WordNet
- the 19th letter of the Roman alphabet (同)s
PrepTutorEJDIC
- sulfurの化学記号 / {略}South[ern]
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/09/02 09:03:10」(JST)
wiki ja
wiki en
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.
- 1. ハンタウイルス心肺症候群 hantavirus cardiopulmonary syndrome
- 2. ハンタウイルス感染の病因 pathogenesis of hantavirus infections
- 3. ハンタウイルス感染の疫学および診断 epidemiology and diagnosis of hantavirus infections
English Journal
- Protective activity of Hertia cheirifolia extracts against DNA damage, lipid peroxidation and protein oxidation.
- Kada S1, Bouriche H1, Senator A1, Demirtaş I2, Özen T3, Çeken Toptanci B4, Kızıl G4, Kızıl M4.
- Pharmaceutical biology.Pharm Biol.2017 Dec;55(1):330-337.
- CONTEXT: Hertia cheirifolia L. (Asteraceae), a perennial shrub widely distributed in Northern Africa, is traditionally used to treat inflammatory disorders.OBJECTIVE: The protective effect of methanol (Met E) and aqueous (Aq E) extracts of Hertia cheirifolia against DNA, lipid and protein oxidation
- PMID 27927074
- Crohn Disease Risk Prediction-Best Practices and Pitfalls with Exome Data.
- Giollo M1, Jones DT1, Carraro M2, Leonardi E3, Ferrari C4, Tosatto SC3,5.
- Human mutation.Hum Mutat.2017 Jan 13. doi: 10.1002/humu.23177. [Epub ahead of print]
- The Critical Assessment of Genome Interpretation (CAGI) experiment is the first attempt to evaluate the state-of-the-art in genetic data interpretation. Among the proposed challenges, Crohn disease (CD) risk prediction has become the most classic problem spanning three editions. The scientific quest
- PMID 28087895
- Genetic Variants Identified from Epilepsy of Unknown Etiology in Chinese Children by Targeted Exome Sequencing.
- Wang Y1, Du X1, Bin R2, Yu S2, Xia Z3, Zheng G4, Zhong J5, Zhang Y1, Jiang YH6,7,8, Wang Y1,9.
- Scientific reports.Sci Rep.2017 Jan 11;7:40319. doi: 10.1038/srep40319.
- Genetic factors play a major role in the etiology of epilepsy disorders. Recent genomics studies using next generation sequencing (NGS) technique have identified a large number of genetic variants including copy number (CNV) and single nucleotide variant (SNV) in a small set of genes from individual
- PMID 28074849
Japanese Journal
- Quantitative Analysis of Salidroside and p-Tyrosol in the Traditional Tibetan Medicine Rhodiola crenulata by Fourier Transform Near-Infrared Spectroscopy
- Chemical and Pharmaceutical Bulletin 64(4), 289-296, 2016
- NAID 130005141020
- Clonality and Micro-Diversity of a Nationwide Spreading Genotype of Mycobacterium tuberculosis in Japan
- PLOS ONE 10(3), e0118495, 2015-03-03
- NAID 120005615579
- 自閉スペクトラム症の遺伝学研究の最近の進歩 (特集 自閉症の生物学)
- 細胞工学 34(5), 453-457, 2015
- NAID 40020456629
Related Links
- At SNV we believe that no-one should have to live in poverty and that all people should have the opportunity to pursue their own sustainable development. Starting out in the Netherlands nearly 50 years ago, we now work in many ...
- SNV is an international not-for-profit development organisation. We believe that no-one should have to live in poverty and that all people should have the opportunity to pursue their own sustainable development. Founded in the ...
Related Pictures
★リンクテーブル★
| リンク元 | 「Sin Nombre virus」 |
| 関連記事 | 「SN」「S」 |
「Sin Nombre virus」
「SN」
「S」