WordNet

move over something with pressure; "rub my hands"; "rub oil into her skin"
the act of rubbing or wiping; "he gave the hood a quick rub" (同)wipe
cause friction; "my sweater scratches" (同)fray, fret, chafe, scratch
scrape or rub as if to relieve itching; "Dont scratch your insect bites!" (同)scratch, itch
a decrease in size of an organ caused by disease or disuse (同)wasting, wasting away
undergo atrophy; "Muscles that are not used will atrophy"
any weakening or degeneration (especially through lack of use) (同)withering

PrepTutorEJDIC

〈物の表面など〉‘を'『こする』,さする / (…に)…‘を'こすりつける《+名+『against(on, over)』+名》;(…に)…‘を'すりこむ《+『名』+『in』(『into, on』)+『名』》 / 〈二つの物〉‘を'こすり合わせる《+『名』+『together,』+『together』+『名』》 / ‥‘を'こすり落とす《+『名』+『away』(『off』)『,』+『away』(『off』)+『名』》 / …‘を'すりむく,ひりひりさせる / (…の表面を)『こする』,すれる《+『against』(『on』)+『名』》;〈二つの物が〉こすれ合う《+『together』》 / 《単数形で》こすること / 当てこすり / 《the rub》やっかいな事,困難
(栄養不良などによる)萎縮(いしゅく) / (一般的に)衰退,退化 / 萎縮する,衰退する / …'を'萎縮させる,衰退させる
(顔・肌などが)青白い,生色のない(pale)

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1. 脊髄性筋萎縮症 spinal muscular atrophy
2. 多系統萎縮症：予後および治療 multiple system atrophy prognosis and treatment
3. 脊髄小脳変性症 the spinocerebellar ataxias
4. アルツハイマー病の臨床症状および診断 clinical manifestations and diagnosis of alzheimer disease
5. パーキンソン病の診断 diagnosis of parkinson disease

Juvenile myoclonic epilepsy is not associated with the DRPLA gene in a European population.

Yapijakis C, Gatzonis S, Youroukos S, Kollia V, Karachristianou S, Anagnostouli M.
In vivo (Athens, Greece). ;28(6)1193-6.
Juvenile myoclonic epilepsy (JME), is an early-onset inherited generalized epilepsy which displays genetic heterogeneity, with at least 10 known loci. Another neurogenetic disease, dentato-rubro-pallido-luysian atrophy (DRPLA) presents three clinical phenotypes, one of which in Japanese displays man
PMID 25398822

Enhanced aggregation of androgen receptor in induced pluripotent stem cell-derived neurons from spinal and bulbar muscular atrophy.

Nihei Y, Ito D, Okada Y, Akamatsu W, Yagi T, Yoshizaki T, Okano H, Suzuki N.
The Journal of biological chemistry. 2013 Mar;288(12)8043-52.
Spinal and bulbar muscular atrophy (SBMA) is an X-linked motor neuron disease caused by a CAG repeat expansion in the androgen receptor (AR) gene. Ligand-dependent nuclear accumulation of mutant AR protein is a critical characteristic of the pathogenesis of SBMA. SBMA has been modeled in AR-overexpr
PMID 23364790

Absence seizures with myoclonic seizures as an early manifestation of dentato-rubro-pallido-luysian atrophy (DRPLA): a follow-up clinical course of twelve years.

Sudo K, Hata D, Yokoyama N, Kawashima J, Yabe I, Tajima Y, Matsumoto A, Tashiro K.
Acta neurologica Belgica. 2010 Mar;110(1)84-8.
Typical absence seizures and isolated myoclonic seizures are both classified as age-related generalized seizures and are considered to be benign neurological manifestations. Concomitance of the two types of seizure is considered benign if it does not accompany other types of seizures or other neurol
PMID 20514931