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
(pathology) a waxy translucent complex protein resembling starch that results from degeneration of tissue
a non-nitrogenous food substance consisting chiefly of starch; any substance resembling starch
inflammation of a nerve accompanied by pain and sometimes loss of function

PrepTutorEJDIC

全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.

1. アミロイドーシスの概要 overview of amyloidosis
2. アミロイド疾患の遺伝的要因 genetic factors in the amyloid diseases
3. アミロイド心筋症の臨床症状および診断 clinical manifestations and diagnosis of amyloid cardiomyopathy
4. 免疫グロブリン軽鎖（AL）アミロイドーシス（原発性アミロイドーシス）の臨床像、検査所見、および診断 clinical presentation laboratory manifestations and diagnosis of immunoglobulin light chain al amyloidosis primary amyloidosis
5. アミロイドーシスの筋骨格系の症状 musculoskeletal manifestations of amyloidosis

Martins F1, Rebelo S2, Santos M1, Cotrim CZ1, da Cruz e Silva EF1, da Cruz e Silva OA1.
Cellular signalling.Cell Signal.2016 Jan;28(1):130-44. doi: 10.1016/j.cellsig.2015.10.012. Epub 2015 Oct 26.
PMID 26515131

Dissecting the role of sortilin receptor signaling in neurodegeneration induced by NGF deprivation.

Capsoni S1, Amato G, Vignone D, Criscuolo C, Nykjaer A, Cattaneo A.
Biochemical and biophysical research communications.Biochem Biophys Res Commun.2013 Feb 15;431(3):579-85. doi: 10.1016/j.bbrc.2013.01.007. Epub 2013 Jan 11.
PMID 23313508

BRI3 inhibits amyloid precursor protein processing in a mechanistically distinct manner from its homologue dementia gene BRI2.

Matsuda S1, Matsuda Y, D'Adamio L.
The Journal of biological chemistry.J Biol Chem.2009 Jun 5;284(23):15815-25. doi: 10.1074/jbc.M109.006403. Epub 2009 Apr 14.
PMID 19366692