Hepatocyte TLR4 triggers inter-hepatocyte Jagged1/Notch signaling to determine NASH-induced fibrosis

A new definition for metabolic dysfunction-associated fatty liver disease: An international expert consensus statement

Eslam, M., Newsome, P. N., Sarin, S. K., Anstee, Q. M., Targher, G., Romero-Gomez, M., Zelber-Sagi, S., Wai-Sun Wong, V., Dufour, J.-F., Schattenberg, J. M., et al. (2020) · Journal of Hepatology · doi:10.1016/j.jhep.2020.03.039 · Cited by 4,472

The Canonical Notch Signaling Pathway: Unfolding the Activation Mechanism

Kopan, R., & Ilagan, M. X. G. (2009) · Cell · doi:10.1016/j.cell.2009.03.045 · Cited by 3,764

Pioglitazone, Vitamin E, or Placebo for Nonalcoholic Steatohepatitis

Sanyal, A. J., Chalasani, N., Kowdley, K. V., McCullough, A., Diehl, A. M., Bass, N. M., Neuschwander-Tetri, B. A., Lavine, J. E., Tonascia, J., Unalp, A., et al. (2010) · New England Journal of Medicine · doi:10.1056/nejmoa0907929 · Cited by 3,327

MAFLD: a consensus-driven proposed nomenclature for metabolic associated fatty liver disease

Eslam, M., Sanyal, A. J., George, J., Sanyal, A., Neuschwander-Tetri, B., Tiribelli, C., Kleiner, D. E., Brunt, E., Bugianesi, E., Yki-Järvinen, H., et al. (2020) · Gastroenterology · doi:10.1053/j.gastro.2019.11.312 · Cited by 3,286

Activating Mutations of NOTCH1 in Human T Cell Acute Lymphoblastic Leukemia

Weng, A. P., Ferrando, A. A., Lee, W., Morris, J. P., Silverman, L. B., Sanchez-Irizarry, C., Blacklow, S. C., Look, A. T., & Aster, J. C. (2004) · Science · doi:10.1126/science.1102160 · Cited by 2,706

Notch signalling: a simple pathway becomes complex

Bray, S. J. (2006) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2009 · Cited by 2,620

Resolving the fibrotic niche of human liver cirrhosis at single-cell level

Ramachandran, P., Dobie, R., Wilson-Kanamori, J. R., Dora, E. F., Henderson, B. E. P., Luu, N. T., Portman, J. R., Matchett, K. P., Brice, M., Marwick, J. A., et al. (2019) · Nature · doi:10.1038/s41586-019-1631-3 · Cited by 1,784

Fibrosis–a common pathway to organ injury and failure

Rockey, D. C., Bell, P. D., & Hill, J. A. (2015) · New England Journal of Medicine · doi:10.1056/nejmra1300575 · Cited by 1,428

From NASH to HCC: current concepts and future challenges

Anstee, Q. M., Reeves, H. L., Kotsiliti, E., Govaere, O., & Heikenwalder, M. (2019) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-019-0145-7 · Cited by 1,392

PROMO: detection of known transcription regulatory elements using species-tailored searches

Messeguer, X., Escudero, R., Farré, D., Núñez, Ó., Martı́nez, J., & Albà, M. M. (2002) · Bioinformatics · doi:10.1093/bioinformatics/18.2.333 · Cited by 1,371

NF-κB in the liver—linking injury, fibrosis and hepatocellular carcinoma

Luedde, T., & Schwabe, R. F. (2011) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2010.213 · Cited by 1,345

Saturated Fatty Acids, but Not Unsaturated Fatty Acids, Induce the Expression of Cyclooxygenase-2 Mediated through Toll-like Receptor 4

Lee, J. Y., Sohn, K. H., Rhee, S. H., & Hwang, D. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m011695200 · Cited by 1,299

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

Li, L., Krantz, I. D., Deng, Y., Genin, A., Banta, A. B., Collins, C. C., Qi, M., Trask, B. J., Kuo, W. L., Cochran, J., et al. (1997) · Nature Genetics · doi:10.1038/ng0797-243 · Cited by 1,281

Duration of Nuclear NF-κB Action Regulated by Reversible Acetylation

Chen, L., Fischle, W., Verdin, E. M., & Greene, W. C. (2001) · Science · doi:10.1126/science.1062374 · Cited by 1,231

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

Oda, T., ELKAHLOUN, A. G., Pike, B. L., Okajima, K., Krantz, I. D., Genin, A., Piccoli, D. A., Meltzer, P. S., Spinner, N. B., Collins, F. S., et al. (1997) · Nature Genetics · doi:10.1038/ng0797-235 · Cited by 1,145

The Notch Ligands Dll4 and Jagged1 Have Opposing Effects on Angiogenesis

Benedito, R., Roca, C., Sörensen, I., Adams, S., Gossler, A., Fruttiger, M., & Adams, R. H. (2009) · Cell · doi:10.1016/j.cell.2009.03.025 · Cited by 1,138

Identification of patterns in biological sequences at the ALGGEN server: PROMO and MALGEN

Farré, D. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg605 · Cited by 1,057

NAFLD, NASH and liver cancer

Michelotti, G. A., Machado, M. V., & Diehl, A. M. (2013) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2013.183 · Cited by 974

Triggering and resolution of inflammation in NASH

Schuster, S., Cabrera, D., Arrese, M., & Feldstein, A. E. (2018) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-018-0009-6 · Cited by 943

Endpoints and clinical trial design for nonalcoholic steatohepatitis

Sanyal, A. J., Brunt, E. M., Kleiner, D. E., Kowdley, K. V., Chalasani, N., Lavine, J. E., Ratziu, V., & McCullough, A. J. (2011) · Hepatology · doi:10.1002/hep.24376 · Cited by 763

Mechanisms of Fibrosis Development in Nonalcoholic Steatohepatitis

Schwabe, R. F., Tabas, I., & Pajvani, U. B. (2020) · Gastroenterology · doi:10.1053/j.gastro.2019.11.311 · Cited by 671

Mastermind Recruits CycC:CDK8 to Phosphorylate the Notch ICD and Coordinate Activation with Turnover

Fryer, C. J., White, B., & Jones, K. A. (2004) · Molecular Cell · doi:10.1016/j.molcel.2004.10.014 · Cited by 627

High-yield and high-purity isolation of hepatic stellate cells from normal and fibrotic mouse livers

Mederacke, I., Dapito, D. H., Affò, S., Uchinami, H., & Schwabe, R. F. (2015) · Nature Protocols · doi:10.1038/nprot.2015.017 · Cited by 548

rax, Hes1, and notch1 promote the formation of Müller glia by postnatal retinal progenitor cells.

Furukawa, T., Mukherjee, S., Bao, Z., Morrow, E. M., & Cepko, C. (2000) · Neuron · doi:10.1016/s0896-6273(00)81171-x · Cited by 545

Targeting the gut-liver axis in liver disease

Wiest, R., Albillos, A., Trauner, M., Bajaj, J. S., & Jalan, R. (2017) · Journal of Hepatology · doi:10.1016/j.jhep.2017.05.007 · Cited by 427

Single-cell transcriptomics uncovers zonation of function in the mesenchyme during liver fibrosis

Dobie, R., Wilson-Kanamori, J. R., Henderson, B. E. P., Smith, J. R., Matchett, K. P., Portman, J. R., Wallenborg, K., Picelli, S., Zagorska, A., Pendem, S. V., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.10.024 · Cited by 420

Hepatocyte TAZ/WWTR1 Promotes Inflammation and Fibrosis in Nonalcoholic Steatohepatitis

Wang, X., Zheng, Z., Caviglia, J. M., Corey, K. E., Herfel, T. M., Cai, B., Masia, R., Chung, R. T., Lefkowitch, J. H., Schwabe, R. F., et al. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.09.016 · Cited by 413

Conditional and inducible transgene expression in mice through the combinatorial use of Cre-mediated recombination and tetracycline induction

Bélteki, G. (2005) · Nucleic Acids Research · doi:10.1093/nar/gni051 · Cited by 382

Increased Liver Localization of Lipopolysaccharides in Human and Experimental NAFLD

Carpino, G., Del Ben, M., Pastori, D., Carnevale, R., Baratta, F., Overi, D., Francis, H., Cardinale, V., Onori, P., Safarikia, S., et al. (2020) · Hepatology · doi:10.1002/hep.31056 · Cited by 381

Heterogeneous distribution of glutamine synthetase among rat liver parenchymal cells in situ and in primary culture.

Gebhardt, R., & Mecke, D. (1983) · The EMBO Journal · doi:10.1002/j.1460-2075.1983.tb01464.x · Cited by 377

Pathological Features of Fatty Liver Disease

Yeh, M. M., & Brunt, E. M. (2014) · Gastroenterology · doi:10.1053/j.gastro.2014.07.056 · Cited by 352

Hepatic Gene Expression Profiles Differentiate Presymptomatic Patients With Mild Versus Severe Nonalcoholic Fatty Liver Disease

Moylan, C. A., Pang, H., Dellinger, A. E., Suzuki, A., Garrett, M. E., Guy, C. D., Murphy, S. K., Ashley‐Koch, A. E., Choi, S. S., Michelotti, G. A., et al. (2013) · Hepatology · doi:10.1002/hep.26661 · Cited by 319

CREB controls hepatic lipid metabolism through nuclear hormone receptor PPAR-γ

Herzig, S., Hedrick, S. A., Morantte, I. G., Koo, S., Galimi, F., & Montminy, M. (2003) · Nature · doi:10.1038/nature02110 · Cited by 317

Molecular mechanisms of NF-κB activation induced by bacterial lipopolysaccharide through Toll-like receptors

Zhang, G., & Ghosh, S. (2000) · Journal of Endotoxin Research · doi:10.1179/096805100101532414 · Cited by 316

Dynamic Ligand Discrimination in the Notch Signaling Pathway

Nandagopal, N., Santat, L. A., LeBon, L., Sprinzak, D., Bronner-Fraser, M. E., & Elowitz, M. B. (2018) · Cell · doi:10.1016/j.cell.2018.01.002 · Cited by 311

Chronic intermittent hypoxia predisposes to liver injury†

Savransky, V., Nanayakkara, A., Vivero, A., Li, J., Bevans‐Fonti, S., Smith, P. L., Torbenson, M. S., & Polotsky, V. Y. (2007) · Hepatology · doi:10.1002/hep.21593 · Cited by 262

Relationship of steatosis grade and zonal location to histological features of steatohepatitis in adult patients with non-alcoholic fatty liver disease

Chalasani, N., Wilson, L., Kleiner, D. E., Cummings, O. W., Brunt, E. M., & Ünalp, A. (2008) · Journal of Hepatology · doi:10.1016/j.jhep.2008.01.016 · Cited by 260

Emerging roles of Notch signaling in liver disease

Geisler, F., & Strazzabosco, M. (2014) · Hepatology · doi:10.1002/hep.27268 · Cited by 255

Hepatocyte Notch activation induces liver fibrosis in nonalcoholic steatohepatitis

Zhu, C., Kim, K., Wang, X., Bartolome, A., Salomao, M., Dongiovanni, P., Meroni, M., Graham, M. J., Yates, K. P., Diehl, A. M., et al. (2018) · Science Translational Medicine · doi:10.1126/scitranslmed.aat0344 · Cited by 250

Jagged1 in the portal vein mesenchyme regulates intrahepatic bile duct development: insights into Alagille syndrome

Hofmann, J. J., Zovein, A. C., Koh, H., Radtke, F., Weinmaster, G., & Iruela‐Arispe, M. L. (2010) · Development · doi:10.1242/dev.052118 · Cited by 249

Mechanism of Hypoxia-Induced NF-κB

Culver, C. A., Sundqvist, A., Mudie, S., Melvin, A., Xirodimas, D. P., & Rocha, S. (2010) · Molecular and Cellular Biology · doi:10.1128/mcb.00409-10 · Cited by 235

Mechanisms of Notch signaling: a simple logic deployed in time and space

Henrique, D., & Schweisguth, F. (2019) · Development · doi:10.1242/dev.172148 · Cited by 208

Hepatic glutamate metabolism: a tale of 2 hepatocytes

Brosnan, M. E., & Brosnan, J. T. (2009) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.2009.27462z · Cited by 199

Inhibition of Notch signaling ameliorates insulin resistance in a FoxO1-dependent manner

Pajvani, U. B., Shawber, C. J., Samuel, V. T., Birkenfeld, A. L., Shulman, G. I., Kitajewski, J., & Accili, D. (2011) · Nature Medicine · doi:10.1038/nm.2378 · Cited by 193

Hypoxia regulates the mitochondrial activity of hepatocellular carcinoma cells through HIF/HEY1/PINK1 pathway

Kung-Chun Chiu, D., Pui-Wah Tse, A., Law, C.-T., Ming-Jing Xu, I., Lee, D., Chen, M., Kit-Ho Lai, R., Wai-Hin Yuen, V., Wing-Sum Cheu, J., Wai-Hung Ho, D., et al. (2019) · Cell Death & Disease · doi:10.1038/s41419-019-2155-3 · Cited by 192

Rel/NF‐κB can trigger the Notch signaling pathway by inducing the expression of Jagged1, a ligand for Notch receptors

Bash, J., Zong, W., Banga, S. S., Rivera, A., Ballard, D. W., Ron, Y., & Gélinas, C. (1999) · The EMBO Journal · doi:10.1093/emboj/18.10.2803 · Cited by 191

NF-κB non-cell-autonomously regulates cancer stem cell populations in the basal-like breast cancer subtype

Yamamoto, M., Taguchi, Y., Ito-Kureha, T., Semba, K., Yamaguchi, N., & Inoue, J. (2013) · Nature Communications · doi:10.1038/ncomms3299 · Cited by 188

Notch is required for wingless signaling in the epidermis of Drosophila

Couso, J. P. (1994) · Cell · doi:10.1016/0092-8674(94)90195-3 · Cited by 179

Inhibition of Notch uncouples Akt activation from hepatic lipid accumulation by decreasing mTorc1 stability

Pajvani, U. B., Qiang, L., Kangsamaksin, T., Kitajewski, J., Ginsberg, H. N., & Accili, D. (2013) · Nature Medicine · doi:10.1038/nm.3259 · Cited by 172

Intestinal Microbiota and Nonalcoholic Steatohepatitis

Brandl, K., & Schnabl, B. (2017) · Current Opinion in Gastroenterology · doi:10.1097/mog.0000000000000349 · Cited by 169

Hypoxia Induced NF-κB

D’Ignazio, L., & Rocha, S. (2016) · Cells · doi:10.3390/cells5010010 · Cited by 168

Hyaluronan synthase 2–mediated hyaluronan production mediates Notch1 activation and liver fibrosis

Yang, Y. M., Noureddin, M., Liu, C., Ohashi, K., Kim, S. Y., Ramnath, D., Powell, E. E., Sweet, M. J., Roh, Y. S., Hsin, I.-F., et al. (2019) · Science Translational Medicine · doi:10.1126/scitranslmed.aat9284 · Cited by 166

Macrophage‐Specific Hypoxia‐Inducible Factor‐1α Contributes to Impaired Autophagic Flux in Nonalcoholic Steatohepatitis

Wang, X., Ribeiro, M. D. C., Iracheta‐Vellve, A., Lowe, P., Ambade, A., Satishchandran, A., Bukong, T. N., Catalano, D., Kodys, K., & Szabó, G. (2018) · Hepatology · doi:10.1002/hep.30215 · Cited by 149

Inhibition of Notch Signaling by a γ-Secretase Inhibitor Attenuates Hepatic Fibrosis in Rats

Chen, Y., Zheng, S., Qi, D., Zheng, S., Guo, J., Zhang, S., & Weng, Z. (2012) · PLoS ONE · doi:10.1371/journal.pone.0046512 · Cited by 140

The Roles of Notch Signaling in Liver Development and Disease

Adams, J., & Jafar‐Nejad, H. (2019) · Biomolecules · doi:10.3390/biom9100608 · Cited by 118

Interspecies NASH disease activity whole-genome profiling identifies a fibrogenic role of PPARα-regulated dermatopontin

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

Hepatocyte Hypoxia Inducible Factor-1 Mediates the Development of Liver Fibrosis in a Mouse Model of Nonalcoholic Fatty Liver Disease

Mesarwi, O. A., Shin, M., Bevans‐Fonti, S., Schlesinger, C., Shaw, J. C., & Polotsky, V. Y. (2016) · PLoS ONE · doi:10.1371/journal.pone.0168572 · Cited by 115

Hepatic Notch Signaling Correlates With Insulin Resistance and Nonalcoholic Fatty Liver Disease

Valenti, L. V. C., Mendoza, R. M., Rametta, R., Maggioni, M., Kitajewski, C., Shawber, C. J., & Pajvani, U. B. (2013) · Diabetes · doi:10.2337/db13-0769 · Cited by 113

Selective regulation of Notch ligands during angiogenesis is mediated by vimentin

Antfolk, D., Sjöqvist, M., Cheng, F., Isoniemi, K. O., Duran, C. L., Rivero‐Müller, A., Antila, C., Niemi, R., Landor, S. K.-J., Bouten, C. V. C., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1703057114 · Cited by 108

Fat uses a TOLL-road to connect inflammation and diabetes

Kim, J. K. (2006) · Cell Metabolism · doi:10.1016/j.cmet.2006.11.008 · Cited by 105

Expression Dynamics and Functions of Hes Factors in Development and Diseases

Kobayashi, T., & Kageyama, R. (2014) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-405943-6.00007-5 · Cited by 98

Real-Time Imaging of Notch Activation with a Luciferase Complementation-Based Reporter

Ilagan, M. X. G., Lim, S., Fulbright, M. C., Piwnica-Worms, D. R., & Kopan, R. (2011) · Science Signaling · doi:10.1126/scisignal.2001656 · Cited by 93

Distinct Tlr4-expressing cell compartments control neutrophilic and eosinophilic airway inflammation

McAlees, J. W., Whitehead, G. S., Harley, I. T. W., Cappelletti, M., Rewerts, C. L., Holdcroft, A. M., Divanovic, S., Wills-Karp, M. A., Finkelman, F. D., Karp, C. L., et al. (2014) · Mucosal Immunology · doi:10.1038/mi.2014.117 · Cited by 93

Bile duct proliferation in liver-specific Jag1 conditional knockout mice: Effects of gene dosage

Loomes, K. M., Russo, P., Ryan, M. J., Nelson, A., Underkoffler, L. A., Glover, C. L., Fu, H. Y., Gridley, T., Kaestner, K. H., & Oakey, R. J. (2007) · Hepatology · doi:10.1002/hep.21460 · Cited by 90

TNF induction of jagged-1 in endothelial cells is NFκB-dependent

Johnston, D. A., Dong, B., & Hughes, C. C. W. (2009) · Gene · doi:10.1016/j.gene.2009.01.003 · Cited by 80

Jag1 Modulates an Oscillatory Dll1-Notch-Hes1 Signaling Module to Coordinate Growth and Fate of Pancreatic Progenitors.

Seymour, P. A., Collin, C. A., Egeskov-Madsen, A., Jørgensen, M. C., Shimojo, H., Imayoshi, I., de Lichtenberg, K. D., Kopan, R., Kageyama, R., & Serup, P. (2020) · Developmental Cell · doi:10.1016/j.devcel.2020.01.015 · Cited by 55

Identification of a novel alpha‐fetoprotein‐expressing cell population induced by the Jagged1/Notch2 signal in murine fibrotic liver

Nakano, Y., Nakao, S., Sumiyoshi, H., Mikami, K., Tanno, Y., Sueoka, M., Kasahara, D., Kimura, H., Moro, T., Kamiya, A., et al. (2017) · Hepatology Communications · doi:10.1002/hep4.1026 · Cited by 34

Jagged1 intracellular domain-mediated inhibition of Notch1 signalling regulates cardiac homeostasis in the postnatal heart

Metrich, M., Pomey, A. B., Berthonneche, C., Sarre, A., Nemir, M., & Pedrazzini, T. (2015) · Cardiovascular Research · doi:10.1093/cvr/cvv209 · Cited by 31

TGF-β1 signaling regulates mouse hepatic stellate cell differentiation via the Jagged1/Notch pathway

Yasen, A., Jin, X., Wang, W., Chen, Z., & Li, D. (2017) · Life Sciences · doi:10.1016/j.lfs.2017.11.018 · Cited by 26

Jagged1 protein processing in the developing mammalian lens

Azimi, M., & Brown, N. L. (2019) · Biology Open · doi:10.1242/bio.041095 · Cited by 17

Reversal effect of Jagged1 signaling inhibition on CCl4-induced hepatic fibrosis in rats

Tang, G., Weng, Z., Song, J., & Chen, Y. (2017) · Oncotarget · doi:10.18632/oncotarget.18484 · Cited by 11

Blocking development of liver fibrosis augments hepatic progenitor cell‐derived liver regeneration in a mouse chronic liver injury model

Kitade, M., Kaji, K., Nishimura, N., Seki, K., Nakanishi, K., Tsuji, Y., Sato, S., Saikawa, S., Takaya, H., Kawaratani, H., et al. (2019) · Hepatology Research · doi:10.1111/hepr.13351 · Cited by 9

In Vivo Zonal Variation and Liver Cell-Type Specific NF-κB Localization after Chronic Adaptation to Ethanol and following Partial Hepatectomy

Nilakantan, H., Kuttippurathu, L., Parrish, A., Hoek, J. B., & Vadigepalli, R. (2015) · PLoS ONE · doi:10.1371/journal.pone.0140236 · Cited by 6

Notch signaling pathway: architecture, disease, and therapeutics

Zhou, B., Lin, W., Long, Y., Yang, Y., Zhang, H., Wu, K., & Chu, Q. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-00934-y · Cited by 1,216

Understanding the cellular interactome of non-alcoholic fatty liver disease

Wallace, S. J., Tacke, F., Schwabe, R. F., & Henderson, N. C. (2022) · JHEP Reports · doi:10.1016/j.jhepr.2022.100524 · Cited by 116

Gut microbiome in metabolic dysfunction-associated steatotic liver disease and associated hepatocellular carcinoma

Lau, H. C.-H., Zhang, X., & Yu, J. (2025) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-025-01089-1 · Cited by 126

Inflammation and immunity in liver homeostasis and disease: a nexus of hepatocytes, nonparenchymal cells and immune cells

(2025) · doi:10.1038/s41423-025-01313-7 · Cited by 97

Pathophysiological underpinnings of metabolic dysfunction-associated steatotic liver disease

Kuchay, M. S., Choudhary, N. S., & Ramos‐Molina, B. (2025) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00951.2024 · Cited by 104

Hepatocyte Notch activation induces liver fibrosis in nonalcoholic steatohepatitis

Zhu, C., Kim, K., Wang, X., Bartolome, A., Salomao, M., Dongiovanni, P., Meroni, M., Graham, M. J., Yates, K. P., Diehl, A. M., et al. (2018) · Science Translational Medicine · doi:10.1126/scitranslmed.aat0344 · Cited by 250

Hepatocyte-targeted siTAZ therapy lowers liver fibrosis in NASH diet-fed chimeric mice with hepatocyte-humanized livers

Wang, X., Moore, M. P., Shi, H., Miyata, Y., Donnelly, S. K., Radiloff, D. R., & Tabas, I. (2023) · Molecular Therapy Methods & Clinical Development · doi:10.1016/j.omtm.2023.101165 · Cited by 21

Notch and Nonalcoholic Fatty Liver and Fibrosis

Romeo, S. (2019) · New England Journal of Medicine · doi:10.1056/nejmcibr1815636 · Cited by 49

Hepatocyte Notch in non-alcoholic steatohepatitis (NASH)-associated liver fibrosis and cancer

Zhu, C. (2019) · doi:10.7916/d8-877b-v389

Jagged-1 signalling is required in liver fibrogensis

Weng, H., Liu, Y., Ilkavets, I., Shen, H., Zimmer, V., Lammert, F., Mueller, A. J., Herweck, F., Stump, C., Mertens, P., et al. (2011) · Zeitschrift für Gastroenterologie · doi:10.1055/s-0030-1269508