c-Myc regulates cell size and ploidy but is not essential for postnatal proliferation in liver

Induction of apoptosis in fibroblasts by c-myc protein

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c-Myc Target Genes Involved in Cell Growth, Apoptosis, and Metabolism

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Inducible Gene Targeting in Mice

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Liver regeneration

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Predictors of morbidity and mortality after the first episode of upper gastrointestinal bleeding in liver cirrhosis

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c-Myc Can Induce DNA Damage, Increase Reactive Oxygen Species, and Mitigate p53 Function

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MYC inactivation uncovers pluripotent differentiation and tumour dormancy in hepatocellular cancer

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Constitutive c-myc expression in an IL-3-dependent myeloid cell line suppresses cell cycle arrest and accelerates apoptosis.

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c-Myc controls the balance between hematopoietic stem cell self-renewal and differentiation

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Drosophila myc Regulates Cellular Growth during Development

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MYC on the Path to Cancer

Dang, C. V. (2012) · Cell · doi:10.1016/j.cell.2012.03.003 · Cited by 3,390

Rapid Loss of Intestinal Crypts upon Conditional Deletion of the Wnt/Tcf-4 Target Gene c-Myc

Muncan, V., Sansom, O. J., Tertoolen, L. G. J., Phesse, T. J., Begthel, H., Sancho, E., Cole, A. M., Gregorieff, A., de Alborán, I. M., Clevers, H. C., et al. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.00821-06 · Cited by 249

The Role for Myc in Coordinating Glycolysis, Oxidative Phosphorylation, Glutaminolysis, and Fatty Acid Metabolism in Normal and Neoplastic Tissues

Goetzman, E. S., & Prochownik, E. V. (2018) · Frontiers in Endocrinology · doi:10.3389/fendo.2018.00129 · Cited by 199

Polyploidization in Liver Tissue

Gentric, G., & Desdouets, C. (2014) · The American Journal of Pathology · doi:10.1016/j.ajpath.2013.06.035 · Cited by 192

Polyploidy in liver development, homeostasis and disease

Donne, R., Saroul-Aïnama, M., Cordier, P., Celton-Morizur, S., & Desdouets, C. (2020) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-020-0284-x · Cited by 188

Focal Adhesion Kinase Is Required for Intestinal Regeneration and Tumorigenesis Downstream of Wnt/c-Myc Signaling

Ashton, G. H. S., Morton, J. P., Myant, K., Phesse, T. J., Ridgway, R. A., Marsh, V. L., Wilkins, J. A., Athineos, D., Muncan, V., Kemp, R., et al. (2010) · Developmental Cell · doi:10.1016/j.devcel.2010.07.015 · Cited by 195

c-Myc depletion inhibits proliferation of human tumor cells at various stages of the cell cycle

Wang, H., Mannava, S., Grachtchouk, V., Zhuang, D., Soengas, M. S., Gudkov, A. V., Prochownik, E. V., & Nikiforov, M. A. (2007) · Oncogene · doi:10.1038/sj.onc.1210823 · Cited by 176

Mechanisms Limiting Body Growth in Mammals

Lui, J. C. K., & Baron, J. (2011) · Endocrine Reviews · doi:10.1210/er.2011-0001 · Cited by 170

Myc controls transcriptional regulation of cardiac metabolism and mitochondrial biogenesis in response to pathological stress in mice

Ahuja, P., Zhao, P., Angelis, E., Ruan, H., Korge, P., Olson, A., Wang, Y., Jin, E. S., Jeffrey, F. M., Portman, M., et al. (2010) · Journal of Clinical Investigation · doi:10.1172/jci38331 · Cited by 157

To divide or not to divide: revisiting liver regeneration

Miyaoka, Y., & Miyajima, A. (2013) · Cell Division · doi:10.1186/1747-1028-8-8 · Cited by 156

C‐Myc and its target FoxM1 are critical downstream effectors of constitutive androstane receptor (CAR) mediated direct liver hyperplasia†

Blanco‐Bose, W. E., Murphy, M. J., Ehninger, A., Offner, S., Dubey, C., Huang, W., Moore, D. D., & Trumpp, A. (2008) · Hepatology · doi:10.1002/hep.22475 · Cited by 138

BCL6 is critical for the development of a diverse primary B cell repertoire

Duy, C., Yu, J. J., Nahar, R. R., Swaminathan, S., Kweon, S.-M., Polo, J. M., Valls, E., Klemm, L., Shojaee, S., Cerchietti, L. C. A., et al. (2010) · The Journal of Experimental Medicine · doi:10.1084/jem.20091299 · Cited by 129

Endogenous Myc controls mammalian epidermal cell size, hyperproliferation, endoreplication and stem cell amplification

Zanet, J., Pibre, S., Jacquet, C., Ramirez, A., de Alborán, I. M., & Gandarillas, A. (2005) · Journal of Cell Science · doi:10.1242/jcs.02298 · Cited by 123

Hypertrophic growth in cardiac myocytes is mediated by Myc through a Cyclin D2‐dependent pathway

Zhong, W., Mao, S., Tobis, S., Angelis, E., Jordan, M. C., Roos, K. P., Fishbein, M. C., de Alborán, I. M., & MacLellan, W. R. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601252 · Cited by 115

Opposing effects of TIGAR- and RAC1-derived ROS on Wnt-driven proliferation in the mouse intestinePreprint

Cheung, E. C., Lee, P., Ceteci, F., Nixon, C., Blyth, K., Sansom, O. J., & Vousden, K. H. (2015) · Genes & Development · doi:10.1101/gad.271130.115 · Cited by 114

Pancreatic Inactivation of c-Myc Decreases Acinar Mass and Transdifferentiates Acinar Cells Into Adipocytes in Mice

Bonal, C., Thorel, F., Ait‐Lounis, A., Reith, W., Trumpp, A., & Herrera, P. L. (2008) · Gastroenterology · doi:10.1053/j.gastro.2008.10.015 · Cited by 112

Cellular plasticity balances the metabolic and proliferation dynamics of a regenerating liver

Chembazhi, U. V., Bangru, S., Hernaez, M., & Kalsotra, A. (2021) · Genome Research · doi:10.1101/gr.267013.120 · Cited by 102

Myc's other life: stem cells and beyond

Laurenti, E., Wilson, A., & Trumpp, A. (2009) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2009.09.006 · Cited by 101

Placental rescue reveals a sole requirement for c-Myc in embryonic erythroblast survival and hematopoietic stem cell function

Dubois, N. C., Adolphe, C., Ehninger, A., Wang, R. A., Robertson, E. J., & Trumpp, A. (2008) · Development · doi:10.1242/dev.022707 · Cited by 95

Cyclin D2–Cyclin-Dependent Kinase 4/6 Is Required for Efficient Proliferation and Tumorigenesis following Apc Loss

Cole, A. M., Myant, K., Reed, K. R., Ridgway, R. A., Athineos, D., van den Brink, G. R., Muncan, V., Clevers, H. C., Clarke, A. R., Siciński, P., et al. (2010) · Cancer Research · doi:10.1158/0008-5472.can-10-0315 · Cited by 90

MicroRNA‐122 regulates polyploidization in the murine liver

Hsu, S., Delgado, E. R., Otero, P. A., Teng, K., Kutay, H., Meehan, K. M., Moroney, J. B., Monga, J. K., Hand, N. J., Friedman, J. R., et al. (2016) · Hepatology · doi:10.1002/hep.28573 · Cited by 84

c-MYC—Making Liver Sick: Role of c-MYC in Hepatic Cell Function, Homeostasis and Disease

Zheng, K., Cubero, F., & Nevzorova, Y. (2017) · Genes · doi:10.3390/genes8040123 · Cited by 84

c-Myc–mediated control of cell fate in megakaryocyte-erythrocyte progenitors

Guo, Y., Niu, C. S., Breslin, P., Tang, M., Zhang, S., Wei, W., Kini, A. R., Paner, G. P., Alkan, S., Morris, S. W., et al. (2009) · Blood · doi:10.1182/blood-2009-01-197947 · Cited by 82

Interactions between Myc and Mediators of Inflammation in Chronic Liver Diseases

Liu, T., Zhou, Y., Ko, K. S., & Yang, H. (2015) · Mediators of Inflammation · doi:10.1155/2015/276850 · Cited by 93

Role of Myc in hepatocellular proliferation and hepatocarcinogenesis

Qu, A., Jiang, C., Cai, Y., Kim, J. H., Tanaka, N., Ward, J. M., Shah, Y. M., & Gonzalez, F. J. (2013) · Journal of Hepatology · doi:10.1016/j.jhep.2013.09.024 · Cited by 80

c-mycin the hematopoietic lineage is crucial for its angiogenic function in the mouse embryo

He, C., Hu, H., Braren, R., Fong, S.-Y., Trumpp, A., Carlson, T. R., & Wang, R. A. (2008) · Development · doi:10.1242/dev.020131 · Cited by 74

Myc Function in DrosophilaPreprint

Gallant, P. (2013) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a014324 · Cited by 74

B-catenin deficiency, but not Myc deletion, suppresses the immediate phenotypes of APC loss in the liver

Reed, K. R., Athineos, D., Méniel, V. S., Wilkins, J. A., Ridgway, R. A., Burke, Z. D., Muncan, V., Clarke, A. R., & Sansom, O. J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0805778105 · Cited by 67

Lessons from Functional Analysis of Genome-Wide Association Studies

Sur, I., Tuupanen, S., Whitington, T., Aaltonen, L. A., & Taipale, J. (2013) · Cancer Research · doi:10.1158/0008-5472.can-13-0789 · Cited by 68

The mysterious human epidermal cell cycle, or an oncogene-induced differentiation checkpoint

Gandarillas, A. (2012) · Cell Cycle · doi:10.4161/cc.22529 · Cited by 61

Universal encoding of pan-cancer histology by deep texture representations

Komura, D., Kawabe, A., Fukuta, K., Sano, K., Umezaki, T., Koda, H., Suzuki, R. H., Tominaga, K., Ochi, M., Konishi, H., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110424 · Cited by 69

Mice deficient of Myc super-enhancer region reveal differential control mechanism between normal and pathological growth

Dave, K., Sur, I., Yan, J., Zhang, J., Kaasinen, E., Zhong, F., Blaas, L., Li, X., Kharazi, S., Gustafsson, C., et al. (2017) · eLife · doi:10.7554/elife.23382 · Cited by 61

Aurora kinase A mediates c‐Myc's oncogenic effects in hepatocellular carcinoma

Lu, L.-F., Han, H., Tian, Y., Li, W., Zhang, J., Feng, M., & Li, Y. (2014) · Molecular Carcinogenesis · doi:10.1002/mc.22223 · Cited by 55

Role of c-Myc in intestinal tumorigenesis of the Apc min/+ mouse1

Ignatenko, N. A., Holubec, H., Besselsen, D. G., Blohm-Mangone, K. A., Padilla‐Torres, J., Nagle, R. B., de Alborán, I. M., Guillen-Rodriguez, J., & Gerner, E. W. (2006) · Cancer Biology & Therapy · doi:10.4161/cbt.5.12.3376 · Cited by 54

MYC in liver cancer: mechanisms and targeted therapy opportunities

Liu, F., Liao, Z., & Zhang, Z. (2023) · Oncogene · doi:10.1038/s41388-023-02861-w · Cited by 53

Dexamethasone-Induced Liver Enlargement Is Related to PXR/YAP Activation and Lipid Accumulation but Not Hepatocyte Proliferation

Jiao, T., Yao, X., Zhao, Y.-Y., Zhou, Y., Gao, Y., Fan, S., Chen, P., Li, X., Jiang, Y., Xiao, Y., et al. (2020) · Drug Metabolism and Disposition · doi:10.1124/dmd.120.000061 · Cited by 49

Somatic polyploidy is associated with the upregulation of c-MYC interacting genes and EMT-like signature

Vázquez‐Martín, A., Anatskaya, O. V., Giuliani, A., Erenpreisa, J. A., Huang, S., Salmiņa, K., Inashkina, I., Huna, A., Nikolsky, N. N., & Vinogradov, A. E. (2016) · Oncotarget · doi:10.18632/oncotarget.12118 · Cited by 48

c-Myc is essential for hematopoietic stem cell differentiation and regulates Lin−Sca-1+c-Kit− cell generation through p21

Baena, E., Ortiz, M., Martínez‐A, C., & de Alborán, I. M. (2007) · Experimental Hematology · doi:10.1016/j.exphem.2007.05.015 · Cited by 51

Myc and ChREBP transcription factors cooperatively regulate normal and neoplastic hepatocyte proliferation in mice

Wang, H., Dolezal, J. M., Kulkarni, S., Lu, J. L., Mandel, J. A., Jackson, L. E., Alencastro, F., Duncan, A. W., & Prochownik, E. V. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.004099 · Cited by 46

Control of Cell Proliferation and Growth by Myc Proteins

Bernard, S., & Eilers, M. (2006) · Springer eBooks · doi:10.1007/400_004 · Cited by 48

Myc heterozygosity attenuates the phenotypes of APC deficiency in the small intestine

Athineos, D., & Sansom, O. J. (2010) · Oncogene · doi:10.1038/onc.2010.5 · Cited by 45

Myc in model organisms: A view from the flyroom

de la Cova, C., & Johnston, L. A. (2006) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2006.07.010 · Cited by 44

Conditional Deletion ofc-mycDoes Not Impair Liver Regeneration

Li, F., Xiang, Y., Potter, J. J., Dinavahi, R., Dang, C. V., & Lee, L. A. (2006) · Cancer Research · doi:10.1158/0008-5472.can-05-4242 · Cited by 44

Role of HNF4alpha-cMyc interaction in liver regeneration and recovery after acetaminophen-induced acute liver injury

Kotulkar, M., Paine‐Cabrera, D., Abernathy, S., Robarts, D. R., Parkes, W. S., Lin‐Rahardja, K., Numata, S., Lebofsky, M., Jaeschke, H., & Apte, U. M. (2023) · Hepatology · doi:10.1097/hep.0000000000000367 · Cited by 44

MYC—an emerging player in mitochondrial diseases

Purhonen, J., Klefström, J. T., & Kallijärvi, J. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1257651 · Cited by 42

Abnormal lipid processing but normal long-term repopulation potential of myc−/− hepatocytes

Edmunds, L. R., Otero, P. A., Sharma, L., D'Souza, S. S., Dolezal, J. M., David, S., Lu, J. L., Lamm, L., Basantani, M. K., Zhang, P., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.8856 · Cited by 37

B Lymphocyte Commitment Program Is Driven by the Proto-Oncogene c-myc

Vallespinós, M., Fernández‐Antorán, D., Rodríguez, L., Álvaro-Blanco, J., Baena, E., Ortiz, M., Dukovska, D., Martínez, D., Rojas, A. M., Campanero, M. R., et al. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1002753 · Cited by 38

Postnatal liver growth and regeneration are independent of c-myc in a mouse model of conditional hepatic c-myc deletion

Sanders, J. A., Schorl, C., Patel, A. J., Sedivy, J. M., & Gruppuso, P. A. (2012) · BMC Physiology · doi:10.1186/1472-6793-12-1 · Cited by 38

c-Myc affects mRNA translation, cell proliferation and progenitor cell function in the mammary gland

Stoelzle, T., Schwarb, P., Trumpp, A., & Hynes, N. E. (2009) · BMC Biology · doi:10.1186/1741-7007-7-63 · Cited by 38

p21 loss blocks senescence following Apc loss and provokes tumourigenesis in the renal but not the intestinal epithelium

Cole, A. M., Ridgway, R. A., Derkits, S., Parry, L., Barker, N., Clevers, H. C., Clarke, A. R., & Sansom, O. J. (2010) · EMBO Molecular Medicine · doi:10.1002/emmm.201000101 · Cited by 35

Polyploidy and Myc Proto-Oncogenes Promote Stress Adaptation via Epigenetic Plasticity and Gene Regulatory Network Rewiring

Anatskaya, O. V., & Vinogradov, A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23179691 · Cited by 27

cMyc increases cell number through uncoupling of cell division from cell size in CHO cells

Kuystermans, D., & Al-Rubeai, M. (2009) · BMC Biotechnology · doi:10.1186/1472-6750-9-76 · Cited by 33

Defining the role of APC in the mitotic spindle checkpoint in vivo: APC-deficient cells are resistant to Taxol

Radulescu, S., Ridgway, R. A., Appleton, P., Kroboth, K., Patel, S., Woodgett, J. R., Taylor, S. S., Näthke, I. S., & Sansom, O. J. (2010) · Oncogene · doi:10.1038/onc.2010.373 · Cited by 32

Deficiency of the oxygen sensor PHD1 augments liver regeneration after partial hepatectomy

Mollenhauer, M., Kiss, J., Dudda, J., Kirchberg, J., Rahbari, N. N., Radhakrishnan, P., Niemietz, T., Rausch, V., Weitz, J., & Schneider, M. A. (2012) · Langenbeck s Archives of Surgery · doi:10.1007/s00423-012-0998-5 · Cited by 31

Growth-promoting and tumourigenic activity of c-Myc is suppressed by Hhex

Marfil, V., Blazquez, M., Serrano, F., Castell, J. V., & Bort, R. (2014) · Oncogene · doi:10.1038/onc.2014.240 · Cited by 30

Excessive hepatomegaly of mice with hepatocyte-targeted elimination of integrin linked kinase following treatment with 1,4-bis [2-(3,5-dichaloropyridyloxy)] benzene

Donthamsetty, S., Bhave, V., Kliment, C. R., Bowen, W. C., Mars, W. M., Bell, A. W., Stewart, R. E., Orr, A. V., Wu, C., & Michalopoulos, G. K. (2010) · Hepatology · doi:10.1002/hep.24040 · Cited by 30

NADPH oxidase 4 (Nox4) deletion accelerates liver regeneration in mice

Herranz‐Itúrbide, M., López‐Luque, J., Gonzalez‐Sanchez, E., Caballero‐Díaz, D., Crosas‐Molist, E., Martín‐Mur, B., Gut, M. O., Esteve‐Codina, A., Jaquet, V., Jiang, J. X., et al. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101841 · Cited by 27

Irs2 Inactivation Suppresses Tumor Progression in Pten+/− Mice

Szabolcs, M. J., Keniry, M. E., Simpson, L., Reid, L. J., Koujak, S., Schiff, S. C., Davidian, G., Licata, S. E., Gruvberger-Saal, S. K., Murty, V. V. V. S., et al. (2008) · American Journal Of Pathology · doi:10.2353/ajpath.2009.080086 · Cited by 24

p27Kip1 Mediates Addiction of Ovarian Cancer Cells to MYCC (c-MYC) and Their Dependence on MYC Paralogs

Prathapam, T., Aleshin, A. A., Guan, Y., Gray, J. W., & Martin, G. S. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.151902 · Cited by 22

Coordinated Cross-Talk Between the Myc and Mlx Networks in Liver Regeneration and Neoplasia

Wang, H., Lu, J. L., Alencastro, F., Roberts, A., Fiedor, J., Carroll, P. A., Eisenman, R. N., Ranganathan, S., Torbenson, M. S., Duncan, A. W., et al. (2022) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2022.02.018 · Cited by 18

Cell size does not always correspond to genome size: Phylogenetic analysis in geckos questions optimal DNA theories of genome size evolution

Starostová, Z., Kratochvíl, L., & Flajšhans, M. (2008) · Zoology · doi:10.1016/j.zool.2007.10.005 · Cited by 20

Regulation of Normal and Neoplastic Proliferation and Metabolism by the Extended Myc Network

Prochownik, E. V. (2022) · Cells · doi:10.3390/cells11243974 · Cited by 17

Computational modeling identifies key gene regulatory interactions underlying phenobarbital-mediated tumor promotion

Luisier, R., Unterberger, E. B., Goodman, J. I., Schwarz, M., Moggs, J. G., Terranova, R., & van Nimwegen, E. (2014) · Nucleic Acids Research · doi:10.1093/nar/gkt1415 · Cited by 18

An E2F5-TFDP1-BRG1 Complex Mediates Transcriptional Activation of MYCN in Hepatocytes

Fan, Z., Kong, M., Miao, X., Guo, Y., Ren, H., Wang, J., Wang, S., Tang, N., Shang, L., Zhu, Z., et al. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.742319 · Cited by 16

Controlling cell length

Kharitonova, M. A., & Vasiliev, J. M. (2008) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2008.07.008 · Cited by 15

Lessons in aging from Myc knockout mouse models

Prochownik, E. V., & Wang, H. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1244321 · Cited by 16

High dietary inorganic phosphate enhances cap-dependent protein translation, cell-cycle progression, and angiogenesis in the livers of young mice

Xu, C., Jin, H., Lim, H.-T., Kim, J., Shin, J., Lee, E.-S., Chung, Y.-S., Lee, Y.-S., Beck, G. R., Lee, K. H., et al. (2008) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.90213.2008 · Cited by 14

Manipulating Myc for reparative regeneration

Ascanelli, C., Dahir, R., & Wilson, C. H. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1357589 · Cited by 15

Myc beyond Cancer: Regulation of Mammalian Tissue Regeneration

Illi, B., & Nasi, S. (2023) · Pathophysiology · doi:10.3390/pathophysiology30030027 · Cited by 13

Hepatocyte-specific C-C motif chemokine ligand 9 signaling promotes liver fibrosis progression in mice

Wang, C., Dong, D., Zhao, N., Zhao, S., Hua, J., Bai, C., Cui, R., Zhao, T., Ji, N., Li, H., et al. (2025) · Hepatology · doi:10.1097/hep.0000000000001393 · Cited by 10

The Role of the Proto-Oncogene c-myc in B Lymphocyte Differentiation

Fernández‐Antorán, D., Lobo, V. J. S.-A., & de Alborán, I. M. (2012) · Critical Reviews in Immunology · doi:10.1615/critrevimmunol.v32.i4.30 · Cited by 6

The fate of pyruvate dictates cell growth by modulating cellular redox potentialPreprint

Toshniwal, A. G., Lam, G., Bott, A. J., Cluntun, A. A., Skabelund, R. A., Nam, H.-J., Wisidagama, D. R., Thummel, C. S., & Rutter, J. P. (2024) · eLife · doi:10.7554/elife.103705 · Cited by 6

A Novel Mouse Model of Combined Hepatocellular-Cholangiocarcinoma Induced by Diethylnitrosamine and Loss of Ppp2r5d

Omella, J. D., Cortesi, E. E., Verbinnen, I., Remmerie, M., Wu, H., Cubero, F. J., Roskams, T., & Janssens, V. (2023) · Cancers · doi:10.3390/cancers15164193 · Cited by 6

Temporal myc dynamics permit mitotic bypass, promoting polyploid phenotypes

Loycano, M. A., Pienta, K. J., & Amend, S. R. (2025) · Cancer Letters · doi:10.1016/j.canlet.2025.217526 · Cited by 6

Hierarchies of Transcriptional Regulation During Liver Regeneration

Kurinna, S. M., & Barton, M. C. (2010) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-385233-5.00007-6 · Cited by 5

ESRP2–microRNA-122 axis promotes the postnatal onset of liver polyploidization and maturation

Bangru, S., Chen, J., Baker, N., Das, D., Chembazhi, U. V., Derham, J. M., Chorghade, S., Arif, W., Alencastro, F., Duncan, A. W., et al. (2025) · Genes & Development · doi:10.1101/gad.352129.124 · Cited by 4

Endomitosis: a new cell fate in the cell cycle leading to polyploidy in megakaryocytes and hepatocytes

Hua, Q.-H., Zhang, X., Tian, R., She, Z., & Huang, Z. (2025) · Journal of Zhejiang University SCIENCE B · doi:10.1631/jzus.b2400127 · Cited by 4

TCR-Independent Metabolic Reprogramming Precedes Lymphoma-Driven Changes in T-cell Fate

Hesterberg, R. S., Liu, M., Elmarsafawi, A. G., Koomen, J. M., Welsh, E. A., Hesterberg, S. G., Ranatunga, S., Yang, C., Li, W., Lawrence, H. R., et al. (2022) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-21-0813 · Cited by 3

The fate of pyruvate dictates cell growth by modulating cellular redox potential

Toshniwal, A. G., Lam, G., Bott, A. J., Cluntun, A. A., Skabelund, R. A., Nam, H.-J., Wisidagama, D. R., Thummel, C. S., & Rutter, J. P. (2025) · eLife · doi:10.7554/elife.103705.3 · Cited by 3

Changes in Hepatocyte Ploidy During Liver Regeneration

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Data from Cyclin D2–Cyclin-Dependent Kinase 4/6 Is Required for Efficient Proliferation and Tumorigenesis following Apc Loss

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Postnatal liver growth and regeneration are independent of c-myc in a mouse model of conditional hepatic c-myc deletion

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