Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Liusong, Wu"'
Autor:
Xuan Shang, Zhiyu Peng, Yuhua Ye, Asan, Xinhua Zhang, Yan Chen, Baosheng Zhu, Wangwei Cai, Shaoke Chen, Ren Cai, Xiaoling Guo, Chonglin Zhang, Yuqiu Zhou, Shuodan Huang, Yanhui Liu, Biyan Chen, Shanhuo Yan, Yajun Chen, Hongmei Ding, Xiaolin Yin, Liusong Wu, Jing He, Dongai Huang, Sheng He, Tizhen Yan, Xin Fan, Yuehong Zhou, Xiaofeng Wei, Sumin Zhao, Decheng Cai, Fengyu Guo, Qianqian Zhang, Yun Li, Xuelian Zhang, Haorong Lu, Huajie Huang, Junfu Guo, Fei Zhu, Yuan Yuan, Li Zhang, Na Liu, Zhiming Li, Hui Jiang, Qiang Zhang, Yijia Zhang, Wan Khairunnisa Wan Juhari, Sarifah Hanafi, Wanjun Zhou, Fu Xiong, Huanming Yang, Jian Wang, Bin Alwi Zilfalil, Ming Qi, Yaping Yang, Ye Yin, Mao Mao, Xiangmin Xu
Publikováno v:
EBioMedicine, Vol 23, Iss C, Pp 150-159 (2017)
Hemoglobinopathies are among the most common autosomal-recessive disorders worldwide. A comprehensive next-generation sequencing (NGS) test would greatly facilitate screening and diagnosis of these disorders. An NGS panel targeting the coding regions
Externí odkaz:
https://doaj.org/article/ddb85bcb4ac24f0987fd7226623d7a62
Publikováno v:
PLoS ONE, Vol 11, Iss 4, p e0154183 (2016)
LNK is an adapter protein negatively regulating the JAK/STAT cell signaling pathway. In this study, we observed the correlation between variation in LNK gene and the clinical type of myeloproliferative neoplasms (MPN).A total of 285 MPN cases were re
Externí odkaz:
https://doaj.org/article/d298ad7aff9e4b349b2cb7e2f515c9eb
Autor:
null Mei Tan, null Yue Bai, null Xiangmei Zhang, null Jian Sun, null Chengshuang Huang, null Runmei Tian, null Yuhang Yang, null Xi Luo, null Qiong Su, null Liusong Wu, null Libo Zheng, null Jing Xia, null Hongmei Murong, null Ping Zhu, null Fan Yang, null Xiaosong Zhong, null Jindong Chen, null Yan Chen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76f73be19714a378a1d9f631c8bd89a5
https://doi.org/10.1111/cge.13923/v3/response1
https://doi.org/10.1111/cge.13923/v3/response1
Autor:
Yonghuai, Feng, Liusong, Wu
The study aimed to investigate the effect of eukaryotic translation initiation factor 3 subunit B (EIF3B) on cell proliferation, migration, and apoptosis as well as the underlying mechanism in acute myeloid leukemia (AML). EIF3B expression was detect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::861f6ad981d19536b529f5ddf9f1e1df
https://europepmc.org/articles/PMC7013369/
https://europepmc.org/articles/PMC7013369/
Autor:
LIUSONG WU1, SEN LU1, MEI TAN1, YING RONG1, RUNMEI TIAN1, YUHANG YANG1, YAN CHEN1, ZHIYU PENG2, JINDONG CHEN3,4
Publikováno v:
Molecular Medicine Reports. Nov2017, Vol. 16 Issue 5, p6552-6557. 6p. 1 Color Photograph, 4 Charts, 1 Graph.
Autor:
Liusong Wu, Yonghuai Feng
Publikováno v:
Biochemical and Biophysical Research Communications. 483:897-903
Although mTOR (mammalian target of rapamycin) activation is frequently observed in acute myeloid leukemia (AML) patients, the precise function and the downstream targets of mTOR are poorly understood. Here we revealed that PFKFB3, but not PFKFB1, PFK
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9df0ddc5ecfe7f1c2caaa2ae19125f31
https://doi.org/10.1016/j.bbrc.2017.01.031
https://doi.org/10.1016/j.bbrc.2017.01.031
Autor:
Qiong, Su, Shiping, Chen, Liusong, Wu, Runmei, Tian, Xiaoqin, Yang, Xiaoyan, Huang, Yan, Chen, Zhiyu, Peng, Jindong, Chen
Publikováno v:
Hemoglobin. 43(1)
Hemoglobinopathies are caused by genetic defects on the globin genes. To date, more than 900 β-globin variants have been recorded worldwide. These gene alterations often cause either a decrease in β-globin synthesis or completely block synthesis, l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f96bde72df922805bd0e8608e30edd28
https://pubmed.ncbi.nlm.nih.gov/31084366
https://pubmed.ncbi.nlm.nih.gov/31084366
Autor:
Zhiming Li, Bin Alwi Zilfalil, Huanming Yang, Fu Xiong, Qiang Zhang, Li Zhang, Jian Wang, Wanjun Zhou, Hongmei Ding, Asan, Yun Li, Dongai Huang, Fengyu Guo, Shaoke Chen, Yaping Yang, Wangwei Cai, Xiaolin Yin, Fei Zhu, Xuelian Zhang, Shuodan Huang, Sarifah Hanafi, Sumin Zhao, Liusong Wu, Na Liu, Xin Fan, Tizhen Yan, Jing He, Xiaoling Guo, Yuhua Ye, Ming Qi, Decheng Cai, Yuehong Zhou, Ye Yin, Xiaofeng Wei, Zhiyu Peng, Ren Cai, Yajun Chen, Xuan Shang, Xinhua Zhang, Yanhui Liu, Hui Jiang, Junfu Guo, Yan Chen, Baosheng Zhu, Mao Mao, Yuqiu Zhou, Biyan Chen, Huajie Huang, Yijia Zhang, Haorong Lu, Qianqian Zhang, Shanhuo Yan, Xiangmin Xu, Sheng He, Wan Khairunnisa Wan Juhari, Chonglin Zhang, Yuan Yuan
Publikováno v:
EBioMedicine
EBioMedicine, Vol 23, Iss C, Pp 150-159 (2017)
EBioMedicine, Vol 23, Iss C, Pp 150-159 (2017)
Hemoglobinopathies are among the most common autosomal-recessive disorders worldwide. A comprehensive next-generation sequencing (NGS) test would greatly facilitate screening and diagnosis of these disorders. An NGS panel targeting the coding regions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::454124f146e23056a4f198aca4452107
https://pubmed.ncbi.nlm.nih.gov/28865746
https://pubmed.ncbi.nlm.nih.gov/28865746