exons

出典: meddic


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出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2014/02/11 01:07:48」(JST)

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英文文献

  • Genome-wide functional analysis of SSR for an edible mushroom Pleurotus ostreatus.
  • Qu J1, Huang C1, Zhang J2.
  • Gene.Gene.2016 Jan 10;575(2P2):524-530. doi: 10.1016/j.gene.2015.09.027. Epub 2015 Sep 18.
  • Simple sequence repeats (SSRs) play specific roles in many biological activities. In this paper, we focused on SSRs in the genome of Pleurotus ostreatus, which is a widely cultivated edible mushroom. The distribution curves of SSRs and exons are opposite throughout the genome, which means that SSRs
  • PMID 26386282
  • Molecular characterization of a novel ovary-specific gene fem-1 homolog from the oriental river prawn, Macrobrachium nipponense.
  • Ma KY1, Liu ZQ1, Lin JY1, Li JL2, Qiu GF3.
  • Gene.Gene.2016 Jan 10;575(2P1):244-252. doi: 10.1016/j.gene.2015.08.070. Epub 2015 Sep 11.
  • The feminization-1 (fem-1) gene is characterized by one of the most common protein-protein interaction motifs, ankyrin repeat motifs, displays many expression patterns in vertebrates and invertebrates, and plays an essential role in the sex-determination/differentiation pathway in Caenorhabditis ele
  • PMID 26367327
  • Comparative molecular approaches in Prader-Willi syndrome diagnosis.
  • Botezatu A1, Puiu M2, Cucu N3, Diaconu CC4, Badiu C5, Arsene C3, Iancu IV4, Plesa A4, Anton G4.
  • Gene.Gene.2016 Jan 10;575(2P1):353-358. doi: 10.1016/j.gene.2015.08.058. Epub 2015 Sep 1.
  • Prader-Willi and Angelman syndromes are two distinct neurogenetic disorders caused by chromosomal deletions, uniparental disomy or loss of the imprinted gene expression in the 15q11-q13 region. PWS results from the lack of the paternally expressed gene contribution in the region. The aim of our stud
  • PMID 26335514

和文文献

  • NF1 single and multi-exons copy number variations in neurofibromatosis type 1
  • Imbard Apolline,Pasmant Eric,Sabbagh Audrey [他]
  • Journal of human genetics 60(4), 221-224, 2015-04
  • NAID 40020433208
  • Mutation Analysis of KCNQ1, KCNH2 and SCN5A Genes in Taiwanese Long QT Syndrome Patients
  • Chang Ya-Sian,Yang Yi-Wen,Lin Yen-Nien,Lin Kuo-Hung,Chang Kuan-Cheng,Chang Jan-Gowth
  • International Heart Journal 56(4), 450-453, 2015
  • … HRM analysis was successfully optimized for 14 of the 16 exons of the KCNQ1, 5 of the 15 exons of the KCNH2, and 23 of the 27 exons of the SCN5A. …
  • NAID 130005087562
  • Mutation Analysis of KCNQ1, KCNH2 and SCN5A Genes in Taiwanese Long QT Syndrome Patients
  • Chang Ya-Sian,Yang Yi-Wen,Lin Yen-Nien,Lin Kuo-Hung,Chang Kuan-Cheng,Chang Jan-Gowth
  • International Heart Journal advpub(0), 2015
  • … HRM analysis was successfully optimized for 14 of the 16 exons of the KCNQ1, 5 of the 15 exons of the KCNH2, and 23 of the 27 exons of the SCN5A. …
  • NAID 130005084052

関連リンク

(ěk'sŏn) A segment of a gene that contains information used in coding for protein synthesis. Genetic information within genes is discontinuous, split among the exons that encode for messenger RNA and absent from the DNA ...
Interupted gene - Introns and exons.mp4, Exons and introns - Melissa Moore (U Mass/HHMI), Exon, Intron and Splicing.flv, Operons Introns and Exons, DNA exons and introns, RNA Splicing, Kreidezeit 76: Intron und Exon

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関連記事exon」「exo

exon」

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WordNet   license wordnet

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


exo」

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