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"
- (genetics) the organic process whereby the DNA sequence in a gene is copied into mRNA; the process whereby a base sequence of messenger RNA is synthesized on a template of complementary DNA
- a sound or television recording (e.g., from a broadcast to a tape recording)
- something written, especially copied from one medium to another, as a typewritten version of dictation (同)written text
- 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
- a coming to an end of a contract period; "the expiry of his drivers license" (同)expiration, expiry
- the act of ending something; "the termination of the agreement" (同)ending, conclusion
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
- 〈U〉(…を)書き写す(書き直す)こと,(…の)転写,謄写《+of+名》 / 〈C〉写し(書き直し)[たもの] / 〈U〉〈C〉編曲[されたもの] / 〈U〉〈C〉(ラジオ・テレビの)録音(録画)
- (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)
- 〈C〉〈U〉(…を)終わること,(…の)終了《+of+名》 / 〈C〉(言葉の)語尾
- =ti
UpToDate Contents
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- 1. 遺伝性疾患の基本原則 basic principles of genetic disease
- 2. Neuroendocrine neoplasms of unknown primary site
- 3. 原発不明の低分化癌 poorly differentiated cancer from an unknown primary site
- 4. 原発不明の腺癌 adenocarcinoma of unknown primary site
- 5. 複合免疫不全 combined immunodeficiencies
English Journal
- Ataluren stimulates ribosomal selection of near-cognate tRNAs to promote nonsense suppression.
- Roy B1, Friesen WJ2, Tomizawa Y2, Leszyk JD3, Zhuo J2, Johnson B2, Dakka J2, Trotta CR2, Xue X4, Mutyam V5, Keeling KM6, Mobley JA7, Rowe SM5, Bedwell DM6, Welch EM2, Jacobson A8.
- Proceedings of the National Academy of Sciences of the United States of America.Proc Natl Acad Sci U S A.2016 Oct 4. pii: 201605336. [Epub ahead of print]
- A premature termination codon (PTC) in the ORF of an mRNA generally leads to production of a truncated polypeptide, accelerated degradation of the mRNA, and depression of overall mRNA expression. Accordingly, nonsense mutations cause some of the most severe forms of inherited disorders. The small-mo
- PMID 27702906
- A meta-analysis of multiple myeloma risk regions in African and European ancestry populations identifies putatively functional loci.
- Rand KA, Song C, Dean E, Serie DJ, Curtin K, Sheng X, Hu D, Huff CA, Bernal-Mizrachi L, Tomasson MH, Ailwadhi S, Singhal S, Pawlish KS, Peters ES, BLock CH, Stram A, Van Den Berg DJ, Edlund CK, Conti DV, Zimmerman TM, Hwang AE, Huntsman S, Graff JJ, Nooka A, Kong Y, Pregja SL, Berndt SI, Blot WJ, Carpten JD, Casey G, Chu LW, Diver WR, Stevens VL, Lieber MR, Goodman PJ, Hennis AJ, Hsing AW, Mehta J, Kittles RA, Kolb S, Klein EA, Leske CM, Murphy AB, Nemesure B, Neslund-Dudas C, Strom SS, Vij R, Rybicki BA, Stanford JL, Signorello L, Witte JS, Ambrosone CB, Bhatti P, John EM, Bernstein L, Zheng W, Olshan AF, Hu JJ, Ziegler RG, Nyante SJ, Bandera EV, Birmann BM, Ingles SA, Press MF, Atanackovic D, Glenn M, Cannon-Albright L, Jones B, Tricot G, Martin TG, Kumar SK, Wolf JL, Deming SL, Rothman N, Brooks-Wilson A, Rajkumar SV, Kolonel LN, Chanock SJ, Slager SL, Severson RK, Janakirman N, Terebelo HJ, Brown EE, De Roos AJ, Mohrbacher A, Colditz GA, Giles GG, Spinelli JJ, Chiu BC, Munshi NC, Anderson KC, Levy J, Zonder JA, Orlowski RZ, Lonial S, Camp NJ, Vachon CM, Ziv E, Stram DO, Hazelett DJ, Cozen W.
- Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.Cancer Epidemiol Biomarkers Prev.2016 Sep 1. pii: cebp.1193.2015. [Epub ahead of print]
- BACKGROUND: Genome-wide association studies (GWAS) in European populations have identified genetic risk variants associated with multiple myeloma (MM).METHODS: We performed association testing of common variation in eight regions in 1,264 MM patients and 1,479 controls of European ancestry (EA) and
- PMID 27587788
- Identification of novel splice site mutation IVS9 + 1(G > A) and novel complex allele G355R/R359X in Type 1 Gaucher patients heterozygous for mutation N370S.
- Hoitsema K1, Amato D2, Khan A3, Sirrs S4, Choy FY1.
- Meta gene.Meta Gene.2016 Mar 23;9:47-51. doi: 10.1016/j.mgene.2016.03.003. eCollection 2016.
- Gaucher disease is an autosomal recessive lysosomal storage disorder resulting from deficient glucocerebrosidase activity. More than 350 mutations that cause Gaucher disease have been described to date. Novel mutations can potentially provide insight into the glucocerebrosidase structure-function re
- PMID 27222815
Japanese Journal
- Nucleosome Distribution near the 3′ Ends of Genes in the Human Genome
- HUANG Huan,LIU Hongde,SUN Xiao
- Bioscience, Biotechnology, and Biochemistry 77(10), 2051-2055, 2013
- … By systematic analysis of high-throughput sequencing datasets from the human genome, we found that protein-coding genes have a specific chromatin structure near transcription termination sites relative to non-coding genes, one related to polyadenylation. … Nucleosome was depleted near the site of cleavage/polyadenylation (polyA site) regardless of its relative position in the gene. …
- NAID 130003381888
- Promoter and Terminator Analysis of 40-kDa Outer Membrane Gene (hbp35) in Porphyromonas gingivalis 381
- Tanaka Hideki,Hiratsuka Koichi,Abiko Yoshimitsu
- International Journal of Oral-Medical Sciences 10(2), 96-102, 2011
- … The transcription start site (+1) was predicted to be located 53 nt upstream from the translation start codon. … Both locations partially overlapped the palindromic sequences, indicating ρ-independent transcription termination in the 3'-noncoding region. …
- NAID 130001088326
- G-to-A mutation at a 5′ splice site of fad3c caused impaired splicing in a low linolenic mutant of canola (Brassica napus L.)
- Hu Xueyi,Sullivan-Gilbert Mandy,Gupta Manju [他],THOMPSON Steven A.
- Plant biotechnology 24(4), 397-400, 2007-09-01
- … The canola mutant line DMS100 carries a G-to-A base substitution at the 5′ splice site, located at +1 G, of fad3c intron 6 and contains reduced C18:3 content in oil seeds. … Reverse transcription (RT) PCR analysis was used to amplify part of the fad3c transcript spanning intron 5, exon 6 and intron 6 using the primers specific to the exon 5 and 7 to investigate whether the mutation caused any abnormal splicing. …
- NAID 10021911864
Related Links
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- Rho-dependent transcription termination: This mechanism requires the presence of rho protein, a RNA-binding protein that forms a hexameric complex at a particular signal site, and races up the RNA strand. Once it reaches the ...
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★リンクテーブル★
| リンク元 | 「転写終結点」 |
| 関連記事 | 「sit」「site」「termination」 |
「転写終結点」
「sit」
- vi.
- (過去-過去分詞sat)座る、位置する
「site」
- n.
「termination」