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:

Mouse model of ischemic acute kidney injury: technical notes and tricks
Qingqing Wei, Zheng Dong
AJP Renal Physiology (2012) Vol. 303, Iss. 11, pp. F1487-F1494
Open Access | Times Cited: 266

Showing 1-25 of 266 citing articles:

Non-Transgenic Mouse Models of Kidney Disease
Michael Rabe, Franz Schaefer
˜The œNephron journals/Nephron journals (2016) Vol. 133, Iss. 1, pp. 53-61
Open Access | Times Cited: 1880

Cellular and molecular mechanisms of kidney fibrosis
Sonja Djudjaj, Peter Boor
Molecular Aspects of Medicine (2018) Vol. 65, pp. 16-36
Closed Access | Times Cited: 379

PINK1-PRKN/PARK2 pathway of mitophagy is activated to protect against renal ischemia-reperfusion injury
Chengyuan Tang, Hailong Han, Mingjuan Yan, et al.
Autophagy (2017) Vol. 14, Iss. 5, pp. 880-897
Open Access | Times Cited: 249

Sustained Activation of Wnt/β-Catenin Signaling Drives AKI to CKD Progression
Liangxiang Xiao, Dong Zhou, Roderick J. Tan, et al.
Journal of the American Society of Nephrology (2015) Vol. 27, Iss. 6, pp. 1727-1740
Open Access | Times Cited: 213

Rodent models of AKI-CKD transition
Ying Fu, Chengyuan Tang, Juan Cai, et al.
AJP Renal Physiology (2018) Vol. 315, Iss. 4, pp. F1098-F1106
Open Access | Times Cited: 206

Pharmacologic ATF6 activation confers global protection in widespread disease models by reprograming cellular proteostasis
Erik A. Blackwood, Khalid Azizi, Donna J. Thuerauf, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 172

Hyperglycemia, p53, and mitochondrial pathway of apoptosis are involved in the susceptibility of diabetic models to ischemic acute kidney injury
Jianping Peng, Xiaoning Li, Dongshan Zhang, et al.
Kidney International (2014) Vol. 87, Iss. 1, pp. 137-150
Open Access | Times Cited: 169

Unilateral Renal Ischemia-Reperfusion as a Robust Model for Acute to Chronic Kidney Injury in Mice
Nathalie Le Clef, Anja Verhulst, Patrick C. D’Haese, et al.
PLoS ONE (2016) Vol. 11, Iss. 3, pp. e0152153-e0152153
Open Access | Times Cited: 151

Tubular GM-CSF Promotes Late MCP-1/CCR2-Mediated Fibrosis and Inflammation after Ischemia/Reperfusion Injury
Leyuan Xu, Diana Sharkey, Lloyd G. Cantley
Journal of the American Society of Nephrology (2019) Vol. 30, Iss. 10, pp. 1825-1840
Open Access | Times Cited: 134

Sonic Hedgehog Is a Novel Tubule-Derived Growth Factor for Interstitial Fibroblasts after Kidney Injury
Dong Zhou, Yingjian Li, Lili Zhou, et al.
Journal of the American Society of Nephrology (2014) Vol. 25, Iss. 10, pp. 2187-2200
Open Access | Times Cited: 131

Changes in Metabolic Profiles during Acute Kidney Injury and Recovery following Ischemia/Reperfusion
Qingqing Wei, Xiao Xiao, Paul Fogle, et al.
PLoS ONE (2014) Vol. 9, Iss. 9, pp. e106647-e106647
Open Access | Times Cited: 128

Renal ischemia/reperfusion injury: An insight on in vitro and in vivo models
Niharika Shiva, Nisha Sharma, Yogesh A. Kulkarni, et al.
Life Sciences (2020) Vol. 256, pp. 117860-117860
Closed Access | Times Cited: 122

应用动物模型探索肾脏疾病作用机制和潜在治疗靶点
Yin-Wu Bao, Yuan Yuan, Jianghua Chen, et al.
动物学研究 (2018) Vol. 39, Iss. 2, pp. 72-86
Open Access | Times Cited: 113

Immune cell landscaping reveals a protective role for regulatory T cells during kidney injury and fibrosis
Fernanda do Valle Durães, Armelle Lafont, Martin Beibel, et al.
JCI Insight (2020) Vol. 5, Iss. 3
Open Access | Times Cited: 111

Caspase-3 Is a Pivotal Regulator of Microvascular Rarefaction and Renal Fibrosis after Ischemia-Reperfusion Injury
Bing Yang, Shanshan Lan, Mélanie Dieudé, et al.
Journal of the American Society of Nephrology (2018) Vol. 29, Iss. 7, pp. 1900-1916
Open Access | Times Cited: 110

MicroRNA-687 Induced by Hypoxia-Inducible Factor-1 Targets Phosphatase and Tensin Homolog in Renal Ischemia-Reperfusion Injury
Kirti Bhatt, Qingqing Wei, Navjotsingh Pabla, et al.
Journal of the American Society of Nephrology (2015) Vol. 26, Iss. 7, pp. 1588-1596
Open Access | Times Cited: 108

OMA1 mediates OPA1 proteolysis and mitochondrial fragmentation in experimental models of ischemic kidney injury
Xiao Xiao, Yanzhong Hu, Pedro M. Quirós, et al.
AJP Renal Physiology (2014) Vol. 306, Iss. 11, pp. F1318-F1326
Open Access | Times Cited: 106

Whole-transcriptome analysis of UUO mouse model of renal fibrosis reveals new molecular players in kidney diseases
Eleni Arvaniti, Panagiotis Moulos, Athina Vakrakou, et al.
Scientific Reports (2016) Vol. 6, Iss. 1
Open Access | Times Cited: 104

Renal Ischaemia Reperfusion Injury: A Mouse Model of Injury and Regeneration
Emily E. Hesketh, Alicja Czopek, Michael Clay, et al.
Journal of Visualized Experiments (2014), Iss. 88
Open Access | Times Cited: 101

Dephosphorylation of AMP-activated protein kinase exacerbates ischemia/reperfusion-induced acute kidney injury via mitochondrial dysfunction
Haijian Ma, Xiaozhen Guo, Shichao Cui, et al.
Kidney International (2021) Vol. 101, Iss. 2, pp. 315-330
Open Access | Times Cited: 98

Progranulin protects against renal ischemia/reperfusion injury in mice
Meng Zhou, Wei Tang, Yi Fu, et al.
Kidney International (2015) Vol. 87, Iss. 5, pp. 918-929
Open Access | Times Cited: 93

Folic acid‐induced animal model of kidney disease
Liang‐Jun Yan
Animal Models and Experimental Medicine (2021) Vol. 4, Iss. 4, pp. 329-342
Open Access | Times Cited: 88

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