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出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2016/10/28 23:04:14」(JST)

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  • Similar frequency of paternal uniparental disomy involving chromosome 20q (patUPD20q) in Japanese and Caucasian patients affected by sporadic pseudohypoparathyroidism type Ib (sporPHP1B).
  • Takatani R1, Minagawa M2, Molinaro A3, Reyes M4, Kinoshita K5, Takatani T6, Kazukawa I2, Nagatsuma M7, Kashimada K7, Sato K8, Matsushita K9, Nomura F9, Shimojo N6, Jüppner H10.
  • Bone.Bone.2015 Oct;79:15-20. doi: 10.1016/j.bone.2015.05.011. Epub 2015 May 19.
  • Pseudohypoparathyroidism type Ib (PHP1B) is caused by proximal tubular resistance to parathyroid hormone that occurs in most cases in the absence of Albright's Hereditary Osteodystrophy (AHO). Familial forms of PHP1B are caused by maternally inherited microdeletions within STX16, the gene encoding s
  • PMID 25997889
  • DlRan3A is involved in hormone, light, and abiotic stress responses in embryogenic callus of Dimocarpus longan Lour.
  • Tian Q1, Lin Y1, Yang M1, Zhang D1, Lai R1, Lai Z2.
  • Gene.Gene.2015 Sep 15;569(2):267-75. doi: 10.1016/j.gene.2015.06.013. Epub 2015 Jun 10.
  • Ras-related nuclear protein (Ran) GTPase plays an important role in nucleo-cytoplasmic transportation of proteins and RNA, mitotic spindle assembly, microtubule assembly and nuclear envelope (NE) assembly. We previously identified the full-length cDNAs and a DNA of DlRan3A from longan (Dimocarpus lo
  • PMID 26071187
  • Wilson's disease caused by alternative splicing and Alu exonization due to a homozygous 3039-bp deletion spanning from intron 1 to exon 2 of the ATP7B gene.
  • Mameli E1, Lepori MB1, Chiappe F1, Ranucci G2, Di Dato F2, Iorio R2, Loudianos G3.
  • Gene.Gene.2015 Sep 15;569(2):276-9. doi: 10.1016/j.gene.2015.05.067. Epub 2015 May 30.
  • We describe a case of Wilson's disease (WD) diagnosed at 5years after routine biochemical test showed increased aminotransferases. Mutation analysis of the ATP7B gene revealed a 3039-bp deletion in the homozygous state spanning from the terminal part of intron 1 to nt position 368 of exon 2. This de
  • PMID 26031236


  • Flux balance impact degree: a new definition of impact degree to properly treat reversible reactions in metabolic networks.
  • Zhao Yang,Tamura Takeyuki,Akutsu Tatsuya,Vert Jean-Philippe
  • Bioinformatics 29(17), 2178-2185, 2013-07-04
  • … We show that the proposed method better predicts the phenotypic impact of single gene deletions on Escherichia coli than existing methods. …
  • NAID 120005333783
  • Testing Subdivision-Freeness: - Property Testing Meets Structural Graph Theory -
  • Ken-ichiKawarabayashi ,Yuichi Yoshida
  • 情報処理学会研究報告. AL, アルゴリズム研究会報告 2013-AL-144(18), 1-5, 2013-05-10
  • … In particular, no global monotone (i.e., closed under edge deletions) property that expander graphs can satisfy has been shown to be testable in constant time so far. …
  • NAID 110009579694
  • A Reduction in Age-Enhanced Gluconeogenesis Extends Lifespan
  • Hachinohe Mayumi,Yamane Midori,Akazawa Daiki,Ohsawa Kazuhiro,Ohno Mayumi,Terashita Yuzu,Masumoto Hiroshi,増本 博司
  • PLoS ONE 8(1), e54011, 2013-01-00
  • … The deletion of TDH2 restores the chronological lifespan of cells with deletions of both the HST3 and HST4 genes, which encode yeast sirtuins, and represses the activation of gluconeogenesis. …
  • NAID 120005246638


Zeroes aka Deletions – Null DNA Markers Deletions occur when a piece of a  , small insertions and small deletions Romance Catalogue Deletions | Social in EP2p deletions - Unique - The Rare Chromosomes 15 and 22: deletions




WordNet   license wordnet

「the act of deleting something written or printed」

WordNet   license wordnet

「the omission that is made when an editorial change shortens a written passage; "an editor''s deletions frequently upset young authors"; "both parties agreed on the excision of the proposed clause"」
excision, cut

WordNet   license wordnet

「(genetics) the loss or absence of one or more nucleotides from a chromosome」

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