出典: meddic

  • ホモ接合の、ホモ接合性の、ホモ接合型の、同型接合性の、同型接合的な、同種接合の

WordNet   license wordnet

「having identical alleles at corresponding chromosomal loci; "these two fruit flies are homozygous for red eye color"」

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出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2016/02/03 22:07:23」(JST)

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  • Pyramiding of three bacterial blight resistance genes for broad-spectrum resistance in deepwater rice variety, Jalmagna.
  • Pradhan SK1, Nayak DK, Mohanty S, Behera L, Barik SR, Pandit E, Lenka S, Anandan A.
  • Rice (New York, N.Y.).Rice (N Y).2015 Dec;8(1):51. doi: 10.1186/s12284-015-0051-8. Epub 2015 May 31.
  • BACKGROUND: Jalmagna is a popular deepwater rice variety with farmers of India because of its good yield under waterlogged condition. However, the variety is highly susceptible to bacterial blight (BB) disease. The development of resistant cultivars has been the most effective and economical strateg
  • PMID 26054243
  • ADIPOQ single nucleotide polymorphism: Association with adiponectin and lipoproteins levels restricted to men.
  • Tureck LV1, Leite N2, Souza RL1, da Silva Timossi L2, Osiecki AC2, Osiecki R2, Alle LF1.
  • Meta gene.Meta Gene.2015 Jun 17;5:98-104. doi: 10.1016/j.mgene.2015.06.003. eCollection 2015.
  • Adiponectin is an adipokine inversely correlated with obesity, which has beneficial effect on insulin resistance and lipid metabolism. Considering its potential as a therapeutic target in the metabolic disorder contexts, and in order to add knowledge in the area, our study evaluated the ADIPOQ 276G�
  • PMID 26137445
  • Genetic model selection for a case-control study and a meta-analysis.
  • Horita N1, Kaneko T1.
  • Meta gene.Meta Gene.2015 May 22;5:1-8. doi: 10.1016/j.mgene.2015.04.003. eCollection 2015.
  • A case-control study often compares the prevalence of a specific disease among persons with normal alleles and persons with variant alleles, which generates an odds ratio (OR). The most common type of allele variation, single-nucleotide polymorphism, consists of a major allele (M) and a minor allele
  • PMID 26042205
  • Paroxysmal nocturnal hemoglobinuria (PNH) and primary p.Cys89Tyr mutation in CD59: Differences and similarities.
  • Mevorach D1.
  • Molecular immunology.Mol Immunol.2015 Sep;67(1):51-55. doi: 10.1016/j.molimm.2015.03.005. Epub 2015 Mar 26.
  • CD59 encodes a 77 amino acid glycosylphosphatidylinositol (GPI)-anchored cell surface glycoprotein that inhibits the final step of membrane attack complex (MAC) formation. CD59 deficiency is a common finding in adult patients with paroxysmal nocturnal hemoglobinuria (PNH). In this condition, there i
  • PMID 25818314


  • Peri-implantation lethality in mice carrying megabase-scale deletion on 5qc3.3 is caused by Exoc1 null mutation
  • Mizuno Seiya,Takami Kohei,Daitoku Yoko,Tanimoto Yoko,Tra Thi Huong Dinh,Mizuno-Iijima Saori,Hasegawa Yoshikazu,Takahashi Satoru,Sugiyama Fumihiro,Yagami Ken-ichi
  • Scientific reports 5, 13632, 2015-09
  • … Interestingly, homozygous mutants (KitWS/WS) showed a peri-implantation lethal phenotype. …
  • NAID 120005661898
  • A novel in-frame deletion in the leucine zipper domain of C/EBPε leads to neutrophil-specific granule deficiency
  • Wada Taizo,Akagi Tadayuki,Muraoka Masahiro,Toma Tomoko,Kaji Kenzo,Agematsu Kazunaga,Koeffler Phillip,Yokota Takashi,Yachie Akihiro
  • Journal of Immunology 195(1), 80-86, 2015-07-01
  • … Defects in a myeloid-specific transcription factor, CCAAT/enhancer binding protein-ε (C/EBPε), have been identified in two cases in which homozygous frameshift mutations led to loss of the leucine zipper domain. … In this study, we report a 55-y-old woman affected with SGD caused by a novel homozygous 2-aa deletion (ΔRS) in the leucine zipper domain of the C/EBPε gene. …
  • NAID 120005647665
  • Hcn1 is a tremorgenic genetic component in a rat model of essential tremor.
  • Ohno Yukihiro,Shimizu Saki,Tatara Ayaka,Imaoku Takuji,Ishii Takahiro,Sasa Masashi,Serikawa Tadao,Kuramoto Takashi
  • PLOS ONE 10(5), 2015-05-13
  • … The TRM rat is homozygous for the tremor (tm) mutation and shows spontaneous tremors resembling human ET. … The TRMR rat also carries a homozygous tm mutation but shows no tremor, leading us to hypothesize that TRM rats carry one or more genes implicated in the development of ET in addition to the tm mutation. …
  • NAID 120005606112
  • Viable Neuronopathic Gaucher Disease Model in Medaka (Oryzias latipes) Displays Axonal Accumulation of Alpha-Synuclein.
  • Uemura Norihito,Koike Masato,Ansai Satoshi,Kinoshita Masato,Ishikawa-Fujiwara Tomoko,Matsui Hideaki,Naruse Kiyoshi,Sakamoto Naoaki,Uchiyama Yasuo,Todo Takeshi,Takeda Shunichi,Yamakado Hodaka,Takahashi Ryosuke
  • PLOS genetics 11(4), 2015-04-02
  • … 2015-04-09.Homozygous mutations in the glucocerebrosidase (GBA) gene result in Gaucher disease (GD), the most common lysosomal storage disease. …
  • NAID 120005593596


homozygousとは。意味や和訳。[形]《生物》同形(接合)の. - goo辞書は国語、英和、和英、中国語、百科事典等からまとめて探せる辞書検索サービスです。 ... 辞書すべて 国語 類語 英和 和英 中日 日中 ※「説明文に含む ...
homozygousの意味は?goo辞書は無料で使える日本最大級の辞書サービスです。国語辞典、英和辞典、和英辞典、類語辞典、中国語辞典、百科事典などを提供しています。 ... 辞書すべて 国語 類語 英和 和英 中日 日中 ※「説明文に ...
homozygous adj. Having the same alleles at a particular gene locus on homologous chromosomes. homozygosity ho ' mozygos ' ity n ... Ask Answer Enter question or phrase... Search: All sources Community Q&A Reference topics



拡張検索homozygous deletion



  • n.

WordNet   license wordnet

「the state of being homozygous; having two identical alleles of the same gene」
















homozygous deletion」