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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/06/05 10:48:38」(JST)
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- 1. 肥大型心筋症の遺伝学 genetics of hypertrophic cardiomyopathy
- 2. 細胞遺伝学的および分子遺伝学的診断ツール cytogenetic and molecular genetic diagnostic tools
- 3. デュシェンヌ型およびベッカー型筋ジストロフィーの臨床的特徴および診断 clinical features and diagnosis of duchenne and becker muscular dystrophy
- 4. 多発性内分泌腫瘍2型の臨床症状および診断 clinical manifestations and diagnosis of multiple endocrine neoplasia type 2
- 5. JAK3欠損を伴う重度複合型免疫不全（SCID） severe combined immunodeficiency scid with jak3 deficiency
English Journal
- A SNP in the 3'-untranslated region of AMPKγ1 may associate with serum ketone body and milk production of Holstein dairy cows.
- Mahmoudi A1, Zargaran A1, Amini HR1, Assadi A2, Vajdi Hokmabad R2, Eghbalsaied S3.
- Gene.Gene.2015 Dec 10;574(1):48-52. doi: 10.1016/j.gene.2015.07.077. Epub 2015 Jul 27.
- AMPK is the key switch for providing the energy balance between cellular anabolic and catabolic processes. In this study, we aimed to screen the PRKAG1 (AMPKγ1) gene in high, moderate, and low producing Holstein dairy cows. A sample of 100 pregnant dairy cows, comprising 41 high, 33 moderate, and 2
- PMID 26226224
- Specific and efficient electrochemical selection of Geoalkalibacter subterraneus and Desulfuromonas acetoxidans in high current-producing biofilms.
- Pierra M1, Carmona-Martínez AA1, Trably E1, Godon JJ1, Bernet N2.
- Bioelectrochemistry (Amsterdam, Netherlands).Bioelectrochemistry.2015 Dec;106(Pt A):221-5. doi: 10.1016/j.bioelechem.2015.02.003. Epub 2015 Feb 17.
- Two different saline sediments were used to inoculate potentiostatically controlled reactors (a type of microbial bioelectrochemical system, BES) operated in saline conditions (35gNaCll(-1)). Reactors were fed with acetate or a mixture of acetate and butyrate at two pH values: 7.0 or 5.5. Electroact
- PMID 25717030
- Mutational analysis of SCN5A gene in long QT syndrome.
- Qureshi SF1, Ali A1, John P1, Jadhav AP1, Venkateshwari A2, Rao H3, Jayakrishnan MP4, Narasimhan C5, Shenthar J6, Thangaraj K7, Nallari P1.
- Meta gene.Meta Gene.2015 Sep 2;6:26-35. doi: 10.1016/j.mgene.2015.07.010. eCollection 2015.
- The SCN5A gene encodes for the INa channel implicated in long QT syndrome type-3 (LQTS-type-3). Clinical symptoms of this type are lethal as most patients had a sudden death during sleep. Screening of SCN5A in South Indian cohort by PCR-SSCP analyses revealed five polymorphisms - A29A (exon-2), H558
- PMID 26401487
Japanese Journal
- 心筋ナトリウムポンプSCN5A遺伝子変異による在胎27週の子宮内胎児死亡の1症例
- 新潟県厚生連医誌 25(1), 115-117, 2016
- NAID 40020905359
- Species identification and strain typing of dermatophytes by single-strand conformation polymorphism (SSCP) analysis of the ribosomal DNA and polymerase chain reaction analysis of subrepeat elements in the intergenic spacer region of Trichophyton rubrum
- 旭川医科大学研究フォーラム 15(1), 27-36, 2015-02
- NAID 120005600794
- ナトリウムポンプαサブユニットSCN5A遺伝子変異をpolymerase chain reaction-single strand conformational polymorphism(PCR-SSCP)手技で同定できた心臓性突然死の4症例
- 新潟県厚生連医誌 24(1), 1-4, 2015
- NAID 40020904638
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★リンクテーブル★
| リンク元 | 「一本鎖DNA高次構造多型」「一本鎖高次構造多型分析法」「single-stranded conformational polymorphism」 |
| 関連記事 | 「SS」 |
「一本鎖DNA高次構造多型」
「一本鎖高次構造多型分析法」
「single-stranded conformational polymorphism」
- 関
- SSCP