- 関
- deletant
WordNet
- exhibiting variation and change; "letters variant in size"
- differing from a norm or standard; "a variant spelling"
- the act of deleting something written or printed
- the omission that is made when an editorial change shortens a written passage; "an editors deletions frequently upset young authors"; "both parties agreed on the excision of the proposed clause" (同)excision, cut
- (genetics) the loss or absence of one or more nucleotides from a chromosome
PrepTutorEJDIC
- (同種のものと)異なった,別の / 異形;(同じ単語の)異なったつづり(発音など)
- 削除;〈C〉削除箇所
UpToDate Contents
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- 1. 先天性の細胞遺伝学的異常 congenital cytogenetic abnormalities
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- 5. 遺伝的変異の概要 overview of genetic variation
English Journal
- Strategies for crystallizing a chromatin protein in complex with the nucleosome core particle.
- Makde RD, Tan S.SourceCenter for Eukaryotic Gene Regulation, Department of Biochemistry & Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA.
- Analytical biochemistry.Anal Biochem.2013 Nov 15;442(2):138-45. doi: 10.1016/j.ab.2013.07.038. Epub 2013 Aug 6.
- The molecular details of how chromatin factors and enzymes interact with the nucleosome are critical to understanding fundamental genetic processes including cell division and gene regulation. A structural understanding of such processes has been hindered by the difficulty in producing diffraction-q
- PMID 23928047
- Association Study of the 2-bp Deletion Polymorphism in Exon 6 of the CHRFAM7A Gene with Idiopathic Generalized Epilepsy.
- Rozycka A, Dorszewska J, Steinborn B, Lianeri M, Winczewska-Wiktor A, Sniezawska A, Wisniewska K, Jagodzinski PP.Source1 Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences , Poznan, Poland .
- DNA and cell biology.DNA Cell Biol.2013 Nov;32(11):640-7. doi: 10.1089/dna.2012.1880. Epub 2013 Sep 11.
- There is evidence of linkage between the 15q13-q14 locus, containing the gene encoding the α7 subunit (CHRNA7) of the neuronal nicotinic acetylcholine receptor (nAChR) and its partially duplicated isoform (CHRFAM7A), and epilepsy. Additionally, a 2-bp deletion polymorphism (c.497-498delTG; rs671586
- PMID 24024466
- The epidermal growth factor receptor variant III (EGFRvIII): where wild things are altered.
- Gan HK, Cvrljevic AN, Johns TG.SourceTumour Targeting Program, Ludwig Institute for Cancer Research, Heidelberg, Victoria, Australia.
- The FEBS journal.FEBS J.2013 Nov;280(21):5350-70. doi: 10.1111/febs.12393. Epub 2013 Jul 8.
- The epidermal growth factor receptor (EGFR) is overexpressed in a variety of human epithelial tumors, often as a consequence of gene amplification. Tumors with EGFR gene amplification frequently contain EGFR gene rearrangements, with the most common extracellular domain mutation being EGFRvIII. This
- PMID 23777544
Japanese Journal
- Val1483Ile polymorphism in the fatty acid synthase gene was associated with depressive symptoms under the influence of psychological stress
- Tsuboi Hirohito,Sakakibara Hiroyuki,Yamakawa-Kobayashi Kimiko,Tatsumi Asami,Inamori Tomoko,Hamamoto Reiko,Suzuki Atsuko,Shimoi Kayoko
- Journal of Affective Disorders 134(1-3), 448-452, 2011-11-01
- … The genotypes of 5-HTTLPR (insertion/deletion; … The S variant of 5-HTTLPR was related with less obese. …
- NAID 120003141899
- A novel y chromosome microdeletion with the loss of an endogenous retrovirus related, testis specific transcript in AZFb region
- Sin Ho-Su,Koh Eitetsu,Taya Masaki,IIjima Masashi,Sugimoto Kazuhiro,Maeda Yuji,Yoshida Atsumi,Iwamoto Teruaki,Namiki Mikio
- Journal of Urology 186(4), 1545-1552, 2011-10
- … Homologous recombination between long terminal repeat of the TTY13 associated human endogenous retrovirus-K14C resulted in TTY13 deletion events. … Specifically 15.63% of the azoospermia group, 10.88% of the oligozoospermia group and 0% of fertile controls had only the deletion variant, indicating an association between the homologous recombination rate and the severity of spermatogenesis failure that was statistically significant (p <0.05). …
- NAID 120003479728
Related Links
- 19 cases well-documented were studied using the in-house duplex polymerase chain reaction (PCR) with probes and primers overlapping 3'end of LMP1 on DNA extracts from whole blood. The results are given on the ...
- The COMT val(158) variant has been associated with impaired cognitive function compared to the met(158) variant yet gene-gene interactions are not well described. In this study we demonstrate an interaction between this COMT ...
Related Pictures
★リンクテーブル★
| リンク元 | 「欠失体」「欠失株」「欠損体」「欠損株」「deletant」 |
| 関連記事 | 「variant」 |
「欠失体」
「欠失株」
- 英
- deletion variant
- 関
- 欠失体、欠損株、欠損体
「欠損体」
- 英
- deletion variant
- 関
- 欠失体、欠失株、欠損株
「欠損株」
- 英
- deletion variant
- 関
- 欠失体、欠失株、欠損体
「deletant」
- n.
- adj.
- 欠失体の
「variant」
- 関
- atypical、atypism、differ、different、disparate、dissimilar、distinct、meta、mutant、mutate、mutation、off-type、transmutation、variation、variational、variety、vary