Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Zhi-wen Pan"'
Autor:
Wen-Ming Cao, Ya-Bing Zheng, Yun Gao, Xiao-Wen Ding, Yan Sun, Yuan Huang, Cai-Jin Lou, Zhi-Wen Pan, Guang Peng, Xiao-Jia Wang
Publikováno v:
BMC Cancer, Vol 19, Iss 1, Pp 1-8 (2019)
Abstract Background Mutated BRCA1/2 genes are associated with hereditary breast and ovarian cancer (HBOC). So far most of the identified BRCA1/2 pathogenic variants are single nucleotide variants (SNVs) or insertions/deletions (Indels). However, larg
Externí odkaz:
https://doaj.org/article/b47b7843ef124fb8ae4d0b9fb9c9cc32
Autor:
Zhi-Wen Pan, Xiao-Jia Wang, Tianhui Chen, Xiao-Wen Ding, Xiyi Jiang, Yun Gao, Wen-Ju Mo, Yuan Huang, Cai-Jin Lou, Wen-Ming Cao
Publikováno v:
Frontiers in Oncology, Vol 9 (2019)
Introduction:FANCC is reported as a novel susceptibility gene for breast cancer, however, its mutation remains unclear in Chinese population. We aimed to identify the germline mutations of FANCC in high-risk breast cancer patients in China.Methods: 2
Externí odkaz:
https://doaj.org/article/dbf7992881b44d80bd3c1f5b9223e936
Autor:
Huai Huang, Wen-Jing Yi, Ji-Cheng Li, Jing Chen, Zhi-Bin Li, Li-Liang Wei, Hui-Hui Tu, Li-Ying Shi, Zhi-Wen Pan, Yu-Ting Hu, Yu-Shuai Han, Ting-Ting Jiang
Publikováno v:
Clinica Chimica Acta. 498:135-142
Background The lack of rapid and efficient diagnostic methods has been one of the most frustrating challenges in controlling the pulmonary tuberculosis (TB) epidemic. This study was aimed to identify novel non-invasive biomarkers for pulmonary TB. Me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::644b09582ab942b53bac698f6f8fe69c
https://doi.org/10.1016/j.cca.2019.08.017
https://doi.org/10.1016/j.cca.2019.08.017
Autor:
Song-xiao Xu, Xiang-dong Cheng, Zhi-wen Pan, Qian Song, Yi-hong Wang, Juan Xiong, Yong-yi Chen, Fan Fan, Jing Zhu, Wan-ying Wu, Xue-ying Deng, Yan-pin Yu, Xiao-hong Xu, Wen-hu Chen, Tao Zhu, Yang Yu, Kai-zhong Liu, Guo-liang Shao, Ming Chen, En-yan Yu
Background: Due to the increased risk of viral infection and the severe shortage of medical resources during the pandemic of COVID-19, most hospitals in the epidemic areas significantly reduced non-emergency admissions and services, if not closed. As
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c571d82ede1bc4205b78f049c589ed30
https://doi.org/10.21203/rs.3.rs-30259/v4
https://doi.org/10.21203/rs.3.rs-30259/v4
Autor:
Yuan Huang, Cai-Jin Lou, Wen-Ju Mo, Xiao-Wen Ding, Tianhui Chen, Xiyi Jiang, Wen-Ming Cao, Xiaojia Wang, Zhi-Wen Pan, Yun Gao
Publikováno v:
Frontiers in Oncology
Frontiers in Oncology, Vol 9 (2019)
Frontiers in Oncology, Vol 9 (2019)
Introduction:FANCC is reported as a novel susceptibility gene for breast cancer, however, its mutation remains unclear in Chinese population. We aimed to identify the germline mutations of FANCC in high-risk breast cancer patients in China.Methods: 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fd6a575588ff43d5e02c3b93ccd1d74
http://europepmc.org/articles/PMC6439399
http://europepmc.org/articles/PMC6439399
Autor:
Ya Bing Zheng, Guang Peng, Yun Gao, Xiao Wen Ding, Xiao Jia Wang, Yan Sun, Cai Jin Lou, Wen-Ming Cao, Yuan Huang, Zhi Wen Pan
Publikováno v:
BMC Cancer
BMC Cancer, Vol 19, Iss 1, Pp 1-8 (2019)
BMC Cancer, Vol 19, Iss 1, Pp 1-8 (2019)
Background Mutated BRCA1/2 genes are associated with hereditary breast and ovarian cancer (HBOC). So far most of the identified BRCA1/2 pathogenic variants are single nucleotide variants (SNVs) or insertions/deletions (Indels). However, large genomic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51654d1cf25642376517530ecba6a300
https://pubmed.ncbi.nlm.nih.gov/31174498
https://pubmed.ncbi.nlm.nih.gov/31174498
Publikováno v:
Applied Mechanics and Materials. :1023-1026
This paper proposes an end-to-end user perception integrated monitoring and analyzing system, the multi-network user perception data by using standard SDK (Software Development Kit), completely solve the terminal abnormal events and the user percepti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80b61b022127b41235b0509201c9e921
https://doi.org/10.4028/www.scientific.net/amm.644-650.1023
https://doi.org/10.4028/www.scientific.net/amm.644-650.1023
Autor:
Wei Wu Ye, Xiao Wen Ding, Yun Gao, Shang Nao Xie, Hong Jian Yang, Zhi Wen Pan, Xiao Jia Wang, Wen-Ming Cao
Publikováno v:
BMC Cancer
Background Germline mutations in the BRCA1 and BRCA2 genes greatly increase a woman’s risk of developing breast and/or ovarian cancer. The prevalence and distribution of such mutations differ across races/ethnicities. Several studies have investiga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35cebcfe4dfa4c370a614ce6d721ac1e
http://europepmc.org/articles/PMC4744435
http://europepmc.org/articles/PMC4744435
Publikováno v:
Journal of Pediatric Surgery. 47:1699-1705
Background Hirschsprung disease (HSCR) is a complex congenital disorder characterized by intestinal obstructions owing to the absence of the intestinal ganglion cells of the nerve plexuses in variable lengths of the digestive tract. Several RET polym
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07b013e2249f68728cc22d5c758fd3a9
https://doi.org/10.1016/j.jpedsurg.2012.03.057
https://doi.org/10.1016/j.jpedsurg.2012.03.057
Publikováno v:
Journal of Pediatric Surgery. 46:1930-1934
Background Hirschsprung disease (HSCR, Online Mendelian Inheritance in Man 142623) is a typical developmental disorder of the enteric nervous system in which ganglion cells fail to innervate the lower gastrointestinal tract during embryonic developme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9036a52e1d46537034549cbd781c669d
https://doi.org/10.1016/j.jpedsurg.2011.05.017
https://doi.org/10.1016/j.jpedsurg.2011.05.017