WordNet

receive from a predecessor; "The new chairman inherited many problems from the previous chair"
obtain from someone after their death; "I inherited a castle from my French grandparents"
receive by genetic transmission; "I inherited my good eyesight from my mother"
the 3rd letter of the Roman alphabet (同)c
(music) the keynote of the scale of C major
a general-purpose programing language closely associated with the UNIX operating system

PrepTutorEJDIC

(…から)〈財産・権利・称号など〉‘を'『相続する』《+『名』+『from』+『名』》 / (…から)〈体質・性質など〉‘を'『受け継ぐ』《+『名』+『from』+『名』》 / (前任者・前代から)…‘を'受け継ぐ,継承ぐ,継承する《+『名』+『from』+『名』》 / 財産を相続する
carbonの化学記号
Chief Justice裁判長

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Watts JC1,2,3, Giles K1,2, Bourkas ME3, Patel S1, Oehler A1, Gavidia M1, Bhardwaj S1, Lee J1, Prusiner SB4,5,6.
Acta neuropathologica.Acta Neuropathol.2016 Jun 28. [Epub ahead of print]
Attempts to model inherited human prion disorders such as familial Creutzfeldt-Jakob disease (CJD), Gerstmann-Sträussler-Scheinker (GSS) disease, and fatal familial insomnia (FFI) using genetically modified mice have produced disappointing results. We recently demonstrated that transgenic (Tg) mice
PMID 27350609

Rare E196A mutation in PRNP gene of three Chinese patients with Creutzfeldt-Jacob disease.

Shi Q1, Zhou W1, Chen C1, Zhang BY1, Xiao K1, Wang Y1, Dong XP1,2.
Prion.Prion.2016 Jun 16:0. [Epub ahead of print]
Inherited prion diseases are characterized by mutations in the PRNP gene, which account for 5-15% of human prion diseases. Here we reported three Chinese genetic Creutzfeldt-Jacob disease cases (gCJD) with a rare mutation in PRNP leading to an exchange of amino acid from glutamic acid (E) to alanine
PMID 27310471

Chen C1,2, Dong XP3,4,5.
Infectious diseases of poverty.Infect Dis Poverty.2016 Jun 2;5(1):47. doi: 10.1186/s40249-016-0143-8.
Human prion diseases are a group of transmissible, progressive, and invariably fatal neurodegenerative disorders, which include Kuru, Creutzfeldt-Jakob disease (CJD), Gerstmann-Sträussler-Scheinker syndrome, and fatal familial insomnia. Human prion diseases affect approximately 1-2 persons per mill
PMID 27251305

萩原健一,山河芳夫,花田賢太郎
ウイルス 59(2), 155-166, 2009
… プリオン病（伝達性海綿状脳症）は，生前の確定診断法・治療法が確立していない致死性神経変性疾患である．ヒトの場合，1）全体の8～9割を占める孤発性クロイツフェルト・ヤコブ病（CJD），2）プリオン蛋白質の遺伝子変異による家族性プリオン病，3）病原体プリオンに汚染された医療用具，生物製剤あるいは食物を介した感染を原因とするプリオン病，が知られている．中枢神経系に蓄積する異常型プリオン蛋 …
NAID 130004470925