amyloid associated
81connective tissue disease — Introduction any of the diseases that affect human connective tissue. Diseases of the connective tissue can be divided into (1) a group of relatively uncommon genetic disorders (genetic disease, human) that affect the primary structure of… …
82Hereditary amyloidosis — A familial (inherited) disorder in which protein deposits (amyloid) accumulate in one or more organ systems in the body. Hereditary amyloidosis is a relatively uncommon cause of amyloidosis. The more common forms of amyloidosis are primary an… …
83Beta-secretase 1 — Beta site APP cleaving enzyme 1 PDB rendering based on 1fkn …
84Gamma secretase — is a multi subunit protease complex, itself an integral membrane protein, that cleaves single pass transmembrane proteins at residues within the transmembrane domain. The most well known substrate of gamma secretase is amyloid precursor protein,… …
85Apolipoprotein A1 — Apolipoprotein A I, also known as APOA1, is a human gene.The protein encoded by this gene is an apolipoprotein. It is the major protein component of high density lipoprotein (HDL) in plasma. The protein promotes cholesterol efflux from tissues to …
86AA amyloidosis — is a form of amyloidosis associated with serum amyloid A protein (SAA), an acute phase protein. cite journal |author=Lachmann HJ, Goodman HJ, Gilbertson JA, et al |title=Natural history and outcome in systemic AA amyloidosis |journal=N. Engl. J.… …
87Amyotrophic lateral sclerosis — This article is about progressive Motor Neuron Disease (MND) affecting both the upper motor neurons and lower motor neurons. For MND affecting either but not necessarily both, see Motor neurone disease. ALS redirects here. For other uses, see ALS …
88Protein — A large molecule composed of one or more chains of amino acids in a specific order determined by the base sequence of nucleotides in the DNA coding for the protein. Proteins are required for the structure, function, and regulation of the body s… …
89Beta sheet — The β sheet (also β pleated sheet) is the second form of regular secondary structure in proteins consisting of beta strands connected laterally by three or more hydrogen bonds, forming a generally twisted, pleated sheet (the most common form of… …
90HSD17B10 — Hydroxysteroid (17 beta) dehydrogenase 10, also known as HSD17B10, is a human gene.cite web | title = Entrez Gene: HSD17B10 hydroxysteroid (17 beta) dehydrogenase 10| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… …
