Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Minyan Jiang"'
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:
Yongxian Shao, Taolin Li, Minyan Jiang, Jianan Xu, Yonglan Huang, Xiuzhen Li, Ruidan Zheng, Li Liu
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-6 (2022)
Abstract Background Pathogenic mutations in the PHKG2 are associated with a very rare disease—glycogen storage disease IXc (GSD-IXc)—and are characterized by severe liver disease. Case presentation Here, we report a patient with jaundice, hypogly
Externí odkaz:
https://doaj.org/article/856e48b9a0f8461dab557f2d6c098b30
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:
Xiuzhen Li, Tzer Hwu Ting, Huiying Sheng, Cui Li Liang, Yongxian Shao, Minyan Jiang, Aijing Xu, Yunting Lin, Li Liu
Publikováno v:
BMC Pediatrics, Vol 18, Iss 1, Pp 1-8 (2018)
Abstract Background There is scarcity of information on the clinical features and genetics of glucokinase-maturity-onset diabetes of the young (GCK-MODY) in China. The aim of the study was to investigate the clinical and molecular characteristics of
Externí odkaz:
https://doaj.org/article/f52edbb5a7854748a13fd0223b694158
Publikováno v:
Interactive Cardiovascular and Thoracic Surgery
A female patient with a right-sided encapsulated pleural effusion was misdiagnosed preoperatively as having an encapsulated empyema. However, a giant mass in the anterior mediastinum was found via thoracoscopy, and a mature teratoma was detected base
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2ac628ebabe02a567f83d1fd0767a63
http://europepmc.org/articles/PMC8782231
http://europepmc.org/articles/PMC8782231
Autor:
Minyan Jiang, Huiying Sheng, Xi Yin, Xiuzhen Li, Ling Su, Yunting Lin, Minzhi Peng, Huifen Mei, Li Liu, Yanna Cai, Yongxian Shao
Publikováno v:
Clinical Biochemistry. 84:63-72
Background Ornithine transcarbamylase deficiency (OTCD) is pleomorphic congenital hyperammonemia, in which the prognosis of the patient is determined both by genotype and environmental factors. This study investigated the clinical and biochemical cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b2056a62d5a326a17863d2395f59e84
https://doi.org/10.1016/j.clinbiochem.2020.06.011
https://doi.org/10.1016/j.clinbiochem.2020.06.011
Autor:
Ting Lyu, Hongyuan Zhou, Yihui Wang, Minyan Jiang, Qian Tao, Juanlin Chen, Yitong Guo, Qiuping Zhang, Xu Wang, Xihan Guo
Publikováno v:
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 165
Epidemiological studies have demonstrated that metformin (a cornerstone of diabetes treatment) has anticancer activity, but the underlying mechanism remains elusive. We aimed to investigate whether metformin elicits anticancer activity via increasing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::041b5c6b46a98d8d6aa3a31f49bec533
https://pubmed.ncbi.nlm.nih.gov/35568294
https://pubmed.ncbi.nlm.nih.gov/35568294
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:
Yongxian Shao, Taolin Li, Minyan Jiang, Jianan Xu, Yonglan Huang, Xiuzhen Li, Ruidan Zheng, Li Liu
Publikováno v:
BMC pediatrics. 22(1)
Background Pathogenic mutations in the PHKG2 are associated with a very rare disease—glycogen storage disease IXc (GSD-IXc)—and are characterized by severe liver disease. Case presentation Here, we report a patient with jaundice, hypoglycaemia, g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a8bbd4fb4aa9c2e6a8a0e2578b292fc
https://pubmed.ncbi.nlm.nih.gov/35549678
https://pubmed.ncbi.nlm.nih.gov/35549678
Autor:
Zongcai Liu, Yonglan Huang, Li Liu, Minyan Jiang, Yunting Lin, Aijing Xu, Ting Xie, Xueying Su, Xiaoyuan Zhao, Yongxian Shao, Huiying Sheng, Wen Zhang
Publikováno v:
Clinica Chimica Acta. 491:114-120
Mucopolysaccharidosis type II (MPS II) is an X-linked recessive lysosomal storage disorder resulting from the deficiency of the enzyme iduronate-2-sulfatase (IDS).This study described the molecular characteristics of 63 Chinese children with MPS II a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::619932b00c6cbe0fff8b13eb02368dd8
https://doi.org/10.1016/j.cca.2019.01.009
https://doi.org/10.1016/j.cca.2019.01.009