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:

Enhanced Cancer Metastasis in Mice Deficient in Vasohibin-1 Gene
Soichi Ito, Hiroki Miyashita, Yasuhiro Suzuki, et al.
PLoS ONE (2013) Vol. 8, Iss. 9, pp. e73931-e73931
Open Access | Times Cited: 25

Showing 25 citing articles:

RETRACTED ARTICLE: N6-methyladenosine induced miR-143-3p promotes the brain metastasis of lung cancer via regulation of VASH1
Hongsheng Wang, Qianqian Deng, Ziyan Lv, et al.
Molecular Cancer (2019) Vol. 18, Iss. 1
Open Access | Times Cited: 204

Pericytes, an overlooked player in vascular pathobiology
David Ferland-McCollough, Sadie C. Slater, J. Stanton Richard, et al.
Pharmacology & Therapeutics (2016) Vol. 171, pp. 30-42
Open Access | Times Cited: 199

Cervical squamous cell carcinoma-secreted exosomal miR-221-3p promotes lymphangiogenesis and lymphatic metastasis by targeting VASH1
Chenfei Zhou, Jing Ma, Lei Huang, et al.
Oncogene (2018) Vol. 38, Iss. 8, pp. 1256-1268
Open Access | Times Cited: 195

The interplay of immunology and cachexia in infection and cancer
Hatoon Baazim, Laura Antonio-Herrera, Andreas Bergthaler
Nature reviews. Immunology (2021) Vol. 22, Iss. 5, pp. 309-321
Open Access | Times Cited: 123

Experimental cancer cachexia: Evolving strategies for getting closer to the human scenario
Fabio Penna, Sı́lvia Busquets, Josep M. Argilés
Seminars in Cell and Developmental Biology (2015) Vol. 54, pp. 20-27
Open Access | Times Cited: 65

DLG5 in Cell Polarity Maintenance and Cancer Development
Jie Liu, Juan Li, Yu Ren, et al.
International Journal of Biological Sciences (2014) Vol. 10, Iss. 5, pp. 543-549
Open Access | Times Cited: 46

Vasohibins: new transglutaminase-like cysteine proteases possessing a non-canonical Cys-His-Ser catalytic triad
Luis Sánchez‐Pulido, Chris P. Ponting
Bioinformatics (2016) Vol. 32, Iss. 10, pp. 1441-1445
Open Access | Times Cited: 40

Age‐associated downregulation of vasohibin‐1 in vascular endothelial cells
Eichi Takeda, Yasuhiro Suzuki, Yasufumi Sato
Aging Cell (2016) Vol. 15, Iss. 5, pp. 885-892
Open Access | Times Cited: 27

Vasohibin-1 expression detected by immunohistochemistry correlates with prognosis in non-small cell lung cancer
Tao Zhang, Tingting Yu, Dongming Zhang, et al.
Medical Oncology (2014) Vol. 31, Iss. 5
Closed Access | Times Cited: 25

Vasohibin-1 suppresses colon cancer
Shuai Liu, Bing Han, Qunyuan Zhang, et al.
Oncotarget (2015) Vol. 6, Iss. 10, pp. 7880-7898
Open Access | Times Cited: 24

Novel Link between Inhibition of Angiogenesis and Tolerance to Vascular Stress
Yasufumi Sato
Journal of Atherosclerosis and Thrombosis (2015) Vol. 22, Iss. 4, pp. 327-334
Open Access | Times Cited: 17

Renal tubular injury exacerbated by vasohibin-1 deficiency in a murine cisplatin-induced acute kidney injury model
Satoshi Tanimura, Katsuyuki Tanabe, H Miyake, et al.
AJP Renal Physiology (2019) Vol. 317, Iss. 2, pp. F264-F274
Open Access | Times Cited: 17

Tubulin carboxypeptidase activity of vasohibin-1 inhibits angiogenesis by interfering with endocytosis and trafficking of pro-angiogenic factor receptors
Miho Kobayashi, Ikumi Wakabayashi, Yasuhiro Suzuki, et al.
Angiogenesis (2020) Vol. 24, Iss. 1, pp. 159-176
Closed Access | Times Cited: 16

High preoperative plasma vasohibin‐1 concentration predicts better prognosis in patients with non–small cell lung carcinoma
Tatsuaki Watanabe, Tomoko Hosaka, Kaori Ohmori‐Matsuda, et al.
Health Science Reports (2018) Vol. 1, Iss. 6
Open Access | Times Cited: 12

Vasohibin-1 rescues erectile function through up-regulation of angiogenic factors in the diabetic mice
Kang‐Moon Song, Woo Jean Kim, Min Ji Choi, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 9

Mechanism of ELL-associated factor 2 and vasohibin 1 regulating invasion, migration, and angiogenesis in colorectal cancer
Mingliang Feng, Ming-Jun Sun, Boyang Xu, et al.
World Journal of Gastroenterology (2023) Vol. 29, Iss. 24, pp. 3770-3792
Open Access | Times Cited: 3

Development of a Novel and Simple Anti-Metastatic Cancer Treatment Targeting Vasohibin-2
Eun‐Seo Lee, Yasuhiro Suzuki, H. Tomioka, et al.
The Tohoku Journal of Experimental Medicine (2023) Vol. 261, Iss. 3, pp. 239-247
Open Access | Times Cited: 2

MicroRNA-10 Family Promotes Renal Fibrosis through the VASH-1/Smad3 Pathway
Yichen Shuai, Na Xu, Chuan Zhao, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 10, pp. 5232-5232
Open Access

Novel Targeted Therapies for Patients with Ovarian Cancer
Samir A. Farghaly
Journal of Cancer Science & Therapy (2014) Vol. 06, Iss. 11
Open Access | Times Cited: 1

Longitudinal transcriptome analysis of cattle infected with Theileria parva
M. Chepkwony, David Wragg, Perle Latré de Laté, et al.
International Journal for Parasitology (2022) Vol. 52, Iss. 13-14, pp. 799-813
Open Access | Times Cited: 1

Angiogenesis in Liver Cancer
Arthur Zimmermann
Springer eBooks (2016), pp. 1-29
Closed Access

Novel Molecular Basis for Vascular Health Regulated by Vasohibin-1
Yasufumi Sato
Journal of Lipid and Atherosclerosis (2016) Vol. 5, Iss. 2, pp. 107-107
Open Access

Determining the Vasohibin-1 Levels of the Serum and Broncoalveolar Lavage Fluid in the Patients with Lung Cancer”
Alev Lazoğlu Özkaya, Mevlüt Sait Keleş, Esra Laloğlu, et al.
Konuralp Tıp Dergisi (2022) Vol. 14, Iss. 2, pp. 298-303
Open Access

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