The force is strong with this one: metabolism (Over)powers stem cell fate

Single Lgr5 stem cells build crypt-villus structures in vitro without a mesenchymal niche

Sato, T., Vries, R. G., Snippert, H. J., van de Wetering, M., Barker, N., Stange, D. E., van Es, J. H., Abo, A., Kujala, P., Peters, P. J., et al. (2009) · Nature · doi:10.1038/nature07935 · Cited by 7,204 · see citing works

Targeting Hypoxia-Inducible Factors for the Treatment of Anemia in Chronic Kidney Disease Patients

Locatelli, F., Fishbane, S. N., Block, G. A., & Macdougall, I. C. (2017) · American Journal of Nephrology · doi:10.1159/000455166 · Cited by 4,834 · see citing works

Paneth cells constitute the niche for Lgr5 stem cells in intestinal crypts

Sato, T., van Es, J. H., Snippert, H. J., Stange, D. E., Vries, R. G., van den Born, M., Barker, N., Shroyer, N. F., van de Wetering, M., & Clevers, H. (2011) · Nature · doi:10.1038/nature09637 · Cited by 2,510 · see citing works

Impact of caloric restriction on health and survival in rhesus monkeys from the NIA study

Mattison, J. A., Roth, G. S., Beasley, T. M., Tilmont, E. M., Handy, A. M., Herbert, R. L., Longo, D. L., Allison, D. B., Young, J. E., Bryant, M., et al. (2012) · Nature · doi:10.1038/nature11432 · Cited by 1,145 · see citing works

The Distinct Metabolic Profile of Hematopoietic Stem Cells Reflects Their Location in a Hypoxic Niche

Simsek, T., Kocabas, F., Zheng, J., DeBerardinis, R. J., Mahmoud, A. I., Olson, E. N., Schneider, J. W., Zhang, C. C., & Sadek, H. A. (2010) · Cell Stem Cell · doi:10.1016/j.stem.2010.07.011 · Cited by 1,101 · see citing works

Metabolic requirements for the maintenance of self-renewing stem cells

Ito, K., & Suda, T. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3772 · Cited by 1,014 · see citing works

Regulation of the HIF-1α Level Is Essential for Hematopoietic Stem Cells

Takubo, K., Goda, N., Yamada, W., Iriuchishima, H., Ikeda, E., Kubota, Y., Shima, H., Johnson, R. S., Hirao, A., Suematsu, M., et al. (2010) · Cell Stem Cell · doi:10.1016/j.stem.2010.06.020 · Cited by 891 · see citing works

The ABC of APC

Fearnhead, N. S. (2001) · Human Molecular Genetics · doi:10.1093/hmg/10.7.721 · Cited by 882 · see citing works

A Mitochondrial Pyruvate Carrier Required for Pyruvate Uptake in Yeast, <i>Drosophila</i> , and Humans

Bricker, D. K., Taylor, E. B., Schell, J. C., Orsak, T., Boutron, A., Chen, Y.-C., Cox, J. E., Cardon, C. M., Van Vranken, J. G., Dephoure, N., et al. (2012) · Science · doi:10.1126/science.1218099 · Cited by 843 · see citing works

High-fat diet enhances stemness and tumorigenicity of intestinal progenitors

Beyaz, S., Mana, M., Roper, J., Kedrin, D., Saadatpour, A., Hong, S., Bauer-Rowe, K. E., Xifaras, M. E., Akkad, A., Arias, E., et al. (2016) · Nature · doi:10.1038/nature17173 · Cited by 840 · see citing works

Regulation of Glycolysis by Pdk Functions as a Metabolic Checkpoint for Cell Cycle Quiescence in Hematopoietic Stem Cells

Takubo, K., Nagamatsu, G., Kobayashi, C. I., Nakamura‐Ishizu, A., Kobayashi, H., Ikeda, E., Goda, N., Rahimi, Y., Johnson, R. S., Soga, T., et al. (2013) · Cell stem cell · doi:10.1016/j.stem.2012.10.011 · Cited by 810 · see citing works

mTORC1 in the Paneth cell niche couples intestinal stem-cell function to calorie intake

Yilmaz, Ö. H., Katajisto, P., Lamming, D. W., Gültekin, Y., Bauer-Rowe, K. E., Sengupta, S., Birsoy, K., Dursun, A., Yilmaz, V. O., Selig, M., et al. (2012) · Nature · doi:10.1038/nature11163 · Cited by 753 · see citing works

Identification and Functional Expression of the Mitochondrial Pyruvate Carrier

Herzig, S., Raemy, E., Montessuit, S., Veuthey, J.-L., Zamboni, N., Westermann, B., Kunji, E. R. S., & Martinou, J.-C. (2012) · Science · doi:10.1126/science.1218530 · Cited by 747 · see citing works

Caloric restriction reduces age-related and all-cause mortality in rhesus monkeys

Colman, R. J., Beasley, T. M., Kemnitz, J. W., Johnson, S. C., Weindruch, R., & Anderson, R. M. (2014) · Nature Communications · doi:10.1038/ncomms4557 · Cited by 711 · see citing works

Energy Metabolism in Human Pluripotent Stem Cells and Their Differentiated Counterparts

Varum, S., Rodrigues, A. S., Moura, M. B., Momcilovic, O., Easley, C. A., Ramalho-Santos, J., Van Houten, B., & Schatten, G. (2011) · PLoS ONE · doi:10.1371/journal.pone.0020914 · Cited by 671 · see citing works

Stem cell metabolism in tissue development and aging

Shyh‐Chang, N., Daley, G. Q., & Cantley, L. C. (2013) · Development · doi:10.1242/dev.091777 · Cited by 573 · see citing works

Interplay between metabolic identities in the intestinal crypt supports stem cell function

Rodríguez-Colman, M. J., Schewe, M., Meerlo, M., Stigter, E., Gerrits, J., Pras-Raves, M., Sacchetti, A., Hornsveld, M., Oost, K. C., Snippert, H. J., et al. (2017) · Nature · doi:10.1038/nature21673 · Cited by 522 · see citing works

Metabolic Regulation in Pluripotent Stem Cells during Reprogramming and Self-Renewal

Zhang, J., Nuebel, E., Daley, G. Q., Koehler, C. M., & Teitell, M. A. (2012) · Cell stem cell · doi:10.1016/j.stem.2012.10.005 · Cited by 465 · see citing works

Structure, mechanism and regulation of pyruvate carboxylase

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A Role for the Mitochondrial Pyruvate Carrier as a Repressor of the Warburg Effect and Colon Cancer Cell Growth

Schell, J. C., Olson, K. A., Jiang, L., Hawkins, A. J., Van Vranken, J. G., Xie, J., Egnatchik, R. A., Earl, E. G., DeBerardinis, R. J., & Rutter, J. (2014) · Molecular Cell · doi:10.1016/j.molcel.2014.09.026 · Cited by 363 · see citing works

Wnt signaling in adult intestinal stem cells and cancer

Krausová, M., & Kořínek, V. (2013) · Cellular Signalling · doi:10.1016/j.cellsig.2013.11.032 · Cited by 362 · see citing works

Control of intestinal stem cell function and proliferation by mitochondrial pyruvate metabolism

Schell, J. C., Wisidagama, D. R., Bensard, C., Zhao, H., Wei, P., Tanner, J., Flores, A., Mohlman, J., Sorensen, L. K., Earl, C. S., et al. (2017) · Nature Cell Biology · doi:10.1038/ncb3593 · Cited by 322 · see citing works

A Fatty Acid Oxidation-Dependent Metabolic Shift Regulates Adult Neural Stem Cell Activity

Knobloch, M., Pilz, G.-A., Ghesquière, B., Kovacs, W. J., Wegleiter, T., Moore, D. L., Hruzova, M., Zamboni, N., Carmeliet, P., & Jessberger, S. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.08.029 · Cited by 322 · see citing works

mTORC1 and SIRT1 Cooperate to Foster Expansion of Gut Adult Stem Cells during Calorie Restriction

Igarashi, M., & Guarente, L. (2016) · Cell · doi:10.1016/j.cell.2016.05.044 · Cited by 302 · see citing works

Lactate dehydrogenase activity drives hair follicle stem cell activation

Flores, A., Schell, J., Krall, A. S., Jelinek, D., Miranda, M., Grigorian, M., Braas, D., White, A. C., Zhou, J. L., Graham, N. A., et al. (2017) · Nature Cell Biology · doi:10.1038/ncb3575 · Cited by 301 · see citing works

Metabolic control of methylation and acetylation

Su, X., Wellen, K. E., & Rabinowitz, J. D. (2015) · Current Opinion in Chemical Biology · doi:10.1016/j.cbpa.2015.10.030 · Cited by 296 · see citing works

Glycolytic Metabolism Plays a Functional Role in Regulating Human Pluripotent Stem Cell State

Gu, W., Gaeta, X., Sahakyan, A., Chan, A. B., Hong, C. S., Kim, R., Braas, D., Plath, K., Lowry, W. E., & Christofk, H. R. (2016) · Cell stem cell · doi:10.1016/j.stem.2016.08.008 · Cited by 275 · see citing works

Impact of age and caloric restriction on neurogenesis in the dentate gyrus of C57BL/6 mice

Bondolfi, L., Ermini, F., Long, J. M., Ingram, D. K., & Jucker, M. (2003) · Neurobiology of Aging · doi:10.1016/s0197-4580(03)00083-6 · Cited by 264 · see citing works

Metabolic trajectory of cellular differentiation in small intestine by Phasor Fluorescence Lifetime Microscopy of NADH

Stringari, C., Edwards, R. A., Pate, K. T., Waterman, M. L., Donovan, P. J., & Gratton, E. (2012) · Scientific Reports · doi:10.1038/srep00568 · Cited by 251 · see citing works

Adult mammalian stem cells: the role of Wnt, Lgr5 and R‐spondins

Schuijers, J., & Clevers, H. C. (2012) · The EMBO Journal · doi:10.1038/emboj.2012.149 · Cited by 247 · see citing works

Pluripotent stem cell energy metabolism: an update

TeSlaa, T. A., & Teitell, M. A. (2014) · The EMBO Journal · doi:10.15252/embj.201490446 · Cited by 212 · see citing works

Wnt pathway regulation of intestinal stem cells

Mah, A. T., Yan, K. S., & Kuo, C. J. (2016) · The Journal of Physiology · doi:10.1113/jp271754 · Cited by 156 · see citing works

Hematopoietic senescence is postponed and hematopoietic stem cell function is enhanced by dietary restriction

Chen, J., Astle, C. M., & Harrison, D. E. (2003) · Experimental Hematology · doi:10.1016/s0301-472x(03)00238-8 · Cited by 106 · see citing works

Energy metabolism in intestinal epithelial cells during maturation along the crypt-villus axis

Yang, H., Wang, X., Xiong, X., & Yin, Y. (2016) · Scientific Reports · doi:10.1038/srep31917 · Cited by 83 · see citing works

Pluripotent Stem Cell Metabolism and Mitochondria: Beyond ATP

Lees, J. G., Gardner, D. K., & Harvey, A. J. (2017) · Stem Cells International · doi:10.1155/2017/2874283 · Cited by 80 · see citing works

Effects of dietary restriction on hematopoietic stem-cell aging are genetically regulated

Ertl, R. P., Chen, J., Astle, C. M., Duffy, T. M., & Harrison, D. E. (2007) · Blood · doi:10.1182/blood-2007-01-069807 · Cited by 71 · see citing works

Influence of Amino Acid Metabolism on Embryonic Stem Cell Function and Differentiation

Kilberg, M. S., Terada, N., & Shan, J. (2016) · Advances in Nutrition · doi:10.3945/an.115.011031 · Cited by 58 · see citing works

Does eating less make you live longer and better? An update on calorie restriction

Picca, A., Pesce, V., & Lezza, A. M. S. (2017) · Clinical Interventions in Aging · doi:10.2147/cia.s126458 · Cited by 54 · see citing works

A metabolic switch controls intestinal differentiation downstream of Adenomatous polyposis coli (APC)

Sandoval, I. T., Delacruz, R. G. C., Miller, B. N., Hill, S., Olson, K. A., Gabriel, A. E., Boyd, K. A., Satterfield, C., Remmen, H. V., Rutter, J. P., et al. (2017) · eLife · doi:10.7554/elife.22706 · Cited by 32 · see citing works

Regulatory Role of Redox Balance in Determination of Neural Precursor Cell Fate

Iqbal, M. A., & Eftekharpour, E. (2017) · Stem Cells International · doi:10.1155/2017/9209127 · Cited by 27 · see citing works

Regulation and function of the mammalian tricarboxylic acid cycle

Arnold, P. K., & Finley, L. W. S. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2022.102838 · Cited by 535 · see citing works

Mitochondria as central regulators of neural stem cell fate and cognitive function

Khacho, M., Harris, R., & Slack, R. S. (2018) · Nature reviews. Neuroscience · doi:10.1038/s41583-018-0091-3 · Cited by 396 · see citing works

Metabolic Pathways Regulating Colorectal Cancer Initiation and Progression

La Vecchia, S., & Sebastián, C. (2020) · Seminars in Cell &amp; Developmental Biology · doi:10.1016/j.semcdb.2019.05.018 · Cited by 349 · see citing works

Integrated analysis of single-cell and bulk RNA sequencing data reveals a pan-cancer stemness signature predicting immunotherapy response

Zhang, Z., Wang, Z., Chen, Y., Wu, H., Yin, L., Zhao, Q., Luo, H., Zeng, Z.-L., Qiu, M., & Xu, R. (2022) · Genome Medicine · doi:10.1186/s13073-022-01050-w · Cited by 279 · see citing works

Stem cell-based bone and dental regeneration: a view of microenvironmental modulation

Zheng, C., Chen, J., Liu, S., & Jin, Y. J. (2019) · International Journal of Oral Science · doi:10.1038/s41368-019-0060-3 · Cited by 242 · see citing works

HNF4 Regulates Fatty Acid Oxidation and Is Required for Renewal of Intestinal Stem Cells in Mice

Chen, L., Vasoya, R. P., Toke, N. H., Parthasarathy, A., Luo, S., Chiles, E. N., Flores, J., Gao, N., Bonder, E. M., Su, X., et al. (2019) · Gastroenterology · doi:10.1053/j.gastro.2019.11.031 · Cited by 235 · see citing works

Metabolism and Colorectal Cancer

Sedlak, J. C., Yilmaz, Ö. H., & Roper, J. (2022) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathmechdis-031521-041113 · Cited by 201 · see citing works

Colorectal Cancer and Metabolism

Brown, R. E., Short, S. P., & Williams, C. S. (2018) · Current Colorectal Cancer Reports · doi:10.1007/s11888-018-0420-y · Cited by 127 · see citing works

Mitochondrial Regulation of Stem Cells in Bone Homeostasis

Zheng, C., Sui, B., Qiu, X., Hu, C., & Jin, Y. J. (2019) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2019.04.008 · Cited by 121 · see citing works

The Rise of Physiologic Media

Cantor, J. R. (2019) · Trends in Cell Biology · doi:10.1016/j.tcb.2019.08.009 · Cited by 100 · see citing works

PRDM16 Maintains Homeostasis of the Intestinal Epithelium by Controlling Region-Specific Metabolism

Stine, R. R., Sakers, A. P., TeSlaa, T. A., Kissig, M., Stine, Z. E., Kwon, C. W., Cheng, L., Lim, H., Kaestner, K. H., Rabinowitz, J. D., et al. (2019) · Cell stem cell · doi:10.1016/j.stem.2019.08.017 · Cited by 99 · see citing works

Quiescence Entry, Maintenance, and Exit in Adult Stem Cells

Mohammad, K., Dakik, P., Medkour, Y., Mitrofanova, D., & Titorenko, V. I. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20092158 · Cited by 90 · see citing works

Signaling pathways in intestinal homeostasis and colorectal cancer: KRAS at centre stage

Ternet, C., & Kiel, C. (2021) · Cell Communication and Signaling · doi:10.1186/s12964-021-00712-3 · Cited by 69 · see citing works

Mitochondria from osteolineage cells regulate myeloid cell-mediated bone resorption

Ding, P., Gao, C., Zhou, J., Mei, J., Li, G., Liu, D., Li, H., Liao, P., Meng, Y., Wang, B., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-49159-3 · Cited by 64 · see citing works

Glycolytic Regulation of Intestinal Stem Cell Self-Renewal and Differentiation

Li, C., Zhou, Y., Wei, R., Napier, D. L., Sengoku, T., Alstott, M. C., Liu, J., Wang, C., Zaytseva, Y. Y., Weiss, H. L., et al. (2022) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2022.12.012 · Cited by 48 · see citing works

A regeneration-triggered metabolic adaptation is necessary for cell identity transitions and cell cycle re-entry to support blastema formation and bone regeneration

Brandão, A. S., Borbinha, J., Pereira, T., Brito, P. H., Lourenço, R., Bensimon‐Brito, A., & Jacinto, A. (2022) · eLife · doi:10.7554/elife.76987 · Cited by 37 · see citing works

Effect of fibronectin, FGF-2, and BMP4 in the stemness maintenance of BMSCs and the metabolic and proteomic cues involved

Chen, L., Carlton, M., Chen, X., Kaur, N., Ryan, H., Parker, T. J., Lin, Z., Xiao, Y., & Zhou, Y. (2021) · Stem Cell Research & Therapy · doi:10.1186/s13287-021-02227-7 · Cited by 34 · see citing works

Annurca Apple Polyphenols Ignite Keratin Production in Hair Follicles by Inhibiting the Pentose Phosphate Pathway and Amino Acid Oxidation

Badolati, N., Sommella, E., Riccio, G., Salviati, E., Heintz, D., Bottone, S., Cicco, E. D., Dentice, M., Tenore, G. C., Campiglia, P., et al. (2018) · Nutrients · doi:10.3390/nu10101406 · Cited by 33 · see citing works

Challenges in Studying Stem Cell Metabolism

Perez-Ramirez, C. A., & Christofk, H. R. (2021) · Cell stem cell · doi:10.1016/j.stem.2021.02.016 · Cited by 29 · see citing works

Mitophagy: A New Player in Stem Cell Biology

Cairns, G., Thumiah-Mootoo, M., Burelle, Y., & Khacho, M. (2020) · Biology · doi:10.3390/biology9120481 · Cited by 29 · see citing works

HDAC11: A novel target for improved cancer therapy

Liu, Y., Tong, X., Hu, W., & Chen, D. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115418 · Cited by 26 · see citing works

Piezo1 regulates colon stem cells to maintain epithelial homeostasis through SCD1-Wnt-β-catenin and programming fatty acid metabolism

Fang, F., Li, G., Li, X., Wu, J., Liu, Y., Xin, H., Wang, Z., Fang, J., Jiang, Y., Qian, W., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115400 · Cited by 24 · see citing works

Taking the road less traveled – the therapeutic potential of CBP/β-catenin antagonists

Kahn, M. (2021) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2021.1992386 · Cited by 19 · see citing works

Reprogramming hormone-sensitive prostate cancer to a lethal neuroendocrine cancer lineage by mitochondrial pyruvate carrier (MPC)

Xu, H., Liu, Z., Gao, D., Li, P., Shen, Y., Sun, Y., Xu, L., Song, N., Wang, Y., Zhan, M., et al. (2022) · Molecular Metabolism · doi:10.1016/j.molmet.2022.101466 · Cited by 20 · see citing works

Metaboverse enables automated discovery and visualization of diverse metabolic regulatory patterns

Berg, J. A., Zhou, Y., Ouyang, Y., Cluntun, A. A., Waller, T. C., Conway, M. E., Nowinski, S. M., Ry, T. V., George, I. D., Cox, J. E., et al. (2023) · Nature Cell Biology · doi:10.1038/s41556-023-01117-9 · Cited by 18 · see citing works

RIPK4-mediated MFN2 degradation drives osteogenesis through mitochondrial fragmentation and restricts myelopoiesis by blocking mitochondrial transfer

Ding, P., Wang, X., Gao, C., Wei, Y., Gan, L., Zhu, W., Wang, N., Fu, W., Fang, Q., Meng, Y., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-61808-9 · Cited by 11 · see citing works

Understanding the “SMART” features of hematopoietic stem cells and beyond

Yuan, S., Sun, G., Zhang, Y., Dong, F., Cheng, H., & Cheng, T. (2021) · Science China Life Sciences · doi:10.1007/s11427-021-1961-1 · Cited by 11 · see citing works

Live cell imaging of metabolic heterogeneity by quantitative fluorescent ATP indicator protein, QUEEN-37CPreprint

Yaginuma, H., & Okada, Y. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.08.463131 · Cited by 10 · see citing works

Differential Kat3 Usage Orchestrates the Integration of Cellular Metabolism with Differentiation

Hu, X., Ono, M., Chimge, N., Chosa, K., Nguyen, C., Melendez, E., Lou, C., Lim, P. P., Termini, J. S., Lai, K. K. Y., et al. (2021) · Cancers · doi:10.3390/cancers13235884 · Cited by 9 · see citing works

Mitochondrial substrate oxidation regulates distinct cell differentiation outcomes

Park, W. Y., Montufar, C., & Zaganjor, E. (2025) · Trends in Cell Biology · doi:10.1016/j.tcb.2025.02.004 · Cited by 5 · see citing works

Effect of Free Long-Chain Fatty Acids on Anagen Induction: Metabolic or Inflammatory Aspect?

Pan, X., Vishnyakova, K. S., Chermnykh, E. S., Jasko, M. V., Zhuravlev, A. D., Verkhova, S. S., Chegodaev, Y. S., Popov, M. A., Nikiforov, N. G., & Yegorov, Y. E. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26062567 · Cited by 4 · see citing works

A niche-dependent redox rheostat regulates epithelial stem cell fate

Chen, X., Raghunathan, K., Bao, B., Ngwa, E. M., Kwong, A., Wu, Z., Babcock, S. J., Baek, C., Ye, G., Muppirala, A. N., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-66636-5 · Cited by 4 · see citing works

Mesenchymal stem cells and exosomes in bone defects treatment

Greben, A. I., Eremin, P. S., Kostromina, E. Y., Александрович, М. П., & Ринатовна, Г. И. (2024) · Genij Ortopedii · doi:10.18019/1028-4427-2024-30-1-124-133 · Cited by 4 · see citing works

An Injectable Composite Hydrogel Enhances Bone Regeneration by Rescuing Impaired Mitochondrial Biogenesis and Fusion of BMSCs under Inflammatory Conditions

Jiang, W., Pan, Z., Zhang, Z., Yan, X., Palasuberniam, P., Xiao, J. Y., Shen, J., Guo, D., Zhang, Y., & Liu, H. (2025) · ACS Applied Polymer Materials · doi:10.1021/acsapm.4c03332 · Cited by 4 · see citing works

Modulation of PKM1/2 Levels by Steric Blocking Morpholinos Alters the Metabolic and Pluripotent State of Murine Pluripotent Stem Cells

Dierolf, J. G., Hunter, H., Watson, A. J., & Betts, D. H. (2022) · Stem Cells and Development · doi:10.1089/scd.2021.0347 · Cited by 3 · see citing works

SOX2‐positive retinal stem cells are identified in adult human pars plicata by single‐cell transcriptomic analyses

Wang, X., Fan, W., Xu, Z., Zhang, Q., Li, N., Li, R., Wang, G., He, S., Li, W., Liao, D., et al. (2022) · MedComm · doi:10.1002/mco2.198 · Cited by 3 · see citing works

The Role of Hypoxia in Metabolism and Nephron Development

Cargill, K. R. (2019) · D-Scholarship@Pitt (University of Pittsburgh)

Hyperbaric oxygen treatment increases intestinal stem cell proliferation through mTORc1 signaling in Mus musculusPreprint

casanova, I., Peña‐Villalobos, I., Arancibia‐Altamirano, D., Lois, P., & Palma, V. (2020) · Research Square · doi:10.21203/rs.3.rs-108513/v1

Role of Mitochondrial pyruvate carrier in ovarian cancer progression

Farook, M. Z. (2022) · doi:10.23889/suthesis.60124

Monitoring ADSC Metabolism Using the Seahorse Analyzer

Rittenhouse, D. J., & Zwezdaryk, K. J. (2024) · Methods in molecular biology · doi:10.1007/978-1-0716-3762-3_24

The One-Dimensional (1D) Numerical Model: An Application to Oxygen Diffusion in Mitochondria Cell

Napitupulu, G., Nagi, A., Putri, M. R., & Radjawane, I. M. (2023) · ComTech Computer Mathematics and Engineering Applications · doi:10.21512/comtech.v14i2.9705

Стовбурові клітини: біологічні властивості та терапевтичний потенціал у регенеративній медицині

Пикалюк, В., Antoniuk, О. P., Романюк, А., Sokolyuk, V. M., & Шварц, Л. О. (2025) · Notes in Current Biology · doi:10.29038/10.29038/ncbio.25.1-7

Additional file 2 of Integrated analysis of single-cell and bulk RNA sequencing data reveals a pan-cancer stemness signature predicting immunotherapy response

Zhang, Z., Wang, Z.-X., Chen, Y.-X., Wu, H.-X., Yin, L., Zhao, Q., Luo, H.-Y., Zeng, Z., Qiu, M., & Xu, R.-H. (2022) · Figshare · doi:10.6084/m9.figshare.19687417

Additional file 5 of Effect of fibronectin, FGF-2, and BMP4 in the stemness maintenance of BMSCs and the metabolic and proteomic cues involved

Chen, L., Carlton, M., Chen, X., Kaur, N., Ryan, H., Parker, T. J., Lin, Z., Xiao, Y., & Zhou, Y. (2021) · Figshare · doi:10.6084/m9.figshare.14175983

Additional file 6 of Effect of fibronectin, FGF-2, and BMP4 in the stemness maintenance of BMSCs and the metabolic and proteomic cues involved

Chen, L., Carlton, M., Chen, X., Kaur, N., Ryan, H., Parker, T. J., Lin, Z., Xiao, Y., & Zhou, Y. (2021) · Figshare · doi:10.6084/m9.figshare.14175986

Additional file 1 of Integrated analysis of single-cell and bulk RNA sequencing data reveals a pan-cancer stemness signature predicting immunotherapy response

Zhang, Z., Wang, Z.-X., Chen, Y.-X., Wu, H.-X., Yin, L., Zhao, Q., Luo, H.-Y., Zeng, Z.-L., Qiu, M., & Xu, R.-H. (2022) · Figshare · doi:10.6084/m9.figshare.19687414

Additional file 1 of Effect of fibronectin, FGF-2, and BMP4 in the stemness maintenance of BMSCs and the metabolic and proteomic cues involved

Chen, L., Carlton, M., Chen, X., Kaur, N., Ryan, H., Parker, T. J., Lin, Z., Xiao, Y., & Zhou, Y. (2021) · Figshare · doi:10.6084/m9.figshare.14175971

Stem cell metabolism in tissue development and aging

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Energy Metabolism Plays a Critical Role in Stem Cell Maintenance and Differentiation

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