Faster access than browser!Similarities between Amyloid and Proteopathy
Amyloid and Proteopathy have 37 things in common (in Unionpedia): Alpha-synuclein, Alzheimer's disease, Amylin, Amyloid, Amyloid beta, Amyloidosis, Apolipoprotein A1, Atrial natriuretic peptide, Beta sheet, Beta-2 microglobulin, Birefringence, Calcitonin, Cerebral amyloid angiopathy, Congo red, Diabetes mellitus type 2, Disease, Electron microscope, Escherichia coli, Gelsolin, Huntington's disease, Inclusion body myositis, Lysozyme, MFGE8, Parkinson's disease, Peptide, Polarization (waves), Prion, Prolactin, Protein, Protein folding, ..., Rudolf Virchow, Senile plaques, Serum amyloid A, TGFBI, Transmissible spongiform encephalopathy, Transthyretin, Trinucleotide repeat disorder. Expand index (7 more) »
Alpha-synuclein
Alpha-synuclein is a protein that, in humans, is encoded by the SNCA gene.
Alpha-synuclein and Amyloid · Alpha-synuclein and Proteopathy ·
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.
Alzheimer's disease and Amyloid · Alzheimer's disease and Proteopathy ·
Amylin
Amylin, or islet amyloid polypeptide (IAPP), is a 37-residue peptide hormone.
Amylin and Amyloid · Amylin and Proteopathy ·
Amyloid
Amyloids are aggregates of proteins that become folded into a shape that allows many copies of that protein to stick together forming fibrils.
Amyloid and Amyloid · Amyloid and Proteopathy ·
Amyloid beta
Amyloid beta (Aβ or Abeta) denotes peptides of 36–43 amino acids that are crucially involved in Alzheimer's disease as the main component of the amyloid plaques found in the brains of Alzheimer patients.
Amyloid and Amyloid beta · Amyloid beta and Proteopathy ·
Amyloidosis
Amyloidosis is a group of diseases in which abnormal protein, known as amyloid fibrils, builds up in tissue.
Amyloid and Amyloidosis · Amyloidosis and Proteopathy ·
Apolipoprotein A1
Apolipoprotein A1 is a protein that in humans is encoded by the APOA1 gene.
Amyloid and Apolipoprotein A1 · Apolipoprotein A1 and Proteopathy ·
Atrial natriuretic peptide
Atrial natriuretic peptide (ANP) or Atrial natriuretic factor (ANF) is a peptide hormone which reduces an expanded extracellular fluid (ECF) volume by increasing renal sodium excretion.
Amyloid and Atrial natriuretic peptide · Atrial natriuretic peptide and Proteopathy ·
Beta sheet
The β-sheet (also β-pleated sheet) is a common motif of regular secondary structure in proteins.
Amyloid and Beta sheet · Beta sheet and Proteopathy ·
Beta-2 microglobulin
β2 microglobulin also known as B2M is a component of MHC class I molecules, MHC class I molecules have α1, α2, and α3 proteins which are present on all nucleated cells (excludes red blood cells).
Amyloid and Beta-2 microglobulin · Beta-2 microglobulin and Proteopathy ·
Birefringence
Birefringence is the optical property of a material having a refractive index that depends on the polarization and propagation direction of light.
Amyloid and Birefringence · Birefringence and Proteopathy ·
Calcitonin
Calcitonin (also known as thyrocalcitonin) is a 32-amino acid linear polypeptide hormone that is produced in humans primarily by the parafollicular cells (also known as C-cells) of the thyroid gland, and in many other animals in the ultimopharyngeal body.
Amyloid and Calcitonin · Calcitonin and Proteopathy ·
Cerebral amyloid angiopathy
Cerebral amyloid angiopathy (CAA), also known as congophilic angiopathy, is a form of angiopathy in which amyloid deposits form in the walls of the blood vessels of the central nervous system.
Amyloid and Cerebral amyloid angiopathy · Cerebral amyloid angiopathy and Proteopathy ·
Congo red
Congo red is an organic compound, the sodium salt of 3,3′-(-4,4′-diyl)bis(4-aminonaphthalene-1-sulfonic acid).
Amyloid and Congo red · Congo red and Proteopathy ·
Diabetes mellitus type 2
Diabetes mellitus type 2 (also known as type 2 diabetes) is a long-term metabolic disorder that is characterized by high blood sugar, insulin resistance, and relative lack of insulin.
Amyloid and Diabetes mellitus type 2 · Diabetes mellitus type 2 and Proteopathy ·
Disease
A disease is any condition which results in the disorder of a structure or function in an organism that is not due to any external injury.
Amyloid and Disease · Disease and Proteopathy ·
Electron microscope
An electron microscope is a microscope that uses a beam of accelerated electrons as a source of illumination.
Amyloid and Electron microscope · Electron microscope and Proteopathy ·
Escherichia coli
Escherichia coli (also known as E. coli) is a Gram-negative, facultatively anaerobic, rod-shaped, coliform bacterium of the genus Escherichia that is commonly found in the lower intestine of warm-blooded organisms (endotherms).
Amyloid and Escherichia coli · Escherichia coli and Proteopathy ·
Gelsolin
Gelsolin is an actin-binding protein that is a key regulator of actin filament assembly and disassembly.
Amyloid and Gelsolin · Gelsolin and Proteopathy ·
Huntington's disease
Huntington's disease (HD), also known as Huntington's chorea, is an inherited disorder that results in death of brain cells.
Amyloid and Huntington's disease · Huntington's disease and Proteopathy ·
Inclusion body myositis
Inclusion body myositis (IBM) is the most common inflammatory muscle disease in older adults.
Amyloid and Inclusion body myositis · Inclusion body myositis and Proteopathy ·
Lysozyme
Lysozyme, also known as muramidase or N-acetylmuramide glycanhydrolase is an antimicrobial enzyme produced by animals that forms part of the innate immune system.
Amyloid and Lysozyme · Lysozyme and Proteopathy ·
MFGE8
Milk fat globule-EGF factor 8 protein (Mfge8), also known as lactadherin, is a protein which in humans is encoded by the MFGE8 gene.
Amyloid and MFGE8 · MFGE8 and Proteopathy ·
Parkinson's disease
Parkinson's disease (PD) is a long-term degenerative disorder of the central nervous system that mainly affects the motor system.
Amyloid and Parkinson's disease · Parkinson's disease and Proteopathy ·
Peptide
Peptides (from Gr.: πεπτός, peptós "digested"; derived from πέσσειν, péssein "to digest") are short chains of amino acid monomers linked by peptide (amide) bonds.
Amyloid and Peptide · Peptide and Proteopathy ·
Polarization (waves)
Polarization (also polarisation) is a property applying to transverse waves that specifies the geometrical orientation of the oscillations.
Amyloid and Polarization (waves) · Polarization (waves) and Proteopathy ·
Prion
Prions are misfolded proteins that are associated with several fatal neurodegenerative diseases in animals and humans.
Amyloid and Prion · Prion and Proteopathy ·
Prolactin
Prolactin (PRL), also known as luteotropic hormone or luteotropin, is a protein that is best known for its role in enabling mammals, usually females, to produce milk.
Amyloid and Prolactin · Prolactin and Proteopathy ·
Protein
Proteins are large biomolecules, or macromolecules, consisting of one or more long chains of amino acid residues.
Amyloid and Protein · Protein and Proteopathy ·
Protein folding
Protein folding is the physical process by which a protein chain acquires its native 3-dimensional structure, a conformation that is usually biologically functional, in an expeditious and reproducible manner.
Amyloid and Protein folding · Protein folding and Proteopathy ·
Rudolf Virchow
Rudolf Ludwig Carl Virchow (13 October 1821 – 5 September 1902) was a German physician, anthropologist, pathologist, prehistorian, biologist, writer, editor, and politician, known for his advancement of public health.
Amyloid and Rudolf Virchow · Proteopathy and Rudolf Virchow ·
Senile plaques
Senile plaques (also known as neuritic plaques) are extracellular deposits of amyloid beta in the grey matter of the brain.
Amyloid and Senile plaques · Proteopathy and Senile plaques ·
Serum amyloid A
Serum amyloid A (SAA) proteins are a family of apolipoproteins associated with high-density lipoprotein (HDL) in plasma.
Amyloid and Serum amyloid A · Proteopathy and Serum amyloid A ·
TGFBI
Transforming growth factor, beta-induced, 68kDa, also known as TGFBI (initially called BIGH3, BIG-H3), is a protein which in humans is encoded by the TGFBI gene, locus 5q31.
Amyloid and TGFBI · Proteopathy and TGFBI ·
Transmissible spongiform encephalopathy
Transmissible spongiform encephalopathies (TSEs), also known as prion diseases, are a group of progressive, invariably fatal, conditions that affect the brain (encephalopathies) and nervous system of many animals, including humans.
Amyloid and Transmissible spongiform encephalopathy · Proteopathy and Transmissible spongiform encephalopathy ·
Transthyretin
Transthyretin (TTR) is a transport protein in the serum and cerebrospinal fluid that carries the thyroid hormone thyroxine (T4) and retinol-binding protein bound to retinol.
Amyloid and Transthyretin · Proteopathy and Transthyretin ·
Trinucleotide repeat disorder
Trinucleotide repeat disorders (also known as trinucleotide repeat expansion disorders, triplet repeat expansion disorders or codon reiteration disorders) are a set of genetic disorders caused by trinucleotide repeat expansion, a kind of mutation where trinucleotide repeats in certain genes or intronsDavid W. Sanders & Clifford P. Brangwynne (2017), Nature, 546, 215–216 (08 June 2017) exceed the normal, stable threshold, which differs per gene.
Amyloid and Trinucleotide repeat disorder · Proteopathy and Trinucleotide repeat disorder ·
The list above answers the following questions
- What Amyloid and Proteopathy have in common
- What are the similarities between Amyloid and Proteopathy
Amyloid and Proteopathy Comparison
Amyloid has 115 relations, while Proteopathy has 123. As they have in common 37, the Jaccard index is 15.55% = 37 / (115 + 123).
References
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