Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Yuejia Tang"'
Autor:
Yang Li, Ting Li, Yuejia Tang, Zhiyan Zhan, Lixia Ding, Lili Song, Tingting Yu, Yi Yang, Jing Ma, Yingwen Zhang, Ying Zhou, Song Gu, Min Xu, Yijin Gao, Yanxin Li
Publikováno v:
PLoS ONE, Vol 15, Iss 6, p e0234262 (2020)
p53 is one of the most extensively studied proteins in cancer research. Mutations in p53 generally abolish normal p53 function, and some mutants can gain new oncogenic functions. However, the mechanisms underlying p53 mutation-driven cancer remains t
Externí odkaz:
https://doaj.org/article/79d6e69f485441d298956d2af327a7cf
Autor:
Hui Xiao, Siqi Wang, Yuejia Tang, Shanshan Li, Yufeng Jiang, Yi Yang, Yinwen Zhang, Yali Han, Xiaoyu Wu, Liang Zheng, Yanxin Li, Yijin Gao
Publikováno v:
International Journal of Cancer. 152:2383-2395
Autor:
Yali Han, Yingwen Zhang, Yanxin Li, Lili Song, Yang Li, Zhou Xv, Shanshan Li, Yi Yang, Liang Zheng, Ting Li, Zhiyan Zhan, Yuejia Tang, Yijin Gao, Siqi wang
Publikováno v:
Journal of Cellular and Molecular Medicine
Patients with relapsed/refractory Burkitt's lymphoma (BL) have a dismal prognosis. Current research efforts aim to increase cure rates by identifying high‐risk patients in need of more intensive or novel therapy. The 8q24 chromosomal translocation
Autor:
Ting Li, Ying Zhou, Min Xu, Yingwen Zhang, Yuejia Tang, Yijin Gao, Lixia Ding, Song Gu, Zhiyan Zhan, Yanxin Li, Jing Ma, Lili Song, Yi Yang, Yang Li, Tingting Yu
Publikováno v:
PLoS ONE, Vol 15, Iss 6, p e0234262 (2020)
PLoS ONE
PLoS ONE
p53 is one of the most extensively studied proteins in cancer research. Mutations in p53 generally abolish normal p53 function, and some mutants can gain new oncogenic functions. However, the mechanisms underlying p53 mutation-driven cancer remains t
Publikováno v:
Journal of pediatric hematology/oncology. 41(5)
Li-Fraumeni syndrome is a kind of hereditary cancer predisposition syndromes, and is caused by TP53 gene mutation. Adrenocortical carcinoma (ACC) is commonly described as the most closely related tumor with this disease. Here, we present a case of a