Tae‐Ju Park

1.6k total citations
45 papers, 1.3k citations indexed

About

Tae‐Ju Park is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, Tae‐Ju Park has authored 45 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 12 papers in Cellular and Molecular Neuroscience and 7 papers in Cell Biology. Recurrent topics in Tae‐Ju Park's work include Ion channel regulation and function (12 papers), Receptor Mechanisms and Signaling (9 papers) and Nicotinic Acetylcholine Receptors Study (9 papers). Tae‐Ju Park is often cited by papers focused on Ion channel regulation and function (12 papers), Receptor Mechanisms and Signaling (9 papers) and Nicotinic Acetylcholine Receptors Study (9 papers). Tae‐Ju Park collaborates with scholars based in United States, South Korea and Japan. Tae‐Ju Park's co-authors include Tom Curran, Kyong‐Tai Kim, Hyunjung Ha, Kelli L. Boyd, Eun‐Mi Hur, Pann‐Ghill Suh, Yong‐Hyun Kim, Young Han Lee, Yongsoo Park and Kwang Jin Baek and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Journal of Neuroscience.

In The Last Decade

Tae‐Ju Park

44 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tae‐Ju Park United States 23 772 269 186 135 131 45 1.3k
Shinichiro Toki Japan 13 1.3k 1.7× 362 1.3× 182 1.0× 127 0.9× 142 1.1× 28 1.9k
Marcel D. Payet Canada 28 1.1k 1.4× 489 1.8× 107 0.6× 111 0.8× 102 0.8× 51 1.8k
Weidong Wang United States 16 691 0.9× 183 0.7× 270 1.5× 151 1.1× 120 0.9× 49 1.3k
Christoph Boehmer Germany 24 1.2k 1.6× 277 1.0× 90 0.5× 132 1.0× 52 0.4× 27 1.6k
Stephanie C. Stotz Canada 23 1.2k 1.5× 629 2.3× 82 0.4× 153 1.1× 65 0.5× 41 1.7k
Athina Tzinia Greece 21 494 0.6× 187 0.7× 89 0.5× 171 1.3× 82 0.6× 35 1.2k
Taehoon G. Lee South Korea 20 1.0k 1.3× 381 1.4× 216 1.2× 73 0.5× 210 1.6× 25 1.7k
Miriam Kolko Denmark 29 1.1k 1.4× 261 1.0× 155 0.8× 114 0.8× 105 0.8× 132 2.6k
Satoshi Tsuzuki Japan 22 928 1.2× 252 0.9× 81 0.4× 79 0.6× 134 1.0× 83 2.1k

Countries citing papers authored by Tae‐Ju Park

Since Specialization
Citations

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

Fields of papers citing papers by Tae‐Ju Park

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tae‐Ju Park. 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 Tae‐Ju Park. The network helps show where Tae‐Ju Park may publish in the future.

Co-authorship network of co-authors of Tae‐Ju Park

This figure shows the co-authorship network connecting the top 25 collaborators of Tae‐Ju Park. A scholar is included among the top collaborators of Tae‐Ju Park 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 Tae‐Ju Park. Tae‐Ju Park 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.
Wu, Bingruo, Pengfei Lu, Tae‐Ju Park, et al.. (2023). Crk and Crkl Are Required in the Endocardial Lineage for Heart Valve Development. Journal of the American Heart Association. 12(18). e029683–e029683. 2 indexed citations
2.
Park, Tae‐Ju, et al.. (2023). Real-Time Quantitative Measurement of Tumor Cell Migration and Invasion Following Synthetic mRNA Transfection. Journal of Visualized Experiments. 1 indexed citations
3.
Mudduluru, Giridhar, et al.. (2020). Impedance-based Real-time Measurement of Cancer Cell Migration and Invasion. Journal of Visualized Experiments. 6 indexed citations
4.
Park, Tae‐Ju & Tom Curran. (2020). Requirement for Crk and CrkL during postnatal lens development. Biochemical and Biophysical Research Communications. 529(3). 603–607. 4 indexed citations
5.
Park, Tae‐Ju, Mateusz Koptyra, & Tom Curran. (2016). Fibroblast Growth Requires CT10 Regulator of Kinase (Crk) and Crk-like (CrkL). Journal of Biological Chemistry. 291(51). 26273–26290. 14 indexed citations
6.
George, Britta, Qingfeng Fan, Jidong Zhang, et al.. (2014). Crk1/2 and CrkL form a hetero-oligomer and functionally complement each other during podocyte morphogenesis. Kidney International. 85(6). 1382–1394. 31 indexed citations
7.
Park, Tae‐Ju & Tom Curran. (2013). Essential roles of Crk and CrkL in fibroblast structure and motility. Oncogene. 33(43). 5121–5132. 26 indexed citations
8.
George, Britta, Rakesh Kumar Verma, Puneet Garg, et al.. (2012). Crk1/2-dependent signaling is necessary for podocyte foot process spreading in mouse models of glomerular disease. Journal of Clinical Investigation. 122(2). 674–692. 83 indexed citations
9.
Austgen, Kathryn, et al.. (2011). The adaptor protein CRK is a pro-apoptotic transducer of endoplasmic reticulum stress. Nature Cell Biology. 14(1). 87–92. 25 indexed citations
10.
Park, Tae‐Ju & Tom Curran. (2008). Crk and Crk-Like Play Essential Overlapping Roles Downstream of Disabled-1 in the Reelin Pathway. Journal of Neuroscience. 28(50). 13551–13562. 125 indexed citations
11.
Park, Tae‐Ju, Kelli L. Boyd, & Tom Curran. (2006). Cardiovascular and Craniofacial Defects in Crk- Null Mice. Molecular and Cellular Biology. 26(16). 6272–6282. 76 indexed citations
12.
Park, Tae‐Ju, et al.. (2003). Inhibition of ubiquitin ligase Siah-1A by disabled-1. Biochemical and Biophysical Research Communications. 302(4). 671–678. 16 indexed citations
13.
Park, Tae‐Ju, et al.. (2001). Inhibition of nicotinic acetylcholine receptors and calcium channels by clozapine in bovine adrenal chromaffin cells. Biochemical Pharmacology. 61(8). 1011–1019. 28 indexed citations
14.
Kim, Yong‐Hyun, Tae‐Ju Park, Young Han Lee, et al.. (1999). Phospholipase C-δ1 Is Activated by Capacitative Calcium Entry That Follows Phospholipase C-β Activation upon Bradykinin Stimulation. Journal of Biological Chemistry. 274(37). 26127–26134. 109 indexed citations
15.
Chae, Hee‐Don, et al.. (1999). Rapid and simple measurement of serotonin N-acetyltransferase activity by liquid biphasic diffusion assay. Neurochemistry International. 35(6). 447–451. 29 indexed citations
16.
17.
Choi, Se‐Young, Hee‐Don Chae, Tae‐Ju Park, Hyunjung Ha, & Kyong‐Tai Kim. (1999). Characterization of high affinity neurotensin receptor NTR1 in HL‐60 cells and its down regulation during granulocytic differentiation. British Journal of Pharmacology. 126(4). 1050–1056. 25 indexed citations
18.
19.
Park, Tae‐Ju, Sook‐Keun Song, & Kyong‐Tai Kim. (1997). A2A Adenosine Receptors Inhibit ATP‐Induced Ca2+ Influx in PC12 Cells by Involving Protein Kinase A. Journal of Neurochemistry. 68(5). 2177–2185. 25 indexed citations
20.
Park, Tae‐Ju, et al.. (1996). Synergistic activation of adenylyl cyclase is dependent upon phospholipase C-mediated processes in human neuroblastoma SK-N-BE(2)C cells. European Journal of Pharmacology. 314(1-2). 235–242. 14 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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