Gabriel Natura

1.3k total citations
18 papers, 966 citations indexed

About

Gabriel Natura is a scholar working on Physiology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Gabriel Natura has authored 18 papers receiving a total of 966 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Physiology, 9 papers in Molecular Biology and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Gabriel Natura's work include Pain Mechanisms and Treatments (11 papers), Ion channel regulation and function (7 papers) and Neuropeptides and Animal Physiology (4 papers). Gabriel Natura is often cited by papers focused on Pain Mechanisms and Treatments (11 papers), Ion channel regulation and function (7 papers) and Neuropeptides and Animal Physiology (4 papers). Gabriel Natura collaborates with scholars based in Germany, United States and France. Gabriel Natura's co-authors include Hans‐Georg Schaible, Gisela Segond von Banchet, Andrea Ebersberger, Frank Richter, Michael Karl Boettger, Susanne Hensellek, Rolf Bräuer, Mieczysław Gajda, Horacio Vanegas and Enrique Vázquez and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Neuroscience and Scientific Reports.

In The Last Decade

Gabriel Natura

18 papers receiving 949 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gabriel Natura Germany 12 510 238 233 182 181 18 966
Sara Kelly United Kingdom 16 434 0.9× 389 1.6× 148 0.6× 296 1.6× 186 1.0× 27 965
Susanne Hensellek Germany 7 336 0.7× 96 0.4× 144 0.6× 97 0.5× 85 0.5× 7 604
Hjalte Holm Andersen Denmark 23 425 0.8× 74 0.3× 196 0.8× 141 0.8× 370 2.0× 57 1.5k
João de Sousa Valente United Kingdom 16 314 0.6× 190 0.8× 211 0.9× 167 0.9× 177 1.0× 25 757
Andreas Bickel Germany 15 697 1.4× 91 0.4× 197 0.8× 203 1.1× 119 0.7× 28 1.4k
Sonia K. Bhangoo United States 9 940 1.8× 119 0.5× 74 0.3× 689 3.8× 233 1.3× 10 1.5k
Anna P. Malykhina United States 21 287 0.6× 53 0.2× 324 1.4× 204 1.1× 308 1.7× 70 1.4k
Lintao Qu United States 17 421 0.8× 49 0.2× 185 0.8× 294 1.6× 262 1.4× 34 1.2k
Jie Su Sweden 14 256 0.5× 78 0.3× 211 0.9× 123 0.7× 205 1.1× 31 804
Steven G. Shimada United States 19 563 1.1× 58 0.2× 319 1.4× 218 1.2× 174 1.0× 38 1.4k

Countries citing papers authored by Gabriel Natura

Since Specialization
Citations

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

Fields of papers citing papers by Gabriel Natura

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gabriel Natura. 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 Gabriel Natura. The network helps show where Gabriel Natura may publish in the future.

Co-authorship network of co-authors of Gabriel Natura

This figure shows the co-authorship network connecting the top 25 collaborators of Gabriel Natura. A scholar is included among the top collaborators of Gabriel Natura 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 Gabriel Natura. Gabriel Natura is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Vázquez, Enrique, Frank Richter, Gabriel Natura, et al.. (2024). Direct Effects of the Janus Kinase Inhibitor Baricitinib on Sensory Neurons. International Journal of Molecular Sciences. 25(22). 11943–11943. 2 indexed citations
2.
Natura, Gabriel, Enrique Vázquez, Frank Richter, et al.. (2024). Antinociceptive interactions between excitatory interferon-γ and interleukin-17 in sensory neurons. Brain Behavior and Immunity. 124. 55–73. 4 indexed citations
3.
Ebbinghaus, Matthias, Gabriel Natura, Gisela Segond von Banchet, et al.. (2017). Interleukin-17A is involved in mechanical hyperalgesia but not in the severity of murine antigen-induced arthritis. Scientific Reports. 7(1). 10334–10334. 40 indexed citations
4.
Natura, Gabriel, Karl‐Jürgen Bär, Annett Eitner, et al.. (2013). Neuronal prostaglandin E 2 receptor subtype EP3 mediates antinociception during inflammation. Proceedings of the National Academy of Sciences. 110(33). 13648–13653. 48 indexed citations
5.
Richter, Frank, Gabriel Natura, Matthias Ebbinghaus, et al.. (2012). Interleukin‐17 sensitizes joint nociceptors to mechanical stimuli and contributes to arthritic pain through neuronal interleukin‐17 receptors in rodents. Arthritis & Rheumatism. 64(12). 4125–4134. 102 indexed citations
6.
Schaible, Hans‐Georg, Andrea Ebersberger, & Gabriel Natura. (2011). Update on peripheral mechanisms of pain: beyond prostaglandins and cytokines. Arthritis Research & Therapy. 13(2). 210–210. 107 indexed citations
7.
Ebersberger, Andrea, et al.. (2011). Effects of prostaglandin D2 on tetrodotoxin-resistant Na+ currents in DRG neurons of adult rat. Pain. 152(5). 1114–1126. 27 indexed citations
8.
Richter, Frank, et al.. (2010). Tumor necrosis factor causes persistent sensitization of joint nociceptors to mechanical stimuli in rats. Arthritis & Rheumatism. 62(12). 3806–3814. 107 indexed citations
9.
Banchet, Gisela Segond von, Michael Karl Boettger, Rolf Bräuer, et al.. (2010). The role of proinflammatory cytokines in the generation and maintenance of joint pain. Annals of the New York Academy of Sciences. 1193(1). 60–69. 157 indexed citations
10.
Schaible, Hans‐Georg, Frank Richter, Andrea Ebersberger, et al.. (2009). Joint pain. Experimental Brain Research. 196(1). 153–162. 164 indexed citations
11.
Natura, Gabriel, et al.. (2008). Functional consequences of leucine and tyrosine mutations in the dual pore motifs of the yeast K+ channel, Tok1p. Pflügers Archiv - European Journal of Physiology. 456(5). 883–896. 6 indexed citations
12.
Natura, Gabriel, et al.. (2005). In the yeast potassium channel, Tok1p, the external ring of aspartate residues modulates both gating and conductance*. Pflügers Archiv - European Journal of Physiology. 451(2). 362–370. 5 indexed citations
13.
Natura, Gabriel, Gisela Segond von Banchet, & Hans‐Georg Schaible. (2005). Calcitonin gene-related peptide enhances TTX-resistant sodium currents in cultured dorsal root ganglion neurons from adult rats. Pain. 116(3). 194–204. 60 indexed citations
14.
Porée, Fabien, Armando Carpaneto, Gabriel Natura, et al.. (2005). Plant Kin and Kout channels: Approaching the trait of opposite rectification by analyzing more than 250 KAT1–SKOR chimeras. Biochemical and Biophysical Research Communications. 332(2). 465–473. 28 indexed citations
15.
16.
Saalbach, Gerhard, et al.. (1999). The  -subunit of a heterotrimeric G-protein from tobacco, NtGP 1, functions in K+ channel regulation in mesophyll cells. Journal of Experimental Botany. 50(330). 53–61. 2 indexed citations
17.
Natura, Gabriel & I. Dahse. (1998). Potassium conductance of Egeria leaf cell protoplasts: Regulation by nedium pH, phosphorylation and G-proteins. Journal of Plant Physiology. 153(3-4). 363–370. 2 indexed citations
18.
Saalbach, Gerhard, et al.. (1997). Over‐expression of plant 14‐3‐3 proteins in tobacco: enhancement of the plasmalemma K+ conductance of mesophyll cells12. FEBS Letters. 413(2). 294–298. 37 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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