Chronic Liver Injury Induces Conversion of Biliary Epithelial Cells into Hepatocytes

Liver fibrosis

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A global double-fluorescent Cre reporter mouse

Muzumdar, M. D., Tasic, B., Miyamichi, K., Li, L., & Luo, L. (2007) · genesis · doi:10.1002/dvg.20335 · Cited by 3,491

Liver cirrhosis

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Liver regeneration

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Lineage Tracing

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Liver regeneration and repair: Hepatocytes, progenitor cells, and stem cells

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Evolving challenges in hepatic fibrosis

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Bipotential Adult Liver Progenitors Are Derived from Chronically Injured Mature Hepatocytes

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Cholangiocytes act as facultative liver stem cells during impaired hepatocyte regeneration

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Robust cellular reprogramming occurs spontaneously during liver regeneration

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The truth lies somewhere in the middle: the cells responsible for liver tissue maintenance finally identified

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Dynamic, IPSC-derived hepatic tissue tri-culture system for the evaluation of liver physiology in vitro

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Lineage plasticity and reprogramming of epithelial cells during tissue injury and regeneration-lessons from the lineage plasticity of hepatocytes and cholangiocytes induced by liver injury–

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The Chromatin Accessibility Landscape in Cell Plasticity and Reprogramming: Understanding and Overcoming the Barriers

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Recapitulating the liver niche in vitro

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Primary cilium‐mediated signaling cascade suppresses age‐related biliary fibrosis

Hong, R., Tian, X., Ma, H., Ni, H., Yang, J. N., Bu, W., Li, T., Yang, S., Li, D., Liu, M., et al. (2023) · Journal of Cellular Physiology · doi:10.1002/jcp.31113 · Cited by 4

Epigenetic regulation in liver regeneration

Li, Z., & Sun, X. (2024) · Life Sciences · doi:10.1016/j.lfs.2024.122924 · Cited by 5

mRNA translational control of regeneration

Amiri, M., Sonenberg, N., & Tahmasebi, S. (2025) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2025.102367 · Cited by 5

Vertebrate lonesome kinase modulates the hepatocyte secretome to prevent perivascular liver fibrosis and inflammation

Pantasis, S., Friemel, J., Brütsch, S. M., Hu, Z., Krautbauer, S., Liebisch, G., Dengjel, J., Weber, A., Werner, S., & Bordoli, M. R. (2022) · Journal of Cell Science · doi:10.1242/jcs.259243 · Cited by 4

Redox experimental medicine and liver regeneration

Bellanti, F., Vendemiale, G., & Serviddio, G. (2022) · Redox Experimental Medicine · doi:10.1530/rem-22-0008 · Cited by 4

Update on Hepatobiliary Plasticity

Kim, M., Rizvi, F., Shin, D., & Gouon–Evans, V. (2023) · Seminars in Liver Disease · doi:10.1055/s-0042-1760306 · Cited by 5

Toward a Reconceptualization of Stem Cells from Cellular Plasticity

Liu, T., Chen, L., Zhao, Z., & Zhang, S.-C. (2019) · International Journal of Stem Cells · doi:10.15283/ijsc18096 · Cited by 5

Cell identity conversion in liver regeneration after injury

He, Q., Cui, L., Yuan, X., Wang, M., & Hui, L. (2022) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2022.101921 · Cited by 4

Biliary-derived hepatocytes in chronic liver injury: Bringing new troops to the battlefield?

Aleksieva, N., & Forbes, S. J. (2019) · Journal of Hepatology · doi:10.1016/j.jhep.2019.03.015 · Cited by 4

Canonical Wnt signalling is activated during BEC-to-hepatocyte conversion in vivo and modulates liver epithelial cell plasticity in hepatic organoidsPreprint

Valle-Encinas, E., Aleksieva, N., Martinez, C. V., Dawes, M., Zverev, M., Müller, M., Offergeld, A., Smalley, M. J., Hogan, C., Forbes, S. J., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.11.09.374462 · Cited by 4

Human embryonic stem cell-derived immunity-and-matrix regulatory cells promote intrahepatic cell renewal to rescue acute liver failure

Chen, L., Li, Z., Wei, W., An, B., Tian, Y., Liu, W., Niu, S., Wang, Y., Wang, L., Li, W., et al. (2023) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2023.04.051 · Cited by 3

Dexmedetomidine facilitates autophagic flux to promote liver regeneration by suppressing GSK3β activity in mouse partial hepatectomy

Yao, X., Liu, Y., Sui, Y., Miao, Z., Zhu, L., Li, Q., Irwin, M. G., Yang, L., Zhan, Q., & Xiao, J. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.117038 · Cited by 3

Modulation of liver regeneration by the nuclear factor erythroid 2-related factor 2

Bellanti, F., Serviddio, G., & Vendemiale, G. (2023) · Advances in Redox Research · doi:10.1016/j.arres.2023.100066 · Cited by 3

Molecular mechanisms of metabolic disease-associated hepatic inflammation in non-alcoholic fatty liver disease and non-alcoholic steatohepatitis

Zhang, C., Sui, Y., Liu, S., & Yang, M. J. (2023) · Exploration of Digestive Diseases · doi:10.37349/edd.2023.00029 · Cited by 3

Mechanobiological stimulation in organ‐on‐a‐chip systems reduces hepatic drug metabolic capacity in favor of regenerative specialization

Scheidecker, B., Poulain, S., Sugimoto, M., Arakawa, H., Kim, S. H., Kawanishi, T., Kato, Y., Danoy, M., Nishikawa, M., & Sakai, Y. (2024) · Biotechnology and Bioengineering · doi:10.1002/bit.28653 · Cited by 3

Cell reprogramming in liver with potential clinical correlations

Wang, Y. C., Wang, Z. J., Zhang, C., & Ning, B. F. (2021) · Journal of Digestive Diseases · doi:10.1111/1751-2980.13072 · Cited by 3

The influence of tissue spatial geometry and functional organisation on liver regeneration

Aloia, L. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.09.011 · Cited by 4

Activation of prep expression by Tet2 promotes the proliferation of bipotential progenitor cells during liver regeneration

Jia, K., Cheng, B., Huang, L., Xu, J., Liu, F., Liao, X., Liao, K., & Lu, H. (2025) · Development · doi:10.1242/dev.204339 · Cited by 2

Periplakin Attenuates Liver Fibrosis via Reprogramming CD44Low Cells into CD44High Liver Progenitor Cells

Zhang, L., Xiong, Z., Chen, Z., Xu, M., Zhao, S., Liu, X., Jiang, K., Hu, Y., Liu, S., Sun, X., et al. (2025) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2025.101498 · Cited by 2

Triggering Mechanisms of Hepatocyte Repopulation during Liver Regeneration

Lee, E. J., Lee, N. Y., Choi, M. G., Ryu, H. J., & Koo, J. H. (2025) · Biomolecules & Therapeutics · doi:10.4062/biomolther.2025.035 · Cited by 2

SOX9 promotes hepatocyte proliferation via upregulating TGF-α expression during liver regeneration

Liu, S., Xiong, H.-L., Yin, C., Deng, X., Ding, K., Nie, M., Xiao, M., Zhu, C., Hong, X.-L., Ding, C., et al. (2025) · Hepatology International · doi:10.1007/s12072-025-10940-1 · Cited by 2

Plastic hepatocyte states limit liver cancer development

Strathearn, L. S., Hayata, Y., Illendula, A., Hewett, C. K., Chen, M., He, G.-S., Escribano-Cebrián, M., Jarboe, B., Gómez-Tomé, L., de Prisco, N., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-66568-0 · Cited by 2

Short‐Term Rapamycin Mitigates the Senescence of Ovaries and Somatic Stem Cells in Multiple Organs in Reproductively Aged Mice

Lu, J., Li, J., Liu, C., Feng, G., Yin, G., Hu, Z., Heng, D., Yu, Y., Jin, K., Wu, Y., et al. (2026) · The FASEB Journal · doi:10.1096/fj.202504132r · Cited by 2

Cholangiocyte biology in primary sclerosing cholangitis and other cholangiopathies: pathogenesis, clinical insights, and experimental tools

Jalan‐Sakrikar, N., Anwar, A. A., Ali, A., Nasser‐Ghodsi, N., Felzen, A., Huebert, R. C., LaRusso, N. F., & O’Hara, S. P. (2026) · Physiological Reviews · doi:10.1152/physrev.00022.2025 · Cited by 5

Arouse potential stemness: Intrinsic and acquired stem cell therapeutic strategies for advanced liver diseases

Song, Y., Lu, Z., Shu, W., Xiang, Z., Wang, Z., Wei, X., & Xu, X. (2023) · Cell Insight · doi:10.1016/j.cellin.2023.100115 · Cited by 2

Establishment of a Fah-LSL mouse model to study BEC-to-hepatocyte conversion

Wang, X., Pu, W., Zhu, H., Zhang, M., & Zhou, B. (2023) · Biophysics Reports · doi:10.52601/bpr.2023.230034 · Cited by 2

Dietary chromium chemical species mitigate inflammation and cholestasis in primary sclerosing cholangitis via regulating bile acid metabolism

Shen, Y., Jiang, B., Hao, Z., Zhang, C., Zhang, Z., Wu, Q., Li, L., & Jiang, P. (2024) · Food Bioscience · doi:10.1016/j.fbio.2024.104887 · Cited by 2

Pseudo-trajectory inference for identifying essential regulations and molecules in cell fate decisions

He, X., Tang, R., Lou, J., & Wang, R. (2024) · Journal of Biological Physics · doi:10.1007/s10867-024-09665-3 · Cited by 2

The Effect of FOXA3 Overexpression on Hepatocyte Differentiation and Liver Regeneration in a Fah cKO Mouse Model

Li, S., Ou, C., Zhang, J., Zeng, M., Liang, K., Peng, Q., & Gao, Y. (2024) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2024.101438 · Cited by 3

Khdrbs1 drives re-differentiation of bipotential progenitor cells by inhibiting p53 in zebrafish biliary-mediated liver regeneration

Gang, K., Chen, Q., Sun, J., Zhang, T., Cai, P., Ni, R., & Ma, J. (2025) · Development · doi:10.1242/dev.204266 · Cited by 2

Dissecting the Cellular Heterogeneity Underlying Liver Diseases Through the Integration of GWASs and Single-Cell RNA Sequencing

Zhou, M., Liu, M., & Xue, C. (2025) · Biology · doi:10.3390/biology14070777 · Cited by 3

To be or not to be: The double-edged sword roles of liver progenitor cells

Yan, Z.-J., Chen, L., & Wang, H. (2023) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2023.188870 · Cited by 2

Liver stem cells

Szkolnicka, D., & Hay, D. C. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-818422-6.00040-x · Cited by 2

Liver Repopulation by Cell Transplantation and the Role of Stem Cells in Liver Biology

Shafritz, D. A., & Grompe, M. (2020) · Wiley eBooks · doi:10.1002/9781119436812.ch44 · Cited by 2

A dual mechanism of enhancer activation by FOXA pioneer factors induces endodermal organ fatesPreprint

Geusz, R. J., Wang, A., Lam, D. K., Vinckier, N. K., Alysandratos, K., Roberts, D. A., Wang, J., Kefalopoulou, S., Qiu, Y., Chiou, J., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.28.263020 · Cited by 2

The rise of RAS: how gradual oncogene activation shapes the OIS spectrumPreprint

Zhu, H., Chan, A. S. L., & Narita, M. (2025) · Genes & Development · doi:10.1101/gad.352761.125 · Cited by 2

Aberrant differentiation and proliferation of hepatocytes in chronic liver injury and liver tumors

Nishikawa, Y. (2024) · Pathology International · doi:10.1111/pin.13441 · Cited by 1

Eltrombopag restores proliferative capacity and adipose-osteogenic balance of mesenchymal stromal cells in low-risk myelodysplastic syndromes

Hong, M., Guo, J., Zhao, Y., Song, L., Zhao, S., Wang, R., Shi, L., Zhang, Z., Wu, D., He, Q., et al. (2024) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2024.177086 · Cited by 1

Adrenal lipoma formation via PI(3,4,5)P 3 /AKT-dependent transdifferentiation of adrenocortical cells into adipocytes

Yanai, S., Sasaki, J., Lee, H., Takahashi, F., Kikuchi, Y., Morioka, S., Yamamoto, T., Yuguchi, K., Oikawa, M., Kajiho, H., et al. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2510306122 · Cited by 1

KANSL3 directs transcriptional programs essential for hepatic metabolism and differentiation

Wiese, M., Rodrigues, C. P., Akbas, M. E., Sun, Y., Holz, H., Greene, J. A. M., Tsang, T. H., Bella, C., Ganter, K., Stehle, T., et al. (2025) · Life Science Alliance · doi:10.26508/lsa.202503238 · Cited by 1

Guilongwan Promoted Diabetic Wound Healing via Inhibition of TLR4/NLRP3 Signaling Pathway in Macrophages

Wang, W., Zhang, X., Lv, X., Wang, F., Yao, Y., Wang, F.-J., & Wang, G. (2025) · Chemistry & Biodiversity · doi:10.1002/cbdv.202501030 · Cited by 1

Establishment and comparative analysis of radiation‐induced liver disease in normal and fibrotic rat models

Jiang, Y., Ding, Y., Wang, F., Chen, D., 钟卫祥, Lu, Z., Wáng, Y. X. J., Yan, S., Liu, X., & Zhao, F. (2026) · Precision Radiation Oncology · doi:10.1002/pro6.70050 · Cited by 1

FXR–YAP signalling maintains biliary epithelial cell identity and preserves liver homeostasis

Sánchez-Sánchez, P., Wang, Z., Zagorac, S., Domínguez, M., Boskovic, J., Nair, A., Macías‐Camero, A., Villaseñor, A., Schwabe, R. F., & Djouder, N. (2026) · Nature Metabolism · doi:10.1038/s42255-026-01521-z · Cited by 1

Spatial transcriptomics supports a role for SOX4-driven signaling throughout the disease course of biliary atresia

Ziogas, I. A., Conover, K. R., Dobrinskikh, E., Al‐Juboori, S. I., Gromer, K. D., Malladi, P., Wright, C. J., Sokol, R. J., Andrews, T. S., & Taylor, S. A. (2026) · Hepatology Communications · doi:10.1097/hc9.0000000000000992 · Cited by 2

The Role of Liver Progenitor Cells in Postembryonic Development of Rana terrestris under Normal Physiological Conditions

Антонова, Е. И., Omarova, D. I., Firsova, N. V., & Krasnikova, K. A. (2024) · Učënye zapiski Kazanskogo universiteta. Seriâ Estestvennye nauki/Učënye zapiski Kazanskogo universiteta. Seriâ Estestvennye nauki/Učenye zapiski Kazanskogo gosudarstvennogo universiteta. Seriâ Estestvennye nauki · doi:10.26907/2542-064x.2024.1.38-65 · Cited by 1

Depression and Suicidal Ideations in Older Adults

Mgbeojedo, U. G., Osiri, E. J., Isaac, F. S., & Anodebe, C. P. (2024) · IntechOpen eBooks · doi:10.5772/intechopen.1006654 · Cited by 1

Experimental models of fibrosis

Косолапов, В. А., Litvinov, R., & Спасов, А. А. (2024) · Journal of Volgograd State Medical University · doi:10.19163/1994-9480-2024-21-3-39-47 · Cited by 1

Hepatic regeneration in aging: Cell type plasticity and redundancies

Li, C., Chalmers, T. J., Wong, A. S. A., Zhou, M., Marinova, M. B., Bertoldo, M. J., & Wu, L. E. (2020) · Advances in stem cells and their niches · doi:10.1016/bs.asn.2020.07.002 · Cited by 1

Clonal dynamics of normal hepatocyte expansions in homeostatic human livers and their association with the biliary epitheliumPreprint

Passman, A. M., Haughey, M. J., Carlotti, E., Williams, M. J., Cereser, B., Lin, M., Devkumar, S., Gabriel, J. P., Russo, F. P., Hoare, M., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.02.450704 · Cited by 1

Hepatic lipid overload potentiates biliary epithelial cell activation via E2FsPreprint

Yıldız, E., Alam, G. E., Perino, A., Jalil, A., Denechaud, P., Huber, K., Lluis Fajas, A., Auwerx, J. H., Sorrentino, G., & Schoonjans, K. (2022) · doi:10.7554/elife.81926.1 · Cited by 1

The proportion of periportal mesenchyme to ductal epithelial cells acts as a proliferative rheostat in liver regenerationPreprint

Cordero-Espinoza, L., Kohler, T. N., Dowbaj, A. M., Strauss, B., Sarlidou, O., Pacini, C., Dobie, R., Wilson‐Kanamori, J. R., Butler, R., Serup, P., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.09.21.306258

Molecular Mechanistic Approach of Important Antileukemic Compounds Present in Honey

Amin, I., Ali, A., Mir, B. A., Ali, R., Ahmad, S. B., Mir, M. R., Qamar, W., Arafah, A. M., Rehman, M. U., & Mir, T. M. (2020) · Springer eBooks · doi:10.1007/978-981-15-7305-7_1

Modelling non-alcoholic fatty liver disease using patient derived liver stem cells and hepatic organoids

Lim, Y. S. (2019) · DR-NTU (Nanyang Technological University) · doi:10.32657/10356/139651

Reviewer #2 (Public Review): Hepatic lipid overload potentiates biliary epithelial cell activation via E2Fs

(2022) · doi:10.7554/elife.81926.1.sa0

Reviewer #1 (Public Review): Hepatic lipid overload potentiates biliary epithelial cell activation via E2Fs

(2022) · doi:10.7554/elife.81926.1.sa1

eLife assessment: Hepatic lipid overload potentiates biliary epithelial cell activation via E2Fs

Tontonoz, P. (2022) · doi:10.7554/elife.81926.1.sa2

The Mechanism and Research Progress of Platelet Affecting Liver Regeneration

王, 鹏. (2023) · Hans Journal of Biomedicine · doi:10.12677/hjbm.2023.132028

Organ Regeneration Without Relying on Regeneration-Dedicated Stem Cells

Kondoh, H. (2024) · Results and problems in cell differentiation · doi:10.1007/978-3-031-39027-2_6

Cholestatic diseases

Carpino, G., Ceci, L., Kennedy, L. L., Gaudio, E., & Baiocchi, L. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-95262-0.00019-x

Author Response: Hepatic lipid overload potentiates biliary epithelial cell activation via E2Fs

Yıldız, E., Alam, G. E., Perino, A., Jalil, A., Denechaud, P., Huber, K., Fajas, L., Auwerx, J. H., Sorrentino, G., & Schoonjans, K. (2022) · doi:10.7554/elife.81926.1.sa3

Engineering principles for rationally design therapeutic strategies against hepatocellular carcinoma

Hernández-Magaña, A., Bensussen, A., Martínez‐García, J. C., & Alvarez-Buylla, E. R. (2024) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2024.1404319

Microanatomy and Immunity in the Liver

Zhang, T., Pan, L., Lei, D., & Liew, P. X. (2024) · Elsevier eBooks · doi:10.1016/b978-0-128-24465-4.00085-5

Single-Cell Transcriptomic Profile Reveals Cholangiocyte Reprogramming in Hepatic Mallory-Denk Bodies FormationPreprint

Fu, W., Pan, J., Yang, X., Zhang, Y., Mo, J., Tang, X., & Liu, H. (2025) · SSRN Electronic Journal · doi:10.2139/ssrn.5170674

Beta-catenin/sirtuin 1/farnesoid X receptor pathway promotion of portal vein ligation and parenchymal transection-induced rapid liver regeneration

Tong, Y., Gu, Q., Dong, B., Ying, H., Ji, T., Shen, X., Shen, B., Yu, H., Feng, L., Cai, X., et al. (2025) · Surgery · doi:10.1016/j.surg.2025.109343

Ontogenetic Anatomy and the Cancer Field Model of Local Tumor Progression

Höckel, M. (2025) · Springer eBooks · doi:10.1007/978-3-031-83030-3_2 · Cited by 1

Dedifferentiation-Dependent Regeneration of the Biliary Ductal Epithelium in Response to Hepatic Injury in TFF1-Deficient Mice

Yamamoto, T., Yamaguchi, J., Kokuryo, T., Yokoyama, Y., Mizuno, T., Onoe, S., Sunagawa, M., Baba, T., & Ebata, T. (2025) · Cells · doi:10.3390/cells14171323

Exploring the role of cellular plasticity in metabolic dysfunction-associated steatosis and related molecular mechanisms

Erçin, M., & Gezginci-Oktayoğlu, S. (2025) · Journal of Translational Medicine · doi:10.1186/s12967-025-06922-4

Additional file 1 of CD24+LCN2+ liver progenitor cells in ductular reaction contributed to macrophage inflammatory responses in chronic liver injury

Huang, W.-J., Qiu, B.-J., Qi, X.-S., Chen, C.-Y., Liu, W.-M., Zhou, S.-A., Ding, M., Lu, F.-F., Zhao, J., Tang, D., et al. (2023) · Figshare · doi:10.6084/m9.figshare.24234232

Additional file 1 of Drug metabolic activity is a critical cell-intrinsic determinant for selection of hepatocytes during long-term culture

Akiyama, S., Saku, N., Miyata, S., Ite, K., Toyoda, M., Kimura, T., Kuroda, M., Nakazawa, A., Kasahara, M., Nonaka, H., et al. (2022) · Figshare · doi:10.6084/m9.figshare.19351367

Additional file 3 of In-organoid single-cell CRISPR screening reveals determinants of hepatocyte differentiation and maturation

Liang, J., Wei, J., Cao, J., Qian, J., Gao, R., Li, X., Wang, D., Gu, Y., Dong, L., Yu, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26634357

Additional file 2 of In-organoid single-cell CRISPR screening reveals determinants of hepatocyte differentiation and maturation

Liang, J., Wei, J., Cao, J., Qian, J., Gao, R., Li, X., Wang, D., Gu, Y., Dong, L., Yu, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26634354

Additional file 1 of In-organoid single-cell CRISPR screening reveals determinants of hepatocyte differentiation and maturation

Liang, J., Wei, J., Cao, J., Qian, J., Gao, R., Li, X., Wang, D., Gu, Y., Dong, L., Yu, J., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26634351

Liver repair and regeneration

Wang, L., Tang, Z., & Xu, H. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-40423-8.00003-8

NRF2 co-opts the SWI/SNF complex to drive liver cell plasticityPreprint

Ong, A. J. S., Wong, C. C., Karamalakis, A. P., Evason, K. J., Brown, K., & Cox, A. G. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.09.704724

Retrorsine impairs liver regeneration by inducing progenitor cell-senescence via ROS after partial hepatectomy

Cui, Y. C., Li, L., He, Y., Shan, S., Liu, L., Ren, J., Wang, H., Yang, M., Zhao, X., Jia, J., et al. (2026) · Annals of Medicine · doi:10.1080/07853890.2026.2635821

The pathoanatomy of cancer: order in paradox

Höckel, M. (2026) · EBioMedicine · doi:10.1016/j.ebiom.2026.106161 · Cited by 1

CellCousin2: an optimized system for partial ablation and tracing of regenerative lineages

Hovhannisyan, G., Akhourbi, T., Eski, S. E., Pirson, I., Gurzov, E. N., & Singh, S. P. (2026) · npj Regenerative Medicine · doi:10.1038/s41536-026-00473-y

Liver pathophysiology at the single cell level : characterization of cellular heterogeneity and identification of novel therapeutic targets for chronic liver diseases and hepatocellular carcinoma

Saviano, A. (2019) · theses.fr (ABES) · doi:10.70675/13a32e69z1eb7z4416za3b9z5e1e77176186

La monoacylglycerol lipase favorise la régénération hépatique en reprogrammant le métabolisme lipidique des macrophages et des hépatocytes

Allaire, M. (2021) · theses.fr (ABES) · doi:10.70675/63c01410z4e9ez41a1za1d1z5413ce87e73c

Medullary adipocytes and age-related osteoporosis

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Modulating hepatic stellate cell senescence: A promising therapeutic strategy for liver fibrosis

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