Mao Xiang Chen

1.3k total citations
22 papers, 1.0k citations indexed

About

Mao Xiang Chen is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Sensory Systems. According to data from OpenAlex, Mao Xiang Chen has authored 22 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 5 papers in Cardiology and Cardiovascular Medicine and 5 papers in Sensory Systems. Recurrent topics in Mao Xiang Chen's work include Ion channel regulation and function (7 papers), Mitochondrial Function and Pathology (5 papers) and Ion Channels and Receptors (5 papers). Mao Xiang Chen is often cited by papers focused on Ion channel regulation and function (7 papers), Mitochondrial Function and Pathology (5 papers) and Ion Channels and Receptors (5 papers). Mao Xiang Chen collaborates with scholars based in United Kingdom, Australia and Denmark. Mao Xiang Chen's co-authors include Patricia T.W. Cohen, Yu Hua Chen, Patricia T.W. Cohen, Philip Cohen, Derek J. Trezise, F. Barry Caudwell, Greg B. G. Moorhead, Dario R. Alessi, David G. Campbell and Catherine M. Shanahan and has published in prestigious journals such as Journal of Neuroscience, Diabetes and FEBS Letters.

In The Last Decade

Mao Xiang Chen

22 papers receiving 1.0k citations

Peers

Mao Xiang Chen
Elaine F. Etter United States
Sandra Mammarella Italy
Hideki Tsumura Japan
J. R. Greenwell United Kingdom
Yoshimasa Shimoto United States
Jesun Lee South Korea
Nanna K. Jørgensen Denmark
M. Wakui Japan
K. Takeda France
Jinhong Wie South Korea
Elaine F. Etter United States
Mao Xiang Chen
Citations per year, relative to Mao Xiang Chen Mao Xiang Chen (= 1×) peers Elaine F. Etter

Countries citing papers authored by Mao Xiang Chen

Since Specialization
Citations

This map shows the geographic impact of Mao Xiang Chen'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 Mao Xiang Chen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mao Xiang Chen more than expected).

Fields of papers citing papers by Mao Xiang Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mao Xiang Chen. 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 Mao Xiang Chen. The network helps show where Mao Xiang Chen may publish in the future.

Co-authorship network of co-authors of Mao Xiang Chen

This figure shows the co-authorship network connecting the top 25 collaborators of Mao Xiang Chen. A scholar is included among the top collaborators of Mao Xiang Chen 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 Mao Xiang Chen. Mao Xiang Chen 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.
Chen, Mao Xiang, Emma Ward, Matilde Caivano, et al.. (2018). Probing Mitochondrial Permeability Transition Pore Activity in Nucleated Cells and Platelets by High-Throughput Screening Assays Suggests Involvement of Protein Phosphatase 2B in Mitochondrial Dynamics. Assay and Drug Development Technologies. 16(8). 445–455. 4 indexed citations
2.
Chen, Mao Xiang, Emma Ward, Helen F. Sneddon, et al.. (2014). Validation and Optimization of Novel High-Throughput Assays for Human Epithelial Sodium Channels. SLAS DISCOVERY. 20(2). 242–253. 8 indexed citations
3.
4.
Ward, Emma, et al.. (2012). A High-Throughput Assay for Connexin 43 (Cx43, GJA1 ) Gap Junctions Using Codon-Optimized Aequorin. Assay and Drug Development Technologies. 11(2). 93–100. 19 indexed citations
5.
Chen, Mao Xiang, et al.. (2006). Novel 384-Well Population Patch Clamp Electrophysiology Assays for Ca2+-Activated K+ Channels. SLAS DISCOVERY. 12(1). 50–60. 36 indexed citations
6.
Bahia, Parmvir K., Rie Suzuki, Amanda Jowett, et al.. (2005). A Functional Role for Small-Conductance Calcium-Activated Potassium Channels in Sensory Pathways Including Nociceptive Processes. Journal of Neuroscience. 25(14). 3489–3498. 65 indexed citations
7.
Furness, John B., Heather L. Robbins, Billie Hunne, et al.. (2004). Intermediate conductance potassium (IK) channels occur in human enteric neurons. Autonomic Neuroscience. 112(1-2). 93–97. 17 indexed citations
8.
Chen, Mao Xiang, Shelby Gorman, Kuljit Singh, et al.. (2004). Small and intermediate conductance Ca 2+ -activated K + channels confer distinctive patterns of distribution in human tissues and differential cellular localisation in the colon and corpus cavernosum. Naunyn-Schmiedeberg s Archives of Pharmacology. 369(6). 602–615. 112 indexed citations
9.
10.
Furness, John B., Heather L. Robbins, Inger-Sofie Selmer, et al.. (2003). Expression of intermediate conductance potassium channel immunoreactivity in neurons and epithelial cells of the rat gastrointestinal tract. Cell and Tissue Research. 314(2). 179–189. 48 indexed citations
11.
Cohen, Philip, et al.. (1997). Identification of the Regions on the M110 Subunit of Protein Phosphatase 1M That Interact with the M21 Subunit and with Myosin. European Journal of Biochemistry. 244(3). 931–939. 78 indexed citations
12.
Chen, Mao Xiang & Patricia T.W. Cohen. (1997). Activation of protein phosphatase 5 by limited proteolysis or the binding of polyunsaturated fatty acids to the TPR domain. FEBS Letters. 400(1). 136–140. 118 indexed citations
13.
Cohen, Patricia T.W., Mao Xiang Chen, & Christopher G. Armstrong. (1996). Novel Protein Phosphatases That May Participate in Cell Signaling. Advances in pharmacology. 36. 67–89. 31 indexed citations
14.
Moorhead, Greg B. G., F. Barry Caudwell, Philip Cohen, et al.. (1996). Identification of Protein‐Phosphatase‐1‐Binding Domains on the Glycogen and Myofibrillar Targetting Subunits. European Journal of Biochemistry. 239(2). 317–325. 129 indexed citations
15.
Hansen, Lars, Torben Hansen, Henrik Vestergaard, et al.. (1995). A widespread amino acid polymorphism at codon 905 of the glycogen-associated regulatory subunit of protein phosphatase-1 is associated with insulin resistance and hypersecretion of insulin. Human Molecular Genetics. 4(8). 1313–1320. 73 indexed citations
16.
Brown, Linda P., Mao Xiang Chen, & Patricia T.W. Cohen. (1994). Identification of a cDNA encoding a Drosophila calcium/calmodulin regulated protein phosphatase, which has its most abundant expression in the early embryo. FEBS Letters. 339(1-2). 124–128. 20 indexed citations
17.
Chen, Yu Hua, Mao Xiang Chen, Dario R. Alessi, et al.. (1994). Molecular cloning of cDNA encoding the 110 kDa and 21 kDa regulatory subunits of smooth muscle protein phosphatase 1M. FEBS Letters. 356(1). 51–55. 114 indexed citations
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Chen, Mao Xiang, Yu Hua Chen, & Patricia T.W. Cohen. (1993). PPQ, a novel protein phosphatase containing a Ser+Asn‐rich amino‐terminal domain, is involved in the regulation of protein synthesis. European Journal of Biochemistry. 218(2). 689–699. 27 indexed citations
20.
Chen, Mao Xiang, Yu Hua Chen, & Patricia T.W. Cohen. (1992). Polymerase chain reactions using Saccharomyces, Drosophila and human DNA predict a large family of protein serine/threonine phosphatases. FEBS Letters. 306(1). 54–58. 41 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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