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  1. Article

    Open Access

    Early progression is associated with worse survival in patients with Waldenström’s macroglobulinemia

    Early progression of disease within 24 months (POD24) of diagnosis is associated with inferior overall survival (OS) in follicular lymphoma, but its prognostic role in Waldenström’s macroglobulinemia (WM) is s...

    Wenjie **ong, Zanzan Wang, Huihan Wang, Chunrui Li in Holistic Integrative Oncology (2024)

  2. Article

    Open Access

    Comparison of different internal fixation models in ankle arthrodesis using 3D finite-element analysis

    The purpose of this study is to use three-dimensional finite-element analysis to better understand the biomechanical features of various internal fixators for ankle arthrodesis.

    Bo Feng, Qing-bo Gao, Guang-ming Dai, Ke-cheng Niu in European Journal of Medical Research (2023)

  3. No Access

    Article

    Associations of SGLT2 genetic polymorphisms with salt sensitivity, blood pressure changes and hypertension incidence in Chinese adults

    Sodium-glucose cotransporter 2 (SGLT2) inhibitors lowers blood pressure (BP) and exert a salutary effect on the salt sensitivity of BP. This study aimed to examine the associations of SGLT2 genetic variants with ...

    Hao Jia, Peng Bao, Shi Yao, ** Zhang, Jian-Jun Mu, Gui-Lin Hu in Hypertension Research (2023)

  4. Article

    Open Access

    Global, regional, and national burdens of myocarditis, 1990–2019: systematic analysis from GBD 2019

    Myocarditis, a health-threatening heart disease, is attracting increasing attention. This systematic study was conducted to study the prevalence of disease through the trends of incidence, mortality, disabilit...

    Yue-Wen-Ying Wang, Run-Ben Liu, Cheng-Yang Huang, Hao-Yang Li in BMC Public Health (2023)

  5. Article

    Open Access

    Serum lnc34a is a potential prediction biomarker for bone metastasis in hepatocellular carcinoma patients

    Early screening and intervention therapies are crucial to improve the prognosis of hepatocellular carcinoma (HCC) patients with bone metastasis. We aimed to identify serum lncRNA as a prediction biomarker in H...

    Li Zhang, Hao Niu, ** Yang, Jie Ma, Bao-Ying Yuan, Zhao-Chong Zeng in BMC Cancer (2021)

  6. No Access

    Article

    S100A14 suppresses metastasis of nasopharyngeal carcinoma by inhibition of NF-kB signaling through degradation of IRAK1

    Nasopharyngeal carcinoma (NPC) is a unique head and neck cancer with highly aggressive and metastatic potential in which distant metastasis is the main reason for treatment failure. Till present, the underlyin...

    Dong-Fang Meng, Rui Sun, Guo-Ying Liu, Li-**a Peng, Li-Sheng Zheng, ** **e in Oncogene (2020)

  7. Article

    Open Access

    Comprehensive functional annotation of susceptibility SNPs prioritized 10 genes for schizophrenia

    Nearly 95% of susceptibility SNPs identified by genome-wide association studies (GWASs) are located in non-coding regions, which causes a lot of difficulty in deciphering their biological functions on disease ...

    Hui-Min Niu, ** Yang, Huan-Huan Chen, Ruo-Han Hao in Translational Psychiatry (2019)

  8. Article

    Open Access

    Clinical and positron emission tomography responses to long-term high-dose interferon-α treatment among patients with Erdheim–Chester disease

    Erdheim–Chester disease (ECD) is a rare multi-systemic form of histiocytosis. Treatment with BRAF inhibitors has markedly improved outcomes of ECD; however, this targeted therapy is expensive (estimated annual...

    **n-xin Cao, Na Niu, Jian Sun, Hao Cai, Feng-dan Wang in Orphanet Journal of Rare Diseases (2019)

  9. No Access

    Article

    Association between genetic variants and characteristic symptoms of type 2 diabetes: A matched case-control study

    To examine the association of genetic variants with characteristic symptoms of type 2 diabetes mellitus (T2DM).

    Hao-ying Dou, Yuan-yuan Wang, Nan Yang in Chinese Journal of Integrative Medicine (2017)

  10. Article

    Open Access

    Globotriaosylsphingosine (lyso-Gb3) might not be a reliable marker for monitoring the long-term therapeutic outcomes of enzyme replacement therapy for late-onset Fabry patients with the Chinese hotspot mutation (IVS4+919G>A)

    In Taiwan, DNA-based newborn screening showed a surprisingly high incidence (1/875 in males and 1/399 in females) of a cardiac Fabry mutation (IVS4 + 919G > A). However, the natural course, long-term treatment...

    Hao-Chuan Liu, Hsiang-Yu Lin, Chia-Feng Yang in Orphanet Journal of Rare Diseases (2014)

  11. Article

    Open Access

    Endomyocardial biopsies in patients with left ventricular hypertrophy and a common Chinese later-onset fabry mutation (IVS4 + 919G > A)

    In Taiwan, DNA-based newborn screening showed a surprisingly high incidence of a cardiac Fabry mutation (IVS4 + 919G > A). The prevalence of this mutation is too high to be believed that it is a real pathogeni...

    Ting-Rong Hsu, Shih-Hsien Sung, Fu-Pang Chang in Orphanet Journal of Rare Diseases (2014)