Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Yanqin Ying"'
Autor:
Huanyu Wang, Shimin Wu, Ying Weng, Xi Yang, Ling Hou, Yan Liang, Wei Wu, Yanqin Ying, Feng Ye, Xiaoping Luo
Publikováno v:
Italian Journal of Pediatrics, Vol 50, Iss 1, Pp 1-9 (2024)
Abstract Background Carboxylesterase 1(CES1) is expressed mainly in the liver and adipose tissue and is highly hypothesized to play an essential role in metabolism. Our study aimed to investigate the association between CES1 and metabolic syndrome (M
Externí odkaz:
https://doaj.org/article/f202d68f5475448f9ffbb669467341ad
Autor:
Shimin Wu, Yuan Gao, Shusen Guo, Lina Fu, Yanqin Ying, Wei Wu, Ling Hou, Yan Liang, Xiaoping Luo
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-9 (2024)
Abstract Objective This study investigated the characteristics of newly diagnosed type 1 diabetes mellitus (T1DM) related to autoimmunity and the frequency of diabetic ketoacidosis (DKA) in children and adolescents from 2017–2022 in China. Research
Externí odkaz:
https://doaj.org/article/b3a027b836c747fda2f247b1d00ff938
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
PurposeTo investigate the effectiveness and safety of gonadotropin-releasing hormone analogue (GnRHa) in combination with recombinant human growth hormone (rhGH) in girls with central precocious puberty (CPP).MethodsClinical data of 80 girls diagnose
Externí odkaz:
https://doaj.org/article/e1f1e105103e488b84b3042966a0ef15
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-6 (2021)
Abstract Background A case of isolated growth hormone deficiency type IA (IGHD IA) caused by novel compound heterozygous mutation in the GH1 gene was reported in this study, which aimed to provide insights that will benefit future diagnosis and treat
Externí odkaz:
https://doaj.org/article/c2c6fd3b5d80427885c044313f381387
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Pearson’s syndrome (PS) is a rare multi-system disorder caused by mitochondrial DNA deletion. Most PS cases in the literature are individual reports, and there is a lack of systematic analysis of clinical features and gene mutations in
Externí odkaz:
https://doaj.org/article/d33a3012f35745079613927b1394feb5
Autor:
Fan Chen, Shan Guo, Xuesong Li, Shengxuan Liu, Li Wang, Victor Wei Zhang, Hui Xu, Zhihua Huang, Yanqin Ying, Sainan Shu
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Niemann–Pick disease is a relatively common lysosomal storage disease. Cholestatic liver disease is a typical clinical phenotype of Niemann–Pick disease in infancy. The diagnosis is traditionally based on Niemann–Pick cells in bone marrow smear
Externí odkaz:
https://doaj.org/article/58785460301943e3966fb0c424d9b24f
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 11, Pp n/a-n/a (2021)
Abstract Background ACAN (OMIM 155760) is located on chromosome 15q26 and encodes the production of aggrecan. Aggrecan is a large chondroitin sulfate proteoglycan with a molecular weight of 254 kDa and contains 2530 amino acids. It is a critical stru
Externí odkaz:
https://doaj.org/article/c83e253187934bb6bac6f6dd419ebd92
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 3, Pp n/a-n/a (2020)
Abstract Background Jansen‐de Vries syndrome is a rare autosomal dominant neurodevelopmental disorder caused by pathogenic variants in the last and penultimate exons of the PPM1D gene. It is characterized by delayed psychomotor development, intelle
Externí odkaz:
https://doaj.org/article/f7f58fb854ee41e8a4fae9cded589c4f
Publikováno v:
Translational Neuroscience, Vol 8, Iss 1, Pp 102-110 (2017)
The present study evaluates the effect of grifolin (GFL) in oxygen/glucose deprivation (OGD) induced white matter lesion. Injury induced with OGD was found to be significant at the 9th h of OGD induction and the effect of GFL on the proliferation of
Externí odkaz:
https://doaj.org/article/23190e07767e4d14af45eca23958a265
Publikováno v:
Translational Neuroscience, Vol 8, Iss 1, Pp 111-116 (2017)
This report evaluates the protective effect of caffeoylquinic acid (CA) injury to oligodendrocyte precursor cells (OPCs) by promoting the formation of oligodendrocytes. Neonatal rat brain was used to isolate primary OPCs and non-lethal CoCl2 was used
Externí odkaz:
https://doaj.org/article/6178bda6b1264b90a37dfda952ec9ed6