Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Fengdie Ma"'
Decreased lipid levels in adult with congenital heart disease: a systematic review and Meta-analysis
Autor:
Fengdie Ma, Peiqiang Li, Shasha Zhang, Wenjing Shi, Jing Wang, Qinglong Ma, Meie Zhao, Ziyan Nie, Handan Xiao, Xinyi Chen, Xiaodong Xie
Publikováno v:
BMC Cardiovascular Disorders, Vol 23, Iss 1, Pp 1-15 (2023)
Abstract Background Metabolic disorders were a health problem for many adults with congenital heart disease, however, the differences in metabolic syndrome-related metabolite levels in adults with congenital heart disease compared to the healthy popu
Externí odkaz:
https://doaj.org/article/ba4cefeacc5745aa86ca336a25706555
Autor:
Jing Wang, Wei Su, Taotao Zhang, Shasha Zhang, Huiwen Lei, Fengdie Ma, Maoning Shi, Wenjing Shi, Xiaodong Xie, Cuixia Di
Publikováno v:
Cell Death and Disease, Vol 14, Iss 4, Pp 1-17 (2023)
Abstract Cyclin D1 (CCND1), a crucial mediator of cell cycle progression, possesses many mutation types with different mutation frequencies in human cancers. The G870A mutation is the most common mutation in CCND1, which produces two isoforms: full-l
Externí odkaz:
https://doaj.org/article/aa05822807a448ed9e34faae2a1cd45a
Autor:
Meie Zhao, Chunxia Wang, Peiqiang Li, Tao Sun, Jing Wang, Shasha Zhang, Qinglong Ma, Fengdie Ma, Wenjing Shi, Maoning Shi, Yapeng Ma, Yunyan Pan, Hui Zhang, Xiaodong Xie
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
The emergence of a vaccine against hepatitis B has proven to be an important milestone in the prevention of this disease; however, 5%–10% of vaccinated individuals do not generate an immune response to the vaccine, and its molecular mechanism has n
Externí odkaz:
https://doaj.org/article/8a0e03a834fa454f943ec179b208872a
Autor:
Shan Li, Juan Li, Wenjing Shi, Ziyan Nie, Shasha Zhang, Fengdie Ma, Jun Hu, Jianjun Chen, Peiqiang Li, Xiaodong Xie
Publikováno v:
Biomolecules, Vol 13, Iss 6, p 988 (2023)
Around 11% of all known gene lesions causing human genetic diseases are nonsense mutations that introduce a premature stop codon (PTC) into the protein-coding gene sequence. Drug-induced PTC readthrough is a promising therapeutic strategy for treatin
Externí odkaz:
https://doaj.org/article/c37fa5157cf349f998eafa5ec0bd0fe2
Autor:
Peiqiang Li, Xiande Huang, Senmao Chai, Dalin Zhu, Huirong Huang, Fengdie Ma, Shasha Zhang, Xiaodong Xie
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Hereditary Spastic Paraplegia (HSP) is considered to be one of the common neurodegenerative diseases with marked genetic heterogeneity. Recently, the mutations in ubiquitin-associated protein 1 (UBAP1) have been described in patients with HSP, known
Externí odkaz:
https://doaj.org/article/1f1bb90d0f7d4cbd978647e0e239dc6d
Autor:
Jing Wang, Jiaxin Zhang, Qinglong Ma, Shasha Zhang, Fengdie Ma, Wei Su, Taotao Zhang, Xiaodong Xie, Cuixia Di
Publikováno v:
Journal of Cellular and Molecular Medicine. 27:991-1005
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b80bbf19aade61f27638a95cb74b7da
https://doi.org/10.1111/jcmm.17716
https://doi.org/10.1111/jcmm.17716