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ANNUAL REVIEW OF NEUROSCIENCE, ISSN 0147-006X, 2007, Volume 30, Issue 1, pp. 317 - 337
Copper and iron are transition elements essential for life. These metals are required to maintain the brain's biochemistry such that deficiency or excess of... 
blood-brain barrier | NEURODEGENERATIVE DISEASE | WILSON DISEASE GENE | NMDA RECEPTOR | OCCIPITAL HORN SYNDROME | neurodegeneration | p-type Atpase | NEUROSCIENCES | CULTURED HIPPOCAMPAL-NEURONS | CYTOCHROME-C-OXIDASE | MENKES-DISEASE | HALLERVORDEN-SPATZ-SYNDROME | HEREDITARY CERULOPLASMIN DEFICIENCY | ferroxidase | Golgi | CENTRAL-NERVOUS-SYSTEM | astrocyte | Friedreich Ataxia - metabolism | Genetic Predisposition to Disease - genetics | Brain Diseases, Metabolic - genetics | Menkes Kinky Hair Syndrome - metabolism | Brain - physiopathology | Humans | Hepatolenticular Degeneration - physiopathology | Menkes Kinky Hair Syndrome - genetics | Brain Diseases, Metabolic - metabolism | Iron - metabolism | Friedreich Ataxia - genetics | Brain - metabolism | Friedreich Ataxia - physiopathology | Iron Metabolism Disorders - physiopathology | Animals | Iron Metabolism Disorders - genetics | Brain Diseases, Metabolic - physiopathology | Menkes Kinky Hair Syndrome - physiopathology | Copper - metabolism | Iron Metabolism Disorders - metabolism | Hepatolenticular Degeneration - genetics | Hepatolenticular Degeneration - metabolism | Homeostasis - genetics | Ferroxidase | Astrocyte | Blood-brain barrier | Neurodegeneration | Genetic disorders | Iron deficiency diseases | Nervous system | Genetic aspects | Degeneration | Research | Risk factors | Brain | Iron | Biochemistry | Copper | Neurological disorders
Journal Article
Neurology, ISSN 0028-3878, 07/2013, Volume 81, Issue 2, pp. e12 - e13
Journal Article
Nature, ISSN 0028-0836, 07/2011, Volume 475, Issue 7354, pp. 59 - 65
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2010, Volume 86, Issue 3, pp. 343 - 352
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 08/2016, Volume 291, Issue 32, pp. 16644 - 16658
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 11/2007, Volume 44, Issue 11, pp. 673 - 688
The trace metal copper is essential for a variety of biological processes, but extremely toxic when present in excessive amounts. Therefore, concentrations of... 
OCCIPITAL-HORN-SYNDROME | ATP7A GENE | TYROLEAN INFANTILE CIRRHOSIS | P-TYPE ATPASE | HAMSTER OVARY CELLS | GENETICS & HEREDITY | N-TERMINAL DOMAIN | COPPER-TRANSPORTING ATPASE | PROTEIN-PROTEIN INTERACTIONS | METAL-BINDING SITES | TOXICOSIS GENE MURR1 | Copper-transporting ATPases | Humans | Cation Transport Proteins - physiology | Male | Structure-Activity Relationship | Mutation, Missense | Rats, Inbred LEC | Mice, Mutant Strains | Adenosine Triphosphate - metabolism | Copper - metabolism | Cation Transport Proteins - genetics | Female | Disease Models, Animal | Protein Structure, Tertiary | Menkes Kinky Hair Syndrome - metabolism | Rats | Genotype | Menkes Kinky Hair Syndrome - genetics | Zebrafish | Protein Interaction Mapping | Phenotype | Animals | Adenosine Triphosphatases - chemistry | Adenosine Triphosphatases - genetics | Hepatolenticular Degeneration - genetics | Mice | Cation Transport Proteins - chemistry | Adenosine Triphosphatases - physiology | Hepatolenticular Degeneration - metabolism | Complications and side effects | Copper in the body | Chromosome abnormalities | Adenosine triphosphatase genes | Physiological aspects | Development and progression | Menkes syndrome | Genetic aspects | Research | Wilson's disease | Pathology, Molecular | Health aspects | Proteins | Enzymes | Disease | Laboratories | Rodents | Mutation | Respiration | Defects | copper | ATP7B | Review | Wilson disease | ATP7A | Menkes disease
Journal Article