Zobrazeno 1 - 10
of 119
pro vyhledávání: '"Yuanlin Zhou"'
Autor:
Shuaishuai Chen, Weibo Zhao, Juping Du, Suyun Chen, Jun Li, Bo Shen, Yuanlin Zhou, Shiyong Chen
Publikováno v:
BMC Genomics, Vol 25, Iss 1, Pp 1-14 (2024)
Abstract Background Recombination signal-binding protein for immunoglobulin kappa J region (RBPJ) is a transcriptional regulator that plays an important role in maintaining immune homeostasis. This study aimed to estimate the expression of RBPJ in rh
Externí odkaz:
https://doaj.org/article/3e1f4e33163c4a238a01e79e0b0639f7
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Charcot-Marie-Tooth disease (CMT) is a hereditary peripheral neuropathy involving approximately 80 pathogenic genes. Whole-exome sequencing (WES) and confirmatory Sanger sequencing analysis was applied to identify the disease-causing mutations in a C
Externí odkaz:
https://doaj.org/article/3eb25a32bc5044cabf7ef773632ab412
Autor:
Anna Ying, Yuanlin Zhou, Chunyue Wang, Tao Wang, Xuan Zhang, Shanshan Wang, Shaofa Ke, Yuyan Bao, Yang Liu, Feng Wang
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
BackgroundCongenital dysfibrinogenemia (CD) is a rare hereditary coagulation disorder resulting from mutations in fibrinogen genes. CD primarily presents with bleeding symptoms, but it can also lead to thrombotic events, including ischemic stroke.Cas
Externí odkaz:
https://doaj.org/article/510b4b89268a4190bcf6dd1b691604d6
Autor:
Shuaishuai Chen, Juping Du, Huihua Jiang, Weibo Zhao, Na Wang, Anna Ying, Jun Li, Shiyong Chen, Bo Shen, Yuanlin Zhou
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 15 (2022)
ObjectivesAutosomal recessive inherited ataxia with oculomotor apraxia type 2 (AOA2), caused by SETX gene mutations, is characterized by early-onset, progressive cerebellar ataxia, peripheral neuropathy, oculomotor apraxia and elevated serum α-fetop
Externí odkaz:
https://doaj.org/article/abe5c1fe3b2e40e483c47f3347b39964
Publikováno v:
Genes and Diseases, Vol 6, Iss 1, Pp 35-42 (2019)
Cyanotic congenital heart disease (CCHD), a term describing the most severe congenital heart diseases are characterized by the anatomic malformation of a right to left shunt. Although the incidence of CCHD are far less than the that of congenital hea
Externí odkaz:
https://doaj.org/article/8677f0cb421f4a2892f116927d5784f5
Autor:
Ao-Shuang Yang, Rong Huang, Zhuoni Jiang, Yongsheng Li, Fangfang He, Quan-Ping Zhang, Yuanlin Zhou, Peng Wang, Guansong He, Wenbin Yang
Publikováno v:
ACS Applied Polymer Materials. 5:1499-1508
Flexible and Mechanically Enhanced Polyurethane Composite for γ-ray Shielding and Thermal Regulation
Autor:
Tianyu Cai, Fangfang He, Yongsheng Li, Yingjun Li, Zhuoni Jiang, Jiale Li, Yuanlin Zhou, Zhengguo Chen, Wenbin Yang
Publikováno v:
ACS Applied Materials & Interfaces. 15:4690-4702
Autor:
Tianyu Cai, Huan Wei, Bonan Ding, Chang Liu, Jiayi An, Yuanlin Zhou, Kai Zhang, Zhengguo Chen, Wenbin Yang
Publikováno v:
International Journal of Energy Research. 46:23273-23286
Publikováno v:
Fullerenes, Nanotubes and Carbon Nanostructures. 30:1109-1115
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
Background: The MTUS1 gene encodes a microtubule-associated protein involved in multiple processes including cell polarity and microtubule balance during myocardial development.Aims: To investigate the association between a de novo c. 2617A->C mutati
Externí odkaz:
https://doaj.org/article/9742823d54f94ade805f3306cf67a024