WordNet

relating to the ciliary body and associated structures of the eye
of or relating to the human eyelash (同)ciliate
of or relating to cilia projecting from the surface of a cell (同)ciliate, cilial
present at birth but not necessarily hereditary; acquired during fetal development (同)inborn, innate
abnormality in performing voluntary muscle movements

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1. 原発性線毛機能不全（線毛不動症候群） primary ciliary dyskinesia immotile cilia syndrome
2. 小児における気管支拡張症の原因 causes of bronchiectasis in children
3. 新生児呼吸促迫の概要：移行の障害 overview of neonatal respiratory distress disorders of transition
4. 小児における気管支拡張症の臨床症状および評価 clinical manifestations and evaluation of bronchiectasis in children
5. 小児における慢性咳嗽に対するアプローチ approach to chronic cough in children

TTC25 Deficiency Results in Defects of the Outer Dynein Arm Docking Machinery and Primary Ciliary Dyskinesia with Left-Right Body Asymmetry Randomization.

Wallmeier J1, Shiratori H2, Dougherty GW1, Edelbusch C1, Hjeij R1, Loges NT1, Menchen T1, Olbrich H1, Pennekamp P1, Raidt J1, Werner C1, Minegishi K2, Shinohara K2, Asai Y2, Takaoka K2, Lee C3, Griese M4, Memari Y5, Durbin R5, Kolb-Kokocinski A5, Sauer S6, Wallingford JB3, Hamada H2, Omran H7.
American journal of human genetics.Am J Hum Genet.2016 Aug 4;99(2):460-9. doi: 10.1016/j.ajhg.2016.06.014.
Multiprotein complexes referred to as outer dynein arms (ODAs) develop the main mechanical force to generate the ciliary and flagellar beat. ODA defects are the most common cause of primary ciliary dyskinesia (PCD), a congenital disorder of ciliary beating, characterized by recurrent infections of t
PMID 27486780

Clinical manifestations in primary ciliary dyskinesia: systematic review and meta-analysis.

Goutaki M1, Meier AB1, Halbeisen FS2, Lucas JS3, Dell SD4, Maurer E2, Casaulta C5, Jurca M2, Spycher BD2, Kuehni CE6.
The European respiratory journal.Eur Respir J.2016 Aug 4. pii: ERJ-00736-2016. doi: 10.1183/13993003.00736-2016. [Epub ahead of print]
Few original studies have described the prevalence and severity of clinical symptoms of primary ciliary dyskinesia (PCD). This systematic review and meta-analysis aimed to identify all published studies on clinical manifestations of PCD patients, and to describe their prevalence and severity stratif
PMID 27492829

Takeuchi K1, Kitano M2, Ishinaga H2, Kobayashi M2, Ogawa S3, Nakatani K4, Masuda S5, Nagao M6, Fujisawa T6.
Auris, nasus, larynx.Auris Nasus Larynx.2016 Jun;43(3):229-36. doi: 10.1016/j.anl.2015.09.012. Epub 2015 Oct 31.
Primary ciliary dyskinesia (PCD) is a genetic disease inherited in an autosomal recessive manner. The prevalence of PCD is estimated to be 1 in 20,000 live births. Congenital abnormality of the primary cilia results in situs inversus in 50% of patients. Decreased function of motile cilia causes chro
PMID 26527516