- 関
- wild strain、wild type、wild-type、wild-type strain、wildtype
WordNet
- the 23rd letter of the Roman alphabet (同)w, double-u
PrepTutorEJDIC
- Watt / West; Western
- wolfram(=tungsten)の原子記号
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2015/08/02 23:51:59」(JST)
[Wiki ja表示]
WT
- ウォーキートーキー (Walkie-Talkie) - 携帯型の双方向無線機。
- ウェルカム・トラスト (Wellcome Trust) - イギリスの公益信託団体。
- ウィキトゥルース (Wikitruth)
- ウィクショナリー (Wiktionary)
- ウィズイン・テンプテーション (Within Temptation) - オランダのシンフォニックメタル / ゴシックメタルバンド。
- ウォークスルー (Walk Through) - 乗用車の内部構成の一形態。
|
このページは曖昧さ回避のためのページです。一つの語句が複数の意味・職能を有する場合の水先案内のために、異なる用法を一覧にしてあります。お探しの用語に一番近い記事を選んで下さい。このページへリンクしているページを見つけたら、リンクを適切な項目に張り替えて下さい。 |
[Wiki en表示]
|
Look up WT in Wiktionary, the free dictionary. |
WT or Wt may refer to:
Contents
- 1 In science
- 2 In technology
- 3 Other uses
In science
- wt%, percentage by weight, in chemistry
- Robert Wight, in botanical taxonomy, abbreviated Wt
- Wildtype (wt), in genetics, denoting a control or unaltered form
- Wilms' tumor, a cancer of the kidneys that typically occurs in children
In technology
- Wt (web toolkit), a web application framework for the C++ programming language
- Wavelet transform, a time-frequency decomposition of a signal or function
- Well tank, a type of locomotive
- Wireless telegraphy or telephony, an early term for radio communications
Other uses
- Washington Territory, a U.S. territory from 1853 to 1889
- Tornado watch, encoded as WT in the US Emergency Alert System
- Watertender, a former petty officer rating in the US Navy
- West Texas A&M University
- Wikitravel, a collaborative travel guide project
- Wiktionary, a collaborative dictionary
UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
English Journal
- Analytical approaches to determination of carnitine in biological materials, foods and dietary supplements.
- Dąbrowska M, Starek M.SourceJagiellonian University, Collegium Medicum, Faculty of Pharmacy, Department of Inorganic and Analytical Chemistry, 9 Medyczna Str., 30-688 Cracow, Poland. Electronic address: mtylka@cm-uj.krakow.pl.
- Food chemistry.Food Chem.2014 Jan 1;142:220-32. doi: 10.1016/j.foodchem.2013.06.137. Epub 2013 Jul 18.
- l-Carnitine is a vitamin-like amino acid derivative, which is an essential factor in fatty acid metabolism as acyltransferase cofactor and in energy production processes, such as interconversion in the mechanisms of regulation of cetogenesis and termogenesis, and it is also used in the therapy of pr
- PMID 24001835
- Reengineered glucose oxidase for amperometric glucose determination in diabetes analytics.
- Arango Gutierrez E, Mundhada H, Meier T, Duefel H, Bocola M, Schwaneberg U.SourceLehrstuhl für Biotechnologie, RWTH Aachen University, Worringerweg 1, 52074 Aachen, Germany. Electronic address: e.arango@biotec.rwth-aachen.de.
- Biosensors & bioelectronics.Biosens Bioelectron.2013 Dec 15;50:84-90. doi: 10.1016/j.bios.2013.06.029. Epub 2013 Jun 20.
- Glucose oxidase is an oxidoreductase exhibiting a high β-d-glucose specificity and high stability which renders glucose oxidase well-suited for applications in diabetes care. Nevertheless, GOx activity is highly oxygen dependent which can lead to inaccuracies in amperometric β-d-glucose determinat
- PMID 23835222
- Modulation of the antioxidant/pro-oxidant balance, cytotoxicity and antiviral actions of grape seed extracts.
- Ignea C, Dorobanţu CM, Mintoff CP, Branza-Nichita N, Ladomery MR, Kefalas P, Chedea VS.SourceDepartment of Food Quality and Chemistry of Natural Products, Mediterranean Agronomic Institute of Chania, Centre International de Hautes Etudes Agronomiques Méditerranéennes, Chania, PO Box 85, 73100 Chania, Crete, Greece. Electronic address: igneacodruta@yahoo.com.
- Food chemistry.Food Chem.2013 Dec 15;141(4):3967-76. doi: 10.1016/j.foodchem.2013.06.094. Epub 2013 Jun 29.
- Grape seed extracts (GSEs) were investigated in yeast cells harbouring defects in their antioxidant system (regarding the cellular growth and growth recovery from H2O2 insult). GSEs antioxidant activity was detected in wild-type and mutant strains Δcta1, Δgsh1 and Δoye2glr1, while pro-oxidant act
- PMID 23993573
Japanese Journal
- Microstructural Evaluation of ZrB2/ZrO2 Ceramic Powders Prepared by Milling-Assisted Magnesiothermic Reduction of Oxide Raw Materials
- Tensile-stress-induced growth of ellipsoidal ω-precipitates in a Ti–20wt%Mo alloy
- ZICOS : New project for neutrinoless double beta decay experiment using zirconium complex in liquid scintillator
- 宮城教育大学紀要 = Bulletin of Miyagi University of Education 50, 135-143, 2016-01-29
- NAID 120005695678
Related Links
- 熱帯魚・海水魚の販売 ... 〒486-0816 愛知県春日井市東野新町2-17-7 光ビル103 TEL.FAX/0568-82-7257 MAIL/info@wt-no1.com
- 自由掲示板/たった今WTやってて顔真っ赤になった奴、事情説明しな。/コメント5 雑談用掲示板/コメント37 2015-07-23 アメリカ雑談掲示板/コメント3 ドイツ雑談掲示板/コメント3 Pz.Kpfw.V Ausf.D/コメント Ki-102 otsu/コメント T-34 1942/コメント ...
Related Pictures
★リンクテーブル★
[★]
- 英
- wild type、WT、wild-type、wildtype
- 関
- 野生株
[★]
- 関
- wild strain、WT
[★]
- 関
- wild type、wild-type、WT
[★]
- 関
- wild type、wildtype、WT
[★]
- 関
- wild-type strain、WT
[★]
- 英
- WT syndrome
参考
- The WT syndrome--a "new" autosomal dominant pleiotropic trait of radial/ulnar hypoplasia with high risk of bone marrow failure and/or leukemia.
- Gonzalez CH, Durkin-Stamm MV, Geimer NF, Shahidi NT, Schilling RF, Rubira F, Opitz JM.AbstractWe report 2 families with an autosomal dominant syndrome of limb and hematologic abnormalities. The W Family was ascertained through AW, a 13-year-old girl, who was purportedly born without congenital anomalies and who was normal until 11 1/2 years when she developed acute lymphoblastic leukemia. She died 2 years later with CNS involvement. Her chromosomes, studied in the first weeks after diagnosis of the disease, were apparently normal. Her father had clinodactyly of both 5th fingers and was found to have panmyelocytopenia refractory to all treatment at 26 years. He died within a year of the onset of his anemia. This man's oldest brother was born with congenital malformations of the elbows and the hands and was healthy until 38 years when he was also found to have an "idopathic anemia" and panmyelocytopenia which was refractory to treatment except for transfusions; he died at age 42 years. Both men were initially thought to have the Fanconi anemia syndrome. Their mother died at 71 years of leukemia. DT, the propositus of the second family, was noted to have malformations of both hands at birth. At 21 months he had anemia for which he received transfusions. Family history reveals that several people on the paternal side have severe hand anomalies and a history of childhood anemia. The paternal grandfather died at age 51 of acute monocytic leukemia. Barring genetic heterogeneity, we think that the trait in the W and T families in the same. It is a pleiotropic autosomal dominant mutant which affects radial and ulnar development of the upper limbs and is associated with a relatively high risk of transient or permanent bone marrow arrest with or without leukemia. We propose the hypothesis that apparently increased risk of leukemia to Fanconi heterozygotes actually represents admixture with the WT syndrome and that Fanconi heterozygotes may not have an increased risk of leukemia.
- Birth defects original article series.Birth Defects Orig Artic Ser.1977;13(3B):31-8.
- We report 2 families with an autosomal dominant syndrome of limb and hematologic abnormalities. The W Family was ascertained through AW, a 13-year-old girl, who was purportedly born without congenital anomalies and who was normal until 11 1/2 years when she developed acute lymphoblastic leukemia. Sh
- PMID 890097
[★]
左室後壁厚 posterior LV wall thickness
[★]
WT1遺伝子 Wilms tumor 1 gene
[★]