Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Binlu Zhu"'
Autor:
Kang An, Ruohan Zhang, Binlu Zhu, Liyun Liu, Jiayu Tang, Yiru Ma, Zengxiang Wu, Lin Zhang, Yi She, Dan Luo, Caizheng Li, Heting Li, Yuehua Ma, Weichang Shi, Qiaoli Su, Shuangqing Li
Publikováno v:
BMC Medical Education, Vol 23, Iss 1, Pp 1-8 (2023)
Abstract Background The insufficient number of general practitioners (GPs) is a major challenge facing China’s healthcare system. The purpose of the GP transfer training programme was to provide training for experienced doctors to transition to gen
Externí odkaz:
https://doaj.org/article/cd242ce989f642fe9fea988eaa13e6b1
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2024)
ObjectivesOsteoporosis, a prevalent skeletal disorder characterized by reduced bone strength, is closely linked to the IGF system, crucial for skeletal metabolism. However, the precise nature of this relationship remains elusive. In this study, we em
Externí odkaz:
https://doaj.org/article/481c82987f3c495bbff0004d061fae6e
Publikováno v:
Biomedicines, Vol 12, Iss 2, p 447 (2024)
Background: Blood lactate is a potentially useful biomarker to predict the mortality and severity of sepsis. The purpose of this study is to systematically review the ability of lactate to predict hierarchical sepsis clinical outcomes and distinguish
Externí odkaz:
https://doaj.org/article/259a7774407847c8a4a1407e0e00157a
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Methylmalonic acidemia (MMA) can display many clinical manifestations, among which acute lymphoblastic leukemia (ALL) has not been reported, and congenital heart disease (CHD) is also rare.Case presentation: We report an MMA case with ALL
Externí odkaz:
https://doaj.org/article/8f6f7a3209ff4045a1f16b91b9a9ec95
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-6 (2019)
Abstract Background Bartter syndrome (BS) is a rare autosomal recessive disorder of salt reabsorption at the thick ascending limb of the Henle loop, characterized by hypokalemia, salt loss, metabolic alkalosis, hyperreninemic hyperaldosteronism with
Externí odkaz:
https://doaj.org/article/c58d10e8f748417bb1c1aba2a0d3045a
Publikováno v:
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-5 (2017)
Abstract Background The pathogenesis of hereditary hyperekplexia is thought to involve abnormalities in the glycinergic neurotransmission system, the most of mutations reported in GLRA1. This gene encodes the glycine receptor α1 subunit, which has a
Externí odkaz:
https://doaj.org/article/b21e0c342b2c485eacf13fbf273b4104
Autor:
Li Zhong, Huiqin Yang, Binlu Zhu, Xueqi Zhao, Meijun Xie, Meiling Cao, Chang Liu, Danyang Zhao, Yuan Lyu, Weiguang Shang, Bo Wang, Ying Wu, Xiuju Sun, Guangrong Qiu, Weineng Fu, Hongkun Jiang
Publikováno v:
Oxidative Medicine and Cellular Longevity, Vol 2022 (2022)
Congenital heart disease (CHD) is the most common noninfectious cause of death during the neonatal stage. T-box transcription factor 1 (TBX1) is the main genetic determinant of 22q11.2 deletion syndrome (22q11.2DS), which is a common cause of CHD. Mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31a0ba1e2e76314497930355a1ce63a6
https://doaj.org/article/77f877e034f1449399f8ccd966741103
https://doaj.org/article/77f877e034f1449399f8ccd966741103
Autor:
Li, Zhong, Huiqin, Yang, Binlu, Zhu, Xueqi, Zhao, Meijun, Xie, Meiling, Cao, Chang, Liu, Danyang, Zhao, Yuan, Lyu, Weiguang, Shang, Bo, Wang, Ying, Wu, Xiuju, Sun, Guangrong, Qiu, Weineng, Fu, Hongkun, Jiang
Publikováno v:
Oxidative Medicine and Cellular Longevity
Congenital heart disease (CHD) is the most common noninfectious cause of death during the neonatal stage. T-box transcription factor 1 (TBX1) is the main genetic determinant of 22q11.2 deletion syndrome (22q11.2DS), which is a common cause of CHD. Mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a653cea3efe56846dc561c5647ee64dd
https://pubmed.ncbi.nlm.nih.gov/35035663
https://pubmed.ncbi.nlm.nih.gov/35035663
Publikováno v:
Cytogenetic and Genome Research. 159:190-200
It is currently believed that the TBX1 gene is one of the core genes of congenital heart disease (CHD). However, there are few studies on the abnormal regulation of TBX1 gene expression. The purpose of this work was to investigate the role of miR-144
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5e6c5bfac9d5edbd43d9d4410c3450b
https://doi.org/10.1159/000505143
https://doi.org/10.1159/000505143
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-6 (2019)
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-6 (2019)
Background Bartter syndrome (BS) is a rare autosomal recessive disorder of salt reabsorption at the thick ascending limb of the Henle loop, characterized by hypokalemia, salt loss, metabolic alkalosis, hyperreninemic hyperaldosteronism with normal bl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6cea2c96e6863bf44cc5ba73f4c9ebf0
http://europepmc.org/articles/PMC6693093
http://europepmc.org/articles/PMC6693093