WordNet

write by means of a keyboard with types; "type the acceptance letter, please" (同)typewrite
a small metal block bearing a raised character on one end; produces a printed character when inked and pressed on paper; "he dropped a case of type, so they made him pick them up"
(biology) the taxonomic group whose characteristics are used to define the next higher taxon
a subdivision of a particular kind of thing; "what type of sculpture do you prefer?"
all of the tokens of the same symbol; "the word `element contains five different types of character"
printed characters; "small type is hard to read"
identify as belonging to a certain type; "Such people can practically be typed" (同)typecast
a pattern of symptoms indicative of some disease
a complex of concurrent things; "every word has a syndrome of meanings"
the 9th letter of the Roman alphabet (同)i
publicize in an exaggerated and often misleading manner
immunological disorder in which some part of the bodys immune system is inadequate and resistance to infectious diseases is reduced

PrepTutorEJDIC

〈C〉(…の)『型』,タイプ,類型,種類(kind)《+of+名》 / 〈C〉(その種類の特質を最もよく表している)『典型』,手本,模範《+of+名》 / 〈U〉《集合的に》活字;〈C〉(1個の)活字 / 〈U〉(印刷された)字体,活字 / 〈C〉(貨幣・メダルなどの)模様,図柄 / 〈C〉血液型(blood group) / …‘を'タイプに打つ / (…として)…‘を'分類する《+名+as+名(doing)》 / …‘の'型を決める / タイプライターを打つ
(疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
『私は』私が
iodineの化学記号
…‘を'刺激する,駆り立てる / (不正な手段で)〈評判など〉‘を'高める,強化する / 不正な手段 / (皮下注射による)麻薬中毒者

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A novel mutation in the CD40 ligand gene in a Chinese boy with X-linked hyper-IgM syndrome.

Liu PN1, Li H, Li Q, Yin ZW, Zhou CY, Jiang MY, Guo X.
Asian Pacific journal of allergy and immunology / launched by the Allergy and Immunology Society of Thailand.Asian Pac J Allergy Immunol.2014 Sep;32(3):270-4. doi: 10.12932/AP0365.32.3.2014.
X-linked hyper-IgM Syndrome (XHIGM) is caused by a mutation of CD40 ligand (CD40L), which is normally expressed on activated CD4+ T cells and is responsible for immunoglobulin class switching. A 7-year-old boy with recurrent sino-pulmonary infections since the age of 3 months had normal CD3+, CD4+,
PMID 25268346

Clinical, molecular, and T cell subset analyses in a small cohort of Chinese patients with hyper-IgM syndrome type 1.

Tang WJ1, An YF1, Dai RX1, Wang QH1, Jiang LP1, Tang XM1, Yang XQ1, Yu J1, Tu WW2, Zhao XD3.
Human immunology.Hum Immunol.2014 Jul;75(7):633-40. doi: 10.1016/j.humimm.2014.04.014. Epub 2014 Apr 24.
Type 1 hyper-IgM syndrome (HIGM1) is a rare primary immunodeficiency disease caused by mutations in the CD40L gene. Patients often present with recurrent infections and autoimmune manifestations. We investigated the clinical and molecular characteristics of HIGM1 in thirteen patients from the Chines
PMID 24768948

[Clinical study on cytomegalovirus infection after hematopoietic stem cell transplantation in 26 patients with primary immunodeficiency diseases].

Que M1, Xiao J1, Guan X1, Xian Y1, Su Y1, Wen X1, Li Y1, Wang Y, Xiao L1, Yu J1.
Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi.Zhonghua Xue Ye Xue Za Zhi.2014 May;35(5):424-7. doi: 10.3760/cma.j.issn.0253-2727.2014.05.010.
OBJECTIVE: To explore the risk factors, and control measures of cytomegalovirus (CMV) infection after hematopoietic stem cell transplantion (HSCT) in children with primary immunodeficiency diseases(PID).METHODS: We retrospectively analyzed results of 26 patients with PID-Wiskott-Aldrich syndrome (WA
PMID 24857213