WordNet

do over; "They would like to take it over again" (同)take_over
an event that repeats; "the events today were a repeat of yesterdays" (同)repetition
to say again or imitate; "followers echoing the cries of their leaders" (同)echo
to say, state, or perform again; "She kept reiterating her request" (同)reiterate, ingeminate, iterate, restate, retell
an impairment of health or a condition of abnormal functioning
the 3rd letter of the Roman alphabet (同)c
(music) the keynote of the scale of C major
a general-purpose programing language closely associated with the UNIX operating system
caused by or altered by or manifesting disease or pathology; "diseased tonsils"; "a morbid growth"; "pathologic tissue"; "pathological bodily processes" (同)morbid, pathologic, pathological

PrepTutorEJDIC

〈自分がすでに一度言ったこと)‘を'『繰り返して言う』 / 〈他人の言ったこと〉‘を'おうむ返しに言う;…‘を'他の人に繰り返して言う / …‘を'『暗記して言う』,暗唱する / …‘を'繰り返して行う(do again) / (食べたあとで)〈食物の〉味が残る / 〈小数が〉循環する / 繰り返すこと,反復すること / 繰り返されるもの,(公演の)再演;(番組の)再放送 / 反復楽節;反復記号(∥: :∥)
(体の)『病気』,疾患 / (精神・道徳などの)病気,病弊
女性の話術芸人 =diseur
carbonの化学記号
病気にかかった / 病的な,不健全な(morbid)
California

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1. 定量的冠動脈造影：臨床応用 quantitative coronary angiography clinical applications
2. 安定冠動脈疾患患者ににおける血行再建術：冠動脈バイパス移植術と経皮的冠動脈形成術の比較 revascularization in patients with stable coronary artery disease coronary artery bypass graft surgery versus percutaneous coronary intervention
3. 診断的心臓カテーテル検査の合併症 complications of diagnostic cardiac catheterization
4. 若年男女における冠動脈疾患および心筋梗塞 coronary heart disease and myocardial infarction in young men and women
5. Cardiovascular sequelae of Kawasaki disease

Detection of huntingtin exon 1 phosphorylation by Phos-Tag SDS-PAGE: Predominant phosphorylation on threonine 3 and regulation by IKKβ.

Bustamante MB1, Ansaloni A2, Pedersen JF1, Azzollini L1, Cariulo C1, Wang ZM2, Petricca L1, Verani M1, Puglisi F1, Park H3, Lashuel H2, Caricasole A4.
Biochemical and biophysical research communications.Biochem Biophys Res Commun.2015 Aug 7;463(4):1317-22. doi: 10.1016/j.bbrc.2015.06.116. Epub 2015 Jun 21.
Expansion of a CAG triplet repeat within the first exon of the HUNTINGTIN gene encoding for a polyglutamine tract is the cause of a progressive neurodegenerative disorder known as Huntington's disease. N-terminal fragments of mutant huntingtin have a strong propensity to form oligomers and aggregate
PMID 26106822

Leoni V1, Caccia C2.
Biochimica et biophysica acta.Biochim Biophys Acta.2015 Aug;1851(8):1095-1105. doi: 10.1016/j.bbalip.2014.12.018. Epub 2015 Jan 14.
Huntington disease (HD), an autosomal dominant neurodegenerative disorder caused by an abnormal expansion of CAG trinucleotide repeat in the Huntingtin (HTT) gene, is characterized by extensive neurodegeneration of striatum and cortex and severe diffuse atrophy at MRI. The expression of genes involv
PMID 25596342

DnaJ-1 and karyopherin α3 suppress degeneration in a new Drosophila model of Spinocerebellar Ataxia Type 6.

Tsou WL1, Hosking RR1, Burr AA2, Sutton JR1, Ouyang M1, Du X3, Gomez CM3, Todi SV4.
Human molecular genetics.Hum Mol Genet.2015 Aug 1;24(15):4385-96. doi: 10.1093/hmg/ddv174. Epub 2015 May 7.
Spinocerebellar ataxia type 6 (SCA6) belongs to the family of CAG/polyglutamine (polyQ)-dependent neurodegenerative disorders. SCA6 is caused by abnormal expansion in a CAG trinucleotide repeat within exon 47 of CACNA1A, a bicistronic gene that encodes α1A, a P/Q-type calcium channel subunit and a
PMID 25954029

Italiano Domenico,Tarantino Patrizia,Valeria De Marco Elvira,Salvatore Calabrò Rocco,Bramanti Placido,Quattrone Aldo,Annesi Grazia
Internal Medicine 51(20), 2953-2955, 2012
… A molecular analysis identified 38 cytosine-adenine-guanine (CAG) repeat expansions within the SCA7 gene. … In this family, the disease is most likely caused by a de novo expansion of a premutated intermediate allele carried by one parent. …
NAID 130002062092

Three Spinocerebellar Ataxia Type 2 Siblings with Ataxia, Parkinsonism, and Motor Neuronopathy

Nishikawa Noriko,Nagai Masahiro,Tsujii Tomoaki,Tanabe Nachi,Takashima Hiroshi,Nomoto Masahiro
Internal Medicine 50(13), 1429-1432, 2011
… Spinocerebellar ataxia type 2 (SCA2) represents a family of dominant neurodegenerative disorders that results from CAG expansion repeat mutations. … Genetic examination revealed expansion to 42, 43, and 42 CAG repeats. … The SCA2 gene should be studied in families with heterogeneous neurodegenerative disorders, including motor neuron disease. …
NAID 130000770521

Direct and accurate measurement of CAG repeat configuration in the ataxin-1 (ATXN-1) gene by "dual-fluorescence labeled PCR-restriction fragment length analysis"

Lin Jiang X.,Ishikawa Kinya,Sakamoto Masaki [他],TSUNEMI Taiji,ISHIGURO Taro,AMINO Takeshi,SHUTA Toru,KONDO Ikuko,MIZUSAWA Hidehiro
Journal of human genetics 53(4), 287-295, 2008-04-01
NAID 10021248419