOGY | MOUSE MODEL | ALS | AMYOTROPHIC-LATERAL-SCLEROSIS | DYSFUNCTION | BONE | NEUROSCIENCES | PAGET-DISEASE | TRANSGENIC MICE | REVEALS | RNA, Small Interfering - genetics | Humans | Middle Aged | Male | Frontotemporal Dementia - metabolism | Neurons - ultrastructure | Muscular Dystrophies, Limb-Girdle - genetics | Adenosine Triphosphate - metabolism | Membrane Potential, Mitochondrial - genetics | Muscular Dystrophies, Limb-Girdle - pathology | NAD - metabolism | Fibroblasts - metabolism | Animals, Newborn | Frontotemporal Dementia - genetics | Magnesium - metabolism | Mitochondria - pathology | Fibroblasts - pathology | Mutation - genetics | Myositis, Inclusion Body - genetics | Osteitis Deformans - pathology | Muscular Dystrophies, Limb-Girdle - metabolism | Analysis of Variance | Luminescent Proteins - genetics | Adenosine Triphosphatases - genetics | Mice | Lipid Peroxidation - genetics | RNA, Small Interfering - metabolism | Valosin Containing Protein | Osteitis Deformans - metabolism | Family Health | Cerebral Cortex - cytology | Case-Control Studies | Osteitis Deformans - genetics | Transfection | Mitochondria - genetics | Cell Cycle Proteins - genetics | Myositis, Inclusion Body - pathology | Adult | Female | Neuroblastoma - pathology | Frontotemporal Dementia - pathology | Adenosine Triphosphatases - deficiency | Mice, Inbred C57BL | Cells, Cultured | Cell Cycle Proteins - deficiency | Mitochondria - metabolism | Animals | Oxygen Consumption - genetics | Myositis, Inclusion Body - metabolism | Aged | Nervous system diseases | Neurosciences | Genes | Amyotrophic lateral sclerosis | Genetic aspects | Adenosine triphosphatase | Dementia | Proteins | Medical research | Phosphorylation | Biomedical research | Disease | Rodents | Respiration | Experiments | Patients | Report
Journal Article
Journal Article
Cell Metabolism, ISSN 1550-4131, 05/2012, Volume 15, Issue 5, pp. 691 - 702
Numerous studies in humans link a nonsynonymous genetic polymorphism (I148M) in adiponutrin (ADPN) to various forms of fatty liver disease and liver cirrhosis.... 
ADIPOSE TRIGLYCERIDE LIPASE | COMPARATIVE GENE IDENTIFICATION-58 | LIPID-METABOLISM | MESSENGER-RNA EXPRESSION | FATTY LIVER-DISEASE | FAMILY-MEMBERS | ENZYMES | ENDOCRINOLOGY & METABOLISM | PNPLA3 | CONGENITAL GENERALIZED LIPODYSTROPHY | CHANARIN-DORFMAN-SYNDROME | CELL BIOLOGY | 1-Acylglycerol-3-Phosphate O-Acyltransferase - genetics | Lysophospholipids - metabolism | Up-Regulation | Lipids - genetics | Humans | Cercopithecus aethiops | Acyl Coenzyme A - genetics | Male | Lipids - biosynthesis | Acyltransferases - metabolism | Acyltransferases - genetics | 1-Acylglycerol-3-Phosphate O-Acyltransferase - metabolism | Cysteine Endopeptidases - metabolism | Liver - drug effects | Lipid Metabolism - genetics | Membrane Proteins - metabolism | Dietary Sucrose - metabolism | Phospholipids - metabolism | Acyl Coenzyme A - metabolism | CHO Cells | Fatty Liver - genetics | Phosphatidic Acids - genetics | Cricetinae | Fatty Liver - metabolism | Membrane Proteins - genetics | Liver - metabolism | Models, Molecular | Phospholipids - genetics | Hep G2 Cells | Mice, Knockout | Polymorphism, Genetic | Triglycerides - metabolism | Lysophospholipids - genetics | Animals | Cysteine Endopeptidases - genetics | Mice | Phosphatidic Acids - metabolism | Triglycerides - genetics | COS Cells | Physiological aspects | Medical colleges | Disease susceptibility | Liver diseases | Liver cirrhosis
Journal Article
eLife, ISSN 2050-084X, 04/2015, Volume 2015, Issue 4, pp. 1 - 61
The conserved MICOS complex functions as a primary determinant of mitochondrial inner membrane structure. We address the organization and functional roles of... 
ORGANIZING SYSTEM | CYTOCHROME-C | OUTER-MEMBRANE | CHAIN SUPERCOMPLEXES | CONTACT SITE | SUPERRESOLUTION FLUORESCENCE | ATP SYNTHASE | BIOLOGY | CRISTAE MORPHOLOGY | PROTEIN BIOGENESIS | SACCHAROMYCES-CEREVISIAE | Saccharomyces cerevisiae - genetics | Mitochondrial Proteins - genetics | Saccharomyces cerevisiae - ultrastructure | Electron Transport Complex I - metabolism | Mitochondria - ultrastructure | Saccharomyces cerevisiae - metabolism | Mitochondria - genetics | Electron Transport Complex I - genetics | Mitochondrial Proteins - metabolism | Recombination, Genetic | Membrane Proteins - metabolism | Electron Transport Complex II - chemistry | Recombinant Proteins - metabolism | Electron Transport Complex II - genetics | Membrane Proteins - genetics | Recombinant Proteins - chemistry | Cardiolipins - metabolism | Mitochondria - metabolism | Recombinant Proteins - genetics | Saccharomyces cerevisiae Proteins - genetics | Cardiolipins - chemistry | Mitochondrial Membranes - metabolism | Electron Transport Complex I - chemistry | Membrane Proteins - chemistry | Electron Transport Complex II - metabolism | Mitochondrial Membranes - ultrastructure | Mitochondrial Proteins - chemistry | Saccharomyces cerevisiae Proteins - metabolism | Protein Binding | Saccharomyces cerevisiae Proteins - chemistry | Cytochrome | Membranes | Membrane structure | Copy number | Cloning | Lipids | Biology | Proteins | Mitochondria | Functional morphology | Dimensional analysis | Cristae | Cardiolipin | Infrared imaging systems | Apoptosis
Journal Article