- 同
- FHC
WordNet
- relating to or having the characteristics of a family; "children of the same familial background"; "familial aggregation"
- occurring among members of a family usually by heredity; "an inherited disease"; "familial traits"; "genetically transmitted features" (同)genetic, hereditary, inherited, transmitted, transmissible
PrepTutorEJDIC
- 家族の,家族特有の / 違伝的な,血統にあらわれる
UpToDate Contents
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English Journal
- Effect of alirocumab, a monoclonal proprotein convertase subtilisin/kexin 9 antibody, on lipoprotein(a) concentrations (a pooled analysis of 150 mg every two weeks dosing from phase 2 trials).
- Gaudet D1, Kereiakes DJ2, McKenney JM3, Roth EM4, Hanotin C5, Gipe D6, Du Y6, Ferrand AC5, Ginsberg HN7, Stein EA8.
- The American journal of cardiology.Am J Cardiol.2014 Sep 1;114(5):711-5. doi: 10.1016/j.amjcard.2014.05.060. Epub 2014 Jun 18.
- Copyright © 2014 The Authors. Published by Elsevier Inc. All rights reserved.
- PMID 25060413
- Common and rare single nucleotide polymorphisms in the LDLR gene are present in a black South African population and associate with low-density lipoprotein cholesterol levels.
- van Zyl T1, Jerling JC1, Conradie KR1, Feskens EJ2.
- Journal of human genetics.J Hum Genet.2014 Feb;59(2):88-94. doi: 10.1038/jhg.2013.123. Epub 2013 Nov 28.
- The LDL receptor has an essential role in regulating plasma LDL-C levels. Genetic variation in the LDLR gene can be associated with either lower or moderately raised plasma levels of LDL-C, or may cause familial hypercholesterolemia. The prevalence of single-nucleotide polymorphisms (SNPs) in the LD
- PMID 24284361
- The emerging role of acyl-CoA thioesterases and acyltransferases in regulating peroxisomal lipid metabolism.
- Hunt MC1, Siponen MI, Alexson SE.
- Biochimica et biophysica acta.Biochim Biophys Acta.2012 Sep;1822(9):1397-410. doi: 10.1016/j.bbadis.2012.03.009. Epub 2012 Mar 23.
- The importance of peroxisomes in lipid metabolism is now well established and peroxisomes contain approximately 60 enzymes involved in these lipid metabolic pathways. Several acyl-CoA thioesterase enzymes (ACOTs) have been identified in peroxisomes that catalyze the hydrolysis of acyl-CoAs (short-,
- PMID 22465940
Related Links
- Nat Genet. 2003 May;34(1):91-6. Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT. Carlton VE, Harris BZ, Puffenberger EG, Batta AK, Knisely AS, Robinson DL, Strauss KA, Shneider BL, Lim WA, ...
- ... B.Z., Puffenberger, E.G., Batta, A.K., Knisely, A.S., Robinson, D.L., Strauss, K.A., Shneider, B.L, Lim, W.A., Salen, G., Morton, D.H., and Bull, L.N.: Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT.
★リンクテーブル★
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家族性肥大心筋症、家族性肥大型心筋症
- 関
- familial hypertrophic cardiomyopathy
- 同
- familial hypercholanemia
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- 関
- family、family member、household、kindred