Comparison of the second consensus statement with the movement disorder society criteria for multiple system atrophy: A single-center analysis

Autor: Sun, Yunchuang, Sun, Wei, Wei, Luhua, Li, Fan, Jiang, Yanyan, Zhai, Fei, Luan, Mingyue, Chen, Jing, Wang, Zhaoxia

Publikováno v: In Parkinsonism and Related Disorders January 2023 106

Novel TUBA4Avariant causes congenital myopathy with focal myofibrillar disorganisation

Autor: Wan, Yalan, Zhou, Chao, Chang, Xingzhi, Wu, Liwen, Zheng, Yilei, Yu, Jiaxi, Bai, Li, Luan, Mingyue, Yu, Meng, Wang, Qi, Zhang, Wei, Yuan, Yun, Deng, Jianwen, Wang, Zhaoxia

Publikováno v: Journal of Medical Genetics (JMG); 2024, Vol. 61 Issue: 7 p626-632, 7p

Ribosomal binding site sequences and promoters for expressing glutamate decarboxylase and producing γ-aminobutyrate in Corynebacterium glutamicum

Autor: Li Yongfu, Feng Shi, Luan Mingyue

Publikováno v: AMB Express
AMB Express, Vol 8, Iss 1, Pp 1-17 (2018)

Glutamate decarboxylase (GAD) converts l-glutamate (Glu) into γ-aminobutyric acid (GABA). Corynebacterium glutamicum that expresses exogenous GAD gene, gadB2 or gadB1, can synthesize GABA from its own produced Glu. To enhance GABA production in C. g

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5a8f6c68e0ab80a1be0867e5e432f04
https://doi.org/10.1186/s13568-018-0595-2

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Novel TUBA4A variant causes congenital myopathy with focal myofibrillar disorganisation.

Autor: Wan Y; Department of Neurology, Peking University First Hospital, Beijing, China., Zhou C; State Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China., Chang X; Department of Pediatrics, Peking University First Hospital, Beijing, China., Wu L; Department of Neurology, Hunan Children's Hospital, Changsha, China., Zheng Y; Department of Neurology, Peking University First Hospital, Beijing, China., Yu J; Department of Neurology, Peking University First Hospital, Beijing, China., Bai L; Department of Neurology, Peking University First Hospital, Beijing, China., Luan M; Department of Neurology, Peking University First Hospital, Beijing, China., Yu M; Department of Neurology, Peking University First Hospital, Beijing, China., Wang Q; Department of Neurology, Peking University First Hospital, Beijing, China., Zhang W; Department of Neurology, Peking University First Hospital, Beijing, China., Yuan Y; Department of Neurology, Peking University First Hospital, Beijing, China., Deng J; Department of Neurology, Peking University First Hospital, Beijing, China drwangzx@163.com jianwendeng@pkufh.com.; Beijing Key Laboratory of Neurovascular Disease Discovery, Beijing, China.; Key Laboratory for Neuroscience, Ministry of Education/National Health Commission, Peking University, Beijing, China., Wang Z; Department of Neurology, Peking University First Hospital, Beijing, China drwangzx@163.com jianwendeng@pkufh.com.; Beijing Key Laboratory of Neurovascular Disease Discovery, Beijing, China.; Key Laboratory for Neuroscience, Ministry of Education/National Health Commission, Peking University, Beijing, China.

Publikováno v: Journal of medical genetics [J Med Genet] 2024 Jun 20; Vol. 61 (7), pp. 626-632. Date of Electronic Publication: 2024 Jun 20.