Zobrazeno 1 - 10
of 68
pro vyhledávání: '"Chaofeng Tu"'
Autor:
Han Gong, Peihe Zhang, Qiang Liu, Yuxuan Tian, Fuxin Chen, Siyi Qian, Chaofeng Tu, Yueqiu Tan, Xingming Hu, Bin Zhang
Publikováno v:
npj Precision Oncology, Vol 8, Iss 1, Pp 1-14 (2024)
Abstract Lung adenocarcinoma (LUAD) is a leading cause of cancer mortality, with many patients facing poor prognosis, particularly those with metastatic or drug-resistant tumors. Homologous recombination genes (HRGs) are crucial in tumor progression
Externí odkaz:
https://doaj.org/article/aab5b71e8c774ac4835276ea060d0099
Autor:
Peihe Zhang, Hui Li, Han Gong, Yuxuan Tian, Fuxin Chen, Xiang Li, Chunbo Xie, Chaofeng Tu, Siyi Qian, Yueqiu Tan, Qiang Liu, Bin Zhang
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 179, Iss , Pp 117315- (2024)
Lung cancer represents one of the most prevalent malignant neoplasms, commanding an alarming incidence and mortality rate globally. Non-small cell lung cancer (NSCLC), constituting approximately 80 %-90 % of all lung cancer cases, is the predominant
Externí odkaz:
https://doaj.org/article/c4090f2ebeba4e9188e777451a0a5650
Publikováno v:
Heliyon, Vol 10, Iss 15, Pp e34945- (2024)
Background: Preimplantation genetic testing (PGT) can reduce the risk of familial genetic diseases, chromosome abnormalities, and recurrent abortions. It is unclear whether genetic counselees with PGT indications understand and accept the implication
Externí odkaz:
https://doaj.org/article/9decc3a806474b909019edc3c220290f
Autor:
Chaofeng Tu, Junfei Wen, Weili Wang, Qifan Zhu, Ying Chen, Jianglu Cheng, Zeye Li, Lanlan Meng, Yong Li, Wenbin He, Chen Tan, Chunbo Xie, Shao-Mei Fu, Juan Du, Guangxiu Lu, Ge Lin, Lan-Tao Gou, Yue-Qiu Tan
Publikováno v:
Cell Discovery, Vol 9, Iss 1, Pp 1-4 (2023)
Externí odkaz:
https://doaj.org/article/92c27d42277248d084a41b9625dd8223
Autor:
Lanlan Meng, Qiang Liu, Chen Tan, Xilin Xu, Wenbin He, Tongyao Hu, Chaofeng Tu, Yong Li, Juan Du, Qianjun Zhang, Guangxiu Lu, Li-Qing Fan, Ge Lin, Hongchuan Nie, Huan Zhang, Yue-Qiu Tan
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 11 (2023)
Introduction: Tracing the genetic causes for male infertility due to asthenoteratozoospermia has revealed at least 40 causative genes, which provides valuable reference for the genetic testing of asthenoteratozoospermia in clinical practice. To ident
Externí odkaz:
https://doaj.org/article/c51f175f0fcd493dab1ac8eeaa88c2c0
Autor:
Haiyu Li, Juan Du, Wen Li, Dehua Cheng, Wenbin He, Duo Yi, Bo Xiong, Shimin Yuan, Chaofeng Tu, Lanlan Meng, Aixiang Luo, Ge Lin, Guangxiu Lu, Yue-Qiu Tan
Publikováno v:
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-8 (2018)
Abstract Background Small supernumerary marker chromosomes (sSMCs) are common structurally abnormal chromosomes that occur in 0.288% of cases of mental retardation. Isodicentric 15 (idic(15)) is common in sSMCs and usually leads to a rare chromosome
Externí odkaz:
https://doaj.org/article/d2def8e0d8bb425cbe52590e2dd2c7ce
Autor:
Caixia He, Shuang Jing, Congling Dai, Chaofeng Tu, Zhenhua Tan, Juan Du, Guang‐Xiu Lu, Ge Lin, Sicong Zeng
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 7, Pp n/a-n/a (2019)
Abstract Background Dyskeratosis congenita (DC) is a rare heritable bone marrow failure syndrome that is associated with telomere dysfunction, and has high genetic heterogeneity and varied features. Objective This study aimed to identify the underlyi
Externí odkaz:
https://doaj.org/article/2b7e65024c2743519d9f4de6d703f0be
Autor:
Jiaxin He, Lilan Su, Weili Wang, Yong Li, Lanlan Meng, Chen Tan, Ge Lin, Yue-Qiu Tan, Qianjun Zhang, Chaofeng Tu
Publikováno v:
Developmental Biology. 497:11-17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ad20696646c5db099aeb258a2b95a89
https://doi.org/10.1016/j.ydbio.2023.02.009
https://doi.org/10.1016/j.ydbio.2023.02.009
Autor:
Chunyu Liu, Wei Si, Chaofeng Tu, Shixiong Tian, Xiaojin He, Shengnan Wang, Xiaoyu Yang, Chencheng Yao, Cong Li, Zine-Eddine Kherraf, Maosen Ye, Zixue Zhou, Yuhua Ma, Yang Gao, Yu Li, Qiwei Liu, Shuyan Tang, Jiaxiong Wang, Hexige Saiyin, Liangyu Zhao, Liqun Yang, Lanlan Meng, Bingbing Chen, Dongdong Tang, Yiling Zhou, Huan Wu, Mingrong Lv, Chen Tan, Ge Lin, Qingpeng Kong, Hong Shi, Zhixi Su, Zheng Li, Yong-Gang Yao, Li Jin, Ping Zheng, Pierre F. Ray, Yue-Qiu Tan, Yunxia Cao, Feng Zhang
Publikováno v:
The American Journal of Human Genetics. 110:516-530
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c9c340fc1745ca73bda9c3881ab3ec8
https://doi.org/10.1016/j.ajhg.2023.01.016
https://doi.org/10.1016/j.ajhg.2023.01.016
Autor:
Yunhao Li, Yong Li, Ying Wang, Lanlan Meng, Chen Tan, Juan Du, Yue-Qiu Tan, Hongchuan Nie, Qianjun Zhang, Guangxiu Lu, Ge Lin, Huanzhu Li, Huan Zhang, Chaofeng Tu
Publikováno v:
Journal of Assisted Reproduction and Genetics. 40:41-51
The aim of this study is to identify the genetic cause of primary ciliary dyskinesia (PCD) and male infertility in two unrelated Han Chinese families.We performed whole-exome sequencing in two unrelated male Han Chinese patients suffering from infert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::952fd94638f1a40cec1bb1dafc11f35c
https://doi.org/10.1007/s10815-022-02681-z
https://doi.org/10.1007/s10815-022-02681-z