Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Ruixia Tian"'
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundThe p120-ctn protein, encoded by CTNND1, is involved in intercellular connections and regulates epithelial–mesenchymal transformation. CTNND1 mutations can lead to blepharocheilodontic syndrome (BCDS). Increasing evidence shows that altho
Externí odkaz:
https://doaj.org/article/06e7796804d946e5b4d5a7ffb8ccd89b
Publikováno v:
BMC Pregnancy and Childbirth, Vol 22, Iss 1, Pp 1-6 (2022)
Abstract Background Ectodermal Dysplasia is a diverse group of inherited disorders characterized by a congenital defect in two or more ectodermal structures. Due to a fairly low incidence, to the best of our knowledge there are few clues that can ass
Externí odkaz:
https://doaj.org/article/ac236243e16348f68185106a3bd24b70
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Barth syndrome (BTHS) is a rare X-linked recessive genetic disease, which appears in infancy with myocardial and skeletal muscle diseases, neutropenia, growth retardation, and other clinical features. TAFAZZIN is the pathogenic gene of BTHS, which en
Externí odkaz:
https://doaj.org/article/b98f5183ebdc4aa29da8d16d59314acd
Autor:
Zhuzi Zhao, Qiyuan Wang, Li Li, Yongming Han, Zhaolian Ye, Siwatt Pongpiachan, Yong Zhang, Suixin Liu, Ruixia Tian, Junji Cao
Publikováno v:
Atmosphere, Vol 10, Iss 11, p 645 (2019)
The Tibetan Plateau (TP) is one of the world’s most sensitive areas for climate change. Previous studies have revealed that air pollutants emitted from South and Southeast Asia can be transported to and have a negative impact on the TP. However, th
Externí odkaz:
https://doaj.org/article/beb67f6c1ff14c0f9cf0a850d11464b4
Autor:
Tian Wang, Zhixue Li, Kewei Gu, Hongming Xie, Tong Liu, Ruixia Tian, Xuejing Hu, Yuan Wei, Fafu Ni, Xiaoxuan Qiu, Yanyu Wang, Junxia Wu
Publikováno v:
IEEE Transactions on Nuclear Science. 70:235-244
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a284c2ed5117bb2768d9a061628a66a7
https://doi.org/10.1109/tns.2023.3243398
https://doi.org/10.1109/tns.2023.3243398
Autor:
Tian Wang, Zhixue Li, Hongming Xie, Junxia Wu, Kewei Gu, Yuan Wei, Jianjun Su, Ruixia Tian, Yanyu Wang, Jin Pan
Publikováno v:
IEEE Transactions on Nuclear Science. 69:1913-1922
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de4dd829372965536a5a2d427f3d68c1
https://doi.org/10.1109/tns.2022.3189683
https://doi.org/10.1109/tns.2022.3189683
Publikováno v:
Molecular Syndromology. 13:511-516
Introduction: Autosomal recessive dystrophic epidermolysis bullosa (RDEB) is a rare disease with an early onset and severe phenotype. The pathogenic mechanism associated with mutations in the gene COL7A1 has been widely studied and many related cases
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1342c8709af7aa9a1022dc315373b800
https://doi.org/10.1159/000525047
https://doi.org/10.1159/000525047
Publikováno v:
Radiation Detection Technology and Methods. 5:440-450
The beam intensity of the High Intensity Heavy-ion Accelerator Facility (HIAF) is converted into current signals by beam intensity detectors and then processed by front-end electronics. The performance of the front-end electronics affects the measure
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0aff98a29335c1b71ac721ac829396c9
https://doi.org/10.1007/s41605-021-00269-2
https://doi.org/10.1007/s41605-021-00269-2
Autor:
Fafu Ni, Zhixue Li, Junxia Wu, Yuan Wei, Xuejing Hu, KeWei Gu, Ruixia Tian, Yong Zhang, Guangyu Zhu, Jianjun Su, Yanyu Wang
Publikováno v:
The Review of scientific instruments. 93(6)
A new digital beam position and phase measurement (BPM) system was designed for the ion-Linac accelerator at the high intensity heavy ion accelerator facility. The fundamental and second harmonic signals are retrieved from the BPM electrodes to simul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e6cd87cc489c2f9f559c00f46b52e15
https://pubmed.ncbi.nlm.nih.gov/35778055
https://pubmed.ncbi.nlm.nih.gov/35778055
Publikováno v:
Cellular and Molecular Life Sciences. 78:129-141
AlkB homologs (ALKBH) are a family of specific demethylases that depend on Fe2+ and α-ketoglutarate to catalyze demethylation on different substrates, including ssDNA, dsDNA, mRNA, tRNA, and proteins. Previous studies have made great progress in det
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70a31c404e912d6541d0c97664133185
https://doi.org/10.1007/s00018-020-03594-9
https://doi.org/10.1007/s00018-020-03594-9