Zobrazeno 1 - 10
of 99
pro vyhledávání: '"Dingyuan Ma"'
Autor:
Yan Wang, Yan Sun, Lulu Meng, Quanze He, Jingyu Zhao, Ran Zhou, Zhonghua Wang, Jianxin Tan, Dingyuan Ma, Linlin Fan, Yunmei Chen, Yuguo Wang, Zhu Jiang, Zhihong Qiao, Xiaojuan Wu, Binbin Shao, Ying Xue, Lijie Song, Ting Wang, Ping Hu, Zhengfeng Xu
Publikováno v:
Clinical and Translational Medicine, Vol 14, Iss 5, Pp n/a-n/a (2024)
Externí odkaz:
https://doaj.org/article/c0d58dc45fb3435b837fd954873b87b7
Autor:
Yang Liu, Xiaowei Zhang, Ping Zhang, Tingting He, Weitao Zhang, Dingyuan Ma, Ping Li, Jun Chen
Publikováno v:
Acta Pharmaceutica Sinica B, Vol 13, Iss 10, Pp 4253-4272 (2023)
It is discovered that activated caspase-3 tends to induce apoptosis in gasdermin E (GSDME)-deficient cells, but pyroptosis in GSDME-sufficient cells. The high GSDME expression and apoptosis resistance of pancreatic ductal adenocarcinoma (PDAC) cells
Externí odkaz:
https://doaj.org/article/577d5a181eba45ffa92a5add7df625b0
Autor:
Xin Wang, Yanyun Wang, Dingyuan Ma, Zhilei Zhang, Yahong Li, Peiying Yang, Yun Sun, Tao Jiang
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-10 (2021)
Abstract Background Hyperphenylalaninemia (HPA) is the most common amino acid metabolic disease involving phenylalanine hydroxylase (PAH, OMIM*612,349) deficiency or coenzyme tetrahydrobiopterin (BH4) deficiency. Patients with severe HPA often have a
Externí odkaz:
https://doaj.org/article/987d7fbf49c347fabb187b5e6e98a4ba
Autor:
Xiaowei Zhang, Ping Zhang, Lin An, Ningyuan Sun, Liying Peng, Weiwei Tang, Dingyuan Ma, Jun Chen
Publikováno v:
Acta Pharmaceutica Sinica B, Vol 10, Iss 8, Pp 1397-1413 (2020)
Pyroptosis is a form of programmed cell death, and recently described as a new molecular mechanism of chemotherapy drugs in the treatment of tumors. Miltirone, a derivative of phenanthrene-quinone isolated from the root of Salvia miltiorrhiza Bunge,
Externí odkaz:
https://doaj.org/article/3574efee0012453da895d0bf2b828330
Autor:
Jingjing Zhang, Dingyuan Ma, Gang Liu, Yuguo Wang, An Liu, Li Li, Chunyu Luo, Ping Hu, Zhengfeng Xu
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-9 (2019)
Abstract Background Duchenne muscular dystrophy (DMD) is a severe X-linked recessive neuromuscular disorder. Patients with DMD usually have severe and fatal symptoms, including progressive irreversible muscle weakness and atrophy complicated with gas
Externí odkaz:
https://doaj.org/article/5603f10269084f1fa9cc3f07f8f6069d
Autor:
Xin Wang, Yanyun Wang, Dingyuan Ma, Zhilei Zhang, Yahong Li, Peiying Yang, Yun Sun, Tao Jiang
Publikováno v:
Frontiers in Genetics, Vol 11 (2021)
Background: Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders encompassing enzyme deficiencies in the adrenal steroidogenesis pathway that leads to impaired cortisol biosynthesis. 21-hydroxylase deficiency (21-OHD) is t
Externí odkaz:
https://doaj.org/article/43d2e1bef8ce4fa59762af238102fccf
Publikováno v:
Journal of Civil Engineering and Management, Vol 26, Iss 8 (2020)
The application capability of international construction standards (ICS) has become a necessary element for the success of contractors in the international market. However, there is a lack of quantitative analysis of the impact of ICS application cap
Externí odkaz:
https://doaj.org/article/db2670a3b8c14c3c8645d3e9f175d33d
Autor:
Dingyuan Ma, Jianxin Tan, Jing Zhou, Jingjing Zhang, Jian Cheng, Chunyu Luo, Gang Liu, Yuguo Wang, Zhengfeng Xu
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 11, Pp n/a-n/a (2019)
Abstract Background X‐linked intellectual disability type Nascimento (XIDTN), caused by mutations in ubiquitin‐conjugating enzyme E2A (UBE2A) gene, is characterized by moderate to severe intellectual disability, impaired speech, urogenital anomal
Externí odkaz:
https://doaj.org/article/755f2005bfce4428896b8a3687f08308
Autor:
Gang Liu, Dingyuan Ma, Jian Cheng, Jingjing Zhang, Chunyu Luo, Yun Sun, Ping Hu, Yuguo Wang, Tao Jiang, Zhengfeng Xu
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-7 (2018)
Abstract Background Wilson’s disease (WD) is an autosomal recessive disorder characterized by copper accumulation. ATP7B gene mutations lead to ATP7B protein dysfunction, which in turn causes Wilson’s disease. Case presentation We describe a male
Externí odkaz:
https://doaj.org/article/66df384b33814b738893348e9434c30f
Autor:
Ping Hu, Fengchang Qiao, Yuan Yuan, Ruihong Sun, Yan Wang, Lulu Meng, Ying Lin, Hang Li, Yaoshen Wang, Rui Han, Dong Liang, Dingyuan Ma, Tao Jiang, Hui Jiang, Zhengfeng Xu
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 56, Iss 5, Pp 686-690 (2017)
Objective: To apply a Hidden Markov Model to test Hemophilia B in a fetus by maternal plasma sequencing only employing proband and maternal haplotypes. Case Report: A family at risk for Hemophilia B was recruited in this study. We performed genetic d
Externí odkaz:
https://doaj.org/article/a2bfa7b4d7c442d9ba7372918ed46d24