- 胎生致死の、胚性致死の
WordNet
- in an early stage of development; "the embryonic government staffed by survivors of the massacre"; "an embryonic nation, not yet self-governing" (同)embryotic
- of an organism prior to birth or hatching; "in the embryonic stage"; "embryologic development" (同)embryologic, embryonal
PrepTutorEJDIC
- =embryo
- 死をもたらす,致死の;死をもたらす目的の
UpToDate Contents
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- 1. サラセミア症候群の分子病理 molecular pathology of the thalassemic syndromes
- 2. レニン－アンギオテンシン系の概要 overview of the renin angiotensin system
- 3. 遺伝的変異の概要 overview of genetic variation
- 4. 補体系の遺伝性疾患 inherited disorders of the complement system
- 5. 先天性赤血球増多症および真性多血症の分子学的病因 molecular pathogenesis of congenital polycythemic disorders and polycythemia vera
English Journal
- PTB Deficiency Causes the Loss of Adherens Junctions in the Dorsal Telencephalon and Leads to Lethal Hydrocephalus.
- Shibasaki T, Tokunaga A, Sakamoto R, Sagara H, Noguchi S, Sasaoka T, Yoshida N.SourceLaboratory of Developmental Genetics, Center for Experimental Medicine and Systems Biology.
- Cerebral cortex (New York, N.Y. : 1991).Cereb Cortex.2013 Aug;23(8):1824-35. doi: 10.1093/cercor/bhs161. Epub 2012 Jun 15.
- Polypyrimidine tract-binding protein (PTB) is a well-characterized RNA-binding protein and known to be preferentially expressed in neural stem cells (NSCs) in the central nervous system; however, its role in NSCs in the developing brain remains unclear. To explore the role of PTB in embryonic NSCs i
- PMID 22705452
- In vivo mutation of pre-mRNA processing factor 8 (Prpf8) affects transcript splicing, cell survival and myeloid differentiation.
- Keightley MC, Crowhurst MO, Layton JE, Beilharz T, Markmiller S, Varma S, Hogan BM, de Jong-Curtain TA, Heath JK, Lieschke GJ.SourceAustralian Regenerative Medicine Institute, Monash University, Clayton, Victoria 3800, Australia.
- FEBS letters.FEBS Lett.2013 Jul 11;587(14):2150-7. doi: 10.1016/j.febslet.2013.05.030. Epub 2013 May 25.
- Mutated spliceosome components are recurrently being associated with perturbed tissue development and disease pathogenesis. Cephalophŏnus (cph), is a zebrafish mutant carrying an early premature STOP codon in the spliceosome component Prpf8 (pre-mRNA processing factor 8). Cph initially develops no
- PMID 23714367
- Structure-Specific Endonucleases Xpf and Mus81 Play Overlapping but Essential Roles in DNA Repair by Homologous Recombination.
- Kikuchi K, Narita T, Pham VT, Iijima J, Hirota K, Keka IS, Mohiuddin, Okawa K, Hori T, Fukagawa T, Essers J, Kanaar R, Whitby MC, Sugasawa K, Taniguchi Y, Kitagawa K, Takeda S.SourceAuthors' Affiliations: Department of Radiation Genetics, and Frontier Technology Center, Graduate School of Medicine, Kyoto University, Sakyo-ku, Kyoto; Department of Molecular Genetics, National Institute of Genetics and Sokendai, Shizuoka; Biosignal Research Center, Organization of Advanced Science and Technology, Kobe University, Hyogo, Japan; Department of Vascular Surgery, Erasmus University Medical Center; Departments of Genetics and Radiation Oncology, Cancer Genomics Center, Erasmus University Medical Center, Rotterdam, the Netherlands; Department of Biochemistry, University of Oxford, Oxford, United Kingdom; and Center for Childhood Cancer, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
- Cancer research.Cancer Res.2013 Jul 5. [Epub ahead of print]
- DNA double-strand breaks (DSB) occur frequently during replication in sister chromatids and are dramatically increased when cells are exposed to chemotherapeutic agents including camptothecin. Such DSBs are efficiently repaired specifically by homologous recombination (HR) with the intact sister chr
- PMID 23576554
Japanese Journal
- Functional Investigation of a Non-coding Variant Associated with Adolescent Idiopathic Scoliosis in Zebrafish: Elevated Expression of the Ladybird Homeobox Gene Causes Body Axis Deformation.
- PLoS genetics 12(1), 2016-01-28
- NAID 120005698038
- 膵管癌におけるWingless/int1（WNT）シグナル伝達経路の臨床病理学的意義について
- Journal of UOEH 38(1), 1-8, 2016
- NAID 130005132763
- Establishment of a tamoxifen-inducible Cre-driver mouse strain for widespread and temporal genetic modification in adult mice
- Experimental Animals advpub(0), 2016
- NAID 130005128424
Related Links
- TDG is a member of the uracil DNA glycosylase family of DNA repair enzymes. It has been implicated in gene regulation but its biological functions have been unclear. Here, a knockout of the Tdg gene in mice reveals functions in ...
- 1. Nature. 2011 Feb 17;470(7334):419-23. doi: 10.1038/nature09672. Epub 2011 Jan 30. Embryonic lethal phenotype reveals a function of TDG in maintaining epigenetic stability. Cortázar D(1), Kunz C, Selfridge J, Lettieri ...
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★リンクテーブル★
| リンク元 | 「胚性致死」「胎生致死」 |
| 拡張検索 | 「embryonic lethality」 |
| 関連記事 | 「embryonic」「lethal」 |
「胚性致死」
「胎生致死」
- 英
- embryonic lethal
- 関
- 胚性致死
「embryonic lethality」
「embryonic」
- adj.
- 胚性の、胚の、胚体の、胚芽の、胎仔の、胎生期の、胎性の、胎児性の
- 関
- embryo、embryonal、embryonic day、embryonic stage、embryonically、fetal、fetal stage、fetus、germ、germinal
「lethal」
- adj.
- 致死的な、致命的な、致死の、致死性の