Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Cuili Liang"'
Publikováno v:
Frontiers in Plant Science, Vol 14 (2023)
MicroRNAs (miRNAs) are widely involved in various aspects of plant growth and development. However, how miRNAs and their targets regulate natural rubber metabolism remains unclear in the rubber-producing dandelions, which are being developed as alter
Externí odkaz:
https://doaj.org/article/3e796cd84c5247af8cdb73a1a0681a3e
Autor:
Yani Zhang, Kelu Zheng, Cuili Liang, Ruidan Zheng, Jinghui Chen, Minyan Jiang, Zhizi Zhou, Yuan Zhao, Min Rao, Sida Yang, Wenxiong Chen, Li Liu
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
ObjectiveNusinersen, an extremely expensive biologic drug (around 100,000 US$ per dose) that needs to be administered intrathecally, is approved for the treatment of 5q-spinal muscular atrophy (SMA). Because of the low muscle tone of the back muscles
Externí odkaz:
https://doaj.org/article/a393fc33f1c047378a094ef8c9609792
Autor:
Aijing Xu, Minyan Jiang, Wen Zhang, Yunting Lin, Yongxian Shao, Huifen Mei, Jing Cheng, Cuili Liang, Cuiling Li, Xiuzhen Li, Li Liu
Publikováno v:
Diabetology & Metabolic Syndrome, Vol 14, Iss 1, Pp 1-8 (2022)
Abstract Background Glucose-6-phosphate dehydrogenase (G6PD) deficiency is one of the most common human genetic abnormalities, with a high prevalence in Guangdong, China. The purpose of this study was to explore the characteristics of newly diagnosed
Externí odkaz:
https://doaj.org/article/ceebfd3306d9408e8e19430bbe9a225d
Autor:
Yunting Lin, Zhihong Guan, Huifen Mei, Wen Zhang, Zhizi Zhou, Ling Su, Jing Cheng, Ruidan Zheng, Cuili Liang, Yanna Cai, Xi Yin, Dongyan Wu, Li Liu, Chunhua Zeng
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
PurposeVitamin D-dependent rickets type 1A (VDDR1A) is a rare autosomal recessive disorder caused by deficiency of the CYP27B1 gene. This study aims to investigate the phenotypic and genotypic features of VDDR1A children in southern China and evaluat
Externí odkaz:
https://doaj.org/article/7482446293424e279c3c186c2d7bd356
Publikováno v:
Frontiers in Plant Science; 2023, Vol. 14, p1-11, 11p
Autor:
Yitong Yan, Cuili Liang, Xing Liu, Yingchao Tan, Yilong Lu, Yuanyuan Zhang, Hongli Luo, Chaozu He, Jie Cao, Chaorong Tang, Kaiye Liu
Publikováno v:
Tropical Plants; 2023, Vol. 2 Issue 1, p1-9, 9p
Publikováno v:
European journal of ophthalmology.
Two siblings from a non-consanguineous Chinese family suffered from isolated congenital cataract. Whole exome sequencing was performed to identify disease-causing variants followed by a confirmatory Sanger sequencing.Whole exome sequencing revealed a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e5499f7cb0f7d8c0da8701b14c4a0c0a
https://pubmed.ncbi.nlm.nih.gov/36262071
https://pubmed.ncbi.nlm.nih.gov/36262071
Autor:
Aijing Xu, Minyan Jiang, Wen Zhang, Yunting Lin, Yongxian Shao, Huifen Mei, Jing Cheng, Cuili Liang, Cuiling Li, Xiuzhen Li, Li Liu
Publikováno v:
Diabetologymetabolic syndrome. 14(1)
Background Glucose-6-phosphate dehydrogenase (G6PD) deficiency is one of the most common human genetic abnormalities, with a high prevalence in Guangdong, China. The purpose of this study was to explore the characteristics of newly diagnosed type 1 d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1deb672abba53579875a977b7b9daaa5
https://pubmed.ncbi.nlm.nih.gov/35313968
https://pubmed.ncbi.nlm.nih.gov/35313968
Autor:
Li Liu, Yunting Lin, Min Rao, Xinjiang Huang, Ling Su, Cuili Liang, Yanna Cai, Wen Zhang, Chunhua Zeng
Publikováno v:
Calcified tissue international. 110(2)
X-linked hypophosphatemic rickets (XLH) is the most common form of hypophosphatemic rickets, which is caused by the deficiencies of PHEX gene with an X-linked dominant inheritance pattern. As at least several thousands of XLH patients have been diagn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::894c640d8db024762e89e68d63b8fe21
https://pubmed.ncbi.nlm.nih.gov/34487203
https://pubmed.ncbi.nlm.nih.gov/34487203
Autor:
Yunting Lin, Huiying Sheng, Xiuzhen Li, Huifen Mei, Li Liu, Chunhua Zeng, Cuiling Li, Cuili Liang, Jing Cheng, Aijing Xu, Tzer Hwu Ting, Wen Zhang
Publikováno v:
Pediatric diabetesREFERENCES. 21(3)
Objective The purpose of this study was to investigate the molecular basis of maturity-onset diabetes of the young (MODY) by whole-exome sequencing (WES) and estimate the frequency and describe the clinical characteristics of MODY in southern China.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ef0db5823d9f6f19105ae4d81850be3
https://pubmed.ncbi.nlm.nih.gov/31957151
https://pubmed.ncbi.nlm.nih.gov/31957151