WordNet

move something or somebody around; usually over long distances
an exchange of molecules (and their kinetic energy and momentum) across the boundary between adjacent layers of a fluid or across cell membranes
move while supporting, either in a vehicle or in ones hands or on ones body; "You must carry your camping gear"; "carry the suitcases to the car"; "This train is carrying nuclear waste"; "These pipes carry waste water into the river" (同)carry
transport commercially (同)send, ship
convert into a sulfate
a salt or ester of sulphuric acid (同)sulphate
a long truck for carrying motor vehicles (同)car transporter
a crane for moving material with dispatch as in loading and unloading ships
abnormal development (of organs or cells) or an abnormal structure resulting from such growth

PrepTutorEJDIC

(ある場所からある場所へ)…‘を'『輸送する』,運搬する《+名+from+名+to+名》 / 《文》《受動態で》(…で)…‘を'夢中にする,有頂天にする《+名+with+名》 / 〈罪人〉‘を'流刑にする / 〈U〉輸送,運送,輸送(交通)機関(transportation) / 〈C〉(軍隊や軍需品を運ぶ)輸送船,輸送機
自動車運搬用大型トラック

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1. 致死的骨格形成異常の出生前診断 prenatal diagnosis of the lethal skeletal dysplasias
2. 遺伝性皮膚症 the genodermatoses
3. 先天性股関節脱臼：治療および転帰 developmental dysplasia of the hip treatment and outcome
4. 小児および思春期における良性骨腫瘍：概要 benign bone tumors in children and adolescents an overview
5. 脳性麻痺の疫学および病因 epidemiology and etiology of cerebral palsy

Effect of SLC26 anion transporter disease-causing mutations on the stability of the homologous STAS domain of E. coli DauA (YchM).

Bai X1, Moraes TF1, Reithmeier RA2.
The Biochemical journal.Biochem J.2016 Mar 1;473(5):615-26. doi: 10.1042/BJ20151025. Epub 2015 Dec 3.
The human solute carrier 26 (SLC26) family of anion transporters consists of ten members that are found in various organs in the body including the stomach, intestine, kidney, thyroid and ear where they transport anions including bicarbonate, chloride and sulfate, typically in an exchange mode. Muta
PMID 26635355

Dysplastic spondylolysis is caused by mutations in the diastrophic dysplasia sulfate transporter gene.

Cai T1, Yang L2, Cai W3, Guo S4, Yu P4, Li J4, Hu X2, Yan M2, Shao Q4, Jin Y5, Sun ZS6, Luo ZJ7.
Proceedings of the National Academy of Sciences of the United States of America.Proc Natl Acad Sci U S A.2015 Jun 30;112(26):8064-9. doi: 10.1073/pnas.1502454112. Epub 2015 Jun 15.
Spondylolysis is a fracture in part of the vertebra with a reported prevalence of about 3-6% in the general population. Genetic etiology of this disorder remains unknown. The present study was aimed at identifying genomic mutations in patients with dysplastic spondylolysis as well as the potential p
PMID 26077908

Al Kaissi A1, Kenis V, Melchenko E, Chehida FB, Ganger R, Klaushofer K, Grill F.
Orthopaedic surgery.Orthop Surg.2014 Nov;6(4):274-9. doi: 10.1111/os.12146.
OBJECTIVE: Accurate understanding of the cause of the underlying pathology in children with diastrophic dysplasia would help in designing targeted management of their locomotion.METHODS: Diastrophic dysplasia was diagnosed in twelve patients (nine girls and three boys; age range 1-14 years), all of
PMID 25430710

A compound heterozygote of novel and recurrent DTDST mutations results in a novel intermediate phenotype of Desbuquois dysplasia, diastrophic dysplasia, and recessive form of multiple epiphyseal dysplasia

Miyake Atsushi,Nishimura Gen,Futami Toru [他],OHASHI Hirofumi,CHIBA Kazuhiro,TOYAMA Yoshiaki,FURUICHI Tatsuya,IKEGAWA Shiro
Journal of human genetics 53(8), 764-768, 2008-08-01
NAID 10021929219

P2-433 Diastrophic dysplasia sulfate transporter (DTDST) geneに変異を認めたatelosteogenesis type IIとdiastrophic dysplasiaの中間的な表現形を示す先天性四肢短縮型骨系統疾患の一症例(Group 169 胎児・新生児X,一般演題,講演要旨,第58回日本産科婦人科学会学術講演会)