OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Dynamic Regulation of the Mitochondrial Proton Gradient during Cytosolic Calcium Elevations
Damon Poburko, Jaime Santo‐Domingo, Nicolas Demaurex
Journal of Biological Chemistry (2011) Vol. 286, Iss. 13, pp. 11672-11684
Open Access | Times Cited: 305

Showing 1-25 of 305 citing articles:

Distinct fission signatures predict mitochondrial degradation or biogenesis
Tatjana Kleele, Timo Rey, Julius Winter, et al.
Nature (2021) Vol. 593, Iss. 7859, pp. 435-439
Open Access | Times Cited: 536

MICU1 Controls Both the Threshold and Cooperative Activation of the Mitochondrial Ca2+ Uniporter
György Csordás, Tünde Golenár, Erin L. Seifert, et al.
Cell Metabolism (2013) Vol. 17, Iss. 6, pp. 976-987
Open Access | Times Cited: 453

Genetically Encoded Fluorescent Biosensors Illuminate the Spatiotemporal Regulation of Signaling Networks
Eric C. Greenwald, Sohum Mehta, Jin Zhang
Chemical Reviews (2018) Vol. 118, Iss. 24, pp. 11707-11794
Open Access | Times Cited: 447

Imaging intraorganellar Ca2+ at subcellular resolution using CEPIA
Junji Suzuki, Kazunori Kanemaru, Kuniaki Ishii, et al.
Nature Communications (2014) Vol. 5, Iss. 1
Open Access | Times Cited: 443

Optogenetic Tools for Subcellular Applications in Neuroscience
Benjamin R. Rost, Franziska Schneider‐Warme, Dietmar Schmitz, et al.
Neuron (2017) Vol. 96, Iss. 3, pp. 572-603
Open Access | Times Cited: 303

Ultrasensitive Genetically Encoded Indicator for Hydrogen Peroxide Identifies Roles for the Oxidant in Cell Migration and Mitochondrial Function
Valeriy V. Pak, Daria Ezeriņa, O. G. Lyublinskaya, et al.
Cell Metabolism (2020) Vol. 31, Iss. 3, pp. 642-653.e6
Open Access | Times Cited: 300

Redox Signaling by Reactive Electrophiles and Oxidants
Saba Parvez, Marcus J. C. Long, Jesse R. Poganik, et al.
Chemical Reviews (2018) Vol. 118, Iss. 18, pp. 8798-8888
Open Access | Times Cited: 297

Mitochondrial Sirtuin Network Reveals Dynamic SIRT3-Dependent Deacetylation in Response to Membrane Depolarization
Wen Yang, Koji Nagasawa, Christian Münch, et al.
Cell (2016) Vol. 167, Iss. 4, pp. 985-1000.e21
Open Access | Times Cited: 293

Redox Nanodomains Are Induced by and Control Calcium Signaling at the ER-Mitochondrial Interface
David M. Booth, Balázs Enyedi, Miklós Geiszt, et al.
Molecular Cell (2016) Vol. 63, Iss. 2, pp. 240-248
Open Access | Times Cited: 264

Red fluorescent genetically encoded indicator for intracellular hydrogen peroxide
Yulia G. Ermakova, Dmitry S. Bilan, Mikhail E. Matlashov, et al.
Nature Communications (2014) Vol. 5, Iss. 1
Open Access | Times Cited: 238

Quantifying ROS levels using CM-H 2 DCFDA and HyPer
Monika Oparka, Jarosław Walczak, Dominika Malińska, et al.
Methods (2016) Vol. 109, pp. 3-11
Closed Access | Times Cited: 179

The redox language in neurodegenerative diseases: oxidative post-translational modifications by hydrogen peroxide
Yew Mun Lee, Weifeng He, Yih‐Cherng Liou
Cell Death and Disease (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 112

Calcium Overload and Mitochondrial Metabolism
Lauren L. Walkon, Jasiel O. Strubbe, Jason N. Bazil
Biomolecules (2022) Vol. 12, Iss. 12, pp. 1891-1891
Open Access | Times Cited: 87

Quantitative measurement of mitochondrial membrane potential in cultured cells: calcium-induced de- and hyperpolarization of neuronal mitochondria
Akos A. Gerencser, Christos Chinopoulos, Matthew J. Birket, et al.
The Journal of Physiology (2012) Vol. 590, Iss. 12, pp. 2845-2871
Open Access | Times Cited: 201

The renaissance of mitochondrial pH
Jaime Santo‐Domingo, Nicolas Demaurex
The Journal of General Physiology (2012) Vol. 139, Iss. 6, pp. 415-423
Open Access | Times Cited: 201

Genetically encoded fluorescent redox sensors
Konstantin A. Lukyanov, Vsevolod V. Belousov
Biochimica et Biophysica Acta (BBA) - General Subjects (2013) Vol. 1840, Iss. 2, pp. 745-756
Closed Access | Times Cited: 190

Reactive oxygen species and redox compartmentalization
Nina Kaludercic, Soni Deshwal, Fabio Di Lisa
Frontiers in Physiology (2014) Vol. 5
Open Access | Times Cited: 174

Mitochondrial Energy and Redox Signaling in Plants
Markus Schwarzländer, Iris Finkemeier
Antioxidants and Redox Signaling (2012) Vol. 18, Iss. 16, pp. 2122-2144
Open Access | Times Cited: 164

Guidelines on experimental methods to assess mitochondrial dysfunction in cellular models of neurodegenerative diseases
Niamh M. C. Connolly, Pierre Theurey, Vera Ádám‐Vizi, et al.
Cell Death and Differentiation (2017) Vol. 25, Iss. 3, pp. 542-572
Open Access | Times Cited: 158

Endoplasmic reticulum: Reduced and oxidized glutathione revisited
Julia Birk, Mariangela Meyer, Isabel Aller, et al.
Journal of Cell Science (2013)
Open Access | Times Cited: 155

Multiparametric optical analysis of mitochondrial redox signals during neuronal physiology and pathology in vivo
Michael O. Breckwoldt, Franz Pfister, Peter Bradley, et al.
Nature Medicine (2014) Vol. 20, Iss. 5, pp. 555-560
Closed Access | Times Cited: 153

NCLX: The mitochondrial sodium calcium exchanger
Liron Boyman, George S.B. Williams, Daniel Khananshvili, et al.
Journal of Molecular and Cellular Cardiology (2013) Vol. 59, pp. 205-213
Open Access | Times Cited: 148

Imaging ROS signaling in cells and animals
Xianhua Wang, Huaqiang Fang, Zhanglong Huang, et al.
Journal of Molecular Medicine (2013) Vol. 91, Iss. 8, pp. 917-927
Open Access | Times Cited: 145

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