WordNet

the main stem of a tree; usually covered with bark; the bole is usually the part that is commercially useful for lumber (同)tree trunk, bole
luggage consisting of a large strong case used when traveling or for storage

PrepTutorEJDIC

(枝および根と区別して樹木の)『幹』 / (人・動物の)胴体 / 『トランク』旅行用箱型の大型かばん) / 象の鼻 / 《複数形で》(文泳などスポーツ競技用の)男子用パンツ,チランクス / 《米》(自動車後部の)荷物入れ,トランク(《英》boot) / =trunk line

全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.

1. 迷走神経切離術 vagotomy
2. 消化性潰瘍の外科的マネージメント surgical management of peptic ulcer disease
3. 総動脈幹 truncus arteriosus
4. 肥満のマネージメントのための肥満手術：適応と術前の準備 bariatric operations for management of obesity indications and preoperative preparation
5. 胃全摘術および消化管再建術 total gastrectomy and gastrointestinal reconstruction

Fink EC, Fisher DE.SourceDepartment of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
The Journal of investigative dermatology.J Invest Dermatol.2013 Apr;133(4):878-80. doi: 10.1038/jid.2012.475.
In this issue, Hacker et al. (2012) report the largest study to date on the association between MC1R variants and BRAF mutant melanoma. Although they did not observe a significant overall correlation, there was a significant negative association between BRAF and MC1R mutations for head/neck melanoma
PMID 23486431

Tarnutzer AA, Bockisch CJ, Straumann D.SourceDepartment of Neurology, University Hospital Zurich, Frauenklinikstrasse 26, 8091, Zurich, Switzerland, alexander.tarnutzer@access.uzh.ch.
Experimental brain research. Experimentelle Hirnforschung. Experimentation cerebrale.Exp Brain Res.2013 Mar 28. [Epub ahead of print]
Body position relative to gravity is continuously updated to prevent falls. Therefore, the brain integrates input from the otoliths, truncal graviceptors, proprioception and vision. Without visual cues estimated direction of gravity mainly depends on otolith input and becomes more variable with incr
PMID 23535837

Clinical and neuropathological features of X-linked spinal muscular atrophy (SMAX2) associated with a novel mutation in the UBA1 gene.

Dlamini N, Josifova DJ, Paine SM, Wraige E, Pitt M, Murphy AJ, King A, Buk S, Smith F, Abbs S, Sewry C, Jacques TS, Jungbluth H.SourceDepartment of Paediatric Neurology - Neuromuscular Service, Evelina Children's Hospital, Guy's & St. Thomas' NHS Foundation Trust, UK. Electronic address: nomazulu.dlamini@gstt.nhs.uk.
Neuromuscular disorders : NMD.Neuromuscul Disord.2013 Mar 18. pii: S0960-8966(13)00052-7. doi: 10.1016/j.nmd.2013.02.001. [Epub ahead of print]
Infantile-onset X-linked spinal muscular atrophy (SMAX2) is a rare lethal disorder linked to mutations in the UBA1 (previously UBE1) gene, encoding ubiquitin-activating enzyme 1 that has an important role in the ubiquitin-proteasome pathway. Published pathological reports are scarce. Here we report
PMID 23518311