Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Baitao Zeng"'
Autor:
Qing Lu, Laipeng Luo, Baitao Zeng, Haiyan Luo, Xianjin Wang, Lijuan Qiu, Yan Yang, Chuanxin Feng, Jihui Zhou, Yanling Hu, Tingting Huang, Pengpeng Ma, Ting Huang, Kang Xie, Huizhen Yuan, Shuhui Huang, Bicheng Yang, Yongyi Zou, Yanqiu Liu
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-11 (2024)
Abstract Background and objectives Congenital heart defect (CHD) is one of the most common birth defects. The aim of this cohort study was to evaluate the prevalence of chromosomal abnormalities and the clinical utility of chromosomal microarray anal
Externí odkaz:
https://doaj.org/article/be0dc194fa524d1fae92b68b64eff4c6
Autor:
Cheng Huang, Haiyan Luo, Baitao Zeng, Chuanxin Feng, Jia Chen, Huizhen Yuan, Shuhui Huang, Bicheng Yang, Yongyi Zou, Yanqiu Liu
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background and purpose: Intellectual disability-7 (MRD7) is a subtype disorder of intellectual disability (MRD) involving feeding difficulties, hypoactivity, and febrile seizures at an age of early onset, then progressive intellectual and physical de
Externí odkaz:
https://doaj.org/article/7fd74913cf8c48adbbe8a18e08c6c879
Autor:
Baitao Zeng, Haoyi Zhang, Qing Lu, Qingzi Fu, Yang Yan, Wan Lu, Pengpeng Ma, Chuanxin Feng, Jiawei Qin, Laipeng Luo, Bicheng Yang, Yongyi Zou, Yanqiu Liu
Publikováno v:
Frontiers in Behavioral Neuroscience, Vol 17 (2023)
BackgroundEpilepsy is characterized by recurrent unprovoked seizures. Mutations in the voltage-gated sodium channel alpha subunit 1 (SCN1A) gene are the main monogenic cause of epilepsy. Type and location of variants make a huge difference in the sev
Externí odkaz:
https://doaj.org/article/9ef41a29de574fdf9c006fd477ca8af7
Autor:
Baitao Zeng, Qing Lu, Shaohong Chen, Huizhen Guan, Xiaolan Xu, Yongyi Zou, Feng Wang, Shuhui Huang, Yanqiu Liu, Bicheng Yang
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: Phenylalanine hydroxylase deficiency (PAHD) is an autosomal recessive disorder of amino acid metabolism and caused by mutations in the phenylalanine hydroxylase (PAH) gene. Without timely and appropriate dietary management, the disturbanc
Externí odkaz:
https://doaj.org/article/9f13985710324df08bb812e70bd5beeb
Autor:
Kang Xie, Baitao Zeng, Liuyang Zhang, Shaohong Chen, Yongyi Zou, Huizhen Yuan, Shuhui Huang, Feng Wang, Qing Lu, Yanqiu Liu, Bicheng Yang
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Hyperphenylalaninemia (HPA) is the most common inborn error in amino acid metabolism. It can be primarily classified into phenylalanine hydroxylase (PAH) deficiency and tetrahydrobiopterin (BH4) deficiency. BH4 deficiency (BH4D) is caused
Externí odkaz:
https://doaj.org/article/c1e4acfc0cf54d3caa450f3dadfd575e
Autor:
Zheng Wu, Wei Liu, Zujia Wang, Baitao Zeng, Guangnan Peng, Hongyan Niu, Linlin Chen, Cong Liu, Qian Hu, Yuxuan Zhang, Mengmeng Pan, Lingqian Wu, Mujun Liu, Xionghao Liu, Desheng Liang
Publikováno v:
Cancer Cell International, Vol 20, Iss 1, Pp 1-10 (2020)
Abstract Background Interleukin-24 (IL-24) is a therapeutic gene for melanoma, which can induce melanoma cell apoptosis. Mesenchymal stem cells (MSCs) show promise as a carrier to delivery anti-cancer factors to tumor tissues. Induced pluripotent ste
Externí odkaz:
https://doaj.org/article/29e52efe4fc3404daf62d088b109797e
Autor:
Nannan Duan, Shuqing Tang, Baitao Zeng, Zhiqing Hu, Qian Hu, Lingqian Wu, Miaojin Zhou, Desheng Liang
Publikováno v:
Life, Vol 11, Iss 11, p 1262 (2021)
(1) Background: Gene editing technology, as represented by CRISPR is a powerful tool used in biomedical science. However, the editing efficiency of such technologies, especially in induced pluripotent stem cells (iPSCs) and other types of stem cells,
Externí odkaz:
https://doaj.org/article/4484a438e67a4695b4475dc04efca9c6
Autor:
Kang, Xie, Baitao, Zeng, Liuyang, Zhang, Shaohong, Chen, Yongyi, Zou, Huizhen, Yuan, Shuhui, Huang, Feng, Wang, Qing, Lu, Yanqiu, Liu, Bicheng, Yang
Publikováno v:
Frontiers in genetics. 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d4e8e37b2ca0f6288fc442a3e9c38a81
https://pubmed.ncbi.nlm.nih.gov/36583021
https://pubmed.ncbi.nlm.nih.gov/36583021
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 16; Pages: 9176
Duchenne muscular dystrophy (DMD) is the most common fatal muscle disease, with an estimated incidence of 1/3500–1/5000 male births, and it is associated with mutations in the X-linked DMD gene encoding dystrophin, the largest known human gene. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85e322e29f9ca107ecf56b36861fd3d0
Autor:
Yiti, Zhang, Baitao, Zeng, Ao, Gu, Qinyu, Kang, Mingri, Zhao, Guangnan, Peng, Miaojin, Zhou, Wanxi, Liu, Min, Liu, Lingjie, Ding, Desheng, Liang, Xionghao, Liu, Mujun, Liu
Publikováno v:
International journal of molecular sciences. 23(19)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::094b00976631834574ee091b28acde75
https://pubmed.ncbi.nlm.nih.gov/36232630
https://pubmed.ncbi.nlm.nih.gov/36232630