Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Xiongwei Cai"'
Autor:
Cong Xiang, Li Chen, Shilei Zhu, Yue Chen, Haodong Huang, Chunmao Yang, Yugang Chi, Yanzhou Wang, Yunlong Lei, Xiongwei Cai
Publikováno v:
Cell Death and Disease, Vol 15, Iss 9, Pp 1-16 (2024)
Abstract Ovarian cancer, the second most leading cause of gynecologic cancer mortality worldwide, is challenged by chemotherapy resistance, presenting a significant hurdle. Pyroptosis, an inflammation-linked programmed cell death mediated by gasdermi
Externí odkaz:
https://doaj.org/article/54fa896369d34128bbc99e9843c151b9
Autor:
Yi Jiang, Dongfang Xiang, Xianmei Wen, Mingmin He, Yan Qin, Xiaoxue Yao, Zexuan Yan, Xiuli Geng, Yong Ren, Xiongwei Cai, Youhong Cui, Yan Wang
Publikováno v:
Genes and Diseases, Vol 11, Iss 2, Pp 564-567 (2024)
Externí odkaz:
https://doaj.org/article/16163480c28f4c75afb3fc22ace885f2
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
BackgroundSepsis is a life-threatening condition that requires rapid assessment to reduce mortality. This study investigates the relationship between the Neutrophil-to-Monocyte/Lymphocyte Ratio (NMLR) upon ICU admission and 28-day mortality in sepsis
Externí odkaz:
https://doaj.org/article/46f0048bffc84f4dabf868c4a0734790
Autor:
Dimitrios Papaioannou, Andreas Petri, Oliver M. Dovey, Sara Terreri, Eric Wang, Frances A. Collins, Lauren A. Woodward, Allison E. Walker, Deedra Nicolet, Felice Pepe, Prasanthi Kumchala, Marius Bill, Christopher J. Walker, Malith Karunasiri, Krzysztof Mrózek, Miranda L. Gardner, Virginia Camilotto, Nina Zitzer, Jonathan L. Cooper, Xiongwei Cai, Xiaoqing Rong-Mullins, Jessica Kohlschmidt, Kellie J. Archer, Michael A. Freitas, Yi Zheng, Robert J. Lee, Iannis Aifantis, George Vassiliou, Guramrit Singh, Sakari Kauppinen, Clara D. Bloomfield, Adrienne M. Dorrance, Ramiro Garzon
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-15 (2019)
LncRNAs at the HOX gene locus are increased in expression in NPM1 mutant acute myeloid leukemia. In this study, the authors show that one such lncRNA, HOX3B-AS3, has a role in regulating gene transcription and protein synthesis in leukemia cells.
Externí odkaz:
https://doaj.org/article/4362506e0cc14ab88f90e66fd4195bb2
Autor:
Zhao Cai, Huang Chen, Jingqiao Bai, Yang Zheng, Jianhui Ma, Xiongwei Cai, Yu Liu, Kaitai Zhang, Jianzhong Shou, Yanning Gao
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
BackgroundFinding effective prognostic signatures is of great urgency due to the high risk of recurrence and progression of bladder cancer (BC). Although a lot of genetic alterations are involved in the carcinogenesis, none of them were referred in t
Externí odkaz:
https://doaj.org/article/c08bf59d655940f5b183bec85b018f82
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 8, Pp n/a-n/a (2020)
Abstract Background Autosomal recessive dystrophic epidermolysis bullosa (RDEB) is an incurable and severe inherited skin disorder characterized by recurrent blistering at the sublamina densa beneath the cutaneous basement membrane. It is caused by b
Externí odkaz:
https://doaj.org/article/6cf0e8ed3add4866b89a4bb44286dd0c
Autor:
Dimitrios Papaioannou, Andreas Petri, Oliver M. Dovey, Sara Terreri, Eric Wang, Frances A. Collins, Lauren A. Woodward, Allison E. Walker, Deedra Nicolet, Felice Pepe, Prasanthi Kumchala, Marius Bill, Christopher J. Walker, Malith Karunasiri, Krzysztof Mrózek, Miranda L. Gardner, Virginia Camilotto, Nina Zitzer, Jonathan L. Cooper, Xiongwei Cai, Xiaoqing Rong-Mullins, Jessica Kohlschmidt, Kellie J. Archer, Michael A. Freitas, Yi Zheng, Robert J. Lee, Iannis Aifantis, George Vassiliou, Guramrit Singh, Sakari Kauppinen, Clara D. Bloomfield, Adrienne M. Dorrance, Ramiro Garzon
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-1 (2020)
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Externí odkaz:
https://doaj.org/article/99c4ed0bb3fa44d68071a84f1b74e8bd
Autor:
Dimitrios Papaioannou, Andreas Petri, Oliver M. Dovey, Sara Terreri, Eric Wang, Frances A. Collins, Lauren A. Woodward, Allison E. Walker, Deedra Nicolet, Felice Pepe, Prasanthi Kumchala, Marius Bill, Christopher J. Walker, Malith Karunasiri, Krzysztof Mrózek, Miranda L. Gardner, Virginia Camilotto, Nina Zitzer, Jonathan L. Cooper, Xiongwei Cai, Xiaoqing Rong-Mullins, Jessica Kohlschmidt, Kellie J. Archer, Michael A. Freitas, Yi Zheng, Robert J. Lee, Iannis Aifantis, George Vassiliou, Guramrit Singh, Sakari Kauppinen, Clara D. Bloomfield, Adrienne M. Dorrance, Ramiro Garzon
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-1 (2020)
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Externí odkaz:
https://doaj.org/article/579218a2e8fe43ea90c3edcd2d6f65f6
Autor:
Xiongwei Cai, Justin J Gaudet, James K Mangan, Michael J Chen, Maria Elena De Obaldia, Zaw Oo, Patricia Ernst, Nancy A Speck
Publikováno v:
PLoS ONE, Vol 6, Iss 12, p e28430 (2011)
RUNX1 encodes a DNA binding subunit of the core-binding transcription factors and is frequently mutated in acute leukemia, therapy-related leukemia, myelodysplastic syndrome, and chronic myelomonocytic leukemia. Mutations in RUNX1 are thought to conf
Externí odkaz:
https://doaj.org/article/b0d378546823416cb18afa21c724ad0f
Publikováno v:
Frontiers in Medicine; 2024, p1-9, 9p