WordNet
- major food fish of Arctic and cold-temperate waters (同)codfish
- lean white flesh of important North Atlantic food fish; usually baked or poached (同)codfish
- a specific sequence of three adjacent nucleotides on a strand of DNA or RNA that specifies the genetic code information for synthesizing a particular amino acid
PrepTutorEJDIC
- =codfish 1
- 〈人〉'を'ばかにする
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- 1. 遺伝性楕円赤血球症：遺伝学と病因 hereditary elliptocytosis genetics and pathogenesis
- 2. 遺伝性疾患の基本原則 basic principles of genetic disease
- 3. 分子遺伝学の原理 principles of molecular genetics
- 4. サラセミア症候群の分子病理 molecular pathology of the thalassemic syndromes
- 5. 慢性B型肝炎ウイルス感染の治療におけるアデホビルジピボキシル adefovir dipivoxil in the treatment of chronic hepatitis b virus infection
English Journal
- Failure of RQC machinery causes protein aggregation and proteotoxic stress.
- Choe YJ1, Park SH1, Hassemer T1, Körner R1, Vincenz-Donnelly L1, Hayer-Hartl M1, Hartl FU1.
- Nature.Nature.2016 Mar 10;531(7593):191-5. doi: 10.1038/nature16973. Epub 2016 Feb 29.
- Translation of messenger RNAs lacking a stop codon results in the addition of a carboxy-terminal poly-lysine tract to the nascent polypeptide, causing ribosome stalling. Non-stop proteins and other stalled nascent chains are recognized by the ribosome quality control (RQC) machinery and targeted for
- PMID 26934223
- Intronic PRRT2 mutation generates novel splice acceptor site and causes paroxysmal kinesigenic dyskinesia with infantile convulsions (PKD/IC) in a three generation family.
- Weber A1, Kreth J2, Müller U3.
- BMC medical genetics.BMC Med Genet.2016 Mar 3;17:16. doi: 10.1186/s12881-016-0281-7.
- BACKGROUND: Mutations in PRRT2 cause autosomal dominant paroxysmal kinesigenic dyskinesia with infantile convulsions (PKD/IC).CASE PRESENTATION: A previously not recognized intronic PRRT2 mutation (c.880-35G > A; p.S294Lfs*29) was found in an 18 month old girl with IC and in her mother with class
- PMID 26936445
- Case report of novel DYRK1A mutations in 2 individuals with syndromic intellectual disability and a review of the literature.
- Luco SM1, Pohl D2, Sell E3, Wagner JD4, Dyment DA5,6, Daoud H7.
- BMC medical genetics.BMC Med Genet.2016 Feb 27;17:15. doi: 10.1186/s12881-016-0276-4.
- BACKGROUND: Chromosomal deletions encompassing DYRK1A have been associated with intellectual disability for several years. More recently, point mutations in DYRK1A have been shown to be responsible for a recognizable syndrome characterized by microcephaly, developmental delay and intellectual disabi
- PMID 26922654
Japanese Journal
- The longer version of Arabidopsis thaliana heat shock protein 18.2 gene terminator contributes to higher expression of stably integrated transgenes in cultured tobacco cells
- Plant Biotechnology 31(2), 191-194, 2014
- NAID 130003391369
- High-level accumulation of recombinant miraculin protein in transgenic tomatoes expressing a synthetic miraculin gene with optimized codon usage terminated by the native miraculin terminator
- Plant cell reports 30(1), 113-124, 2011-01
- NAID 120002771204
- Promoter and Terminator Analysis of 40-kDa Outer Membrane Gene (hbp35) in Porphyromonas gingivalis 381
- International Journal of Oral-Medical Sciences 10(2), 96-102, 2011
- NAID 130001088326
Related Links
- terminator codon [′tər·mə‚nād·ər ′kō‚dän] (genetics) A UAA, UAG, or UGA trinucleotide in messenger ribonucleic acid (mRNA) that specifies termination of synthesis of the polypeptide (protein) product of the gene. Also known as stop ...
- 英語をクリック → Terminator Codon との組み合わせでEntrez を検索 翻訳領域 (Open Reading Frame); タンパク質生合成 (Protein Biosynthesis); リボソーム (Ribosome); 大腸菌 (Escherichia coli); 転移RNA (Transfer RNA); 変異 ); (); ...
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★リンクテーブル★
| リンク元 | 「終結コドン」「termination codon」 |
| 関連記事 | 「terminator」「cod」 |
「終結コドン」
「termination codon」
「terminator」
「cod」