The biology of hypoxia: the role of oxygen sensing in development, normal function, and disease

Targeting HIF-1 for cancer therapy

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The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis

Maxwell, P. H., Wiesener, M. S., Chang, G.-W., Clifford, S. C., Vaux, E. C., Cockman, M. E., Wykoff, C. C., Pugh, C. W., Maher, E. R., & Ratcliffe, P. J. (1999) · Nature · doi:10.1038/20459 · Cited by 5,180

Exploiting tumour hypoxia in cancer treatment

Brown, J. M., & Wilson, W. R. (2004) · Nature Reviews Cancer · doi:10.1038/nrc1367 · Cited by 2,828

Purification and Characterization of Hypoxia-inducible Factor 1

Wang, G. L., & Semenza, G. L. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.3.1230 · Cited by 2,094

Oxygen sensing by HIF hydroxylases

Schofield, C. J., & Ratcliffe, P. J. (2004) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1366 · Cited by 2,068

The CBP co-activator is a histone acetyltransferase

Bannister, A. J., & Kouzarides, T. (1996) · Nature · doi:10.1038/384641a0 · Cited by 1,828

Tumor Response to Radiotherapy Regulated by Endothelial Cell Apoptosis

Garcı́a-Barros, M., Paris, F., Cordon‐Cardo, C., Lyden, D. C., Rafii, S., Haimovitz‐Friedman, A., FUKS, Z. Y., & Kolesnick, R. (2003) · Science · doi:10.1126/science.1082504 · Cited by 1,591

Ubiquitination of hypoxia-inducible factor requires direct binding to the β-domain of the von Hippel–Lindau protein

Ohh, M., Park, C. W., Ivan, M., Hoffman, M. A., Kim, T.-Y., Huang, L. E., Pavletich, N., Chau, V., & Kaelin, W. G. (2000) · Nature Cell Biology · doi:10.1038/35017054 · Cited by 1,577

Asparagine Hydroxylation of the HIF Transactivation Domain: A Hypoxic Switch

Lando, D., Peet, D. J., Whelan, D. A., Gorman, J. J., & Whitelaw, M. L. (2002) · Science · doi:10.1126/science.1068592 · Cited by 1,558

FIH-1 is an asparaginyl hydroxylase enzyme that regulates the transcriptional activity of hypoxia-inducible factor

Lando, D., Peet, D. J., Gorman, J. J., Whelan, D. A., Whitelaw, M. L., & Bruick, R. K. (2002) · Genes & Development · doi:10.1101/gad.991402 · Cited by 1,550

Emerging paradigms and questions on pro-angiogenic bone marrow-derived myelomonocytic cells

Laurent, J., Touvrey, C., Botta, F., Kuonen, F., & Rüegg, C. (2011) · The International Journal of Developmental Biology · doi:10.1387/ijdb.103228jl · Cited by 21

Kinetics of oxygen uptake by cells potentially used in a tissue engineered trachea

Curcio, E., Piscioneri, A., Morelli, S., Salerno, S., Macchiarini, P., & Bartolo, L. D. (2014) · Biomaterials · doi:10.1016/j.biomaterials.2014.04.100 · Cited by 21

Hypoxia-based strategies for regenerative dentistry—Views from the different dental fields

Müller, A. S., Janjić, K., Lilaj, B., Edelmayer, M., & Agis, H. (2017) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2017.04.029 · Cited by 20

The Toxicity of Iodinated Radiographic Contrast Agents in the Clinical Practice

Andreucci, M., Faga, T., Sarro, G. D., & Michael, A. (2015) · Journal Of Nephrology Advances · doi:10.14302/issn.2574-4488.jna-14-601 · Cited by 20

Myocardial Adaptation in Pseudohypoxia: Signaling and Regulation of mPTP via Mitochondrial Connexin 43 and Cardiolipin

Ferko, M., Andelová, N., Bačová, B. S., & Jasova, M. (2019) · Cells · doi:10.3390/cells8111449 · Cited by 19

HIF-1α and growth plate development: what we really know

Schipani, E., Mangiavini, L., & Merceron, C. (2015) · BoneKEy Reports · doi:10.1038/bonekey.2015.99 · Cited by 21

Chronic hypoxia upregulates adenosine 2a receptor expression in chromaffin cells via hypoxia inducible factor-2α: Role in modulating secretion

Brown, S. T., Reyes, E. P., & Nurse, C. A. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2011.07.122 · Cited by 20

Drosophila dMRP4regulates responsiveness to O2deprivation and development under hypoxia

Huang, H., & Haddad, G. G. (2007) · Physiological Genomics · doi:10.1152/physiolgenomics.00166.2006 · Cited by 20

Very low oxygen concentration (0.1%) reveals two FDCP-Mix cell subpopulations that differ by their cell cycling, differentiation and p27KIP1 expression

Guitart, A. V., Debeissat, C., Hermitte, F., Villacreces, A., Ivanović, Z., Bœuf, H., & Praloran, V. (2010) · Cell Death and Differentiation · doi:10.1038/cdd.2010.85 · Cited by 20

Expression of hypoxia-inducible factor-1alpha (HIF-1alpha) related to oxidative stress in liver of rat-induced by systemic chronic normobaric hypoxia.

Jusman, S. W. A., Halim, A., Wanandi, S. I., & Sadikin, M. (2010) · PubMed · Cited by 20

Differential Expression of Transcription Factors and Inflammation-, ROS-, and Cell Death-Related Genes in Organotypic Cultures in the Modiolus, the Organ of Corti and the Stria Vascularis of Newborn Rats

Gross, J., Olze, H., & Mazurek, B. (2014) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-014-0036-y · Cited by 19

A Genetically Encoded FRET Sensor for Hypoxia and Prolyl Hydroxylases

Youssef, S., Ren, W., & Ai, H. (2016) · ACS Chemical Biology · doi:10.1021/acschembio.6b00330 · Cited by 19

MicroRNA regulation in hypoxic environments: differential expression of microRNAs in the liver of largemouth bass (Micropterus salmoides)

Sun, J., Zhao, L., He, K., Liu, Q., Luo, J., Zhang, D. M., Liang, J., Liao, L., Ma, J. D., & Yang, S. Y. (2020) · Fish Physiology and Biochemistry · doi:10.1007/s10695-020-00877-7 · Cited by 19

Molecular expression and functional activity of efflux and influx transporters in hypoxia induced retinal pigment epithelial cells

Vadlapatla, R. K., Vadlapudi, A. D., Ponnaluri, V. K. C., Pal, D., Mukherji, M., & Mitra, A. K. (2013) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2013.06.044 · Cited by 19

Shiga Toxin-Producing Escherichia coli Infections during Pregnancy

Sacerdoti, F., Scalise, M. L., Burdet, J., Amaral, M. M., Franchi, A. M., & Ibarra, C. (2018) · Microorganisms · doi:10.3390/microorganisms6040111 · Cited by 19

Deletion of a subgroup of ribosome-related genes minimizes hypoxia-induced changes and confers hypoxia tolerance

Shah, A. N., Cadinu, D., Henke, R. M., Xin, X., Dastidar, R. G., & Li, Z. (2011) · Physiological Genomics · doi:10.1152/physiolgenomics.00232.2010 · Cited by 17

Late neuroprogenitors contribute to normal retinal vascular development in a Hif2a-dependent manner

Cristante, E., Liyanage, S. E., Sampson, R. D., Kalargyrou, A. A., Rossi, G. D., Rizzi, M., Hoke, J., Ribeiro, J., Maswood, R. N., Durán, Y., et al. (2018) · Development · doi:10.1242/dev.157511 · Cited by 18

ROS-ATM-CHK2 axis stabilizes HIF-1α and promotes tumor angiogenesis in hypoxic microenvironment

Bai, M., Xu, P., Cheng, R., Li, N., Cao, S., Guo, Q., Wang, X., Li, C., Bai, N., Jiang, B., et al. (2025) · Oncogene · doi:10.1038/s41388-025-03336-w · Cited by 20

The close interaction between hypoxia-related proteins and metastasis in pancarcinomas

López‐Cortés, A., Prathap, L., Ortiz‐Prado, E., Kyriakidis, N. C., Cáceres, Á. L., Armendáriz‐Castillo, I., Vera-Guapi, A., Yumiceba, V., Simbaña‐Rivera, K., Echeverría‐Garcés, G., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-15246-y · Cited by 17

Mutations in EPAS1 in congenital heart disease in Tibetans

Pan, H., Chen, Q., Qi, S., Li, T., Liu, B., Liu, S., Ma, X., & Wang, B. (2018) · Bioscience Reports · doi:10.1042/bsr20181389 · Cited by 18

Molecular Characterization and Response of Prolyl Hydroxylase Domain (PHD) Genes to Hypoxia Stress in Hypophthalmichthys molitrix

Li, X., Zhang, M., Ling, C., Sha, H., Zou, G., & Liang, H. (2022) · Animals · doi:10.3390/ani12020131 · Cited by 18

The Choice of the Iodinated Radiographic Contrast Media to Prevent Contrast-Induced Nephropathy

Andreucci, M., Faga, T., Pisani, A., Sabbatini, M., Russo, D., & Michael, A. (2014) · Advances in Nephrology · doi:10.1155/2014/691623 · Cited by 17

Oxidative Stress in Liver Tissue of Rat Induced by Chronic Systemic Hypoxia

Jusman, S. A. W. A., & Halim, A. (2010) · Makara Journal of Health Research · doi:10.7454/msk.v13i1.346 · Cited by 17

An Oxygen Molecular Sensor, the HIF Prolyl 4-Hydroxylase, in the Marine Protist Perkinsus olseni

Leite, R. B., Bensimon‐Brito, A., & Cancela, M. L. (2008) · Protist · doi:10.1016/j.protis.2008.03.002 · Cited by 17

ANTIOXIDANT ENZYMES AS DEFENSE MECHANISM AGAINST OXIDATIVE STRESS IN MIDGUT TISSUE AND HEMOCYTES OF Bombyx mori LARVAE SUBJECTED TO VARIOUS STRESSORS

Micheal, A. S., & Subramanyam, M. V. V. (2013) · Archives of Insect Biochemistry and Physiology · doi:10.1002/arch.21138 · Cited by 16

Pathogenesis of Acute Renal Failure Induced by Iodinated Radiographic Contrast Media

Andreucci, M., Faga, T., Sabbatini, M., & Michael, A. (2014) · Cited by 16

Discretizing Three‐Dimensional Oxygen Gradients to Modulate and Investigate Cellular Processes

Blatchley, M. R., Hall, F. D., Ntekoumes, D., Cho, H., Kailash, V., Vázquez-Duhalt, R., & Gerecht, S. (2021) · Advanced Science · doi:10.1002/advs.202100190 · Cited by 15

Acute Prenatal Hypoxia in Rats Affects Physiology and Brain Metabolism in the Offspring, Dependent on Sex and Gestational Age

Graf, A. V., Maslova, M. V., Artiukhov, A. V., Ksenofontov, A. L., Aleshin, V. A., & Bunik, V. I. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052579 · Cited by 16

Oxygen Depletion Speeds and Simplifies Diffusion in HeLa Cells

Edwald, E., Stone, M. B., Gray, E. M., Wu, J., & Veatch, S. L. (2014) · Biophysical Journal · doi:10.1016/j.bpj.2014.08.023 · Cited by 17

The metalloendopeptidase gene Pitrm1 is regulated by hedgehog signaling in the developing mouse limb and is expressed in muscle progenitors

Town, L., McGlinn, E., Fiorenza, S., Metzis, V., Butterfield, N. C., Richman, J. M., & Wicking, C. (2009) · Developmental Dynamics · doi:10.1002/dvdy.22126 · Cited by 15

A translational program that suppresses metabolism to shield the genome

Balukoff, N. C., Ho, J. J. D., Theodoridis, P. R., Wang, M., Bokros, M., Llanio, L., Krieger, J. R., Schatz, J. H., & Lee, S. (2020) · Nature Communications · doi:10.1038/s41467-020-19602-2 · Cited by 16

Posttranslational modifications of collagens as targets of hypoxia and Hif‐1α in endochondral bone development

Schipani, E. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.05236.x · Cited by 15

Size restricted silymarin suspension evokes integrated adaptive response against acute hypoxia exposure in rat lung

Paul, S., Arya, A., Gangwar, A., Bhargava, K., & Ahmad, Y. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.04.020 · Cited by 15

Hypoxia and Anoxia Tolerance in the Annual KillifishAustrofundulus limnaeus

Podrabsky, J. E., & Wilson, N. E. (2016) · Integrative and Comparative Biology · doi:10.1093/icb/icw092 · Cited by 15

Hypoxia-Induced Epithelial-to-Mesenchymal Transition in Proximal Tubular Epithelial Cells through miR-545-3p–TNFSF10

Kuo, M., Chang, W., Wu, L., Tsai, Y., & Hsu, Y. (2021) · Biomolecules · doi:10.3390/biom11071032 · Cited by 15

HIF-1α-induced microRNA-210 reduces hypoxia-induced osteoblast MG-63 cell apoptosis

Sun, G., & Peng, H. (2015) · Bioscience Biotechnology and Biochemistry · doi:10.1080/09168451.2014.1003128 · Cited by 14

Injectable Oxygen: Interfacing Materials Chemistry with Resuscitative Science

Peng, Y., Kheir, J. N., & Polizzotti, B. D. (2018) · Chemistry - A European Journal · doi:10.1002/chem.201802054 · Cited by 14

Ethanol Dehydrogenase I Contributes to Growth and Sporulation Under Low Oxygen Condition via Detoxification of Acetaldehyde in Metarhizium acridum

Zhang, E., Cao, Y., & Xia, Y. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.01932 · Cited by 14

Sphingosine-1-phosphate pretreatment amends hypoxia-induced metabolic dysfunction and impairment of myogenic potential in differentiating C2C12 myoblasts by stimulating viability, calcium homeostasis and energy generation

Rahar, B., Chawla, S., Pandey, S., Bhatt, A. N., & Saxena, S. (2017) · The Journal of Physiological Sciences · doi:10.1007/s12576-016-0518-4 · Cited by 13

TRP channels as sensors of oxygen availability

Numata, T., Ogawa, N., Takahashi, N., & Mori, Y. (2013) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-013-1237-9 · Cited by 13

Amphiphilic Fluorine-Containing Block Copolymers as Carriers for Hydrophobic PtTFPP for Dissolved Oxygen Sensing, Cell Respiration Monitoring and In Vivo Hypoxia Imaging with High Quantum Efficiency and Long Lifetime

Li, J., Qiao, Y., Pan, T., Zhong, K., Wen, J., Wu, S., Su, F., & Tian, Y. (2018) · Sensors · doi:10.3390/s18113752 · Cited by 13

Transcriptional elongation control of hypoxic response

Soliman, S. H. A., Iwanaszko, M., Zheng, B., Gold, S. R., Howard, B. C., Das, M., Chakrabarty, R. P., Chandel, N. S., & Shilatifard, A. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2321502121 · Cited by 13

Localization of erythropoietin in and around growing cartilage

Spiegelaere, W. D., Cornillie, P., & Broeck, W. V. D. (2009) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-009-0310-3 · Cited by 11

Moderate hypoxia modulates ABCG2 to promote the proliferation of mouse spermatogonial stem cells by maintaining mild ROS levels

Wang, J., Xue, X., Fan, K. C., Liu, Q., Zhang, S., Peng, M., Zhou, J., & Cao, Z. (2019) · Theriogenology · doi:10.1016/j.theriogenology.2019.10.007 · Cited by 12

Subchronic perinatal asphyxia in rats: Embryo–foetal assessment of a new model of oxidative stress during critical period of development

Ujházy, E., Dubovický, M., Navarová, J., Sedláčková, N., Danihel, Ľ., Brucknerová, I., & Mach, M. (2013) · Food and Chemical Toxicology · doi:10.1016/j.fct.2013.07.023 · Cited by 13

Structural Analysis of Redox-sensing Transcriptional Repressor Rex from Thermotoga maritima

Park, Y. W., Jang, Y. Y., Joo, H. K., & Lee, J. Y. (2018) · Scientific Reports · doi:10.1038/s41598-018-31676-z · Cited by 12

Molecular Characterization and Functional Analysis of Hypoxia-Responsive Factor Prolyl Hydroxylase Domain 2 in Mandarin Fish (Siniperca chuatsi)

Yu, Y., He, J., Liu, W., Li, Z., Weng, S., He, J., & Guo, C.-J. (2023) · Animals · doi:10.3390/ani13091556 · Cited by 12

Oxygen Sensing in Neurodegenerative Diseases: Current Mechanisms, Implication of Transcriptional Response, and Pharmacological Modulation

Rey, F., Messa, L., Maghraby, E., Casili, G., Ottolenghi, S., Barzaghini, B., Raimondi, M. T., Cereda, C., Cuzzocrea, S., Zuccotti, G., et al. (2022) · Antioxidants and Redox Signaling · doi:10.1089/ars.2022.0046 · Cited by 11

Transcriptome and hypoxia-responsive gene expression analyses reveal the physiological reaction to acute hypoxia and reoxygenation in Epinephelus coioides

Wu, Y., Lai, X., Bing, L., Lin, Y., Yang, Y., Zhang, M., Liu, S., Wu, J., Fu, X., & Shu, H. (2023) · Aquaculture Reports · doi:10.1016/j.aqrep.2023.101655 · Cited by 10

Hypoxia signaling in bone physiology and energy metabolism

Valle-Tenney, R., Melis, S., & Maes, C. (2023) · Current Opinion in Endocrine and Metabolic Research · doi:10.1016/j.coemr.2023.100473 · Cited by 11

Identification of new TSGA10 transcript variants in human testis with conserved regulatory RNA elements in 5'untranslated region and distinct expression in breast cancer

Salehipour, P., Nematzadeh, M., Mobasheri, M. B., Afsharpad, M., Mansouri, K., & Modarressi, M. H. (2017) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2017.07.007 · Cited by 10

Chapter 15 Cell differentiation as a response to oxidative stress

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Particulate cytoplasmic structures with high concentration of ubiquitin-proteasome accumulate in myeloid neoplasms

Pecci, A., Necchi, V., Barozzi, S., Vitali, A., Boveri, E., Elena, C., BERNASCONI, P. P., Noris, P., & Solcia, E. (2015) · Journal of Hematology & Oncology · doi:10.1186/s13045-015-0169-6 · Cited by 9

Polyubiquitinated proteins, proteasome, and glycogen characterize the particle-rich cytoplasmic structure (PaCS) of neoplastic and fetal cells

Necchi, V., Sommi, P., Vitali, A., Vanoli, A., Savoia, A., Ricci, V., & Solcia, E. (2014) · Histochemistry and Cell Biology · doi:10.1007/s00418-014-1202-5 · Cited by 9

Hypoxia promotes a perinatal-like progenitor state in the adult murine epicardium

Sayed, A., Turoczi, S., Soares‐da‐Silva, F., Marazzi, G., Hulot, J., Sassoon, D. A., & Valente, M. (2022) · Scientific Reports · doi:10.1038/s41598-022-13107-2 · Cited by 9

U2AF - Hypoxia-induced fas alternative splicing regulator

Vilys, L., Pečiulienė, I., Jakubauskienė, E., Zinkevičiūtė, R., Makino, Y., & Kanopka, A. (2020) · Experimental Cell Research · doi:10.1016/j.yexcr.2020.112444 · Cited by 9

Hypoxia and Tumour Angiogenesis

Brahimi-Horn, M. C., Laferrière, J., Mazure, N. M., & Pouysségur, J. (2007) · Springer eBooks · doi:10.1007/978-3-540-33177-3_10 · Cited by 8

Autoinflammation Around AES Total Ankle Replacement Implants

Koivu, H., Takakubo, Y., Mackiewicz, Z., Al‐Samadi, A., Soininen, A., Peled, N., Kukis, M., Trokovic, N., & Konttinen, Y. T. (2015) · Foot & Ankle International · doi:10.1177/1071100715596608 · Cited by 8

Does cardiac development provide heart research with novel therapeutic approaches?

Sayed, A., Valente, M., & Sassoon, D. A. (2018) · F1000Research · doi:10.12688/f1000research.15609.1 · Cited by 8

Naringin Affects Caspase-3, IL-1β, and HIF-1α Levels in Experimental Kidney Ischemia-Reperfusion in Rats

Danis, E. G., Acar, G., Dasdelen, D., Solmaz, M., Moğulkoç, R., & Baltacı, A. K. (2024) · Current Pharmaceutical Design · doi:10.2174/0113816128324562240816095551 · Cited by 7

Ultrasonic Measurement of Blood Flow Velocity and Applications for Cardiovascular Assessments

Bashford, G. R. (2016) · Springer eBooks · doi:10.1007/978-94-007-7678-4_18 · Cited by 7

Selecting the appropriate indirect viability assay for 3D paper-based cultures: a data-driven study

Sitte, Z. R., Larson, T. S., McIntosh, J. C., Sinanian, M., & Lockett, M. R. (2023) · The Analyst · doi:10.1039/d3an00283g · Cited by 8

First Dual Red–Near-Infrared Emissive Solution-Processed Organic Light-Emitting Diode Based on Europium–Ytterbium Mixed-Ligand Complexes for Pulse Oximetry

Kornikov, A. I., Kozlov, M. I., Vashchenko, A. A., Pavlov, A. A., Gordeeva, E. O., Latipov, E. V., Lepnev, L. S., Kozhevnikova, V. Y., & Utochnikova, V. V. (2023) · ACS Applied Optical Materials · doi:10.1021/acsaom.3c00124 · Cited by 7

A Dye‐Sensitized Sensor for Oxygen Detection under Visible Light

Wettstein, L., Specht, J., Kesselring, V., Sieben, L., Pan, Y., Käch, D., Baster, D., Krumeich, F., Kazzi, M. E., & Bezdek, M. J. (2024) · Advanced Science · doi:10.1002/advs.202405694 · Cited by 7

β3‐Adrenoceptor Agonism to Mimic the Biological Effects of Intrauterine Hypoxia: Taking Great Strides Toward a Pharmacological Artificial Placenta

Filippi, L., Innocenti, F., Pascarella, F., Scaramuzzo, R. T., Morganti, R., Bagnoli, P., Cammalleri, M., Monte, M. D., Calvani, M., & Pini, A. (2024) · Medicinal Research Reviews · doi:10.1002/med.22092 · Cited by 8

Computational EPAS1 rSNP Analysis, Transcriptional Factor Binding Sites and High Altitude Sickness or Adaptation

Buroker, N. E. (2016) · Journal of Proteomics and Genomics research · doi:10.14302/issn.2326-0793.jpgr-15-889 · Cited by 7

Expression pattern and functional analysis of fundc1 in rare minnow ( Gobiocypris rarus )

Xu, G., Li, Z., Xiao, J., Li, F., Ye, W., Zhao, H., Zhou, Q., & Zhong, X. (2017) · Gene · doi:10.1016/j.gene.2017.05.015 · Cited by 7

Neuronal cell fate decisions

Petersen, J. G., & Pocock, R. (2013) · Worm · doi:10.4161/worm.27284 · Cited by 7

Cooperativity between inhibition of cytosolic K+ efflux and AMPK activation during suppression of hypoxia-induced cellular apoptosis

Gopalani, N. K., Meena, R. N., Prasad, D. N., Ilavazhagan, G., & Sharma, M. (2011) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2011.10.018 · Cited by 7

Distribution of Gemcitabine Is Nearly Homogenous in Two Orthotopic Murine Models of Pancreatic Cancer

Kramer, R. M., Russell, J., & Humm, J. L. (2015) · Cancer Biotherapy and Radiopharmaceuticals · doi:10.1089/cbr.2015.1869 · Cited by 7

Metabolic Regulation and Related Molecular Mechanisms in Various Stem Cell Functions

Lee, H., & Hong, I. (2020) · Current Stem Cell Research & Therapy · doi:10.2174/1574888x15666200512105347 · Cited by 7

Diallyl Trisulfide Suppresses High-Glucose-Induced Cardiomyocyte Apoptosis by Targeting Reactive Oxygen Species-Mediated Hypoxia-Inducible Factor-1α/Insulin-like Growth Factor Binding Protein 3 Activation

Lin, K., Wei, Y.-M., Liu, C., Liu, J., Huang, I., Viswanadha, V. P., Huang, C., & Kuo, W. (2021) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.1c02384 · Cited by 7

Exposure to tobacco smoke increases bone loss in spontaneously hypertensive rats

Xu, J., Qiu, X., Liang, Z., Smiley‐Jewell, S. M., Lu, F., Yu, M., Pinkerton, K. E., Zhao, D., & Shi, B. (2018) · Inhalation Toxicology · doi:10.1080/08958378.2018.1506838 · Cited by 6

The effects of smoking on adolescent trauma patients: a propensity-score-matched analysis

Kojayan, G. G., Grigorian, A., Schubl, S. D., Kuza, C. M., Dolich, M. O., Bashir, R., & Nahmias, J. T. (2020) · Pediatric Surgery International · doi:10.1007/s00383-020-04654-8 · Cited by 6

Protein–Protein Interactions of Seryl-tRNA Synthetases with Emphasis on Human Counterparts and Their Connection to Health and Disease

Dulić, M., Mikulčić, V. G., Kekez, M., Ević, V., & Rokov‐Plavec, J. (2024) · Life · doi:10.3390/life14010124 · Cited by 6

Influence of Hypoxia on Endothelium-Derived NO-Mediated Relaxation in Rat Carotid, Mesenteric and Iliac Arteries

Tawa, M., Shimosato, T., Geddawy, A., Imamura, T., & Okamura, T. (2013) · Pharmacology · doi:10.1159/000351706 · Cited by 6

HAHmiR.DB: a server platform for high-altitude human miRNA–gene coregulatory networks and associated regulatory circuits

Khurana, P., Gupta, A., Sugadev, R., Sharma, Y. K., & Kumar, B. (2020) · Database · doi:10.1093/database/baaa101 · Cited by 6

Cyanide contaminated water treatment by di-nuclear Cu(II)-cryptate: A supramolecular approach

Ghosh, T. K., Ghosh, R., Chakraborty, S., Saha, P., Sarkar, S., & Ghosh, P. (2020) · Journal of Water Process Engineering · doi:10.1016/j.jwpe.2020.101364 · Cited by 6

Redox-sensing transcriptional repressor Rex

Park, Y. W., Jang, Y. Y., Joo, H. K., & Lee, J. Y. (2018) · Worldwide Protein Data Bank · doi:10.2210/pdb5zz6/pdb · Cited by 6

HIF1 and ID1 Interplay Confers Adaptive Survival to HIF1α-Inhibition

Geng, H., Ko, H., Pittsenbarger, J., Harvey, C. T., Xue, C., Liu, Q., Wiens, S., Kachhap, S. K., Beer, T. M., & Qian, D. Z. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.724059 · Cited by 5

Intrarenal urothelial transformation after obstruction: a novel metaplasia

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A novel cross-communication of HIF-1α and HIF-2α with Wnt signaling in TNBC and influence of hypoxic microenvironment in the formation of an organ-on-chip model of breast cancer

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