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 fibrous band of scar tissue that binds together normally separate anatomical structures
abnormal union of bodily tissues; most common in the abdomen
blood cells that engulf and digest bacteria and fungi; an important part of the bodys defense system (同)leucocyte, white_blood_cell, white_cell, white blood corpuscle, white_corpuscle, WBC
writing done with a typewriter (同)typewriting

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
〈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
粘着,付着

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1. 炎症の病因における白血球内皮細胞接着 leukocyte endothelial adhesion in the pathogenesis of inflammation
2. 白血球粘着不全症 leukocyte adhesion deficiency
3. 貧食細胞機能の原発性疾患：概要 primary disorders of phagocytic function an overview
4. 好中球増多症の原因 causes of neutrophilia

Lentiviral Vector-Mediated Correction of a Mouse Model of Leukocyte Adhesion Deficiency Type I.

Leon-Rico D1,2, Aldea M1,2, Sanchez-Baltasar R1,2, Mesa-Nuñez C1,2, Record J3, Burns SO4,5, Santilli G3, Thrasher AJ3,6, Bueren JA1,2, Almarza E1,2.
Human gene therapy.Hum Gene Ther.2016 Sep;27(9):668-78. doi: 10.1089/hum.2016.016. Epub 2016 May 5.
Leukocyte adhesion deficiency type I (LAD-I) is a primary immunodeficiency caused by mutations in the ITGB2 gene and is characterized by recurrent and life-threatening bacterial infections. These mutations lead to defective or absent expression of β2 integrins on the leukocyte surface, compromising
PMID 27056660

Mutations of Cystic Fibrosis Transmembrane Conductance Regulator Gene Cause a Monocyte-Selective Adhesion Deficiency.

Sorio C1,2, Montresor A1, Bolomini-Vittori M1,2,3, Caldrer S1,2, Rossi B1, Dusi S1, Angiari S1, Johansson JE1,2, Vezzalini M1,2, Leal T4, Calcaterra E1,2, Assael BM5, Melotti P5, Laudanna C1.
American journal of respiratory and critical care medicine.Am J Respir Crit Care Med.2016 May 15;193(10):1123-33. doi: 10.1164/rccm.201510-1922OC.
RATIONALE: Cystic fibrosis (CF) is a common genetic disease caused by mutations of the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Persistent lung inflammation, characterized by increasing polymorphonuclear leukocyte recruitment, is a major cause of the decline in respiratory fu
PMID 26694899

Leukocyte Calpain Deficiency Reduces Angiotensin II-Induced Inflammation and Atherosclerosis But Not Abdominal Aortic Aneurysms in Mice.

Howatt DA1, Balakrishnan A1, Moorleghen JJ1, Muniappan L1, Rateri DL1, Uchida HA1, Takano J1, Saido TC1, Chishti AH1, Baud L1, Subramanian V2.
Arteriosclerosis, thrombosis, and vascular biology.Arterioscler Thromb Vasc Biol.2016 May;36(5):835-45. doi: 10.1161/ATVBAHA.116.307285. Epub 2016 Mar 10.
OBJECTIVE: Angiotensin II (AngII) infusion profoundly increases activity of calpains, calcium-dependent neutral cysteine proteases, in mice. Pharmacological inhibition of calpains attenuates AngII-induced aortic medial macrophage accumulation, atherosclerosis, and abdominal aortic aneurysm in mice.
PMID 26966280