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Artykuły w czasopismach na temat "FAT10"
Hipp, Mark Steffen, Birte Kalveram, Shahri Raasi, Marcus Groettrup i Gunter Schmidtke. "FAT10, a Ubiquitin-Independent Signal for Proteasomal Degradation". Molecular and Cellular Biology 25, nr 9 (1.05.2005): 3483–91. http://dx.doi.org/10.1128/mcb.25.9.3483-3491.2005.
Pełny tekst źródłaSchnell, Leonie, Alina Zubrod, Nicola Catone, Johanna Bialas i Annette Aichem. "Tumor necrosis factor mediates USE1-independent FAT10ylation under inflammatory conditions". Life Science Alliance 6, nr 11 (21.08.2023): e202301985. http://dx.doi.org/10.26508/lsa.202301985.
Pełny tekst źródłaJia, Yue, Ping Ji i Samuel W. French. "The Role of FAT10 in Alcoholic Hepatitis Pathogenesis". Biomedicines 8, nr 7 (1.07.2020): 189. http://dx.doi.org/10.3390/biomedicines8070189.
Pełny tekst źródłaMah, Mei Min, Nicola Roverato i Marcus Groettrup. "Regulation of Interferon Induction by the Ubiquitin-Like Modifier FAT10". Biomolecules 10, nr 6 (23.06.2020): 951. http://dx.doi.org/10.3390/biom10060951.
Pełny tekst źródłaArshad, Maria, Nazefah Abdul Hamid, Mun Chiang Chan, Fuad Ismail, Geok Chin Tan, Francesco Pezzella i Ka-Liong Tan. "NUB1 and FAT10 Proteins as Potential Novel Biomarkers in Cancer: A Translational Perspective". Cells 10, nr 9 (24.08.2021): 2176. http://dx.doi.org/10.3390/cells10092176.
Pełny tekst źródłaCanaan, Allon, Xiaofeng Yu, Carmen J. Booth, Jin Lian, Isaac Lazar, Serwa L. Gamfi, Katrina Castille i in. "FAT10/Diubiquitin-Like Protein-Deficient Mice Exhibit Minimal Phenotypic Differences". Molecular and Cellular Biology 26, nr 13 (1.07.2006): 5180–89. http://dx.doi.org/10.1128/mcb.00966-05.
Pełny tekst źródłaSchregle, Richard, Stefanie Mueller, Daniel F. Legler, Jérémie Rossy, Wolfgang A. Krueger i Marcus Groettrup. "FAT10 localises in dendritic cell aggresome-like induced structures and contributes to their disassembly". Journal of Cell Science 133, nr 14 (16.06.2020): jcs240085. http://dx.doi.org/10.1242/jcs.240085.
Pełny tekst źródłaBoehm, Annika N., Johanna Bialas, Nicola Catone, Almudena Sacristan-Reviriego, Jacqueline van der Spuy, Marcus Groettrup i Annette Aichem. "The ubiquitin-like modifier FAT10 inhibits retinal PDE6 activity and mediates its proteasomal degradation". Journal of Biological Chemistry 295, nr 42 (14.08.2020): 14402–18. http://dx.doi.org/10.1074/jbc.ra120.013873.
Pełny tekst źródłaSaxena, Kritika, Nicola Domenico Roverato, Melody Reithmann, Mei Min Mah, Richard Schregle, Gunter Schmidtke, Ivan Silbern, Henning Urlaub i Annette Aichem. "FAT10 is phosphorylated by IKKβ to inhibit the antiviral type-I interferon response". Life Science Alliance 7, nr 1 (8.11.2023): e202101282. http://dx.doi.org/10.26508/lsa.202101282.
Pełny tekst źródłaYao, Yi, Weikun Jia, Xiaofei Zeng, Yali Wang, Qiuxia Hu, Shiran Yu, Dongsheng He i Ying Li. "FAT10 Combined with Miltefosine Inhibits Mitochondrial Apoptosis and Energy Metabolism in Hypoxia-Induced H9C2 Cells by Regulating the PI3K/AKT Signaling Pathway". Evidence-Based Complementary and Alternative Medicine 2022 (18.08.2022): 1–10. http://dx.doi.org/10.1155/2022/4388919.
Pełny tekst źródłaRozprawy doktorskie na temat "FAT10"
Bialas, Johanna [Verfasser]. "The influence of FAT10 on the ubiquitin pathway and The search for FAT10-specific E3 ligases / Johanna Bialas". Konstanz : KOPS Universität Konstanz, 2018. http://d-nb.info/1215032919/34.
Pełny tekst źródłaRyu, Stella [Verfasser]. "Investigation of the FAT10 conjugation pathway / Stella Ryu". Konstanz : Bibliothek der Universität Konstanz, 2012. http://d-nb.info/105034880X/34.
Pełny tekst źródłaAhmad, Faiz [Verfasser]. "The Search for Deconjugating Enzymes of FAT10 / Faiz Ahmad". Konstanz : Bibliothek der Universität Konstanz, 2016. http://d-nb.info/1159513368/34.
Pełny tekst źródłaBürger, Stefanie [Verfasser]. "The Ubiquitin-like modifier FAT10 in tolerance induction / Stefanie Bürger". Konstanz : Bibliothek der Universität Konstanz, 2013. http://d-nb.info/1110770529/34.
Pełny tekst źródłaSchwab, Ricarda [Verfasser]. "Investigation of the interaction of FAT10 and VCP (p97) / Ricarda Schwab". Konstanz : Bibliothek der Universität Konstanz, 2015. http://d-nb.info/1144178703/34.
Pełny tekst źródłaMah, Mei Min [Verfasser]. "The Role of FAT10 in Regulating the Interferon Response / Mei Min Mah". Konstanz : KOPS Universität Konstanz, 2019. http://d-nb.info/1202012833/34.
Pełny tekst źródłaSpinnenhirn, Valentina [Verfasser]. "Functional analysis of the ubiquitin-like modifier FAT10 in autophagy / Valentina Spinnenhirn". Konstanz : Bibliothek der Universität Konstanz, 2015. http://d-nb.info/1112604391/34.
Pełny tekst źródłaKluge, Kathrin Christiane [Verfasser]. "Characterisation of the Interaction between FAT10 and its Substrate Protein p62 / Kathrin Christiane Kluge". Konstanz : Bibliothek der Universität Konstanz, 2014. http://d-nb.info/1112745238/34.
Pełny tekst źródłaSchregle, Richard [Verfasser]. "The Ubiquitin-like Modifier FAT10 in Dendritic Cell Aggresome-like Induced Structures / Richard Schregle". Konstanz : KOPS Universität Konstanz, 2018. http://d-nb.info/121985266X/34.
Pełny tekst źródłaBernard, Lucie. "Rôle de FAT10 dans la sénescence des hépatocytes et le développement de la NASH". Electronic Thesis or Diss., Université de Lille (2022-....), 2023. https://pepite-depot.univ-lille.fr/ToutIDP/EDBSL/2023/2023ULILS039.pdf.
Pełny tekst źródłaThe accumulation of senescent hepatocytes has been identified as a key factor in the progression of non-alcoholic fatty liver diseases (NAFLDs), which correspond to a spectrum of chronic liver pathologies, ranging from simple steatosis to the development of non-alcoholic steatohepatitis (NASH), cirrhosis or even hepatocellular carcinoma (HCC). However, the mechanisms and actors involved in the regulation of senescence during NASH are still poorly described. The objective of this thesis was therefore to study the mechanisms controlling hepatocyte senescence during the development of NASH. Using transcriptomic and protein analyses, we have shown in the livers of patients and mice that the protein FAT10 (human leukocyte antigen-F Adjacent Transcript 10), also called UBD (Ubiquitin D), is induced during NASH. However, FAT10 is an ubiquitin-like protein that interacts with different partners playing a role in metabolism and senescence, we therefore hypothesized that FAT10 could be involved in the development of NASH, as well as in the induction and spread of hepatocyte senescence. First, we showed in the livers of NASH patients a positive correlation between the expression of FAT10 and the severity of the disease. Conversely, FAT10 expression decreases when the disease regresses. We showed specifically in hepatocytes of NASH mice that the expression of Fat10 negatively correlates with lipid metabolism pathways, and that interestingly, the decrease of Fat10 expression in NASH mice hepatocytes decreases hepatic steatosis, by reducing the size and number of lipid droplets. Secondly, we showed a positive correlation between the expression of FAT10 and of senescence genes in the livers of NASH patients. This correlation is found specifically in hepatocytes in mice. Furthermore, in this mouse model of NASH, Fat10 expression positively correlates with liver SA-β-Gal (Senescence Associated-β-Galactosidase) activity. In vitro, the induction of senescence in human hepatocytes by an irradiation or a treatment with H2O2 induces FAT10 protein as a SASP (Senescence Associated Secretory Phenotype) actor. Interestingly, FAT10 inhibition in this model promotes the induction and propagation of senescence, through an increase of SA-β-Gal activity, an induction of SASP genes, an accelerated cell proliferation arrest, an induction of the DNA damage response system and a greater accumulation of lipid droplets. Conversely, stable overexpression of FAT10 in senescent hepatocytes accelerates the loss of senescent status (decreased SA-β-Gal activity), and promotes the senescence escape and the acquisition of a pro-cancerous phenotype. In the end, all of these data suggest that the induction of FAT10 within hepatocytes during the development of NASH promotes the progression of the disease, on one hand by altering lipid metabolism within steatotic hepatocytes, and on the other hand by gradually promoting the escape of senescent hepatocytes, which could lead to the development of HCC
Książki na temat "FAT10"
Nayak, R. V., N. A. Mousa i International Joint Power Generation Conference (1990 Boston, Mass.). Combustion Modeling and Burner Replacement Strategies/Fact10/No G00523: Presented at the 1990 International Joint Power Generation Conference, Boston, ... 21-25, 1990 (Fact (Series), Vol. 10,). Amer Society of Mechanical, 1992.
Znajdź pełny tekst źródłaCzęści książek na temat "FAT10"
Pelzer, Christiane, i Marcus Groettrup. "FAT10". W Subcellular Biochemistry, 238–46. New York, NY: Springer New York, 2010. http://dx.doi.org/10.1007/978-1-4419-6676-6_19.
Pełny tekst źródłaAichem, Annette, i Marcus Groettrup. "Detection and Analysis of FAT10 Modification". W Methods in Molecular Biology, 125–32. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-474-2_7.
Pełny tekst źródłaLukasiak, Sebastian, Kai Breuhahn, Claudia Schiller, Gunter Schmidtke i Marcus Groettrup. "Quantitative Analysis of Gene Expression Relative to 18S rRNA in Carcinoma Samples Using the LightCycler® Instrument and a SYBR GreenI-based Assay: Determining FAT10 mRNA Levels in Hepatocellular Carcinoma". W Methods in Molecular Biology, 59–72. Totowa, NJ: Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-040-3_5.
Pełny tekst źródłaAichem, Annette, Annika N. Boehm, Nicola Catone, Gunter Schmidtke i Marcus Groettrup. "Analysis of modification and proteolytic targeting by the ubiquitin-like modifier FAT10". W Methods in Enzymology, 229–56. Elsevier, 2019. http://dx.doi.org/10.1016/bs.mie.2018.12.040.
Pełny tekst źródłaAdams, Susan. ""And the Sun Refused to Shine"". W Final Acts: The End of Life: Hospice and Palliative Care. Baywood Publishing Company, Inc., 2013. http://dx.doi.org/10.2190/fatc10.
Pełny tekst źródłaB. Pathak, Anand, i Satyam Satyarthi. "Head Neck Squamous Cell Cancer Genomics: Oncogenes, Tumor Suppressor Genes and Clinical Implications". W Molecular Mechanisms in Cancer. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.101044.
Pełny tekst źródłaStreszczenia konferencji na temat "FAT10"
Noymai, Anukool, Urachada Ketprom i Chaichana Mitrpant. "Increasing memory in FAT16 removable media of RFID handheld reader". W 2008 5th International Conference on Electrical Engineering/Electronics, Computer, Telecommunications and Information Technology (ECTI-CON). IEEE, 2008. http://dx.doi.org/10.1109/ecticon.2008.4600538.
Pełny tekst źródłaIrshad, Khushboo, Chitrangda Srivastava, Nargis Malik, Yakhlesh Gupta, Vaishali Suri, Swati Mahajan, Deepak Gupta i in. "Abstract 3175: FAT1 and the immunosuppressive milieu in glioblastoma tumors". W Proceedings: AACR Annual Meeting 2021; April 10-15, 2021 and May 17-21, 2021; Philadelphia, PA. American Association for Cancer Research, 2021. http://dx.doi.org/10.1158/1538-7445.am2021-3175.
Pełny tekst źródłaDikshit, Bhawana, Parthaprasad Chattopadhyay, Subrata Sinha i Kunzang Chosdol. "Abstract 4102: FAT1: A novel regulator of cancer and inflammation." W Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-4102.
Pełny tekst źródłaSrivastava, Chitrangda, Khushboo Irshad, Parthaprasad Chattopadhyay, Chitra Sarkar, Ashish Suri, Subrata Sinha i Kunzang Chosdol. "Abstract 3534: FAT1: A potential target of NFkB (RelA) in GBM". W Proceedings: AACR Annual Meeting 2017; April 1-5, 2017; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-3534.
Pełny tekst źródłaHalimah, Nova Nur. "KARAKTERISASI SENSOR HY-SRF05 DAN LOAD CELL SINGLE-POINT SEBAGAI PARAMETER PENGUKURAN ANTROPOMETRI PADA SISTEM PEMANTAUAN STATUS GIZI BAYI". W SEMINAR NASIONAL FISIKA 2016 UNJ. PRODI Pendidikan Fisika dan Fisika UNJ, 2024. http://dx.doi.org/10.21009/03.1201.fa10.
Pełny tekst źródłaArafahnti, Bestari Laksmi, Umiatin Umiatin i Heru Prasetio. "PENGARUH ENERGI LINAC TERHADAP RESPON FILM DOSIMETRI GAFCHROMIC". W SEMINAR NASIONAL FISIKA 2016 UNJ. PRODI Pendidikan Fisika dan Fisika UNJ, 2023. http://dx.doi.org/10.21009/03.1101.fa10.
Pełny tekst źródłaGupta, Y., SS Shivajirao, K. Irshad, B. Dikshit, T. Srivastav, PP Chattopadhyay, S. Sinha i K. Chosdol. "PO-125 FAT1 on salvador-warts-hippo (SWH) pathway in human glioblastoma". W Abstracts of the 25th Biennial Congress of the European Association for Cancer Research, Amsterdam, The Netherlands, 30 June – 3 July 2018. BMJ Publishing Group Ltd, 2018. http://dx.doi.org/10.1136/esmoopen-2018-eacr25.166.
Pełny tekst źródłaKrasteva, V. M., G. H. Sigel, S. L. Semjonov, M. M. Bubnov i M. I. Belovolov. "Pr3+ -doped Ge-S-I glasses and fibers for PDFA applications". W Optical Amplifiers and Their Applications. Washington, D.C.: OSA, 1997. http://dx.doi.org/10.1364/oaa.1997.faw10.
Pełny tekst źródłaConnor, Ashton A., Jordan Lerner-Ellis, Mohammad R. Akbari, Cezary Cybulski, J. Lubinski, Caroline Badouel, Helen McNeill, James G. Dowty, Mark Clendenning i Daniel D. Buchanan. "Abstract A23: Rare variants in the FAT1 gene may predispose to familial colorectal cancer". W Abstracts: AACR Special Conference: Colorectal Cancer: From Initiation to Outcomes; September 17-20, 2016; Tampa, FL. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.crc16-a23.
Pełny tekst źródłaKasahara, Shunji, i Ryo Yamamoto. "HIGH-RESOLUTION LASER SPECTROSCOPY OF THE S1 ← S0 TRANSITION OF Cl-NAPHTHALENES". W 70th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2015. http://dx.doi.org/10.15278/isms.2015.fa10.
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