BPG is committed to discovery and dissemination of knowledge
Cited by in CrossRef
For: Baumert JT, Sparmann G, Emmrich J, Liebe S, Jaster R. Inhibitory effects of interferons on pancreatic stellate cell activation. World J Gastroenterol 2006; 12(6): 896-901 [PMID: 16521217 DOI: 10.3748/wjg.v12.i6.896]
URL: https://www.wjgnet.com/1948-5204/full/v12/i6/896.htm
Number Citing Articles
1
Soumya Jagannath, Pramod Kumar Garg. Novel and Experimental Therapies in Chronic PancreatitisDigestive Diseases and Sciences 2017; 62(7): 1751 doi: 10.1007/s10620-017-4604-0
2
Rupjyoti Talukdar, Rakesh K Tandon. Pancreatic stellate cells: New target in the treatment of chronic pancreatitisJournal of Gastroenterology and Hepatology 2008; 23(1): 34 doi: 10.1111/j.1440-1746.2007.05206.x
3
Atsushi Masamune, Tooru Shimosegawa. Signal transduction in pancreatic stellate cellsJournal of Gastroenterology 2009; 44(4): 249 doi: 10.1007/s00535-009-0013-2
4
Brit Fitzner, Stephanie-Anna Holzhueter, Saleh Ibrahim, Horst Nizze, Robert Jaster. Interferon-Gamma Treatment Accelerates and Aggravates Autoimmune Pancreatitis in the MRL/Mp-MousePancreatology 2009; 9(3): 233 doi: 10.1159/000199434
5
Jaganmay Sarkar, Hiranmoy Das. Handbook of Oxidative Stress in Cancer: Therapeutic Aspects2022; : 3987 doi: 10.1007/978-981-16-5422-0_272
6
Robin Bülow, Brit Fitzner, Gisela Sparmann, Jörg Emmrich, Stefan Liebe, Robert Jaster. Antifibrogenic effects of histone deacetylase inhibitors on pancreatic stellate cellsBiochemical Pharmacology 2007; 74(12): 1747 doi: 10.1016/j.bcp.2007.08.023
7
Divya Thomas, Prakash Radhakrishnan. Tumor MicroenvironmentAdvances in Experimental Medicine and Biology 2020; 1234: 57 doi: 10.1007/978-3-030-37184-5_5
8
Falko Lange, Katja Rateitschak, Brit Fitzner, Ralf Pöhland, Olaf Wolkenhauer, Robert Jaster. Studies on mechanisms of interferon-gamma action in pancreatic cancer using a data-driven and model-based approachMolecular Cancer 2011; 10(1) doi: 10.1186/1476-4598-10-13
9
Katja Rateitschak, Felix Winter, Falko Lange, Robert Jaster, Olaf Wolkenhauer, Scott Markel. Parameter Identifiability and Sensitivity Analysis Predict Targets for Enhancement of STAT1 Activity in Pancreatic Cancer and Stellate CellsPLoS Computational Biology 2012; 8(12): e1002815 doi: 10.1371/journal.pcbi.1002815
10
Anika Jonitz, Brit Fitzner, Robert Jaster. Molecular determinants of the profibrogenic effects of endothelin-1 in pancreatic stellate cellsWorld Journal of Gastroenterology 2009; 15(33): 4143-4149 doi: 10.3748/wjg.15.4143
11
Lennard Spanehl, Denis Revskij, Karen Bannert, Luise Ehlers, Robert Jaster. YAP activates pancreatic stellate cells and enhances pancreatic fibrosisHepatobiliary & Pancreatic Diseases International 2022; 21(6): 583 doi: 10.1016/j.hbpd.2022.06.004
12
Voddu Suresh, Pujarini Dash, Sujit Suklabaidya, Krushna Chandra Murmu, Prakash K. Sasmal, Gajendra M. Jogdand, Deepti Parida, Manisha Sethi, Biswajit Das, Debasish Mohapatra, Subha Saha, Punit Prasad, Abhay Satoskar, Shantibhusan Senapati. MIF confers survival advantage to pancreatic CAFs by suppressing interferon pathway‐induced p53‐dependent apoptosis The FASEB Journal 2022; 36(8) doi: 10.1096/fj.202101953R
13
Andrew Cannon, Christopher Michael Thompson, Rakesh Bhatia, Katharine Anne Armstrong, Joyce Christopher Solheim, Sushil Kumar, Surinder Kumar Batra. Molecular mechanisms of pancreatic myofibroblast activation in chronic pancreatitis and pancreatic ductal adenocarcinomaJournal of Gastroenterology 2021; 56(8): 689 doi: 10.1007/s00535-021-01800-4
14
Siri Dunér, Jacob Lopatko Lindman, Daniel Ansari, Chinmay Gundewar, Roland Andersson. Pancreatic Cancer: The Role of Pancreatic Stellate Cells in Tumor ProgressionPancreatology 2011; 10(6): 673 doi: 10.1159/000320711
15
Daniel Ansari, Ellen Andersson, Bodil Andersson, Roland Andersson. Chronic pancreatitis: potential future interventionsScandinavian Journal of Gastroenterology 2010; 45(9): 1022 doi: 10.3109/00365521003734174
16
Despina Bazou, Nir Maimon, Lance Munn, Iciar Gonzalez. Effects of Low Intensity Continuous Ultrasound (LICU) on Mouse Pancreatic Tumor ExplantsApplied Sciences 2017; 7(12): 1275 doi: 10.3390/app7121275
17
S. Bolivar, J.A. Espitia-Corredor, F. Olivares-Silva, P. Valenzuela, C. Humeres, R. Anfossi, E. Castro, R. Vivar, A. Salas-Hernández, V. Pardo-Jiménez, G. Díaz-Araya. In cardiac fibroblasts, interferon-beta attenuates differentiation, collagen synthesis, and TGF-β1-induced collagen gel contractionCytokine 2021; 138: 155359 doi: 10.1016/j.cyto.2020.155359
18
Morgan K. Groover, Jillian M. Richmond. Potential therapeutic manipulations of the CXCR3 chemokine axis for the treatment of inflammatory fibrosing diseasesF1000Research 2020; 9: 1197 doi: 10.12688/f1000research.26728.1
19
Ratnakar R Bynigeri, Aparna Jakkampudi, Ramaiah Jangala, Chivukula Subramanyam, Mitnala Sasikala, G Venkat Rao, D Nageshwar Reddy, Rupjyoti Talukdar. Pancreatic stellate cell: Pandora's box for pancreatic disease biologyWorld Journal of Gastroenterology 2017; 23(3): 382-405 doi: 10.3748/wjg.v23.i3.382
20
Robert Jaster, Jörg Emmrich. Crucial role of fibrogenesis in pancreatic diseasesBest Practice & Research Clinical Gastroenterology 2008; 22(1): 17 doi: 10.1016/j.bpg.2007.10.004
21
Katja Rateitschak, Anna Karger, Brit Fitzner, Falko Lange, Olaf Wolkenhauer, Robert Jaster. Mathematical modelling of interferon-γ signalling in pancreatic stellate cells reflects and predicts the dynamics of STAT1 pathway activityCellular Signalling 2010; 22(1): 97 doi: 10.1016/j.cellsig.2009.09.019
22
Jaganmay Sarkar, Hiranmoy Das. Handbook of Oxidative Stress in Cancer: Therapeutic Aspects2022; : 1 doi: 10.1007/978-981-16-1247-3_272-1
23
Brit Fitzner, Peter Brock, Hana Nechutova, Änne Glass, Thomas Karopka, Dirk Koczan, Hans-Jürgen Thiesen, Gisela Sparmann, Jörg Emmrich, Stefan Liebe, Robert Jaster. Inhibitory effects of interferon-γ on activation of rat pancreatic stellate cells are mediated by STAT1 and involve down-regulation of CTGF expressionCellular Signalling 2007; 19(4): 782 doi: 10.1016/j.cellsig.2006.10.002