WordNet
- serve in a specific professional capacity; "the priest sat for confession"; "she sat on the jury"
- be around, often idly or without specific purpose; "The object sat in the corner"; "We sat around chatting for another hour" (同)sit around
- be seated (同)sit_down
- be in session; "When does the court of law sit?"
- be located or situated somewhere; "The White House sits on Pennsylvania Avenue"
- join together so as to form new genetic combinations; "splice genes"
- a junction where two things (as paper or film or magnetic tape) have been joined together; "the break was due to an imperfect splice" (同)splicing
- join by interweaving strands; "Splice the wires"
- join the ends of; "splice film"
- the piece of land on which something is located (or is to be located); "a good site for the school" (同)land site
- physical position in relation to the surroundings; "the sites are determined by highly specific sequences of nucleotides" (同)situation
- (genetics) any event that changes genetic structure; any alteration in the inherited nucleic acid sequence of the genotype of an organism (同)genetic mutation, chromosomal_mutation
- a change or alteration in form or qualities
PrepTutorEJDIC
- (…に)『座る』,座っている《+『at』(『on, in』)+『名』》・着席する《+『down』》・(…に)〈鳥などが〉『止まる』,休む《+『on』+『名』》・〈めんどりが〉卵を抱く,巣に就く / 《場所の副詞[句]を伴って》(ある場所に)『位置する』・ (画家・写真家のために)ポーズをとる・しっとしている,動かないでいる・(議員・委員などの)職に就いている《+『on』+『名』》・〈議会・法廷などが〉開会(開廷)される・(…に)負担となる,重荷となる《+『on』(『upon』)+『名』》・〈衣服などが〉(…に)合う,似合う《+『on』+『名』》・〈人〉‘を'座らせる,着席させる《+『down』+『名,』+『名』+『down』》・〈馬〉‘に'乗る・《英》〈試験〉‘を'受ける
- 〈綱などの端と端と〉‘を'組み(より)継ぎする;〈材木など)‘を'重ね継ぐ,〈フィルム・テープ〉‘を'つなぐ / 《受動態で》《話》〈二人〉‘を'結婚させる / (綱の)より継ぎ;(材木の)重ね継ぎ;(フィルム・テープの)接合 / より(重ね)継ぎ目
- (町・建物などの)『場所』;敷地,用地 / 遺跡;(事件などの)現場 / 〈建物など〉‘を'位置させる(locate)
- 変化,俸転 / (生物の)突然変異;その変種
- =ti
UpToDate Contents
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English Journal
- The ARMC5 gene shows extensive genetic variance in primary macronodular adrenocortical hyperplasia.
- Correa R1, Zilbermint M1, Berthon A1, Espiard S1, Batsis M1, Papadakis GZ1, Xekouki P1, Lodish MB1, Bertherat J1, Faucz FR2, Stratakis CA1.
- European journal of endocrinology / European Federation of Endocrine Societies.Eur J Endocrinol.2015 Oct;173(4):435-40. doi: 10.1530/EJE-15-0205. Epub 2015 Jul 10.
- OBJECTIVE: Primary macronodular adrenal hyperplasia (PMAH) is a rare type of Cushing's syndrome (CS) that results in increased cortisol production and bilateral enlargement of the adrenal glands. Recent work showed that the disease may be caused by germline and somatic mutations in the ARMC5 gene, a
- PMID 26162405
- Alterations of the CD58 gene in classical Hodgkin lymphoma.
- Schneider M1, Schneider S1, Zühlke-Jenisch R2, Klapper W3, Sundström C4, Hartmann S5, Hansmann ML5, Siebert R2, Küppers R1, Giefing M2,6,7.
- Genes, chromosomes & cancer.Genes Chromosomes Cancer.2015 Oct;54(10):638-45. doi: 10.1002/gcc.22276. Epub 2015 Jul 21.
- Immune evasion plays a central role in the pathophysiology of classical Hodgkin lymphoma (cHL). As mutations of the CD58 gene contribute to immune evasion of diffuse large B cell lymphoma tumor cells, we studied whether alterations of the CD58 gene also occur in Hodgkin and Reed/Sternberg (HRS) cell
- PMID 26194173
- Novel CDKN2A mutations in Austrian melanoma patients.
- Burgstaller-Muehlbacher S1, Marko M, Müller C, Wendt J, Pehamberger H, Okamoto I.
- Melanoma research.Melanoma Res.2015 Oct;25(5):412-20. doi: 10.1097/CMR.0000000000000179.
- CDKN2A is the most prominent familial melanoma gene, with mutations occurring in up to 40% of the families. Numerous mutations in the gene are known, several of them representing regional founder mutations. We sought to determine, for the first time, germline mutations in CDKN2A in Austria to identi
- PMID 26225579
Japanese Journal
- In vitro transcription of compound heterozygous hypofibrinogenemia Matsumoto IX; first identification of FGB IVS6 deletion of 4 nucleotides and FGG IVS3-2A > G causing abnormal RNA splicing
- Terasawa Fumiko,Kamijyo Yuka,Fujihara Noriko,Yamauchi Kazuyoshi,Kumagai Toshiko,Honda Takayuki,Shigematsu Satoshi,Okumura Nobuo,山内 一由
- Clinica chimica acta 411(17-18), 1325-1329, 2010-09
- … BackgroundWe reported a case of hypofibrinogenemia Matsumoto IX (M IX) caused by a novel compound heterozygous mutation involving an FGB IVS6 deletion of 4 nucleotides (Δ4b) (three T, one G; …
- NAID 120002353821
- Analysis of LDLR mRNA in patients with familial hypercholesterolemia revealed a novel mutation in intron 14, which activates a cryptic splice site
- Kulseth Mari Ann,Berge Knut Erik,Bogsrud Martin Proven [他]
- Journal of human genetics 55(10), 676-680, 2010-10
- NAID 40017332002
Related Links
- A splice site mutation is a genetic mutation that inserts or deletes a number of nucleotides in the specific site at which splicing of an intron takes place during the processing of precursor messenger RNA into mature messenger RNA. ...
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★リンクテーブル★
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- 関
- lie、locate、location、loci、locus、map、position、rank、seat、situated、situation、stand、topo
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- 関
- location、loci、locus、place、topo
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- 関
- splicing