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
autosomal dominant disease characterized by numerous neurofibromas and by spots on the skin and often by developmental abnormalities (同)von Recklinghausen''s disease
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

出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/02/08 02:02:22」(JST)

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1. 神経線維腫症I型（NF1）：病因、臨床的特徴、および診断 neurofibromatosis type 1 nf1 pathogenesis clinical features and diagnosis
2. 神経線維腫症I型（NF1）：マネージメントおよび予後 neurofibromatosis type 1 nf1 management and prognosis
3. 神経線維腫症2型 neurofibromatosis type 2
4. 色素沈着過剰を有する患者へのアプローチ approach to the patient with hyperpigmentation disorders
5. 硬膜内神経鞘腫 intradural nerve sheath tumors

Johansson G1, Andersson U1, Melin B1.
Acta oncologica (Stockholm, Sweden).Acta Oncol.2016 Apr;55(4):401-11. doi: 10.3109/0284186X.2015.1107190. Epub 2015 Dec 3.
The etiologies of brain tumors are in the most cases unknown, but improvements in genetics and DNA screening have helped to identify a wide range of brain tumor predisposition disorders. In this review we are discussing some of the most common predisposition disorders, namely: neurofibromatosis type
PMID 26634384

Loss of H3K27me3 Expression Is a Highly Sensitive Marker for Sporadic and Radiation-induced MPNST.

Prieto-Granada CN1, Wiesner T, Messina JL, Jungbluth AA, Chi P, Antonescu CR.
The American journal of surgical pathology.Am J Surg Pathol.2016 Apr;40(4):479-89. doi: 10.1097/PAS.0000000000000564.
Most malignant peripheral nerve sheath tumors (MPNSTs) exhibit combined inactivation of NF1, CDKN2A, and polycomb repressive complex 2 component genes (Embryonic Ectoderm Development [EED] and Suppressor of Zeste 12 [SUZ12]). Mutations in EED and SUZ12 induce loss of trimethylation at lysine 27 of h
PMID 26645727

Risk of optic pathway glioma in children with neurofibromatosis type 1 and optic nerve tortuosity or nerve sheath thickening.

Levin MH1, Armstrong GT2, Broad JH3, Zimmerman R4, Bilaniuk LT5, Feygin T4, Li Y6, Liu GT7, Fisher MJ8.
The British journal of ophthalmology.Br J Ophthalmol.2016 Apr;100(4):510-4. doi: 10.1136/bjophthalmol-2015-306958. Epub 2015 Aug 20.
BACKGROUND/AIMS: Optic nerve tortuosity and nerve and sheath thickening are observed on MRI in some patients with neurofibromatosis type 1 (NF-1). This study aimed to determine if tortuosity and thickening are associated with the development of optic pathway glioma (OPG) and subsequent vision loss.M
PMID 26294105

惣田哲次,奥見雅由,宮川康 [他],中紀文,辻村晃,野々村祝夫
泌尿器科紀要 = Acta urologica Japonica 59(5), 293-296, 2013-05
… Since he had a past history of neurofibroma of cauda equina, we suspected neurofibromatosis type 1. …
NAID 120005245085