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Cell Metabolism Under Microenvironmental Low Oxygen Tension Levels in Stemness, Proliferation and Pluripotency

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Acute hypoxia to endothelial cells induces activating transcription factor 3 (ATF3) expression that is mediated via nitric oxide

Chen, S.-C., Liu, Y., Shyu, K., & Wang, D. L. (2008) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2008.02.014 · Cited by 43 · see citing works

Placenta growth factor induces 5-lipoxygenase–activating protein to increase leukotriene formation in sickle cell disease

Patel, N. N., Gonsalves, C. S., Yang, M., Malik, P., & Kalra, V. K. (2008) · Blood · doi:10.1182/blood-2008-07-169821 · Cited by 43 · see citing works

The toxic mechanism and bioactive components of Chinese leek root exudates acting against Fusarium oxysporum f. sp. cubense tropical race 4

Zuo, C., Li, C., Li, B., Wei, Y., Hu, C., Yang, Q., Yang, J., Sheng, O., Kuang, R., Deng, G., et al. (2015) · European Journal of Plant Pathology · doi:10.1007/s10658-015-0697-5 · Cited by 42 · see citing works

Characterization of Jumping translocation breakpoint (JTB) gene product isolated as a TGF-β1-inducible clone involved in regulation of mitochondrial function, cell growth and cell death

Kanome, T., Itoh, N., Ishikawa, F., Mori, K., Kim‐Kaneyama, J., Nose, K., & Shibanuma, M. (2007) · Oncogene · doi:10.1038/sj.onc.1210423 · Cited by 38 · see citing works

Nitric oxide, interorganelle communication, and energy flow: a novel route to slow aging

Valerio, A., & Nisoli, E. (2015) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2015.00006 · Cited by 37 · see citing works

Prolyl hydroxylase domain enzymes and their role in cell signaling and cancer metabolism

Nguyen, T.-L., & Durán, R. V. (2016) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2016.09.026 · Cited by 37 · see citing works

Redox modification of proteins as essential mediators of CNS autophagy and mitophagy

Lizama, B. N., & McLaughlin, B. (2013) · FEBS Letters · doi:10.1016/j.febslet.2013.06.007 · Cited by 37 · see citing works

Protective conditioning of the brain: expressway or roadblock?

Mergenthaler, P., & Dirnagl, U. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2011.209718 · Cited by 35 · see citing works

Biological mechanisms and clinical significance of endoplasmic reticulum oxidoreductase 1 alpha (ERO1α) in human cancer

Chen, P., Sharma, A., Weiher, H., & Schmidt‐Wolf, I. G. H. (2024) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-024-02990-4 · Cited by 37 · see citing works

A novel 4‐mRNA signature predicts the overall survival in acute myeloid leukemia

Chen, Z., Song, J., Wang, W., Bai, J., Zhang, Y., Shi, J., Bai, J., & Zhou, Y. (2021) · American Journal of Hematology · doi:10.1002/ajh.26309 · Cited by 35 · see citing works

Multimodal polymer encapsulated CdSe/Fe3O4 nanoplatform with improved biocompatibility for two-photon and temperature stimulated bioapplications

Antoniak, M. A., Pązik, R., Bazylińska, U., Wiwatowski, K., Tomaszewska, A., Kulpa-Greszta, M., Adamczyk‐Grochala, J., Wnuk, M., Maćkowski, S., Lewińska, A., et al. (2021) · Materials Science and Engineering C · doi:10.1016/j.msec.2021.112224 · Cited by 31 · see citing works

Hypoxia Increases β-Cell Death by Activating Pancreatic Stellate Cells within the Islet

Kim, J. J., Lee, E., Ryu, G. R., Ko, S., Ahn, Y., & Song, K. (2020) · Diabetes & Metabolism Journal · doi:10.4093/dmj.2019.0181 · Cited by 29 · see citing works

Prolyl Hydroxylase Inhibition During Hyperoxia Prevents Oxygen-Induced Retinopathy in the Rat 50/10 Model

Trichonas, G., Lee, T. J., Hoppe, G., Au, J. D., & Sears, J. E. (2013) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.13-12171 · Cited by 30 · see citing works

Hipoxia tumoral. Papel del factor inducible por hipoxia

Fraga, A. M., Ribeiro, R. J. T., & Medeiros, R. (2009) · Actas Urológicas Españolas · doi:10.1016/s0210-4806(09)72891-8 · Cited by 37 · see citing works

Fibrillin-1-regulated miR-122 has a critical role in thoracic aortic aneurysm formation

Zhang, R., Tiedemann, K., Muthu, M. L., Dinesh, N. E. H., Komarova, S. V., Ramkhelawon, B., & Reinhardt, D. P. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04337-8 · Cited by 28 · see citing works

In Vivo Hypoxia PET Imaging Quantifies the Severity of Arthritic Joint Inflammation in Line with Overexpression of Hypoxia-Inducible Factor and Enhanced Reactive Oxygen Species Generation

Fuchs, K., Kuehn, A., Mahling, M., Guenthoer, P., Hector, A., Schwenck, J., Hartl, D., Laufer, S., Kohlhofer, U., Quintanilla‐Martínez, L., et al. (2017) · Journal of Nuclear Medicine · doi:10.2967/jnumed.116.185934 · Cited by 28 · see citing works

Engineering nanomedicines to inhibit hypoxia-inducible Factor-1 for cancer therapy

Zhang, X., He, C., & Xiang, G. (2022) · Cancer Letters · doi:10.1016/j.canlet.2022.01.012 · Cited by 28 · see citing works

pVHL interacts with Ceramide kinase like (CERKL) protein and ubiquitinates it for oxygen dependent proteasomal degradation

Chen, J., Liu, F., Li, H., Archacki, S. R., Gao, M., Liu, Y., Liao, S., Huang, M. N., Wang, J., Yu, S., et al. (2015) · Cellular Signalling · doi:10.1016/j.cellsig.2015.08.011 · Cited by 25 · see citing works

Advances in polyphenol-based carbon dots for biomedical engineering applications

Han, J., Hong, J., Lee, H., Choi, S., Shin, K., Gu, M., & Kim, S. (2023) · European Polymer Journal · doi:10.1016/j.eurpolymj.2023.112354 · Cited by 25 · see citing works

Reactive oxygen species and cellular oxygen sensing

Cash, T. P., Pan, Y., & Simon, M. C. (2007) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2007.07.001 · Cited by 186 · see citing works

Mitochondrial oxygen sensing: regulation of hypoxia-inducible factor by mitochondrial generated reactive oxygen species

Bell, E. L., & Chandel, N. S. (2007) · Essays in Biochemistry · doi:10.1042/bse0430017 · Cited by 90 · see citing works

Reactive oxygen species: important regulators of the oxygen sensing pathway

Wenner, J., Plate, K. H., & Acker, T. (2006) · Aktuelle Neurologie · doi:10.1055/s-2006-953496

Oxygen sensing requires mitochondrial ROS but not oxidative phosphorylation

Brunelle, J. K., Bell, E. L., Quesada, N. M., Vercauteren, K., Tiranti, V., Zeviani, M., Scarpulla, R. C., & Chandel, N. S. (2005) · Cell Metabolism · doi:10.1016/j.cmet.2005.05.002 · Cited by 763 · see citing works

Reactive oxygen species in the control of hypoxia-inducible factor-mediated gene expression

Kietzmann, T., & Görlach, A. (2005) · Seminars in Cell &amp; Developmental Biology · doi:10.1016/j.semcdb.2005.03.010 · Cited by 295 · see citing works