Detection of gene mutation responsible for Huntington's disease by terahertz attenuated total reflection microfluidic spectroscopy.

Tang, Mingjie; Zhang, Mingkun; Xia, Liangping; Wei, Dongshan; Yang, Zhongbo; Yan, Shihan; Du, Chunlei; Cui, Hong-Liang

Tang, Mingjie; Zhang, Mingkun; Xia, Liangping; Wei, Dongshan; Yang, Zhongbo; Yan, Shihan; Du, Chunlei; Cui, Hong-Liang.

Affiliation

Tang M; Chongqing Institute of Green and Intelligent Technology, Chinese Academy of Sciences, Chongqing, China.
Zhang M; University of Chinese Academy of Sciences, Beijing, China.
Xia L; Chongqing Institute of Green and Intelligent Technology, Chinese Academy of Sciences, Chongqing, China.
Wei D; Chongqing Institute of Green and Intelligent Technology, Chinese Academy of Sciences, Chongqing, China.
Yang Z; Key Laboratory of Micro Nano Optoelectronic Devices and Intelligent Perception Systems, Yangtze Normal University, Chongqing, China.
Yan S; Chongqing Institute of Green and Intelligent Technology, Chinese Academy of Sciences, Chongqing, China.
Du C; School of Electronic Engineering, Dongguan University of Technology, Dongguan, China.
Cui HL; Chongqing Institute of Green and Intelligent Technology, Chinese Academy of Sciences, Chongqing, China.

J Biophotonics ; 14(1): e202000315, 2021 01.

Article de En | MEDLINE | ID: mdl-32981137

Sujet(s)
Mots clés

ATR; DNA oligonucleotides; microfluidic cell; repeated sequence; terahertz absorption

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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Maladie de Huntington / Spectroscopie térahertz Type d'étude: Diagnostic_studies Limites: Humans Langue: En Journal: J Biophotonics Sujet du journal: BIOFISICA Année: 2021 Type de document: Article Pays d'affiliation: Chine

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