exon

出典: meddic

エクソン

WordNet   license wordnet

「sequence of a gene''s DNA that transcribes into protein structures; "exons are interspersed with introns"」
coding DNA

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出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2014/10/25 13:14:42」(JST)

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英文文献

  • A signature protein-based method to distinguish Mediterranean water buffalo and foreign breed milk.
  • Caira S, Pinto G, Balteanu VA, Chianese L, Addeo F.SourceUniversità degli Studi di Napoli "Federico II", Facoltà di Agraria Via Università, 100 80055 Portici, Napoli, Italy. caira@unina.it
  • Food chemistry.Food Chem.2013 Nov 1;141(1):597-603. doi: 10.1016/j.foodchem.2013.02.033. Epub 2013 Mar 15.
  • A novel genetic variant at the αs1-casein locus of water buffalo (WB), 8-residue shorter than its wild-type has been found and sequenced. The internal deletion of the peptide E(35)KVNELsT(42) was confirmed by the isolation of the junction peptide. The 8-residue deletion mutant has a molecular weigh
  • PMID 23768399
  • Exonic sequencing revealed no causative mutation in the BST1 gene in patients with Parkinson's disease.
  • Wang C, Feng X, Xie S, Gu Z, Chan P.SourceDepartment of Neurobiology, Beijing Institute of Geriatrics, Xuanwu Hospital, Capital Medical University, Beijing, China; Department of Neurology, Beijing Institute of Geriatrics, Xuanwu Hospital, Capital Medical University, Beijing, China; Key Laboratory on Neurodegenerative Disease of Ministry of Education, Beijing, China; Key Laboratory on Parkinson's Disease of Beijing, Beijing, China; Department of Neurology, The Affiliated Sanming First Hospital, Fujian Medical University, Sanming, Fujian, China.
  • Neurobiology of aging.Neurobiol Aging.2013 Nov;34(11):2695.e9-2695.e10. doi: 10.1016/j.neurobiolaging.2013.05.024. Epub 2013 Jul 2.
  • Genome-wide association and large-scale replication studies have linked Parkinson's disease (PD) to a locus on 4p15 encompassing a single gene encoding bone marrow stromal cell antigen 1 (BST1). To screen for causative mutations of BST1 in PD, we have directly sequenced all the 9 exons of BST1 in a
  • PMID 23827523
  • Clearance of the mutant androgen receptor in motoneuronal models of spinal and bulbar muscular atrophy.
  • Rusmini P, Crippa V, Giorgetti E, Boncoraglio A, Cristofani R, Carra S, Poletti A.SourceSezione di Biomedicina e Endocrinologia, Dipartimento di Scienze Farmacologiche e Biomolecolari (DiSFeB), Centro di Eccellenza sulle Malattie Neurodegenerative, Universita' degli Studi di Milano, Milan, Italy; Centro InterUniversitario sulle Malattie Neurodegenerative, Universita' degli Studi di Firenze, Milano, Genova e Roma Tor Vergata, Sede di Milano, Italy.
  • Neurobiology of aging.Neurobiol Aging.2013 Nov;34(11):2585-603. doi: 10.1016/j.neurobiolaging.2013.05.026. Epub 2013 Jun 28.
  • Spinal and bulbar muscular atrophy (SBMA) is an X-linked motoneuron disease caused by an abnormal expansion of a tandem CAG repeat in exon 1 of the androgen receptor (AR) gene that results in an abnormally long polyglutamine tract (polyQ) in the AR protein. As a result, the mutant AR (ARpolyQ) misfo
  • PMID 23810450

和文文献

  • Polymorphism of DNA sequences of cryptochrome genes is not associated with the photoperiodic flowering of wild soybean along a latitudinal cline.
  • Ishibashi Nobuchika,Setoguchi Hiroaki
  • Journal of plant research 125(4), 483-488, 2012-07
  • … Although CRY1a did not show neutral evolution, balancing selection was recognized in the intron while not in the exon. …
  • NAID 40019329711
  • Four parameters increase the sensitivity and specificity of the exon array analysis and disclose 25 novel aberrantly splice exons in myotonic dystrophy
  • Yamashita Yoshihiro,Matsuura Tohru,Shinmi Jun [他]
  • Journal of human genetics 57(6), 368-374, 2012-06
  • NAID 40019311719

関連リンク

株式会社エクソンは、千葉市花見川区幕張町にある会社です。人・企業・地域・日本のイノベーションを主導を目指します。 ... 2013.10.24 Thu 弊社代表荒巻が、千葉商工会議所の講師として登録されました。詳細はこちらをご覧ください。 2013 ...
株式会社エクソンは、千葉市花見川区幕張町にある会社です。人・企業・地域・日本のイノベーションを主導を目指します。 ... Layer Thinkingという考え方に感動! 荒巻社長の講義の中で出てきたLayer Thinkingという考え方。とても斬新で非常 ...

関連画像

File:Exon shuffling.pnghide exon an exon is the portion of a gene Exon skipping is a strategy in which an removal of introns : role of snRNP and the might consider exon during the exon Exon-skipping strategies using antisense


★リンクテーブル★
リンク元エクソン」「エキソン」「mini-exon」「exonic
拡張検索exonerate」「exoneration」「DNA exonuclease」「first exon」「exon trapping
関連記事exo」「ex

エクソン」

  [★]

exonexonic
エキソン
イントロンスプライシング



エキソン」

  [★]

[[]]
exon
[[]]


-エクソン
exon


mini-exon」

  [★]

ミニエクソンミニエキソン

exon


exonic」

  [★]

  • エクソンの、エキソンの
exon


exonerate」

  [★]

PrepTutorEJDIC   license prepejdic

「〈人〉‘の'無罪を証明する,‘に'無罪を言い渡す / (非難・嫌疑などから)〈人〉‘を'解放する《+『名』+『from』+『名』》」


exoneration」

  [★]

WordNet   license wordnet

「the condition of being relieved from blame or obligation」

PrepTutorEJDIC   license prepejdic

「免罪,罪を晴らすこと」


DNA exonuclease」

  [★]

DNAエキソヌクレアーゼ

exodeoxyribonuclease

first exon」

  [★]


exon trapping」

  [★] エキソントラッピング


exo」

  [★]

エキソエクソ

externalexternallyextra


ex」

  [★]

PrepTutorEJDIC   license prepejdic

「先妻,先夫」


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