WordNet
- (genetics) any event that changes genetic structure; any alteration in the inherited nucleic acid sequence of the genotype of an organism (同)genetic mutation, chromosomal_mutation
- a change or alteration in form or qualities
- the 4th letter of the Roman alphabet (同)d
PrepTutorEJDIC
- 変化,俸転 / (生物の)突然変異;その変種
- deuteriumの化学記号
- deoxyribonucleic acidディオキシリボ核酸
UpToDate Contents
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- 1. ミトコンドリアの構造、機能、および遺伝学 mitochondrial structure function and genetics
- 2. ミトコンドリア細胞症における腎病変 renal involvement in the mitochondrial cytopathies
- 3. ミトコンドリアミオパシー：臨床的特徴および診断 mitochondrial myopathies clinical features and diagnosis
- 4. 先天異常の遺伝学的および環境的原因 genetic and environmental causes of birth defects
- 5. 全身疾患と関連した遺伝性ニューロパチー hereditary neuropathies associated with generalized disorders
English Journal
- Evaluation of cytotoxicity, genotoxicity, and apoptosis of wastewater before and after disinfection with performic acid.
- Ragazzo P1, Feretti D2, Monarca S3, Dominici L3, Ceretti E2, Viola G2, Piccolo V4, Chiucchini N4, Villarini M3.
- Water research.Water Res.2017 Jun 1;116:44-52. doi: 10.1016/j.watres.2017.03.016. Epub 2017 Mar 7.
- PMID 28292679
- A neurodevelopmental disorder with a nonsense mutation in the Ox-2 antigen domain of the amyloid precursor protein (APP) gene.
- Nguyen KV1,2, Leydiker K3, Wang R3, Abdenur J3, Nyhan WL2.
- Nucleosides, nucleotides & nucleic acids.Nucleosides Nucleotides Nucleic Acids.2017 May 4;36(5):317-327. doi: 10.1080/15257770.2016.1267361. Epub 2017 Jan 19.
- PMID 28102781
- Primer in Genetics and Genomics, Article 3-Explaining Human Diversity: The Role of DNA.
- Read CY1.
- Biological research for nursing.Biol Res Nurs.2017 May;19(3):350-356. doi: 10.1177/1099800417698798. Epub 2017 Mar 14.
- PMID 28413933
Japanese Journal
- Macular thickness changes in a patient with Leber's hereditary optic neuropathy
- BMC ophthalmology 15, 27, 2015-03-18
- NAID 120005606032
- A Specific Nuclear DNA Background Is Required for High Frequency Lymphoma Development in Transmitochondrial Mice with G13997A mtDNA
- PLoS ONE 10(3), e0118561, 2015-03
- NAID 120005604045
- A Patient with an Extra-adrenal Pheochromocytoma and Germ-line SDHB Mutation Accompanied by an Atypical Meningioma
- Internal Medicine 54(18), 2355-2360, 2015
- NAID 130005099675
Related Links
- Recently an attempt was made to estimate the age of the human race using mitochondrial DNA. This material is inherited always from mother to children only. By measuring the difference in mitochondrial DNA among many ...
- Mitochondrial DNA (mtDNA) mutations are an important cause of genetic disease and have been proposed to play a role in the ageing process. Quantification of total mtDNA mutation load in ageing tissues is difficult as mutational ...
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★リンクテーブル★
| リンク元 | 「ミトコンドリアDNA突然変異」 |
| 拡張検索 | 「mitochondrial DNA mutations」 |
| 関連記事 | 「D」「DNA」「mitochondrial」「mitochondrial DNA」 |
「ミトコンドリアDNA突然変異」
「mitochondrial DNA mutations」
「D」
- アスパラギン酸
- ジヒドロウリジン
- 遠位の distal,
- うつ病 depression
- 下行結腸 descending colon(大腸内視鏡検査の結果を記載するときに用いる)
「DNA」
- 英
- deoxyribonucleic acid
- 同
- デオキシリボ核酸
- 関
- リボ核酸 RNA
「mitochondrial」
- adj.
- ミトコンドリアの