heterozygote

出典: meddic



WordNet   license wordnet

「(genetics) an organism having two different alleles of a particular gene and so giving rise to varying offspring」

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出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2014/05/08 11:49:38」(JST)

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英文文献

  • Plasma homocysteine levels, methylene tetrahydrofolate reductase A1298C gene polymorphism and risk of retinal vein thrombosis.
  • Ghaznavi H1, Soheili Z, Samiei S, Soltanpour MS.
  • Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.Blood Coagul Fibrinolysis.2016 Sep;27(6):679-83. doi: 10.1097/MBC.0000000000000476.
  • There are limited data regarding the role of methylene tetrahydrofolate reductase (MTHFR) A1298C polymorphism and hyperhomocysteinemia as risk factors for retinal vein thrombosis (RVT) in Iranians. This study aimed to examine a possible association between fasting plasma total homocysteine (tHcy) le
  • PMID 26650461
  • Mitochondrial DNA deletions in patients with chronic suppurative otitis media.
  • Tatar A1, Tasdemir S2, Sahin I2, Bozoglu C3, Erdem HB2, Yoruk O4, Tatar A2.
  • European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery.Eur Arch Otorhinolaryngol.2016 Sep;273(9):2473-9. doi: 10.1007/s00405-015-3839-7. Epub 2015 Nov 30.
  • The aim of this study was to investigate the 4977 and 7400 bp deletions of mitochondrial DNA in patients with chronic suppurative otitis media and to indicate the possible association of mitochondrial DNA deletions with chronic suppurative otitis media. Thirty-six patients with chronic suppurative o
  • PMID 26620342
  • Two transgenic mouse models for beta subunit components of succinate-CoA ligase yielding pleiotropic metabolic alterations.
  • Kacso G1, Ravasz D1, Doczi J1, Nemeth B1, Madgar O1, Saada A2, Ilin P3, Miller C3, Ostergaard E4, Iordanov I1, Adams D1, Vargedo Z1, Araki M5, Araki K5, Nakahara M5, Ito H5, Gal A1, Molnar MJ1, Nagy Z1, Patocs A1, Adam-Vizi V1, Chinopoulos C6.
  • The Biochemical journal.Biochem J.2016 Aug 5. pii: BCJ20160594. [Epub ahead of print]
  • Succinate-CoA ligase is a heterodimer enzyme composed of Suclg1 -alpha- and a substrate-specific Sucla2 or Suclg2 -beta- subunit yielding ATP or GTP, respectively. In humans, the deficiency of this enzyme leads to encephalomyopathy with, or without methylmalonyl aciduria, in addition to resulting in
  • PMID 27496549

和文文献

  • 3500xL Genetic Analyzer による AmpFlSTR<sup>®</sup> Identifiler<sup>®</sup> PCR Amplification Kit を用いた口腔内細胞からの STR 型検査法の評価
  • Flower color polymorphism maintained by overdominant selection in Sisyrinchium sp.
  • 今月の症例 腎移植を契機に診断されたFabry病ヘテロ接合体からヘミ接合体への生体腎移植症例

関連リンク

heterozygote /het·ero·zy·gote/ (-zi´gōt) an individual having different alleles in regard to a given character. manifesting heterozygote a female heterozygous for an X-linked disorder in whom, because of unfavorable X inactivation, the ...
heterozygoteとは。意味や和訳。[名]《生物》異型接合体:対立遺伝子が互いに異なる配偶子からできた個体.hètero・zýgous[形]異型(接合体)の. - goo英和辞書は14万項目以上を収録し、発音、音声、慣用句、例文が分かる英和辞書 ...

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★リンクテーブル★
リンク元heterozygous」「異種接合体」「異型接合体」「ヘテロ接合体

heterozygous」

  [★]

  • adj.
  • ヘテロ接合性の、ヘテロ接合の、異型接合的な、異型接合の、異型接合性の、異種接合体の
heterozygosityheterozygoteheterozygoticheterozygously

WordNet   license wordnet

「having dissimilar alleles at corresponding chromosomal loci; "heterozygous for eye color"」


異種接合体」

  [★]

heterozygousheterozygote
異型接合異型接合性異型接合体異型接合的ヘテロ接合ヘテロ接合性ヘテロ接合体

異型接合体」

  [★]

heterozygote
異種接合体ヘテロ接合体
-homozygote


ヘテロ接合体」

  [★]

heterozygote
異型接合体
[[]]





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