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There is a page named "Familial defective apolipoprotein B-100" on Wikipedia
R.; Ahmad, Zahid; Andersen, Rolf L. (November 2016). "Familial defective apolipoprotein B-100: A review". Journal of Clinical Lipidology. 10 (6): 1297–1302...40 KB (4,875 words) - 14:08, 5 May 2024
Apolipoprotein B deficiency is an autosomal dominant disorder resulting from a missense mutation which reduces the affinity of apoB-100 for the low-density...2 KB (144 words) - 04:10, 19 January 2024
homozygous familial hypercholesterolemia. In January 2013, The US FDA also approved mipomersen, which inhibits the action of the gene apolipoprotein B, for...48 KB (5,456 words) - 18:52, 29 May 2024
hyperlipoproteinemia) Familial defective apolipoprotein B-100 Familial dysbetalipoproteinemia (broad beta disease, remnant removal disease) Familial hypertriglyceridemia...198 KB (17,958 words) - 01:24, 6 July 2024
Apolipoprotein D (ApoD) is a protein that in humans is encoded by the APOD gene. Unlike other lipoproteins, which are mainly produced in the liver, apolipoprotein...44 KB (4,897 words) - 14:15, 11 June 2024- Dabbing Syndrome Defect in synthesis of adenosylcobalamin Defective apolipoprotein B-100 Defective expression of HLA class 2 Degenerative motor system disease...13 KB (1,155 words) - 22:52, 28 April 2024
- David C. Rubinsztein (category EngvarB from August 2017)Rubinsztein completed his Bachelor of Medicine, Bachelor of Surgery (MB ChB) in 1986 and PhD in 1993 in the Medical Research Council/University of Cape...17 KB (1,277 words) - 13:26, 20 April 2024
mechanism, including Aβ amyloidosis, amyloid A (AA) amyloidosis, and apolipoprotein AII amyloidosis, tauopathy, synucleinopathy, and the aggregation of...62 KB (4,594 words) - 04:36, 14 July 2024
insoluble forms of alpha-synuclein accumulate as inclusions in Lewy bodies. Familial Parkinson's disease is associated with mutations in the -synuclein (SNCA)...83 KB (9,383 words) - 03:57, 6 July 2024- control subjects, together with an increased expression of an isoforms of apolipoprotein E in RR-MS. Expression of some specific proteins in circulating CD4+...66 KB (7,797 words) - 16:19, 8 June 2024
Enemark EJ (May 2015). "Cancer-associated mutants of RNA helicase DDX3X are defective in RNA-stimulated ATP hydrolysis". Journal of Molecular Biology. 427 (9):...183 KB (12,458 words) - 20:40, 1 July 2024
macrophage fatty-acid–binding protein aP2 protects mice deficient in apolipoprotein E against atherosclerosis". Nature Medicine. 7 (6): 699–705. doi:10...67 KB (7,848 words) - 01:42, 11 December 2023
- delivered mRNA–LNP complexes mainly target the liver owing to binding of apolipoprotein E and subsequent receptor-mediated uptake by hepatocytes, and intradermal
- susceptibility gene has so far been identified: the epsilon 4 allele of the apolipoprotein E gene. Age of onset itself has a heritability of around 50%. The changes