WordNet
- any of several fat-soluble organic compounds having as a basis 17 carbon atoms in four rings; many have important physiological effects
PrepTutorEJDIC
- ステロイド(脂肪溶解性の有機化合物の総称)
UpToDate Contents
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- 1. β-ラクタマーゼ阻害剤、カルバペネム系、およびモノバクタム系抗菌薬の併用 combination beta lactamase inhibitors carbapenems and monobactams
- 2. 基質特異性拡張型β-ラクタマーゼ extended spectrum beta lactamases
- 3. 第ⅩＩ因子欠乏症 factor xi deficiency
- 4. 成人における褐色細胞腫の治療 treatment of pheochromocytoma in adults
- 5. 12歳未満の小児における慢性喘息：コントローラ剤 chronic asthma in children younger than 12 years controller medications
Japanese Journal
- Functional zonation of the rat adrenal cortex : the development and maintenance
- MITANI Fumiko
- Proceedings of the Japan Academy. Ser. B, Physical and Biological Sciences 90(5), 163-183, 2014-05
- NAID 40020079455
- ステロイド11β-水酸化酵素欠損症 : 原因遺伝子として最近発見されたCYP11B2/CYP11B1キメラを中心に
- 栗林 功雄
- 生化学 78(8), 749-755, 2006-08-25
- NAID 10019282969
- Immunohistochemical Localization of Cytochrome P450 Enzymes in the Rat Brain, Considering the Steroid-Synthesis in the Neurons
- YAMADA Hisao,KOMINAMI Shiro,TAKEMORI Shigeki,KITAWAKI Jo,KATAOKA Yosky
- Acta histochemica et cytochemica 30(5), 609-616, 1997-10-01
- … To elucidate the steroid-synthesis in the mammalian brain (i. … The primary antibodies used in this study were rabbit polyclonal antibodies to cholesterol side-chain cleavage (SCC), C21-hydroxylase (C21), 11β-hydroxylase (11β), 17α-hydroxylase/C17-20 lyase (17α) and aromatase (AROM). …
- NAID 10008608025
Related Links
- Congenital adrenal hyperplasia (CAH) is one of the most common autosomal recessive inherited endocrine disease. Steroid 11β-Hydroxylase deficiency (11β-OHD) is the second most common form of CAH. The aim of the study was ...
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★リンクテーブル★
| リンク元 | 「11β-水酸化酵素」 |
「11β-水酸化酵素」
- 英
- 11β-hydroxylase, 11beta-hydroxylase
- 同
- 11β水酸化酵素、11βヒドロキシラーゼ、11β-ヒドロキシラーゼ
- ステロイド11β-水酸化酵素 steroid 11β-hydroxylase、ステロイド11β-モノオキシゲナーゼ steroid 11β-monooxygenase、P-450C11、P-45011β
- 関
- 副腎皮質ホルモン
蓄積
症状
- デオキシコルチコステロン：高血圧
- 過剰のアンドロゲン：男性：性早熟、女性：外陰部の男性化
臨床関連
- 同
- P450Cll欠損症