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Differential gene expression in periportal and perivenous mouse hepatocytes
Open accessAbstract
Hepatocytes located in the periportal and perivenous zones of the liver lobule show remarkable differences in the levels and activities of various enzymes and other proteins. To analyze global gene expression patterns of periportal and perivenous hepatocytes, enriched populations of the two cell types were isolated by combined collagenase/digitonin perfusion from mouse liver and used for microarray analysis. In total, 198 genes and expressed sequences were identified that demonstrated a ≥ 2‐fold difference in expression between hepatocytes from the two different zones of the liver. A subset of 20 genes was additionally analyzed by real‐time RT‐PCR, validating the results obtained by the microarray analysis. Several of the differentially expressed genes encoded key enzymes of intermediary metabolism, including those involved in glycolysis and gluconeogenesis, fatty acid degradation, cholesterol and bile acid metabolism, amino acid degradation and ammonia utilization. In addition, several enzymes of phase I and phase II of xenobiotic metabolism were differentially expressed in periportal and perivenous hepatocytes. Our results confirm previous findings on metabolic zonation in liver, and extend our knowledge of the regulatory mechanisms at the transcriptional level.
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“Collectively, these observations are consistent with the classic zonation described in human and mouse liver4,24–26, supporting our MERFISH measurements.”
From Spatial transcriptomics of healthy and fibrotic human liver at single-cell resolution (2025) · cites this paper as [24]
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“SDS was enriched in zone 1 (periportal), while CYP2E1 expression increased in zone 3 (pericentral), as previously described in mouse24–27 (Fig. 1c, e, f; Supplementary Fig. 5a).”
From Spatial transcriptomics of healthy and fibrotic human liver at single-cell resolution (2025) · cites this paper as [24]
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Citations
Cites
Functional specialization of different hepatocyte populations
Jungermann, K. A., & Katz, N. R. (1989) · Physiological Reviews · doi:10.1152/physrev.1989.69.3.708 · Cited by 655
Metabolic zonation of the liver: Regulation and implications for liver function
Gebhardt, R. (1992) · Pharmacology & Therapeutics · doi:10.1016/0163-7258(92)90055-5 · Cited by 607
Zonation of parenchymal and nonparenchymal metabolism in liver.
Jungermann, K., & Keitzmann, T. (1996) · Annual Review of Nutrition · doi:10.1146/annurev.nu.16.070196.001143 · Cited by 589
Apc Tumor Suppressor Gene Is the “Zonation-Keeper” of Mouse Liver
Benhamouche, S., Decaens, T., Godard, C., Chambrey, R., Rickman, D. S., Moinard, C., Vasseur-Cognet, M., Kuo, C. J., Kahn, A., Perret, C., et al. (2006) · Developmental Cell · doi:10.1016/j.devcel.2006.03.015 · Cited by 543
Rider, M. H., Bertrand, L., Vertommen, D., Michels, P. A. M., Rousseau, G. G., & Hue, L. (2004) · Biochemical Journal · doi:10.1042/bj20040752 · Cited by 435
New targets of β-catenin signaling in the liver are involved in the glutamine metabolism
Cadoret, A., Ovejero, C., Terris, B., Souil, E., Lévy, L., Lamers, W. H., Kitajewski, J., Kahn, A., & Perret, C. (2002) · Oncogene · doi:10.1038/sj.onc.1206118 · Cited by 412
Gebhardt, R., & Mecke, D. (1983) · The EMBO Journal · doi:10.1002/j.1460-2075.1983.tb01464.x · Cited by 377
Zonation of hepatic cytochrome P-450 expression and regulation
Oinonen, T., & LINDROS, O. K. (1998) · Biochemical Journal · doi:10.1042/bj3290017 · Cited by 227
Zonal gene expression in murine liver: Lessons from tumors
Hailfinger, S., Jaworski, M., Braeuning, A., Buchmann, A., & Schwarz, M. (2006) · Hepatology · doi:10.1002/hep.21082 · Cited by 149
Self-citationWeiner, I. D., Miller, R. T., & Verlander, J. W. (2003) · Gastroenterology · doi:10.1016/s0016-5085(03)00277-4 · Cited by 121
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Godoy, P., Hewitt, N. J., Albrecht, U., Andersen, M. E., Ansari, N., Bhattacharya, S., Bode, J. G., Bolleyn, J., Borner, C., Böttger, J., et al. (2013) · Archives of Toxicology · doi:10.1007/s00204-013-1078-5 · Cited by 1,280
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Halpern, K. B., Shenhav, R., Matcovitch-Natan, O., Tóth, B., Lemze, D., Golan, M., Massasa, E. E., Baydatch, S., Landen, S., Moor, A. E., et al. (2017) · Nature · doi:10.1038/nature21065 · Cited by 1,059
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Wang, B., Zhao, L., Fish, M., Logan, C. Y., & Nusse, R. (2015) · Nature · doi:10.1038/nature14863 · Cited by 674
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Kietzmann, T. (2017) · Redox Biology · doi:10.1016/j.redox.2017.01.012 · Cited by 499
Cairo, S., Armengol, C., de Reyniès, A., Yu, W., Thomas, E., Renard, C.-A., Goga, A., Balakrishnan, A., Semeraro, M., Gresh, L., et al. (2008) · Cancer Cell · doi:10.1016/j.ccr.2008.11.002 · Cited by 530
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Ben-Moshe, S., & Itzkovitz, S. (2019) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-019-0134-x · Cited by 485
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Halpern, K. B., Shenhav, R., Massalha, H., Toth, B., Egozi, A., Massasa, E. E., Medgalia, C., David, E., Giladi, A., Moor, A. E., et al. (2018) · Nature Biotechnology · doi:10.1038/nbt.4231 · Cited by 368
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Marro, S. G., Pang, Z. P., Yang, N., Tsai, M.-C., Qu, K., Chang, H. Y., Südhof, T. C., & Wernig, M. (2011) · Cell stem cell · doi:10.1016/j.stem.2011.09.002 · Cited by 343
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Gola, A., Dorrington, M. G., Speranza, E. E., Sala, C., Shih, R. M., Radtke, A. J., Wong, H. S., Baptista, A. P., Hernandez, J. M., Castellani, G., et al. (2020) · Nature · doi:10.1038/s41586-020-2977-2 · Cited by 286
Liver zonation: Novel aspects of its regulation and its impact on homeostasis
Gebhardt, R. (2014) · World Journal of Gastroenterology · doi:10.3748/wjg.v20.i26.8491 · Cited by 275
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Halpern, K. B., Tanami, S., Landen, S., Chapal, M., Szlak, L., Hutzler, A., Nizhberg, A., & Itzkovitz, S. (2015) · Molecular Cell · doi:10.1016/j.molcel.2015.01.027 · Cited by 251
YAP Inhibition Restores Hepatocyte Differentiation in Advanced HCC, Leading to Tumor Regression
Fitamant, J., Kottakis, F., Benhamouche, S., Tian, H. S., Chuvin, N., Parachoniak, C. A., Nagle, J. M., Perera, R. M., Lapouge, M., Deshpande, V., et al. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.02.027 · Cited by 248
Wilson, G. K., Tennant, D. A., & McKeating, J. A. (2014) · Journal of Hepatology · doi:10.1016/j.jhep.2014.08.025 · Cited by 205
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Rocha, A. S., Vidal, V., Mertz, M., Kendall, T. J., Charlet, A., Okamoto, H., & Schedl, A. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.10.049 · Cited by 194
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Diggle, C. P., Shires, M., Leitch, D., Brooke, D., Carr, I., MARKHAM, A. F., Hayward, B. E., Asipu, A., & Bonthron, D. T. (2009) · Journal of Histochemistry & Cytochemistry · doi:10.1369/jhc.2009.953190 · Cited by 197
Hildebrandt, F., Andersson, A., Saarenpää, S., Larsson, L., Hul, N. V., Kanatani, S., Masek, J., Ellis, E. C. S., Barragán, A., Mollbrink, A., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-27354-w · Cited by 191
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Gougelet, A., Torre, C., Veber, P., Sartor, C., Bachelot, L., Denechaud, P.-D., Godard, C., Moldes, M., Burnol, A.-F., Dubuquoy, C., et al. (2014) · Hepatology · doi:10.1002/hep.26924 · Cited by 190
Self-citationAmino acid metabolism, transport and signalling in the liver revisited
Paulusma, C. C., Lamers, W. H., Bröer, S., & van de Graaf, S. F. J. (2022) · Biochemical Pharmacology · doi:10.1016/j.bcp.2022.115074 · Cited by 185
In Situ Lipidomic Analysis of Nonalcoholic Fatty Liver by Cluster TOF-SIMS Imaging
Debois, D., Bralet, M., Naour, F. L., Brunelle, A., & Laprévôte, O. (2009) · Analytical Chemistry · doi:10.1021/ac900045m · Cited by 168
Paris, J., & Henderson, N. C. (2022) · Hepatology · doi:10.1002/hep.32408 · Cited by 177
Liver Zonation – Revisiting Old Questions With New Technologies
Cunningham, R. P., & Porat‐Shliom, N. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.732929 · Cited by 181
Single-cell RNA sequencing of human liver reveals hepatic stellate cell heterogeneity
Payen, V. L., Lavergne, A., Alevra Sarika, N., Colonval, M., Karim, L., Deckers, M., Najimi, M., Coppieters, W., Charloteaux, B., Sokal, E. M., et al. (2021) · JHEP Reports · doi:10.1016/j.jhepr.2021.100278 · Cited by 160
Liver tissue engineering in the evaluation of drug safety
Dash, A., Inman, W., Hoffmaster, K. A., Sevidal, S., Kelly, J., Obach, R. S., Griffith, L. G., & Tannenbaum, S. R. (2009) · Expert Opinion on Drug Metabolism & Toxicology · doi:10.1517/17425250903160664 · Cited by 157
The Liver–α-Cell Axis and Type 2 Diabetes
Albrechtsen, N. J. W., Pedersen, J., Galsgaard, K. D., Winther‐Sørensen, M., Suppli, M. P., Janah, L., Gromada, J., Vilstrup, H., Knop, F. K., & Holst, J. J. (2019) · Endocrine Reviews · doi:10.1210/er.2018-00251 · Cited by 154
Kubota, N., Kubota, T., Kajiwara, E., Iwamura, T., Kumagai, H., Watanabe, T., Inoue, M., Takamoto, I., Sasako, T., Kumagai, K., et al. (2016) · Nature Communications · doi:10.1038/ncomms12977 · Cited by 143
McCommis, K. S., Hodges, W. T., Brunt, E. M., Nalbantoglu, I., McDonald, W. G., Holley, C. L., Fujiwara, H., Schaffer, J. E., Colca, J. R., & Finck, B. N. (2016) · Hepatology · doi:10.1002/hep.29025 · Cited by 139
Mfsd2a+ hepatocytes repopulate the liver during injury and regeneration
Pu, W., Zhang, H., Huang, X., Tian, X., He, L., Wang, Y., Zhang, L., Liu, Q., Li, Y., Li, Y., et al. (2016) · Nature Communications · doi:10.1038/ncomms13369 · Cited by 136
Désert, R., Rohart, F., Canal, F., Sicard, M., Desille, M., Renaud, S., Turlin, B., Bellaud, P., Perret, C., Clément, B., et al. (2017) · Hepatology · doi:10.1002/hep.29254 · Cited by 148
Wnt signaling and hepatocarcinogenesis: The hepatoblastoma model
Armengol, C., Cairo, S., Fabrè, M., & Buendia, M. (2009) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2009.07.012 · Cited by 137
Spatial transcriptomics of healthy and fibrotic human liver at single-cell resolution
Watson, B. R., Paul, B., Rahman, R. U., Amir-Zilberstein, L., Segerstolpe, Å., Epstein, E. T., Murphy, S., Geistlinger, L., Lee, T., Shih, A., et al. (2025) · Nature Communications · doi:10.1038/s41467-024-55325-4 · Cited by 123
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Garrido, A., & Djouder, N. (2020) · Trends in cancer · doi:10.1016/j.trecan.2020.08.005 · Cited by 123
Angiocrine Wnt signaling controls liver growth and metabolic maturation in mice
Leibing, T., Géraud, C., Augustin, I., Boutros, M., Augustin, H. G., Okun, J. G., Langhans, C., Zierow, J., Wohlfeil, S. A., Olsavszky, V., et al. (2018) · Hepatology · doi:10.1002/hep.29613 · Cited by 116
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Martini, T., Naef, F., & Tchorz, J. S. (2023) · Annual Review of Pathology: Mechanisms of Disease · doi:10.1146/annurev-pathmechdis-031521-024831 · Cited by 113
Lefebvre, P., Lalloyer, F., Baugé, E., Pawlak, M., Gheeraert, C., Dehondt, H., Vanhoutte, J., Woitrain, E., Hennuyer, N., Mazuy, C., et al. (2017) · JCI Insight · doi:10.1172/jci.insight.92264 · Cited by 117
Temporal analyses of postnatal liver development and maturation by single-cell transcriptomics
Liang, Y., Kaneko, K., Xin, B., Lee, J., Sun, X., Zhang, K., & Feng, G.-S. (2022) · Developmental Cell · doi:10.1016/j.devcel.2022.01.004 · Cited by 116
Smith, L., Villaret, J., Claus, S. P., Canlet, C., Guillou, H., Cabaton, N. J., & Ellero‐Simatos, S. (2020) · Metabolites · doi:10.3390/metabo10030104 · Cited by 121
Intersection of AHR and Wnt Signaling in Development, Health, and Disease
Schneider, A. J., Branam, A. M., & Peterson, R. E. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms151017852 · Cited by 109
Ang, C. H., Hsu, S. H., Guo, F., Tan, C. T., Yu, V. C., Visvader, J. E., Chow, P. K. H., & Fu, N. Y. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1908099116 · Cited by 102
Torre, C., Perret, C., & Colnot, S. (2009) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2009.11.004 · Cited by 106
Gupte, A. A., Liu, J. Z., Ren, Y., Minze, L. J., Wiles, J. R., Collins, A. R., Lyon, C. J., Praticò, D., Finegold, M. J., Wong, S. T. C., et al. (2010) · Hepatology · doi:10.1002/hep.23941 · Cited by 98
Molecular Determinants of Liver Zonation
Torre, C., Perret, C., & Colnot, S. (2010) · Progress in Molecular Biology and Translational Science · doi:10.1016/b978-0-12-385233-5.00005-2 · Cited by 97
Norton, L., Fourcaudot, M. J., Abdul-Ghani, M. A., Winnier, D. A., Mehta, F. F., Jenkinson, C. P., & DeFronzo, R. A. (2011) · Diabetologia · doi:10.1007/s00125-011-2289-z · Cited by 93
Dynamic zonation of liver polyploidy
Tanami, S., Ben-Moshe, S., Elkayam, A., Mayo, A., Bahar Halpern, K., & Itzkovitz, S. (2017) · Cell and Tissue Research · doi:10.1007/s00441-016-2427-5 · Cited by 77
Glucagon contributes to liver zonation
Cheng, X., Kim, S. Y., Okamoto, H., Xin, Y., Yancopoulos, G. D., Murphy, A. J., & Gromada, J. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1721403115 · Cited by 90
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Wattacheril, J. J., Seeley, E. H., Angel, P. M., Chen, H., Bowen, B. P., Lanciault, C., Caprioli, R. M., Abumrad, N. N., & Flynn, C. R. (2013) · PLoS ONE · doi:10.1371/journal.pone.0057165 · Cited by 88
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Daujat‐Chavanieu, M., & Gerbal‐Chaloin, S. (2020) · Cells · doi:10.3390/cells9112395 · Cited by 87
Budinsky, R. A., Schrenk, D., Simon, T. W., van den Berg, M., Reichard, J. F., Silkworth, J. B., Aylward, L. L., Brix, A., Gasiewicz, T. A., Kaminski, N. E., et al. (2013) · Critical Reviews in Toxicology · doi:10.3109/10408444.2013.835787 · Cited by 87
Dicer is required for proper liver zonation
Sekine, S., Ogawa, R., McManus, M. T., Kanai, Y., & Hebrok, M. (2009) · The Journal of Pathology · doi:10.1002/path.2606 · Cited by 85
Truong, X. T., & Lee, D. H. (2025) · Diabetes & Metabolism Journal · doi:10.4093/dmj.2025.0644 · Cited by 84
“Insulin receptor substrate 1 (IRS1) and IRS2 among IRS1–6 are the main adaptor proteins in the liver, activating phosphatidylinositol-3 kinase (PI3K) [9,11,15,19].”
Braeuning, A., Sanna, R., Huelsken, J., & Schwarz, M. (2009) · Drug Metabolism and Disposition · doi:10.1124/dmd.108.026179 · Cited by 82
Self-citationDual modulation of human hepatic zonation via canonical and non-canonical Wnt pathways
McEnerney, L., Duncan, K., Bang, B.-R., Elmasry, S., Li, M., Miki, T., Ramakrishnan, S. K., Shah, Y. M., & Saito, T. (2017) · Experimental & Molecular Medicine · doi:10.1038/emm.2017.226 · Cited by 81
Lan, T., Hu, Y., Hu, F., Li, H., Chen, Y., Zhang, J., Yu, Y., Jiang, S., Weng, Q., Tian, S., et al. (2022) · Journal of Hepatology · doi:10.1016/j.jhep.2021.09.040 · Cited by 75
Novel aspects of glutamine synthetase in ammonia homeostasis
Zhou, Y., Eid, T., Hassel, B., & Danbolt, N. C. (2020) · Neurochemistry International · doi:10.1016/j.neuint.2020.104809 · Cited by 80
Hepatic zonation of carbon and nitrogen fluxes derived from glutamine and ammonia transformations
Comar, J. F., Suzuki‐Kemmelmeier, F., Constantin, J., & Bracht, A. (2010) · Journal of Biomedical Science · doi:10.1186/1423-0127-17-1 · Cited by 71
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Ghallab, A., Myllys, M., Holland, C. H., Zaza, A., Murad, W., Hassan, R. A. R. A., Ahmed, Y. A., Abbas, T., Abdelrahim, E. A., Schneider, K. M., et al. (2019) · Cells · doi:10.3390/cells8121556 · Cited by 74
Selective Insulin Resistance in the Kidney
Horita, S., Nakamura, M., Suzuki, M., Satoh, N., Suzuki, A., & Seki, G. (2016) · BioMed Research International · doi:10.1155/2016/5825170 · Cited by 71
Schleicher, J., Tokarski, C., Marbach, E., Matz‐Soja, M., Zellmer, S., Gebhardt, R., & Schuster, S. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2015.02.004 · Cited by 75
Antitumour activity of an inhibitor of miR-34a in liver cancer with β-catenin-mutations
Gougèlet, A., Sartor, C., Bachelot, L., Godard, C., Marchiol, C., Renault, G., Torès, F., Nitschké, P., Cavard, C., Terris, B., et al. (2015) · Gut · doi:10.1136/gutjnl-2014-308969 · Cited by 75
Gerbal‐Chaloin, S., Dumé, A., Briolotti, P., Klieber, S., Raulet, E., Duret, C., Fabre, J., Ramos, J., Maurel, P., & Daujat‐Chavanieu, M. (2014) · Molecular Pharmacology · doi:10.1124/mol.114.094797 · Cited by 71
Liver regeneration: Cellular origin and molecular mechanisms
Huang, R. C. C., Zhang, X., Gracia‐Sancho, J., & Xie, W. (2022) · Liver International · doi:10.1111/liv.15174 · Cited by 69
Sun, X., Wu, J., Liu, L., Chen, Y., Tang, Y., Liu, S., Chen, H., Jiang, Y., Liu, Y., Yuan, H., et al. (2022) · Journal of Hepatology · doi:10.1016/j.jhep.2022.02.028 · Cited by 68
Cellular and molecular basis of liver regeneration
Bangru, S., & Kalsotra, A. (2020) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2019.12.004 · Cited by 67
Molecular mechanisms of liver and bile duct development
Zong, Y., & Stanger, B. Z. (2012) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.47 · Cited by 65
Torre, C., Benhamouche, S., Mitchell, C., Godard, C., Veber, P., Letourneur, F., Cagnard, N., Jacques, S., Finzi, L., Perret, C., et al. (2011) · Journal of Hepatology · doi:10.1016/j.jhep.2010.10.021 · Cited by 60
Yang, S., Liu, C., Jiang, M., Liu, X., Geng, L., Zhang, Y., Sun, S., Wang, K., Yin, J. B., Ma, S., et al. (2023) · Protein & Cell · doi:10.1093/procel/pwad039 · Cited by 65
Giera, S., Braeuning, A., Köhle, C., Bursch, W., Metzger, U., Buchmann, A., & Schwarz, M. (2010) · Toxicological Sciences · doi:10.1093/toxsci/kfq033 · Cited by 66
Self-citation13N as a tracer for studying glutamate metabolism
Cooper, A. J. L. (2010) · Neurochemistry International · doi:10.1016/j.neuint.2010.11.011 · Cited by 62
Regulation of hepatocyte identity and quiescence
Berasain, C., & Avila, M. A. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-1970-7 · Cited by 64
Cell-type diversity and regionalized gene expression in the planarian intestine
Forsthoefel, D. J., Cejda, N. I., Khan, U. W., & Newmark, P. A. (2020) · eLife · doi:10.7554/elife.52613 · Cited by 54
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Berndt, N., Kolbe, E., Gajowski, R., Eckstein, J., Ott, F., Meierhofer, D., Holzhütter, H., & Matz‐Soja, M. (2020) · Hepatology · doi:10.1002/hep.31274 · Cited by 55
Marx‐Stoelting, P., Knebel, C., & Braeuning, A. (2020) · Cells · doi:10.3390/cells9051192 · Cited by 54
Self-citationRole and Regulation of Wnt/β-Catenin in Hepatic Perivenous Zonation and Physiological Homeostasis
Goel, C., Monga, S. P., & Nejak-Bowen, K. (2022) · The American Journal of Pathology · doi:10.1016/j.ajpath.2021.09.007 · Cited by 53
Nault, J., Couchy, G., Caruso, S., Meunier, L., Caruana, L., Letouzé, É., Rebouissou, S., Paradis, V., Caldéraro, J., & Zucman‐Rossi, J. (2018) · Hepatology · doi:10.1002/hep.29884 · Cited by 52
Colnot, S., & Perret, C. (2010) · Molecular pathology library · doi:10.1007/978-1-4419-7107-4_2 · Cited by 58
Braeuning, A., Menzel, M., Kleinschnitz, E., Harada, N., Tamai, Y., Köhle, C., Buchmann, A., & Schwarz, M. (2007) · FEBS Journal · doi:10.1111/j.1742-4658.2007.06002.x · Cited by 50
Self-citationOrganismal complexity, cell differentiation and gene expression: human over mouse
Vinogradov, A. E., & Anatskaya, O. V. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm723 · Cited by 50
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Rojas, I. Y., Moyer, B. J., Ringelberg, C. S., & Tomlinson, C. R. (2020) · International Journal of Obesity · doi:10.1038/s41366-019-0512-z · Cited by 51
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Schwimmer, J. B., Biddinger, S. B., & Ibrahim, S. H. (2025) · Journal of Clinical Investigation · doi:10.1172/jci186422 · Cited by 49
Pridans, C., Sauter, K. A. D., Irvine, K. M., Davis, G. M., Lefèvre, L., Raper, A., Rojo, R., Nirmal, A. J., Beard, P. M., Cheeseman, M. T., et al. (2017) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00343.2017 · Cited by 46
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Trinh, V. Q.-H., Lee, T.-F., Lemoinne, S., Ray, K. C., Ybanez, M. D., Tsuchida, T., Carter, J. K., Agudo, J., Brown, B. D., Akat, K. M., et al. (2023) · Science Signaling · doi:10.1126/scisignal.adf6696 · Cited by 45
Walenbergh, S. M. A., Houben, T., Rensen, S. S., Bieghs, V., Hendrikx, T., van Gorp, P. J., Oligschlaeger, Y., Jeurissen, M. L. J., Gijbels, M. J., Buurman, W. A., et al. (2016) · Scientific Reports · doi:10.1038/srep38278 · Cited by 44
Kumar, B. S. (2023) · Analytical Methods · doi:10.1039/d3ay00867c · Cited by 45
Braeuning, A., Ittrich, C., Köhle, C., Buchmann, A., & Schwarz, M. (2007) · Drug Metabolism and Disposition · doi:10.1124/dmd.106.013656 · Cited by 42
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Region-specific cellular and molecular basis of liver regeneration after acute pericentral injury.
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Spatial metabolic gradients in the liver and small intestine
Samarah, L. Z., Zheng, C., Xing, X., Lee, W. D., Afriat, A., Chitra, U., MacArthur, M. R., Lu, W., Jankowski, C. S. R., Ma, C., et al. (2025) · Nature · doi:10.1038/s41586-025-09616-5 · Cited by 53
Mechanisms of RAS/β-catenin interactions
Zeller, E., Hammer, K., Kirschnick, M., & Braeuning, A. (2013) · Archives of Toxicology · doi:10.1007/s00204-013-1035-3 · Cited by 40
Self-citationβ-Catenin as a multilayer modulator of zonal cytochrome P450 expression in mouse liver
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Self-citationSexual dimorphisms in zonal gene expression in mouse liver
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Inflammation-associated suppression of metabolic gene networks in acute and chronic liver disease
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Ha‐ras and β‐catenin oncoproteins orchestrate metabolic programs in mouse liver tumors
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Self-citationSignal integration by the CYP1A1 promoter -- a quantitative study
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Self-citation
Metadata
- Authors
- Braeuning, A., Ittrich, C., Köhle, C., Hailfinger, S., Bonin, M., Buchmann, A., & Schwarz, M.
- Affiliations
- University of Tübingen (DE)
- German Cancer Research Center (DE)
- Venue
- The FEBS Journal
- Publisher
- Wiley
- Published
- 2006-10-20
- Volume
- 273
- Issue
- 22
- Pages
- 5051-5061
- ISSN
- 1742-464X (ISSN-L)
- 1742-4658
- OpenAlex
- W2031402631
- Cited by
- 240
- References
- 27
- Citations by year
- 2026: 8 · 2025: 14 · 2024: 15 · 2023: 18 · 2022: 13 · 2021: 15 · 2020: 28 · 2019: 14 · 2018: 16 · 2017: 12 · 2016: 12 · 2015: 11 · 2014: 12 · 2013: 11 · 2012: 3
- FWCI
- 5.46
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- FEBS Journal (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Deutsche Krebshilfe
- Topics
- Health Sciences › Medicine › Hepatology › Liver physiology and pathology
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Pharmacogenetics and Drug Metabolism
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Drug-Induced Hepatotoxicity and Protection
- Keywords
- periportal hepatocytes, perivenous hepatocytes, differential gene expression, hepatocyte isolation, xenobiotic metabolism, transcriptional regulation, mouse liver
- MeSH terms
- Amino Acids, Ammonia, Animals, Cholesterol, Fatty Acids, Gene Expression Regulation, Gluconeogenesis, Glycolysis, Hepatic Veins, Liver, Male, Mice, Inbred C3H, Models, Biological, Portal Vein, Protein Denaturation, Xenobiotics, Gene Expression Regulation, Enzymologic, Gene Expression Profiling, Hepatocytes, Mice
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