Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Suwei Hu"'
Publikováno v:
Cancer Medicine, Vol 8, Iss 6, Pp 2979-2993 (2019)
Abstract Introduction Lung large cell neuroendocrine carcinoma (L‐LCNEC) is a rare, aggressive tumor, for which the optimal treatment strategies for LCNEC have not yet been established. In order to explore how to improve the outcome of prognosis fo
Externí odkaz:
https://doaj.org/article/3e04599980ca4ccdb21899dc773748c7
Autor:
Yutu, Luo, Suwei, Hu, Fang, Wang, Junjun, Yang, Daohui, Gong, Wenjing, Xu, Xingxiang, Xu, Lingfeng, Min
Publikováno v:
Translational Cancer Research. 11:3803-3813
Lung cancer is a common malignant tumor, with, non-small cell lung cancer (NSCLC) accounting for about 80-85% of cases. This study investigated the expression of miR-137 in NSCLC tissues and cells and its effects on the migration and invasion of NSCL
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 39(11)
To carry out genetic testing and prenatal diagnosis for a Chinese pedigree with Lesch-Nyhan syndrome (LNS) but no specimen from the affected probands.All affected individuals in this pedigrees were male and had deceased during childhood, with no biol
Autor:
Yuxiu Wang, Xingxiang Xu, Junjun Yang, Jianjun Gu, Suwei Hu, Ying Li, Beiyuan Chi, Lingfeng Min, Jun Zhang, Daohui Gong
Publikováno v:
OncoTargets and Therapy. 13:5967-5977
Purpose AMP-activated protein kinase α1 (AMPK α1) associates closely with cancers. However, the relationship between AMPK α1 and non-small cell lung cancer (NSCLC) is not fully understood. In this study, we aim to explore the role and mechanism of
Publikováno v:
Cancer Medicine
Cancer Medicine, Vol 8, Iss 6, Pp 2979-2993 (2019)
Cancer Medicine, Vol 8, Iss 6, Pp 2979-2993 (2019)
Introduction Lung large cell neuroendocrine carcinoma (L‐LCNEC) is a rare, aggressive tumor, for which the optimal treatment strategies for LCNEC have not yet been established. In order to explore how to improve the outcome of prognosis for patient
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 38(2)
To explore the genetic basis for a Chinese pedigree affected with autosomal dominant late-onset non-syndromic hearing loss (NSHL).Clinical data of the pedigree were collected. Genomic DNA was extracted from peripheral blood samples of the proband and
Autor:
Jianjun Gu, Jixin Jiang, Daohui Gong, Liping Wang, Xiaolin Wang, Yuxiu Wang, Xingxiang Xu, Yusheng Shu, Suwei Hu, Lingfeng Min
Background: Genome-wide association studies of lung cancer have shown a common variation at 15q24-25.1 as a determinant of risk, but the role of specific genes has not been proven. This study aims to explore the expression of mutations and the progno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d21357f010875eb9c8657ebc9fbe411b
https://doi.org/10.21203/rs.3.rs-26978/v3
https://doi.org/10.21203/rs.3.rs-26978/v3
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 37(4)
To explore the genetic basis for a Chinese pedigree affected with split hand/foot malformation (SHFM).Genomic DNA of the proband and other affected members was extracted from peripheral blood samples. Chromosomal microarray analysis was employed to d
Autor:
Daohui, Gong, Ying, Li, Yuxiu, Wang, Beiyuan, Chi, Jun, Zhang, Jianjun, Gu, JunJun, Yang, Xingxiang, Xu, Suwei, Hu, Lingfeng, Min
Publikováno v:
OncoTargets and therapy
Purpose AMP-activated protein kinase α1 (AMPK α1) associates closely with cancers. However, the relationship between AMPK α1 and non-small cell lung cancer (NSCLC) is not fully understood. In this study, we aim to explore the role and mechanism of
Autor:
Yuxiu Wang, Xiaolin Wang, Liping Wang, Jianjun Gu, Daohui Gong, Jixin Jiang, Xingxiang Xu, Suwei Hu, Yusheng Shu, Lingfeng Min
Background To explore the mutations expression and prognostic significance of 15q25 (CHRNA5 and PSMA4) mRNA in lung adenocarcinoma (LAC) based on immunohistochemistry, TCGA and bioinformatics.Methods Mutations expression on chromosome 15q25 of 576 pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0fc44d6fc549789608b5444827295b0
https://doi.org/10.21203/rs.2.12982/v1
https://doi.org/10.21203/rs.2.12982/v1