Zobrazeno 1 - 10
of 156
pro vyhledávání: '"Yazhou Cui"'
Autor:
Fei Li, Yanling Zhu, Tianyu Wang, Jun Tang, Yuhua Huang, Jiaming Gu, Yuchan Mai, Mingquan Wang, Zhishuai Zhang, Jiaying Ning, Baoqiang Kang, Junwei Wang, Tiancheng Zhou, Yazhou Cui, Guangjin Pan
Publikováno v:
Cell Regeneration, Vol 13, Iss 1, Pp 1-18 (2024)
Abstract Human hematopoiesis starts at early yolk sac and undergoes site- and stage-specific changes over development. The intrinsic mechanism underlying property changes in hematopoiesis ontogeny remains poorly understood. Here, we analyzed single-c
Externí odkaz:
https://doaj.org/article/6fd29a7879b54401a05389d64d7d3a0f
Publikováno v:
Genes and Diseases, Vol 11, Iss 3, Pp 101002- (2024)
Externí odkaz:
https://doaj.org/article/48bfcdae1d3c4738a554d8bbcbfc6acb
Publikováno v:
Thoracic Cancer, Vol 14, Iss 16, Pp 1451-1466 (2023)
Abstract Objective Cuproptosis‐related genes are closely related to lung adenocarcinoma (LUAD), which can be analyzed via the analysis of long noncoding RNA (lncRNA). To date, the clinical significance and function of cuproptosis‐related lncRNAs
Externí odkaz:
https://doaj.org/article/3e3f37334496467e86354b60c7208bff
Autor:
Jiafang Fu, Jingli Shan, Yazhou Cui, Chuanzhu Yan, Qinzhou Wang, Jinxiang Han, Guangxiang Cao
Publikováno v:
Cell & Bioscience, Vol 13, Iss 1, Pp 1-14 (2023)
Abstract Objective Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is a rare acquired immune-mediated neuropathy. Although microbial infection is potentially a contributing factor, a causative link between CIDP and microbial infectio
Externí odkaz:
https://doaj.org/article/f5864f75f69544b28150c420b06f4874
Autor:
Qingzhi Hou, Hui Zou, Shuping Zhang, Jiujing Lin, Wenying Nie, Yazhou Cui, Sijin Liu, Jinxiang Han
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
AimsNeonatal metabolites are very important in neonatal disease screening, and maternal thyroid hormones play an important role in fetal and neonatal health. Our study aimed to explore the association of maternal thyroid hormones with neonatal metabo
Externí odkaz:
https://doaj.org/article/54e6b6888e6f4e25a918819df9c82bb9
Publikováno v:
Stem Cell Research, Vol 63, Iss , Pp 102852- (2022)
The human induced pluripotent stem cell (iPSC) line SMBCi017-A was derived from urine cells of a 20 year old male healthy control donor. The generated iPSCs had normal karyotype, expressed chromosomal stability pluripotency hallmarks and differentiat
Externí odkaz:
https://doaj.org/article/120ec18219784ee7aa453417a7b862f4
Publikováno v:
Stem Cell Research, Vol 62, Iss , Pp 102821- (2022)
Methylmalonic acidemia(MMA) is an autosomal recessive hereditary disease caused by methylmalonyl-CoA mutase defect or its coenzyme cobalamin metabolism defect. The mutation of the MMACHC gene leads to metabolic disorder of coenzyme cobalamin, resulti
Externí odkaz:
https://doaj.org/article/bf4efdc1a87f4653abd6cd798f10f77f
Publikováno v:
Stem Cell Research, Vol 62, Iss , Pp 102827- (2022)
Osteogenesis imperfecta (OI) is a group of genetic disorders characterized mainly by fractures and bone deformities. It has been established that gene mutations, particularly those in COL1A1 and COL1A2, account for most phenotypes. Here, we generated
Externí odkaz:
https://doaj.org/article/03b6f47ae24e4d8a8aa99b812fcf4736
Publikováno v:
Stem Cell Research, Vol 62, Iss , Pp 102814- (2022)
Congenital talipes equinovarus (CTEV) is a congenital malformation affecting approximately 1/700-1/1000 of live borns. To date extensive epidemiological and biological studies have been operated to solve this issue, the most meaningful findings in cl
Externí odkaz:
https://doaj.org/article/d71d9daabd874d498f40a30454f28c3a
Publikováno v:
Stem Cell Research, Vol 60, Iss , Pp 102695- (2022)
Prader–Willi syndrome (PWS) is a neurodevelopmental disorder caused by deficiency of paternal gene expression in the 15q11.2-q13 chromosome imprinted region. Hyperphagia and dysgnosia are typical clinical features in the early-childhood of patient.
Externí odkaz:
https://doaj.org/article/94e11b24523e4af98cf3f9165f1d35ef