Miduo Tan

904 total citations
21 papers, 662 citations indexed

About

Miduo Tan is a scholar working on Molecular Biology, Epidemiology and Cancer Research. According to data from OpenAlex, Miduo Tan has authored 21 papers receiving a total of 662 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 8 papers in Epidemiology and 5 papers in Cancer Research. Recurrent topics in Miduo Tan's work include Autophagy in Disease and Therapy (7 papers), Heavy Metal Exposure and Toxicity (3 papers) and MicroRNA in disease regulation (3 papers). Miduo Tan is often cited by papers focused on Autophagy in Disease and Therapy (7 papers), Heavy Metal Exposure and Toxicity (3 papers) and MicroRNA in disease regulation (3 papers). Miduo Tan collaborates with scholars based in China, United States and Tanzania. Miduo Tan's co-authors include Li Song, Huifeng Pi, Wen Li, Yan Deng, Nongyue He, Zhu Chen, Ziyu He, Taotao Li, Yuan Liu and Elingarami Sauli and has published in prestigious journals such as The Science of The Total Environment, Biochemical and Biophysical Research Communications and Environmental Pollution.

In The Last Decade

Miduo Tan

21 papers receiving 658 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Miduo Tan China 15 365 151 146 72 64 21 662
Guanghai Yan China 19 550 1.5× 62 0.4× 101 0.7× 77 1.1× 28 0.4× 64 1.2k
Dongyun Shi China 14 470 1.3× 78 0.5× 152 1.0× 61 0.8× 15 0.2× 22 793
Lakhan Kma India 10 274 0.8× 106 0.7× 111 0.8× 42 0.6× 13 0.2× 13 580
Bonan Chen China 18 529 1.4× 117 0.8× 179 1.2× 151 2.1× 30 0.5× 43 960
Zhenhua Ni China 17 494 1.4× 65 0.4× 219 1.5× 115 1.6× 26 0.4× 44 801
Emilie Dubois‐Deruy France 14 410 1.1× 70 0.5× 87 0.6× 44 0.6× 23 0.4× 25 922
Xingkai Liu China 15 366 1.0× 162 1.1× 97 0.7× 116 1.6× 12 0.2× 39 692
Paola Vergara Italy 7 426 1.2× 74 0.5× 65 0.4× 50 0.7× 18 0.3× 7 716
Tomasz Dziaman Poland 19 539 1.5× 56 0.4× 158 1.1× 107 1.5× 82 1.3× 23 1.0k

Countries citing papers authored by Miduo Tan

Since Specialization
Citations

This map shows the geographic impact of Miduo Tan's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Miduo Tan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Miduo Tan more than expected).

Fields of papers citing papers by Miduo Tan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Miduo Tan. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Miduo Tan. The network helps show where Miduo Tan may publish in the future.

Co-authorship network of co-authors of Miduo Tan

This figure shows the co-authorship network connecting the top 25 collaborators of Miduo Tan. A scholar is included among the top collaborators of Miduo Tan based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Miduo Tan. Miduo Tan is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
Yang, Yue, Huadong Zhang, Ping Deng, et al.. (2023). Environmental cadmium exposure facilitates mammary tumorigenesis via reprogramming gut microbiota-mediated glutamine metabolism in MMTV-Erbb2 mice. The Science of The Total Environment. 897. 165348–165348. 13 indexed citations
3.
Hong, Huihui, Jia Xu, Xue Wang, et al.. (2022). Cadmium perturbed metabolomic signature in pancreatic beta cells correlates with disturbed metabolite profile in human urine. Environment International. 161. 107139–107139. 24 indexed citations
4.
Long, Jing, et al.. (2022). NUPR1 promotes the proliferation and migration of breast cancer cells by activating TFE3 transcription to induce autophagy. Experimental Cell Research. 418(1). 113234–113234. 16 indexed citations
5.
Yang, Yue, Miduo Tan, Yan Luo, et al.. (2022). miR-3614–5p downregulation promotes cadmium-induced breast cancer cell proliferation and metastasis by targeting TXNRD1. Ecotoxicology and Environmental Safety. 247. 114270–114270. 6 indexed citations
6.
Liang, Yidan, Huifeng Pi, Miduo Tan, et al.. (2021). Cadmium promotes breast cancer cell proliferation, migration and invasion by inhibiting ACSS2/ATG5-mediated autophagy. Environmental Pollution. 273. 116504–116504. 36 indexed citations
7.
Yang, Yue, Ping Deng, Heng Xiao, et al.. (2021). N6-methyladenosine-mediated downregulation of miR-374c-5p promotes cadmium-induced cell proliferation and metastasis by targeting GRM3 in breast cancer cells. Ecotoxicology and Environmental Safety. 229. 113085–113085. 26 indexed citations
8.
Gong, Liang, Miduo Tan, Ting Pan, et al.. (2021). Two-Photon Fluorescent Nanomaterials and Their Applications in Biomedicine. Journal of Biomedical Nanotechnology. 17(4). 509–528. 20 indexed citations
9.
10.
Deng, Ping, Miduo Tan, Wei Zhou, et al.. (2020). Bisphenol A promotes breast cancer cell proliferation by driving miR-381-3p-PTTG1-dependent cell cycle progression. Chemosphere. 268. 129221–129221. 39 indexed citations
11.
He, Ziyu, Zhu Chen, Miduo Tan, et al.. (2020). A review on methods for diagnosis of breast cancer cells and tissues. Cell Proliferation. 53(7). e12822–e12822. 142 indexed citations
12.
Jiang, Pengfei, et al.. (2020). A novel electrochemical DNA detection method based on bio-barcode/gold label silver stain dual amplification. Materials Express. 10(2). 206–213. 5 indexed citations
13.
Tan, Miduo, Bin Jiang, Haihua Wang, et al.. (2019). Dihydromyricetin induced lncRNA MALAT1-TFEB-dependent autophagic cell death in cutaneous squamous cell carcinoma. Journal of Cancer. 10(18). 4245–4255. 30 indexed citations
14.
Wu, Bowen, et al.. (2018). Arsenic trioxide induces autophagic cell death in osteosarcoma cells via the ROS-TFEB signaling pathway. Biochemical and Biophysical Research Communications. 496(1). 167–175. 40 indexed citations
15.
Tan, Miduo, et al.. (2018). Inhibiting ROS-TFE3-dependent autophagy enhances the therapeutic response to metformin in breast cancer. Free Radical Research. 52(8). 872–886. 21 indexed citations
16.
Zeng, Wei, Tao Xiao, Huanhuan Liu, et al.. (2017). Inhibiting ROS-TFEB-Dependent Autophagy Enhances Salidroside-Induced Apoptosis in Human Chondrosarcoma Cells. Cellular Physiology and Biochemistry. 43(4). 1487–1502. 27 indexed citations
17.
Fan, Tengfei, Huifeng Pi, Min Li, et al.. (2017). Inhibiting MT2‐TFE3‐dependent autophagy enhances melatonin‐induced apoptosis in tongue squamous cell carcinoma. Journal of Pineal Research. 64(2). 72 indexed citations
18.
Chen, Xun, Miduo Tan, Zhiqin Xie, et al.. (2016). Inhibiting ROS-STAT3-dependent autophagy enhanced capsaicin–induced apoptosis in human hepatocellular carcinoma cells. Free Radical Research. 50(7). 744–755. 57 indexed citations
19.
Tan, Miduo, Yaqing Zhang, Yan Cheng, et al.. (2015). SIRT1/PGC-1α signaling protects hepatocytes against mitochondrial oxidative stress induced by bile acids. Free Radical Research. 49(8). 935–945. 52 indexed citations
20.
Epstein, Wallace V., et al.. (1968). Effect of renal homotransplantation on the metabolism of the light chains of immunoglobulins. Transplantation. 6(5). 749–749. 4 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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