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the 4th letter of the Roman alphabet (同)d

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deuteriumの化学記号

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1. 微細欠失症候群（1番～11番染色体）microdeletion syndromes chromosomes 1 to 11 [show details]
…some cases, a single gene. This topic reviews microdeletion syndromes involving chromosomes 1 through 11. Microdeletion syndromes involving chromosomes 12 through 22 are discussed separately, as are microduplication …
2. 糖尿病症例解説11：2型糖尿病を有する妊娠中の34歳女性interactive diabetes case 11 a 34 year old pregnant woman with type 2 diabetes [show details]
…before lunch, 284 mg/dL before supper, and 244 mg/dL at bedtime. Her most recent dilated eye exam, 11 months ago, revealed moderate nonproliferative retinopathy with scattered microaneurysms and exudates…
3. 副腎ステロイド生合成adrenal steroid biosynthesis [show details]
…chromosome 6p21.3 , but only one is active . The last step in cortisol biosynthesis is the 11-beta-hydroxylation of 11-deoxycortisol, a reaction catalyzed by the mitochondrial enzyme CYP11B1. Like CYP11A1, …
4. 7～18歳の小児におけるジフテリア、破傷風、および百日咳ワクチンdiphtheria tetanus and pertussis immunization in children 7 through 18 years of age [show details]
…routinely recommended at age 11 through 12 years . Thereafter, booster doses of Td vaccine should be given every 10 years. The adolescent Tdap booster is recommended for children age 11 through 12 years even …
5. まれな先天性副腎過形成uncommon congenital adrenal hyperplasias [show details]
…the reasons described below. Deficiency of 11-beta-hydroxylase activity in the zona fasciculata blocks the conversions of 11-deoxycorticosterone (DOC) and 11-deoxycortisol to corticosterone and cortisol …

English Journal

In Vitro Enzyme Assay of CYP21A2 Mutation (R483Q) by A Novel Method Using Liquid Chromatography-Electrospray Ionization Tandem Mass Spectrometry (LC-ESI-MS/MS).

Ono M, Kashimada K, Miyai K, Onishi T, Takagi M, Honma S, Mizutani S.
Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology. 2008 ;17(2)49-56.
Congenital adrenal hyperplasia (CAH) is one of the most common autosomal recessive disorders in humans, and 21-hydroxylase deficiency (21-OHD) accounts for 90 to 95% of all cases of CAH. Approximately 95% mutations are a consequence of recombination between the CYP21A2 and its highly homologous pseu
PMID 24790362

Japanese Journal

受動車輪を用いた省自由度脚車輪ロボットの開発:―グライド推進による等速移動の検討―

野原健斗,稲垣克彦
ロボティクス・メカトロニクス講演会講演概要集 2018(0), 1P2-H01, 2018
… <p>This paper presents a new type of leg-wheeled robot designed to reduce the degree of freedom (DOF). … The main element of the design to reduce the DOF is to use a passive wheel and a 6-joints closing link mechanism. … By using these elements, it is possible to construct a leg-wheeled robot with 11 DOF despite having 6 legs. …
NAID 130007551370

Grasp synthesis based on tactile sensation in robot manipulation of arbitrary located object

Yussof Hanafiah,Wada Jiro,Ohka Masahiro
IEEE/ASME International Conference on Advanced Intelligent Mechatronics (AIM 2009), 560-565, 2009-07-14
… We developed an 11-dof multi-fingered arm and a novel optical three-axis tactile sensor system based on an optical waveguide transduction method. …
NAID 120002277464

In Vitro Enzyme Assay of CYP21A2 Mutation (R483Q) by A Novel Method Using Liquid Chromatography-Electrospray Ionization Tandem Mass Spectrometry (LC-ESI-MS/MS)

ONO Makoto,KASHIMADA Kenichi,MIYAI Kentaro,ONISHI Toshikazu,TAKAGI Masatoshi,HONMA Seijiro,MIZUTANI Shuki,Department of Pediatrics and Developmental Biology Tokyo Medical and Dental University,Department of Pediatrics and Developmental Biology Tokyo Medical and Dental University,Department of Pediatrics and Developmental Biology Tokyo Medical and Dental University,Department of Pediatrics and Developmental Biology Tokyo Medical and Dental University,Department of Pediatrics and Developmental Biology Tokyo Medical and Dental University,Teikoku Hormone Medical Co. Ltd.,Department of Pediatrics and Developmental Biology Tokyo Medical and Dental University
Clinical pediatric endocrinology 17(2), 49-56, 2008-04-01
NAID 110006794360