mutations

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出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2013/12/05 12:12:52」(JST)

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出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2017/08/18 09:01:53」(JST)

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英文文献

  • C3 Glomerulonephritis/CFHR5 Nephropathy Is an Endemic Disease in Cyprus: Clinical and Molecular Findings in 21 Families.
  • Deltas C, Gale D, Cook T, Voskarides K, Athanasiou Y, Pierides A.SourceMolecular Medicine Research Center and Laboratory of Molecular and Medical Genetics, Department of Biological Sciences, University of Cyprus, Kallipoleos 75, 1678, Nicosia, Cyprus, deltas@ucy.ac.cy.
  • Advances in experimental medicine and biology.Adv Exp Med Biol.2013;734:189-96.
  • Microscopic haematuria is the presenting symptom of several conditions, either heritable or acquired. A well-recognized familial condition is Alport syndrome, either of X-linked or autosomal recessive inheritance, as well as thin basement membrane nephropathy (TBMN) because of heterozygous collagen
  • PMID 22990703
  • Paroxysmal nocturnal hemoglobinuria and the complement system: recent insights and novel anticomplement strategies.
  • Risitano AM.SourceDivision of Hematology, Department of Biochemistry and Medical Biotechnologies, Federico II University of Naples, Via Pansini 5, 80131, Naples, Italy, amrisita@unina.it.
  • Advances in experimental medicine and biology.Adv Exp Med Biol.2013;734:155-72.
  • Paroxysmal nocturnal hemoglobinuria (PNH) is a hematological disorder characterized by complement-mediated hemolytic anemia, thrombophilia, and bone marrow failure. PNH is due to a somatic, acquired mutation in the X-linked phosphatidylinositol glycan class A (PIG-A) gene, which impairs the membrane
  • PMID 22990701

和文文献

  • 放線菌の転写及び翻訳系の改変による潜在能力の開発と抗生物質の探索
  • 保坂 毅,今井 優,藤原 達也
  • 信州大学農学部紀要 48(1-2), 9-15, 2012-03-27
  • … these drug-resistance mutations dramatically alter gene expression in actinomycetes by modulating the transcriptional and translational apparatus or both (i. …
  • NAID 120003988808
  • Novel mutations of cholesteryl ester transfer protein (CETP) gene in Japanese hyperalphalipoproteinemic subjects
  • Ohtani Rumiko,Inazu Akihiro,Noji Yoshihiro,Wakasugi Takanobu,Miwa Kenji,Tada Hayato,Kawashiri Masa-aki,Noguchi Tohru,Nohara Atsushi,Kobayashi Junji,Koizumi Junji,Yamagishi Masakazu,Mabuchi Hiroshi
  • Clinica Chimica Acta 413(5-6), 537-543, 2012-03-22
  • … Background: The half of hyperalphalipoproteinemia (HALP) in Japan is caused by CETP gene mutations. … Other than two prevalent mutations (D442G and Intron 14 splicing donor site +. … 1G>A), some rare CETP mutations are found in Japanese HALP subjects. … Mutations which were suspected to cause a splicing defect or a protein secretion defect were investigated in COS-1 cells transfected with a CETP minigene construct or a cDNA expression vector. …
  • NAID 120004026116

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 types of mutations such as macro mutationsDNA MutationsDNA - the mtDNA Mitochondrial Mutations Mutations - PowerPoint by zhangyunAIP Gene Mutationsve been building a list of mutations


★リンクテーブル★
拡張検索mitochondrial DNA mutations
関連記事mutation

mitochondrial DNA mutations」

  [★] ミトコンドリアDNA異常


mutation」

  [★] 突然変異

WordNet   license wordnet

「(genetics) any event that changes genetic structure; any alteration in the inherited nucleic acid sequence of the genotype of an organism」
genetic mutation, chromosomal mutation

WordNet   license wordnet

「a change or alteration in form or qualities」

PrepTutorEJDIC   license prepejdic

「変化,俸転 / (生物の)突然変異;その変種」




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