Accès ouvert
2026
article
OpenAlex
Xiaoke Chen, Liqiang Qian, Jia Huang, Wei Mao et autres
Background: Patients with both primary simultaneous squamous cell carcinoma (SQ) and peripheral-type small-cell lung cancer (SCLC) are extremely rare clinically, and an in-depth molecular characterization and tumor microenvironment (TME) analysis are urgently needed. This study aimed to characterize the mutational landscape, epigenetic …
cn
(code pays fourni par la source)
Accès ouvert
2025
article
OpenAlex
Xiaoling Weng, Na Huang, Bihua Zeng, Haiyan Deng
Cleft palate is a common congenital malformation of the maxillofacial region, and its postoperative speech disorders (such as hypernasality, nasal air escape, and articulation errors) can significantly impact patients’ communication abilities and psychological well-being. Traditional speech-language therapy faces challenges such as insufficient …
cn
(code pays fourni par la source)
Accès ouvert
2025
preprint
OpenAlex
Guan‐Tian Lang, San-Jian Yu, Xiaoling Weng, Yun Liu et autres
cn
(code pays fourni par la source)
Accès ouvert
2025
article
OpenAlex
Mao Yang, Yuhao Zhao, Chen Li, Xiaoling Weng et autres
cn
(code pays fourni par la source)
Accès ouvert
2024
article
OpenAlex
Wenpeng Ni, Ji Liu, Kunyi Deng, Zhouyu Zeng et autres
Acute lymphoblastic leukemia (ALL) with granular blasts was historically referred to as "granular ALL", but this is not recognized as a distinct entity in the current WHO classification. This rare morphological feature is predominantly associated with a B-cell immunophenotype, while T-ALL with …
cn
(code pays fourni par la source)
2024
article
OpenAlex
Guo-Wen Lin, Feng Tian, Qiwei Yu, Xiaoling Weng et autres
cn, us
(code pays fourni par la source)
2024
article
OpenAlex
Guo-Wen Lin, Feng Zhang, Xiaoling Weng, Zhe Hong et autres
cn
(code pays fourni par la source)
Accès ouvert
2024
preprint
OpenAlex
Honglian Wang, Haoran Wang, Xiaoling Weng, Fa-tao Liu et autres
2023
article
OpenAlex
Guoqiang Li, Peng Pu, Mengqiao Pan, Xiaoling Weng et autres
cn
(code pays fourni par la source)
Accès ouvert
2023
other
OpenAlex
Xiaomin Niu, Fatao Liu, Yi Zhou, Zhen Zhou et autres
Sixty erlotinib-related aberrant DNA methylation genes in both patients discovered with the the methyl-sensitive cut counting sequencing (MSCC) screening method.
Accès ouvert
2023
other
OpenAlex
Xiaomin Niu, Fatao Liu, Yi Zhou, Zhen Zhou et autres
Data summary of methyl-sensitive cut counting sequencing (MSCC) sequencing of the 4 samples (8 libraries).
Accès ouvert
2023
other
OpenAlex
Xiaomin Niu, Fatao Liu, Yi Zhou, Zhen Zhou et autres
DNA methylation results of GABAA receptor families was relatively conservative before and after erlotinib treatment in both patients using methyl-sensitive cut counting sequencing (MSCC) screening method.