変異マウス、遺伝子変異マウス、変異体マウス、ミュータントマウス
- 関
- mutant mouse
WordNet
- tending to undergo or resulting from mutation; "a mutant gene"
- an animal that has undergone mutation
- (biology) an organism that has characteristics resulting from chromosomal alteration (同)mutation, variation, sport
- the syllable naming the third (mediant) note of any major scale in solmization
PrepTutorEJDIC
- 突然変異種(堤)
- ミ(全音階の第3音)
- mouseの複数形
UpToDate Contents
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- 1. マウス遺伝子：育種戦略と遺伝子工学 mouse genetics breeding strategies and genetic engineering
- 2. 筋萎縮性側索硬化症の疫学および病因 epidemiology and pathogenesis of amyotrophic lateral sclerosis
- 3. 肥満の病因 pathogenesis of obesity
- 4. 結核の免疫学 immunology of tuberculosis
- 5. ハンチントン病：遺伝学と病因 huntington disease genetics and pathogenesis
English Journal
- Splicing factor TRA2B is required for neural progenitor survival.
- Roberts JM, Ennajdaoui H, Edmondson C, Wirth B, Sanford JR, Chen B.SourceDepartment of Molecular, Cell, and Developmental Biology, University of California, Santa Cruz, California, 95064.
- The Journal of comparative neurology.J Comp Neurol.2014 Feb;522(2):372-92. doi: 10.1002/cne.23405.
- Alternative splicing of pre-mRNAs can rapidly regulate the expression of large groups of proteins. The RNA binding protein TRA2B (SFRS10) plays well-established roles in developmentally regulated alternative splicing during Drosophila sexual differentiation. TRA2B is also essential for mammalian emb
- PMID 23818142
- Autonomous functions of murine thyroid hormone receptor TRα and TRβ in cochlear hair cells.
- Dettling J, Franz C, Zimmermann U, Lee SC, Bress A, Brandt N, Feil R, Pfister M, Engel J, Flamant F, Rüttiger L, Knipper M.SourceMolecular Physiology of Hearing, Hearing Research Centre Tübingen (THRC), Department of Otolaryngology, University of Tübingen, Elfriede-Aulhorn-Str. 5, 72076 Tübingen, Germany.
- Molecular and cellular endocrinology.Mol Cell Endocrinol.2014 Jan 25;382(1):26-37. doi: 10.1016/j.mce.2013.08.025. Epub 2013 Sep 6.
- Thyroid hormone acts on gene transcription by binding to its nuclear receptors TRα1 and TRβ. Whereas global deletion of TRβ causes deafness, global TRα-deficient mice have normal hearing thresholds. Since the individual roles of the two receptors in cochlear hair cells are still unclear, we gene
- PMID 24012852
- Mitochondrial mutations and ageing: Can mitochondrial deletion mutants accumulate via a size based replication advantage?
- Kowald A, Dawson M, Kirkwood TB.SourceCentre for Integrated Systems Biology of Ageing and Nutrition, Institute for Ageing and Health, Newcastle University, Newcastle upon Tyne NE4 5PL, United Kingdom. Electronic address: Axel.Kowald@ncl.ac.uk.
- Journal of theoretical biology.J Theor Biol.2014 Jan 7;340:111-8. doi: 10.1016/j.jtbi.2013.09.009. Epub 2013 Sep 17.
- The mitochondrial theory of ageing is one of the main contenders to explain the biochemical basis of the ageing process. An important line of support comes from the observation that mtDNA deletions accumulate over the life course in post-mitotic cells of many species. A single mutant expands clonall
- PMID 24055401
Japanese Journal
- Behavioural and Anatomical Characterization of Mutant Mice With Targeted Deletion of D?
- Daniela Babovic,Jiang Luning,Goto Satoshi
- Journal of pharmacological sciences 121(1), 39-47, 2013-01
- NAID 40019554447
- Wx/ae Double-Mutant Brown Rice Prevents the Rise in Plasma Lipid and Glucose Levels in Mice
- MATSUMOTO Kenji,MAEKAWA Masashi,NAKAYA Makoto
- Bioscience, Biotechnology, and Biochemistry 76(11), 2112-2117, 2012-11
- NAID 40019498958
- Somatic Reactivation of Expression of the Silent Maternal Mest Allele and Acquisition of Normal Reproductive Behaviour in a Colony of Peg1/Mest Mutant Mice
- INESON Jessica,STAYNER Cherie,HAZLETT Jody,SLOBBE Lynn,ROBSON Ewan,LEGGE Michael,ECCLES Michael R.
- The Journal of reproduction and development 58(4), 490-500, 2012-08-01
- … In humans and mice the Peg1/Mest gene (Mest) is maternally repressed, and paternally expressed. … Here we report an occurrence of post-embryonic somatic variability of Mest allelic expression in a colony of mice where heterozygotes at the imprinted Mest locus for a mutation inherited from the father spontaneously expressed the normally silenced allele from the mother. …
- NAID 10031067254
Related Links
- Mice harboring spontaneous mutations have long been a major source for animal models of human genetic disorders, particularly mendelian diseases. The Mouse Mutant Resource maintains over 700 established mutant strains and ...
- Nature is the international weekly journal of science: a magazine style journal that publishes full-length research papers in all disciplines of science, as well as News and Views, reviews, news, features, commentaries, web focuses ...
★リンクテーブル★
[★]
- 英
- mutant mouse、mutant mice
- 関
- ミュータントマウス、遺伝子変異マウス、変異体マウス
[★]
- 関
- mutant mice
[★]
- 英
- mutant mouse、mutant mice
- 関
- ミュータントマウス、遺伝子変異マウス、変異マウス
[★]
- 英
- mutant mouse、mutant mice
- 関
- ミュータントマウス、変異マウス、変異体マウス
[★]
- 英
- mutant mouse、mutant mice
- 関
- 遺伝子変異マウス、変異マウス、変異体マウス
[★]
- mi-, mio-
- ？
- MI
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