- 関
- dominantly-inherited spinocerebellar ataxia、SCA1、spinocerebellar ataxia、spinocerebellar ataxia type 2、spinocerebellar ataxia type 4、spinocerebellar ataxia type 5、spinocerebellar ataxia type 6、spinocerebellar ataxia type 7、spinocerebellar atrophy
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
- inability to coordinate voluntary muscle movements; unsteady movements and staggering gait (同)ataxy, dyssynergia, motor_ataxia
- 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
UpToDate Contents
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- 1. 脊髄小脳変性症 the spinocerebellar ataxias
- 2. 遺伝性運動失調の概要 overview of the hereditary ataxias
- 3. 舞踏病の概要 overview of chorea
- 4. 遺伝性疾患に伴う神経障害 neuropathies associated with hereditary disorders
- 5. 片麻痺性片頭痛 hemiplegic migraine
English Journal
- The optic nerve: a "mito-window" on mitochondrial neurodegeneration.
- Maresca A, la Morgia C, Caporali L, Valentino ML, Carelli V.SourceIRCCS Istituto delle Scienze Neurologiche di Bologna, University of Bologna, Via Ugo Foscolo 7, 40123 Bologna, Italy.
- Molecular and cellular neurosciences.Mol Cell Neurosci.2013 Jul;55:62-76. doi: 10.1016/j.mcn.2012.08.004. Epub 2012 Aug 15.
- Retinal ganglion cells (RGCs) project their long axons, composing the optic nerve, to the brain, transmitting the visual information gathered by the retina, ultimately leading to formed vision in the visual cortex. The RGC cellular system, representing the anterior part of the visual pathway, is vul
- PMID 22960139
- H1152 promotes the degradation of polyglutamine-expanded ataxin-3 or ataxin-7 independently of its ROCK-inhibiting effect and ameliorates mutant ataxin-3-induced neurodegeneration in the SCA3 transgenic mouse.
- Wang HL, Hu SH, Chou AH, Wang SS, Weng YH, Yeh TH.SourceDepartment of Physiology and Pharmacology, Chang Gung University School of Medicine, 259 Wen-Hwa 1 Road, Kwei-San, Tao-Yuan, Taiwan, ROC. Electronic address: hlwns@mail.cgu.edu.tw.
- Neuropharmacology.Neuropharmacology.2013 Jul;70:1-11. doi: 10.1016/j.neuropharm.2013.01.006. Epub 2013 Jan 21.
- Spinocerebellar ataxia type 3 (SCA3) caused by polyglutamine-expanded ataxin-3 is the most prevalent subtype of spinocerebellar ataxias. A compound, which decreases protein level of mutant ataxin-3 in SCA3 affected CNS regions, should be a promising therapeutic agent for SCA3. SCA3 and Huntington's
- PMID 23347954
- Aggregation of polyQ-extended proteins is promoted by interaction with their natural coiled-coil partners.
- Petrakis S, Schaefer MH, Wanker EE, Andrade-Navarro MA.SourceNeuroproteomics, Max Delbrueck, Center for Molecular Medicine, Berlin, Germany; Aristotle University of Thessaloniki, Thessaloniki, Greece.
- BioEssays : news and reviews in molecular, cellular and developmental biology.Bioessays.2013 Jun;35(6):503-7. doi: 10.1002/bies.201300001. Epub 2013 Mar 11.
- Polyglutamine (polyQ) diseases are genetically inherited neurodegenerative disorders. They are caused by mutations that result in polyQ expansions of particular proteins. Mutant proteins form intranuclear aggregates, induce cytotoxicity and cause neuronal cell death. Protein interaction data suggest
- PMID 23483542
- Expression of Expanded CAG Transcripts Triggers Nucleolar Stress in Huntington's Disease.
- Tsoi H, Chan HY.SourceLaboratory of Drosophila Research, School of Life Sciences, Faculty of Science, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong, China.
- Cerebellum (London, England).Cerebellum.2013 Jun;12(3):310-2. doi: 10.1007/s12311-012-0447-6.
- Polyglutamine (polyQ) diseases, including several types of spinocerebellar ataxias and Huntington's disease (HD), are dominantly inherited neurodegenerative disorders caused by the expansion of the glutamine-coding CAG repeat in the open reading frame of the disease gene. Apart from being translated
- PMID 23315009
Japanese Journal
- 症例報告 痙性対麻痺様の症候を呈した脊髄小脳失調症2型の1例
- 宮地 洋輔,土井 宏,児矢野 繁 [他]
- 臨床神経学 50(9), 641-644, 2010-09
- NAID 40017328813
- Congo Red, an Amyloid-Inhibiting Compound, Alleviates Various Types of Cellular Dysfunction Triggered by Mutant Protein Kinase Cγ That Causes Spinocerebellar Ataxia Type 14 (SCA14) by Inhibiting Oligomerization and Aggregation
- Seki Takahiro,Takahashi Hideyuki,Yamamoto Kazuhiro [他],Ogawa Kota,Onji Tomoya,Adachi Naoko,Tanaka Shigeru,Hide Izumi,Saito Naoaki,Sakai Norio
- Journal of Pharmacological Sciences advpub(0), 1010010456, 2010
- … Several missense mutations in the protein kinase Cγ (γPKC) gene have been found to cause spinocerebellar ataxia type 14 (SCA14), an autosomal dominant neurodegenerative disease. …
- NAID 130000439860
- Prevalence of Autosomal Dominant Cerebellar Ataxia in Aomori, the Northernmost Prefecture of Honshu, Japan
- Yamamoto-Watanabe Yukiko,Watanabe Mitsunori,Hikichi Motofumi,Ikeda Yoshio,Jackson Mandy,Wakasaya Yasuhito,Matsubara Etsuro,Kawarabayashi Takeshi,Kannari Kazuya,Shoji Mikio
- Internal Medicine 49(22), 2409-2414, 2010
- … Objective The frequency of autosomal dominant cerebellar ataxia (ADCA) varies between different regions of Japan. … Methods and Patients Sixty-five familial spinocerebellar ataxia (SCA) patients and 15 sporadic SCA patients were genetically examined. … Results Spinocerebellar ataxia (SCA) type 6 was often observed (77.7% of cases), with SCA2 (10.6% of cases) being the next most common form. …
- NAID 130000413368
Related Links
- Spinocerebellar ataxia type 1 (SCA1) is a condition characterized by progressive problems with movement. People with this condition initially experience problems with coordination and balance (ataxia). Other signs and ...
- NATIONALF ATAAXIAQ FOUNDATION What is spinocerebellar ataxia type 1? Spinocerebellar ataxia type 1 (SCA1) is one specific type of ataxia among a group of inherited diseases of the central nervous system. In SCA1, genetic ...
- 164400 - SPINOCEREBELLAR ATAXIA 1; SCA1 - SPINOCEREBELLAR ATROPHY I;; OLIVOPONTOCEREBELLAR ATROPHY I; OPCA1;; OPCA I;; CEREBELLOPARENCHYMAL DISORDER I; CPD1;; MENZEL TYPE ...
Related Pictures
★リンクテーブル★
| リンク元 | 「脊髄小脳失調症1型」「spinocerebellar ataxia type 2」「spinocerebellar ataxia type 4」「spinocerebellar ataxia type 5」「spinocerebellar ataxia type 6」 |
| 関連記事 | 「type」「spinocerebellar ataxia」「typed」「typing」 |
「脊髄小脳失調症1型」
- 英
- spinocerebellar ataxia type 1
- 関
- 脊髄小脳変性症、脊髄小脳変性症1型、脊髄小脳失調症2型、脊髄小脳失調症7型、脊髄小脳失調症4型、脊髄小脳失調症5型、脊髄小脳失調症6型、脊髄小脳萎縮症、優性遺伝性脊髄小脳失調症
「spinocerebellar ataxia type 2」
- 関
- dominantly-inherited spinocerebellar ataxia、spinocerebellar ataxia、spinocerebellar ataxia type 1、spinocerebellar ataxia type 4、spinocerebellar ataxia type 5、spinocerebellar ataxia type 6、spinocerebellar ataxia type 7、spinocerebellar atrophy
「spinocerebellar ataxia type 4」
- 関
- dominantly-inherited spinocerebellar ataxia、spinocerebellar ataxia、spinocerebellar ataxia type 1、spinocerebellar ataxia type 2、spinocerebellar ataxia type 5、spinocerebellar ataxia type 6、spinocerebellar ataxia type 7、spinocerebellar atrophy
「spinocerebellar ataxia type 5」
- 関
- dominantly-inherited spinocerebellar ataxia、spinocerebellar ataxia、spinocerebellar ataxia type 1、spinocerebellar ataxia type 2、spinocerebellar ataxia type 4、spinocerebellar ataxia type 6、spinocerebellar ataxia type 7、spinocerebellar atrophy
「spinocerebellar ataxia type 6」
- 関
- dominantly-inherited spinocerebellar ataxia、spinocerebellar ataxia、spinocerebellar ataxia type 1、spinocerebellar ataxia type 2、spinocerebellar ataxia type 4、spinocerebellar ataxia type 5、spinocerebellar ataxia type 7、spinocerebellar atrophy
「type」
- n.
- (windows)ファイル内容表示(linux -> cat])
- ex. type report_20111118.jp.htm | php a.php > report_20111118.jp.jp.jp.html
「spinocerebellar ataxia」
[★] 脊髄小脳変性症 spinocerebellar degeneration SCD = SCA
「typed」
- adj.
- 型の
「typing」
- n.
- タイプで打つこと、タイピング。分類