WordNet

any state or process known through the senses rather than by intuition or reasoning
a remarkable development

PrepTutorEJDIC

〈U〉〈C〉(…の)(量・額などの)不足,欠乏《+『of』(『in』)+『名』》 / 〈C〉不足分,不足量,不足額 / 〈C〉(精神・肉体などの)欠陥
『現象』 / 驚くべきこと(物),非凡な人

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. ホスホグリセリン酸キナーゼ欠損症およびホスホグリセリン酸ムターゼ欠損症 phosphoglycerate kinase deficiency and phosphoglycerate mutase deficiency
2. 選択的IgA欠損症：臨床症状、病態生理、および診断 selective iga deficiency clinical manifestations pathophysiology and diagnosis
3. IgG サブクラス欠乏症 igg subclass deficiency
4. アデノシンデアミナーゼ欠損症：治療 adenosine deaminase deficiency treatment
5. 免疫不全症を引き起こすミエロペルオキシダーゼ欠損症および酵素白血球欠損症 myeloperoxidase deficiency and other enzymatic wbc defects causing immunodeficiency

English Journal

Hypercarotenodermia in Zambia: which children turned orange during mango season?

Tanumihardjo SA1, Gannon BM1, Kaliwile C2, Chileshe J3.
European journal of clinical nutrition.Eur J Clin Nutr.2015 Dec;69(12):1346-9. doi: 10.1038/ejcn.2015.143. Epub 2015 Sep 2.
Vitamin A (VA) deficiency is a public health problem in many countries. The World Health Organization recommends high-dose VA supplements to children aged 6-59 months based on unequivocal evidence that supplements decreased mortality risk. VA supplements were meant as a temporary intervention until
PMID 26330146

Tequila Regulates Insulin-Like Signaling and Extends Life Span in Drosophila melanogaster.

Huang CW1, Wang HD2, Bai H3, Wu MS4, Yen JH5, Tatar M3, Fu TF6, Wang PY7.
The journals of gerontology. Series A, Biological sciences and medical sciences.J Gerontol A Biol Sci Med Sci.2015 Dec;70(12):1461-9. doi: 10.1093/gerona/glv094. Epub 2015 Aug 11.
The aging process is a universal phenomenon shared by all living organisms. The identification of longevity genes is important in that the study of these genes is likely to yield significant insights into human senescence. In this study, we have identified Tequila as a novel candidate gene involved
PMID 26265729

Redistribution of soil water by a saprotrophic fungus enhances carbon mineralization.

Guhr A1, Borken W2, Spohn M2, Matzner E2.
Proceedings of the National Academy of Sciences of the United States of America.Proc Natl Acad Sci U S A.2015 Nov 24;112(47):14647-51. doi: 10.1073/pnas.1514435112. Epub 2015 Nov 9.
The desiccation of upper soil horizons is a common phenomenon, leading to a decrease in soil microbial activity and mineralization. Recent studies have shown that fungal communities and fungal-based food webs are less sensitive and better adapted to soil desiccation than bacterial-based food webs. O
PMID 26554004

Japanese Journal

家族性グルコーストランスポーター1欠損症症候群

伊藤康,小国弘量,大澤眞木子,ITO Yasushi,OGUNI Hirokazu,OSAWA Makiko
東京女子医科大学雑誌 83(E1), E9-E13, 2013-01-31
… グルコーストランスポーター1欠損症症候群(Glucose transporter type 1 deficiency syndrome; …
NAID 110009559421

銅および亜鉛キレート形成によるangiotensin-converting enzyme (ACE) 阻害剤エナラプリラトの脂溶性増加

藤岡晴人,稗田雄三,倉本康弘,小西華那世,木下恵美子,木下英司,小池透
YAKUGAKU ZASSHI, 2013
… Some side effects such as neurodegeneration and taste disorder can be related to copper or zinc deficiency, which would be caused by the metal complex formation of dianionic elalaprilat (L2−). … For a better understanding of this phenomenon, we investigated the solution species of enalaprilat in the presence of copper(II) or zinc(II) ions by pH titration analysis with I = 0.10 M (NaCl) at 25℃. …
NAID 130003361996

Survival motor neuron (SMN) protein in the spinal anterior horn cells of patients with sporadic amyotrophic lateral sclerosis

Piao Yingshan,Hashimoto Tomoyo,Takahama Sachiko,Kakita Akiyoshi,Komori Takashi,Morita Takashi,Takahashi Hitoshi,Mizutani Toshio,Oyanagi Kiyomitsu
BRAIN RESEARCH 1372, 152-159, 2011-02-04
… The disease is caused by deficiency of SMN protein induced by mutation of one of the SMA-associated genes, SMN1. … These findings suggest that: 1) the amount of SMN protein in the cytoplasm of AHCs is strictly controlled in accordance with cell size, in both sALS patients and controls, 2) the amount of SMN protein in the AHCs of sALS patients may be reduced when the AHCs are atrophic, and 3) decrease of SMN protein in the AHCs of sALS patients may be a secondary, and not primary, phenomenon according to their sizes. …
NAID 120005248074

Related Pictures

Estrogen And Arthritis Symptoms Symptoms Finger Are Little ~ Dcss Arthritis Studiodoc Raynaud's phenomenon Symptoms Of Vitamin B12 Deficiency Include Pale Complexion - #B12 #complexion # Raynaud's Phenomenon and Raynaud's Syndrome Results | Healthmark Foot & Ankle Associates Iron deficiency: everything you need to know about the phenomenon Pin on Autoimmune Disease پدیده رینود (Raynaud's phenomenon)