Mitochondria and Endothelial Function

Apoptosis: A Review of Programmed Cell Death

Elmore, S. (2007) · Toxicologic Pathology · doi:10.1080/01926230701320337 · Cited by 13,853

PGC-1α-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes

Mootha, V. K., Lindgren, C. M., Eriksson, K.-F., Subramanian, A., Sihag, S., Lehar, J., Puigserver, P., Carlsson, E., Ridderstråle, M., Laurila, E., et al. (2003) · Nature Genetics · doi:10.1038/ng1180 · Cited by 10,197

Biochemistry and molecular cell biology of diabetic complications

Brownlee, M. (2001) · Nature · doi:10.1038/414813a · Cited by 9,107

How mitochondria produce reactive oxygen species

Murphy, M. P. (2009) · Biochemical Journal · doi:10.1042/bj20081386 · Cited by 8,207

Hydroperoxide metabolism in mammalian organs.

Chance, B., Sies, H., & Boveris, A. (1979) · Physiological Reviews · doi:10.1152/physrev.1979.59.3.527 · Cited by 5,827

The BCL-2 protein family: opposing activities that mediate cell death

Youle, R. J., & Strasser, A. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2308 · Cited by 4,806

Normalizing mitochondrial superoxide production blocks three pathways of hyperglycaemic damage

Nishikawa, T., Edelstein, D., Du, X. L., Yamagishi, S.-I., Matsumura, T., Kaneda, Y., Yorek, M. A., Beebe, D., Oates, P. J., Hammes, H.-P., et al. (2000) · Nature · doi:10.1038/35008121 · Cited by 4,277

Therapeutic potential of resveratrol: the in vivo evidence

Baur, J. A., & Sinclair, D. A. (2006) · Nature Reviews Drug Discovery · doi:10.1038/nrd2060 · Cited by 3,958

Mechanisms of mitophagy

Youle, R. J., & Narendra, D. P. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3028 · Cited by 3,273

Nutrient control of glucose homeostasis through a complex of PGC-1α and SIRT1

Rodgers, J. T., Lerin, C., Haas, W., Gygi, S. P., Spiegelman, B. M., & Puigserver, P. (2005) · Nature · doi:10.1038/nature03354 · Cited by 3,160

Intercellular Mitochondrial Transfer and Mitochondrial Transplantation in Cardiovascular Disease

Farhid, F., Heydari, F., Hamblin, M. R., Masoudifar, S., Sahebkar, A., & Naghinezhad, J. (2026) · Canadian Journal of Cardiology · doi:10.1016/j.cjca.2026.06.032 · Cited by 3

Vascular Endothelial Function

Widlansky, M. E., & Malik, M. A. (2014) · Springer eBooks · doi:10.1007/978-3-642-37393-0_8-1 · Cited by 3

Mitochondria, a Therapeutic Target of Aerobic Exercise for the Vascular Homeostasis

Lee, H., Kim, K., Lee, M. C., Byun, K., & Kim, J. (2018) · Exercise Science · doi:10.15857/ksep.2018.27.3.177 · Cited by 2

Повреждение гематоэнцефалического барьера при стрессе и нейродегенерации: биохимические механизмы и новые модели для трансляционных исследований

Salmina, A. B., Комлева, Ю. К., Малиновская, Н. А., Morgun, A. V., Тепляшина, Е. А., Lopatina, O. L., Gorina, Y. V., Kharitonova, E. V., Хилажева, Е. Д., & Shuvaev, А. N. (2021) · Biochemistry (Moscow) · doi:10.31857/s0320972521060130 · Cited by 3

Postprandial lipemia and the relationship to health

Huggins, C. E., James, A. P., Bonham, M. P., Clark, K., & Lee, S. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-823914-8.00019-7 · Cited by 3

Disorders of Mitochondrial Homeostasis, Dynamics, Protein Import, and Quality Control

de Boer, L., de Vries, M. C., Smeitink, J. A. M., & Koopman, W. J. H. (2022) · Springer eBooks · doi:10.1007/978-3-030-67727-5_46 · Cited by 3

Peptides GWN and GW protect kidney cells against Dasatinib induced mitochondrial injury in a SIRT1 dependent manner

Bhullar, K. S., Ashkar, F., & Wu, J. (2021) · Food Chemistry Molecular Sciences · doi:10.1016/j.fochms.2021.100069 · Cited by 3

The Translational Proteome Modulated by 20(S)-Protopanaxadiol in Endothelial Cells.

Ying-Hua, S., Chen, C. C., Li, F., Cheng, J. K., Lin, M. C., & Huang, B. (2014) · PubMed Central · Cited by 3

Non-hematopoietic erythropoietin-derived peptides for atheroprotection and treatment of cardiovascular diseases

Belyaeva, V. S., Stepenko, Y. V., Lyubimov, I. I., Kulikov, A. L., Tietze, A. A., Kochkarova, I. S., Martynova, O. V., Pokopeyko, O. N., Крупенькина, Л. А., Nagikh, A. S., et al. (2020) · Research Results in Pharmacology · doi:10.3897/rrpharmacology.6.58891 · Cited by 4

Ex Vivo Placental Explant Flow Culture - Mimicking the Dynamic Conditions In Utero

Kupper, N., Pritz, E., Siwetz, M., Guettler, J., & Huppertz, B. (2023) · Journal of Visualized Experiments · doi:10.3791/65919 · Cited by 2

Ginsenoside Rg1 ameliorates the senescence and neurite injury of retinal ganglion cells in DR via targeting VDR and promoting mitochondrial biogenesis

Tang, K., Huang, C., Huang, Z., Lin, Z., Wang, Z., & Tan, N. (2025) · Journal of Ginseng Research · doi:10.1016/j.jgr.2025.05.006 · Cited by 3

Temporal Effects of Lipid Oversupply on Energy Metabolism and Mitochondrial Homeostasis in Hepatocytes

Chuang, C.-C., Chen, Y.-H., Chu, F., Yang, C.-P., Ho, H., Chang, F., Lo, Y., Chen, C., & Chang, Y.-H. (2025) · International Journal of Medical Sciences · doi:10.7150/ijms.104128 · Cited by 2

Endothelial RAB5IF is required for pathological and developmental retinal angiogenesis

Bai, W., Yin, D.-P., Chen, G., Lu, Y., Jiang, Q., Li, K., Yao, J., & Cao, C. (2025) · Nature Communications · doi:10.1038/s41467-025-66212-x · Cited by 2

15-Hydroxyprostaglandin Dehydrogenase Inhibitor Restores Endothelial Function Under Dihydrotestosterone-Induced Stress in Human Dermal Microvascular Endothelial Cells

Kim, M., Kim, H. J., Lee, Y., Lee, S., Lim, D., Park, H. D., & Shin, D. W. (2025) · Molecules · doi:10.3390/molecules31010123 · Cited by 2

Bioconverted Blueberry Extract Potentiates the Angiogenic and Endothelial Functions in Human Dermal Microvascular Endothelial Cells Under Oxidative Stress

Shin, J. U., Jo, Y. H., Jeong, S. A., Jeong, Y. H., Son, M. G., Jeong, Y. J., Lim, B. O., & Shin, D. W. (2026) · Current Issues in Molecular Biology · doi:10.3390/cimb48020224 · Cited by 2

Endothelial mitochondrial homeostasis in the development and progression of atherosclerosis

Remex, N. S., Miah, M. S., Islam, T., Aishwarya, R., Sinha, M. H., Dhar, P., Dhaou, C. B., Orr, A. W., & Bhuiyan, M. S. (2026) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2026.1813122 · Cited by 2

In-Utero Neurotoxicity of Nanoparticles

Siddiqi, N. J., Fatima, S., Sharma, B., & Elrobh, M. S. (2022) · IntechOpen eBooks · doi:10.5772/intechopen.101452 · Cited by 3

Updates on Endoplasmic Reticulum

Favero, G. (2022) · Biochemistry · doi:10.5772/intechopen.100952 · Cited by 2

Angiogenic activity of mitochondria; beyond the sole bioenergetic organelle

Sadeghsoltani, F., Hassanpour, P., Safari, M., Haiaty, S., Rahbarghazi‬, R., Rahmati, M., & Mota, A. (2024) · Journal of Cellular Physiology · doi:10.1002/jcp.31185 · Cited by 3

Gestational diabetus mellitus and its complications, role of desynchronosis in pathogenesis (a review)

Хара, М. Р., Korda, I. V., & Podilska, T. I. (2023) · Pathologia · doi:10.14739/2310-1237.2023.2.282626 · Cited by 3

The effect of Ashwagandha Versus Amitriptyline on the Histological Structure of Submandibular Glands in Albino Rats

Idrees, I., Taqa, G. A., & ALtaaye, S. (2022) · Egyptian Journal of Veterinary Science · doi:10.21608/ejvs.2022.156115.1381 · Cited by 2

Mitochondrial genome and aging of cardiomyocytes

Николаевна, К. С., Свеклина, Т. С., Борисович, Ш. С., Семёнович, Ч. В., Ovchinnikov, D. V., & Eliseeva, M. I. (2021) · Genes and Cells · doi:10.23868/202112002 · Cited by 2

[Acetaldehyde dehydrogenase 2 ameliorates lung endothelial barrier and balances mitochondrial dynamics in mice with acute lung injury].

Wang, L., Tian, M., Li, R., Wu, Y. Z., Wang, S., Lü, H., Liu, Z., & Yu, Y. (2023) · PubMed Central · doi:10.12122/j.issn.1673-4254.2023.08.16 · Cited by 2

Oxidant-Dependent and Oxidant-Independent Proangiogenic and Vasomotor Signaling in Coronary Vascular Endothelium

Aldosari, S., Awad, M. A., Gao, M. Z., McCormack, I. G., Sellke, F. W., & Abid, M. R. (2019) · Springer eBooks · doi:10.1007/978-981-13-8946-7_2 · Cited by 2

Assessing the Heterogeneity of Cardiac Non-myocytes and the Effect of Cell Culture with Integrative Single Cell AnalysisPreprint

Iskra, B. S., Davis, L., Miller, H. E., Chiu, Y., Bishop, A. J. R., Chen, Y., & Aune, G. J. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.03.04.975177 · Cited by 2

Exacerbation of mitochondrial fission in human CD34 + cells halts erythropoiesis and hemoglobin biosynthesisPreprint

Gonzalez-Ibañez, A. M., Ruíz, L. M., Jensen, E. L., Echeverría, C., Romero, V., Stiles, L., Shirihai, O. S., & Elorza, Á. A. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.07.31.230961 · Cited by 2

A mitochondrion-targeted poly(N-isopropylacrylamide-coacrylic acid) nanohydrogel with a fluorescent bioprobe for ferrous ion imaging in vitro and in vivo

Xiao, W., Wang, F., Wang, X., & Wang, X. (2025) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2025.125725 · Cited by 1

Mitochondrial Dysfunction in the Cardiovascular Disease Continuum: Problems of Studying the Progression During the Follow-Up of the Pathologies

Невойт, Г. В., Potyazhenko, M., Mintser, O. P., Jaruševičius, G., & Vainoras, A. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262110497 · Cited by 3

Redox‐Responsive Mitochondrial Delivery from Functionalized Vascular Stent Surfaces

Tang, F., Applewhite, B. C., Wang, B., & Jiang, B. (2025) · Advanced NanoBiomed Research · doi:10.1002/anbr.202500202 · Cited by 1

Zinc finger CCCH-type containing 13–mediated N6-methyladenosine methylation mitigates endothelial injury in venous thrombosis by inhibiting elevated mitochondrial fission

Lu, H. J., Cai, Y., Tao, Y., Xia, Y., Wu, T., Hu, Y., & Tang, L. V. (2025) · Journal of Thrombosis and Haemostasis · doi:10.1016/j.jtha.2025.11.007 · Cited by 1

Paeoniflorin alleviates hypobaric hypoxia-triggered lung injury through targeting MEK2 to modulate ERK2–SGK1 signaling

Wu, Z., Wang, Y., Wang, R., Gao, R. B., Li, S., Tu, B., Yin, X.-R., Li, M., Zhou, W. J., Xu, H., et al. (2025) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2025.12.024 · Cited by 1

Peripheral blood mononuclear cell mitochondrial bioenergetics are related to vascular endothelial function in young and older adults

Wolf, S. T., Bangle, J. F., Jennings, W. E., Albino, G. R., Gorejena, M., Clary, B. L., Heo, J., & Call, J. A. (2026) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00262.2025 · Cited by 1

Sodium-glucose Co-transporter 2 (SGLT2) inhibitor dapagliflozin acutely activates cardiomyocyte HIF-1α signaling via succinate, a signaling metabolite

Sato, T., Isagawa, T., Sugiura, Y., Sawaki, D., Nakagama, Y., Kuchimaru, T., Minatsuki, S., Sato, S., Ono, K., Chuluun-Erdene, A., et al. (2026) · Journal of Pharmacological Sciences · doi:10.1016/j.jphs.2026.01.008 · Cited by 2

RNA-seq analysis reveals altered gene expression profiles in HMEC-1 cells overexpressing KRAS gene associated with brain arteriovenous malformation

Yuan, K., Zhao, Y., Zhang, H., Wang, K., Zhou, Y., Chen, Y., Chen, X., Zhao, Y., & Hao, Q. (2026) · Chinese Neurosurgical Journal · doi:10.1186/s41016-026-00427-9 · Cited by 1

Pink1-mediated mitophagy in the endothelium releases proteins encoded by mitochondrial DNA and activates neutrophil responses during inflammation

Gajwani, P., Wang, L. X., Debnath, K., Danos-Diaz, P., Kim, Y.-M., Srivastava, S., Ye, Z., Krantz, S., Wang, D.-M., Tiruppathì, C., et al. (2026) · eLife · doi:10.7554/elife.82205 · Cited by 1

Alterations of endothelial cell bioenergetics in congenital diaphragmatic hernia

Emrick, B. F., Zhevlakova, I., Novotny, M., Mavrakis, L. A., Mulya, A., Cass, D. L., Miyasaka, E. A., Byzova, T. V., Asosingh, K., ERZURUM, S. C., et al. (2026) · Pediatric Research · doi:10.1038/s41390-026-05447-w · Cited by 1

Mechanisms of Cardiovascular Aging

Paneni, F., Costantino, S., Cosentino, F., & Lüscher, T. F. (2013) · Current Translational Geriatrics and Experimental Gerontology Reports · doi:10.1007/s13670-013-0061-6 · Cited by 1

Effects of In Vitro Laminar Shear Stress as an Exercise Mimetic on Endothelial Cell Health

Brown, M. D., & Park, J. (2015) · Molecular and translational medicine · doi:10.1007/978-3-319-17076-3_7 · Cited by 1

Mitochondrial Dysfunction in Stem Cell Aging

Meiliana, A., Dewi, N. M., & Wijaya, A. (2015) · The Indonesian Biomedical Journal · doi:10.18585/inabj.v7i1.18 · Cited by 1

Organelles Stress and their Crosstalk within Diabetic Myocardium

Popov, D. (2015) · ATHENS JOURNAL OF HEALTH & MEDICAL SCIENCES · doi:10.30958/ajh.2-2-3 · Cited by 1

Environmental stress influences mitochondrial metabolism in vascular cells: consequences for angiogenesis

Bowen, T. S., & Egginton, S. (2019) · Vascular Biology · doi:10.1530/vb-19-0018 · Cited by 1

Mitochondrial biogenesis for the treatment of spinal cord injury

Simmons, E. C., Scholpa, N. E., Crossman, J. D., & Schnellmann, R. G. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-822498-4.00028-2 · Cited by 1

Advanced Glycation End Product Induced Endothelial Dysfunction through ER Stress: Unravelling the Role of Paraoxonase 2

Ravi, R., & Rajesh, B. S. (2022) · Biochemistry · doi:10.5772/intechopen.106018 · Cited by 2

Effects of Glutamine Starvation on SHVV Replication by Quantitative Proteomics Analysis

Liu, J., Zhang, Y., Liu, X., Zhang, H., Liu, Y., Chen, K., Tang, M., & Sun, L. (2022) · Fishes · doi:10.3390/fishes7060315 · Cited by 1

SERUM HUMANIN IN PEDIATRIC SEPTIC SHOCK–ASSOCIATED MULTIPLE-ORGAN DYSFUNCTION SYNDROME

Atreya, M. R., Piraino, G., Cvijanovich, N. Z., Fitzgerald, J. C., Weiss, S. L., Bigham, M. T., Jain, P., Schwarz, A. J., Lutfi, R., Nowak, J. E., et al. (2023) · Shock · doi:10.1097/shk.0000000000002266 · Cited by 3

Age-Induced Endothelial Dysfunction and Intima–Media Thickening

Kozàkovà, M., & Schmidt-Truksäss, A. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-801387-8.00014-4 · Cited by 1

Mitochondrial Depolarization in Endothelial and Other Vascular Cells and Their Role in the Regulation of Cerebral Vascular Tone

Busija, D. W., Rutkai, I., & Katakam, P. V. G. (2016) · Springer eBooks · doi:10.1007/978-3-319-29635-7_3 · Cited by 1

Mitochondrial Dysfunction Signature in Diabetic Vascular Endothelium

Popov, L. (2018) · Journal of Clinical & Experimental Pathology · doi:10.4172/2161-0681.1000334 · Cited by 1

Endothelial dysfunction and cardiovascular diseases through oxidative stress pathways

Guzmán, R. R., Miranda, E. M. C., & Guzmán-Díaz, P. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-816196-8.00012-6 · Cited by 1

The Role of Heme Synthesis in Endothelial Mitochondrial Function and Ocular Angiogenesis

Shetty, T. (2020) · IUScholarWorks (Indiana University) · doi:10.7912/c2/342 · Cited by 1

TERTing the hyperoxic lung

Vellingiri, V., & Mehta, D. (2021) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00580.2021 · Cited by 1

Chronic Nucleoside Reverse Transcriptase Inhibitors Disrupt Mitochondrial Homeostasis and Promote Premature Endothelial Senescence

Chen, Y. (2019) · Louisiana State University · doi:10.31390/gradschool_dissertations.4974 · Cited by 1

Pink1-mediated mitophagy in the endothelium releases proteins encoded by mitochondrial DNA and activates neutrophil responsesPreprint

Gajwani, P., Wang, L., Srivastava, S., Ye, Z., Kim, Y.-M., Krantz, S., Wang, D., Tiruppathì, C., Tóth, P. T., & Rehman, J. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.08.07.503084 · Cited by 1

BAM15, a mitochondrial uncoupler regulates mitochondrial function by FUNDC1 dependently in hyperglycemiaPreprint

Rethineswaran, V. K., Jang, W. B., Choi, J., Lim, H. J., Park, S., Lee, E. J., Ha, J. S., Yun, J., & Kwon, S. (2023) · Research Square · doi:10.21203/rs.3.rs-2903880/v1 · Cited by 1

Ephedra protects vascular endothelium cells from vinorelbine‐induced cytotoxicity by preserving endothelial nitric oxide synthase activity

Konaka, K., Moriyama, K., Okada, N., Nishisako, H., Shono, M., Kawazoe, K., & Ishizawa, K. (2015) · Traditional & Kampo Medicine · doi:10.1002/tkm2.1024

The responses of endothelium to insult : does endothelial heterogeneity play a role in in vitro cell models

Mthethwa, M. (2015) · SUNScholar (Stellenbosch University)

Mechanisms of vascular protection in chronic inflammatory disease

Thornton, C. C. (2014) · Spiral (Imperial College London) · doi:10.25560/26595

Mitochondrial oxidative stress and antioxidant therapy in arterial aging

Gioscia‐Ryan, R. A. (2016) · CU Scholar (University of Colorado Boulder)

The Effects of Autophagic Deficiencies on the Leukemia Mitochondrial Phenotype and Implications in Strategic Drug Targeting

Rodrigo, R. (2016) · UWSpace (University of Waterloo)

Shear Stress-Induced Mitochondrial Biogenesis Decreases the

Kim, J., Kim, B., Lee, H., Thakkar, S. R., Babbitt, D. M., Eguchi, S., Michael, D., & Park, J. (2015)

Endothelial Alterations in Chronic Coronary Disease

de Moraes, A. A. I., Chagas, A. C. P., Faria‐Neto, J. R., & da Luz, P. L. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-812348-5.00030-1

Mechanisms of S1P-Induced Endothelial Barrier Enhancement

Alves, N. G. (2018) · Digital Commons - University of South Florida (University of South Florida)

Митохондрии клеток церебрального эндотелия как потенциальная мишень для нейропротекторного действия коэнзима Q10

Шаповал, Н. С., Os, M., Васильевич, М. А., Константиновна, А. С., & Салмина, А. Б. (2020) · Экспериментальная и клиническая фармакология · doi:10.30906/0869-2092-2020-83-3-40-46

Mechanical View on the Mitochondria

Mierke, C. T. (2020) · Biological and medical physics, biomedical engineering · doi:10.1007/978-3-030-58532-7_6

Mitochondrial Dysfunction in Neurodegenerative Dis-orders and Atherosclerosis: Pathophysiological Mecha-nisms and innovative Protocol Towards an Elegant New Era Of Health

Abdulgader, A. A. A. (2020) · American Journal of Biomedical Science & Research · doi:10.34297/ajbsr.2020.11.001582

Mitochondrial content and oxidative damage in full-term placentas from SGA, LGA and AGA infants pregnant women

Ramı́rez-Emiliano, J., Barbosa‐Sabanero, G., Solı́s-Martı́nez, M. O., Mina-Bravo, M., Edgar Martínez-Escamilla Edgar, A., & Pérez‐Vázquez, V. (2021) · Archives of Medical Science · doi:10.5114/aoms/132681

Caveolin-1 Alleviates Angiotensin Ⅱ Induced Endothelial Injury and Cerebral Microbleed Via Mitochondrial ProtectionPreprint

Li, C., Tang, X., Wang, J., Duan, H.-J., Xia, M., Guo, C., Chen, Y.-J., Wang, B., Chen, Y., Yin, Y., et al. (2021) · Research Square · doi:10.21203/rs.3.rs-709689/v1

Prospective Advances in Exercise-Induced Autophagy on Health

Liang, J., Kirberger, M., & Chen, N. (2021) · Springer eBooks · doi:10.1007/978-981-16-4525-9_11

Hydrogen-Rich Medium Ameliorates Lipopolysaccharides-Induced Mitochondrial Fission and Dysfunction in Human Umbilical Vein Endothelial Cells (Huvecs) via Up-Regulating HO-1 ExpressionPreprint

Xie, K., Mao, X., Lian, N., Wang, Y., Wang, Y., Chen, H., Zhu, R., Yu, Y., & Wang, G. (2021) · Research Square · doi:10.21203/rs.3.rs-1020841/v1

Efeitos das erva-mate (Ilex paraguariensis) na modulação do metabolismo energético mitocondrial associado à obesidade

dos Santos, T. W. (2018) · doi:10.47749/t/unicamp.2018.1051961

Transplantation of Viable Allogeneic Mitochondria Improves Gas Exchange and Alveolar-Capillary Permeability in Rats with Endotoxin-Induced Acute Lung InjuryPreprint

Pang, Y.-L., FANG, S.-Y., Cheng, T.-T., Huang, C.-C., Lin, M., Lam, C., & Chen, K. (2022) · Research Square · doi:10.21203/rs.3.rs-1236978/v1

Altersbedingte Dysfunktion von Mitochondrien – Ursache und therapeutisches Ziel kardiovaskulärer Erkrankungen

Dihlmann, S., Böckler, D., & Peters, A. S. (2022) · Gefässchirurgie · doi:10.1007/s00772-022-00887-0

2 типті қант диабеті бар науқастарда эндотелиальды дисфункциямен байланысты тамырлы асқынулар

Duisenbek, A., Аблайханова, Н. Т., Қалдықараева, А. Т., Есенбекова, А. Е., Mukhitdin, B., Беркутовна, Е. З., & Кожамжарова, Л. С. (2022) · Bulletin of the Karaganda University “Biology medicine geography Series” · doi:10.31489/2022bmg3/176-184

Caveolin-1 alleviates angiotensin Ⅱ induced endothelial injury and cerebral microbleed via mitochondrial protectionPreprint

Li, C., Tang, X., Wang, J., Duan, H.-J., Xia, M., Guo, C., Chen, Y.-J., Wang, B., Chen, Y., Yi, Y., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-709689/v2

Vascular Endothelial Cells Perform Distinct Sensing and Signaling of Laminar and Disturbed Flows across Plasma Membranes and MitochondriaPreprint

Yamamoto, K., Maeno, R., Kawabe, K., Shimogonya, Y., & Ando, J. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.04.20.537745

JoVE Video Dataset

Kupper, N., Pritz, E., Siwetz, M., Guettler, J., & Huppertz, B. (2023) · doi:10.3791/65919-v

Effects of moderate - intensity exercise training on cardiac angiogenic capacity and fibrosis in middle-aged and aged rats

Mekrungruangwong, T., Patumraj, S., & Viboolvorakul, S. (2019) · doi:10.58837/chula.the.2019.368

Age-Induced Endothelial Dysfunction and Intima–Media Thickening

Kozàkovà, M., & Schmidt‐Trucksäss, A. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15512-3.00029-5

Prolonged Hypoxic Exposure Impairs Endothelial Functions: Possible Mechanism of HIF-1α Signaling

Hong, J., & Shin, J. (2024) · Exercise Science · doi:10.15857/ksep.2024.00262

Mitochondria in Endothelial Dysfunction and The Relation to Cardiovascular Disease

Poznyak, A. V., Khotina, V. A., Sukhorukov, V. N., Sobenin, I. A., Popov, M. A., Postnov, A. Y., & Orekhov, A. A. N. (2024) · Journal of Angiotherapy · doi:10.25163/angiotherapy.859557

Laminar Shear Stress Increases the Cytosolic Pool of PINK1 in Endothelial Cells and Enhances Mitophagic Sensitivity Toward Dysfunctional MitochondriaPreprint

Hong, S., Shin, J., Saredy, J., Choi, S. Y., Wang, H., & Park, J. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.06.21.660867

Integration of artificial intelligence and high-content screening enabled identification of drugs for long-term treatment of cerebral cavernous malformation diseasePreprint

Frías-Anaya, E., Gallego-Gutiérrez, H., Bui, C., Birrueta, J. O., Steinberg, J. D., Niesman, I. R., Gongol, B., Nguyen, B., Sawhney, A., Mizushima, Z., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.08.693036 · Cited by 1

Additional file 1 of Liver sinusoidal endothelial cells rely on oxidative phosphorylation but avoid processing long-chain fatty acids in their mitochondria

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Additional file 2 of FGF21 alleviates endothelial mitochondrial damage and prevents BBB from disruption after intracranial hemorrhage through a mechanism involving SIRT6

Wang, R., Wang, J., Zhang, Z., Ma, B., Sun, S., Gao, L., & Gao, G. (2024) · Figshare · doi:10.6084/m9.figshare.26649429

Additional file 2 of Liver sinusoidal endothelial cells rely on oxidative phosphorylation but avoid processing long-chain fatty acids in their mitochondria

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Additional file 3 of FGF21 alleviates endothelial mitochondrial damage and prevents BBB from disruption after intracranial hemorrhage through a mechanism involving SIRT6

Wang, R., Wang, J., Zhang, Z., Ma, B., Sun, S., Gao, L., & Gao, G. (2024) · Figshare · doi:10.6084/m9.figshare.26649432

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