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36 relations: Aceruloplasminemia, Acute-phase protein, Alzheimer's disease, Angina, Ataxia, ATP7A, Cirrhosis, Cis-regulatory element, Copper, Copper toxicity, Dementia, Endocrine system, Endoplasmic reticulum, Enzyme, Extrapyramidal symptoms, Ferroxidase, GAIT element, Gene, Golgi apparatus, Hepatocyte, Hephaestin, Human iron metabolism, Inflammation, Lymphoma, Malnutrition, Menkes disease, Obsessive–compulsive disorder, Occipital horn syndrome, Oral contraceptive pill, Pregnancy, Rheumatoid arthritis, Schizophrenia, Transferrin, Wilson disease protein, Wilson's disease, Zinc deficiency.
Aceruloplasminemia
Aceruloplasminemia is a rare autosomal recessive disorder in which iron gradually accumulates in the retina, basal ganglia, and other organs.
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Acute-phase protein
Acute-phase proteins (APPs) are a class of proteins whose plasma concentrations increase (positive acute-phase proteins) or decrease (negative acute-phase proteins) in response to inflammation.
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Alzheimer's disease
Alzheimer's disease (AD), also referred to simply as Alzheimer's, is a chronic neurodegenerative disease that usually starts slowly and worsens over time.
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Angina
Angina, also known as angina pectoris, is chest pain or pressure, usually due to not enough blood flow to the heart muscle.
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Ataxia
Ataxia is a neurological sign consisting of lack of voluntary coordination of muscle movements that includes gait abnormality.
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ATP7A
ATP7A, also known as Menkes' protein (MNK), is a copper-transporting P-type ATPase which uses the energy arising from ATP hydrolysis to transport Cu(I) across cell membranes.
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Cirrhosis
Cirrhosis is a condition in which the liver does not function properly due to long-term damage.
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Cis-regulatory element
Cis-regulatory elements (CREs) are regions of non-coding DNA which regulate the transcription of neighboring genes.
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Copper
Copper is a chemical element with symbol Cu (from cuprum) and atomic number 29.
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Copper toxicity
Copper toxicity, also called copperiedus, is a type of metal poisoning caused by an excess of copper in the body.
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Dementia
Dementia is a broad category of brain diseases that cause a long-term and often gradual decrease in the ability to think and remember that is great enough to affect a person's daily functioning.
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Endocrine system
The endocrine system is a chemical messenger system consisting of hormones, the group of glands of an organism that carry those hormones directly into the circulatory system to be carried towards distant target organs, and the feedback loops of homeostasis that the hormones drive.
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Endoplasmic reticulum
The endoplasmic reticulum (ER) is a type of organelle found in eukaryotic cells that forms an interconnected network of flattened, membrane-enclosed sacs or tube-like structures known as cisternae.
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Enzyme
Enzymes are macromolecular biological catalysts.
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Extrapyramidal symptoms
Extrapyramidal symptoms (EPS), also known as extrapyramidal side effects (EPSE), are drug-induced movement disorders that include acute and tardive symptoms.
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Ferroxidase
Ferroxidase also known as Fe(II):oxygen oxidoreductase is an enzyme that catalyzes the oxidization of iron II to iron III.
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GAIT element
The gamma interferon inhibitor of translation element or GAIT element is a cis-acting RNA element located in the 3'-UTR of the ceruloplasmin (Cp) mRNA.
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Gene
In biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.
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Golgi apparatus
The Golgi apparatus, also known as the Golgi complex, Golgi body, or simply the Golgi, is an organelle found in most eukaryotic cells.
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Hepatocyte
A hepatocyte is a cell of the main parenchymal tissue of the liver.
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Hephaestin
Hephaestin, also known as HEPH, is a protein which in humans is encoded by the HEPH gene.
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Human iron metabolism
Human iron metabolism is the set of chemical reactions that maintain human homeostasis of iron at the systemic and cellular level.
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Inflammation
Inflammation (from inflammatio) is part of the complex biological response of body tissues to harmful stimuli, such as pathogens, damaged cells, or irritants, and is a protective response involving immune cells, blood vessels, and molecular mediators.
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Lymphoma
Lymphoma is a group of blood cancers that develop from lymphocytes (a type of white blood cell).
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Malnutrition
Malnutrition is a condition that results from eating a diet in which one or more nutrients are either not enough or are too much such that the diet causes health problems.
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Menkes disease
Menkes disease (MNK), also known as Menkes syndrome, is an X-linked recessive disorder caused by mutations in genes coding for the copper-transport protein ATP7A, leading to copper deficiency.
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Obsessive–compulsive disorder
Obsessive–compulsive disorder (OCD) is a mental disorder where people feel the need to check things repeatedly, perform certain routines repeatedly (called "rituals"), or have certain thoughts repeatedly (called "obsessions").
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Occipital horn syndrome
Occipital horn syndrome (OHS), formerly considered a variant of Ehlers-Danlos syndrome, is an X-linked recessive mitochondrial and connective tissue disorder.
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Oral contraceptive pill
Oral contraceptives, abbreviated OCPs, also known as birth control pills, are medications taken by mouth for the purpose of birth control.
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Pregnancy
Pregnancy, also known as gestation, is the time during which one or more offspring develops inside a woman.
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Rheumatoid arthritis
Rheumatoid arthritis (RA) is a long-term autoimmune disorder that primarily affects joints.
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Schizophrenia
Schizophrenia is a mental disorder characterized by abnormal social behavior and failure to understand reality.
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Transferrin
Transferrins are iron-binding blood plasma glycoproteins that control the level of free iron (Fe) in biological fluids.
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Wilson disease protein
Wilson disease protein (WND), also known as ATP7B protein, is a copper-transporting P-type ATPase which is encoded by the ATP7B gene.
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Wilson's disease
Wilson's disease is a genetic disorder in which copper builds up in the body.
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Zinc deficiency
Zinc deficiency is defined either as insufficient zinc to meet the needs of the body, or as a serum zinc level below the normal range.
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Redirects here:
CP (gene), Caeruloplasmin, Cp-2, Holo-ceruloplasmin.
References
[1] https://en.wikipedia.org/wiki/Ceruloplasmin
