228 related articles for article (PubMed ID: 20975683)
21. Ufmylation and FATylation pathways are downregulated in human alcoholic and nonalcoholic steatohepatitis, and mice fed DDC, where Mallory-Denk bodies (MDBs) form.
Liu H; Li J; Tillman B; French BA; French SW
Exp Mol Pathol; 2014 Aug; 97(1):81-8. PubMed ID: 24893112
[TBL] [Abstract][Full Text] [Related]
22. Analysis of modification and proteolytic targeting by the ubiquitin-like modifier FAT10.
Aichem A; Boehm AN; Catone N; Schmidtke G; Groettrup M
Methods Enzymol; 2019; 618():229-256. PubMed ID: 30850054
[TBL] [Abstract][Full Text] [Related]
23. The FAT10 post-translational modification is involved in the lytic replication of Kaposi's sarcoma-associated herpesvirus.
Sugimoto A; Abe Y; Watanabe T; Hosokawa K; Adachi J; Tomonaga T; Iwatani Y; Murata T; Fujimuro M
J Virol; 2021 Apr; 95(10):. PubMed ID: 33627385
[TBL] [Abstract][Full Text] [Related]
24. Association of Uba6-Specific-E2 (USE1) With Lung Tumorigenesis.
Kim SJ; Hyeong Lee T; Hee Nam S; Kim JH; Oh S; Sook Cho Y; Sup Lee M; Choi S; Lee PC
J Natl Cancer Inst; 2017 Mar; 109(3):1-11. PubMed ID: 28376205
[TBL] [Abstract][Full Text] [Related]
25. The inherited blindness protein AIPL1 regulates the ubiquitin-like FAT10 pathway.
Bett JS; Kanuga N; Richet E; Schmidtke G; Groettrup M; Cheetham ME; van der Spuy J
PLoS One; 2012; 7(2):e30866. PubMed ID: 22347407
[TBL] [Abstract][Full Text] [Related]
26. FAT10 and NUB1L bind to the VWA domain of Rpn10 and Rpn1 to enable proteasome-mediated proteolysis.
Rani N; Aichem A; Schmidtke G; Kreft SG; Groettrup M
Nat Commun; 2012 Mar; 3():749. PubMed ID: 22434192
[TBL] [Abstract][Full Text] [Related]
27. Degradation of FAT10 by the 26S proteasome is independent of ubiquitylation but relies on NUB1L.
Schmidtke G; Kalveram B; Groettrup M
FEBS Lett; 2009 Feb; 583(3):591-4. PubMed ID: 19166848
[TBL] [Abstract][Full Text] [Related]
28. FAT10 and NUB1L cooperate to activate the 26S proteasome.
Brockmann F; Catone N; Wünsch C; Offensperger F; Scheffner M; Schmidtke G; Aichem A
Life Sci Alliance; 2023 Aug; 6(8):. PubMed ID: 37188463
[TBL] [Abstract][Full Text] [Related]
29. The ubiquitin-like modifier FAT10 is required for normal IFN-γ production by activated CD8
Mah MM; Basler M; Groettrup M
Mol Immunol; 2019 Apr; 108():111-120. PubMed ID: 30818228
[TBL] [Abstract][Full Text] [Related]
30. Newly translated proteins are substrates for ubiquitin, ISG15, and FAT10.
Spinnenhirn V; Bitzer A; Aichem A; Groettrup M
FEBS Lett; 2017 Jan; 591(1):186-195. PubMed ID: 27926780
[TBL] [Abstract][Full Text] [Related]
31. The FAT10- and ubiquitin-dependent degradation machineries exhibit common and distinct requirements for MHC class I antigen presentation.
Ebstein F; Lehmann A; Kloetzel PM
Cell Mol Life Sci; 2012 Jul; 69(14):2443-54. PubMed ID: 22349260
[TBL] [Abstract][Full Text] [Related]
32. Grsf1-induced translation of the SNARE protein Use1 is required for expansion of the erythroid compartment.
Nieradka A; Ufer C; Thiadens K; Grech G; Horos R; van Coevorden-Hameete M; van den Akker E; Sofi S; Kuhn H; von Lindern M
PLoS One; 2014; 9(9):e104631. PubMed ID: 25184340
[TBL] [Abstract][Full Text] [Related]
33. The ubiquitin-like modifier FAT10 interacts with HDAC6 and localizes to aggresomes under proteasome inhibition.
Kalveram B; Schmidtke G; Groettrup M
J Cell Sci; 2008 Dec; 121(Pt 24):4079-88. PubMed ID: 19033385
[TBL] [Abstract][Full Text] [Related]
34. Activating the ubiquitin family: UBA6 challenges the field.
Groettrup M; Pelzer C; Schmidtke G; Hofmann K
Trends Biochem Sci; 2008 May; 33(5):230-7. PubMed ID: 18353650
[TBL] [Abstract][Full Text] [Related]
35. E1-L2 activates both ubiquitin and FAT10.
Chiu YH; Sun Q; Chen ZJ
Mol Cell; 2007 Sep; 27(6):1014-23. PubMed ID: 17889673
[TBL] [Abstract][Full Text] [Related]
36. NEDD8 ultimate buster-1L interacts with the ubiquitin-like protein FAT10 and accelerates its degradation.
Hipp MS; Raasi S; Groettrup M; Schmidtke G
J Biol Chem; 2004 Apr; 279(16):16503-10. PubMed ID: 14757770
[TBL] [Abstract][Full Text] [Related]
37. The UBA domains of NUB1L are required for binding but not for accelerated degradation of the ubiquitin-like modifier FAT10.
Schmidtke G; Kalveram B; Weber E; Bochtler P; Lukasiak S; Hipp MS; Groettrup M
J Biol Chem; 2006 Jul; 281(29):20045-54. PubMed ID: 16707496
[TBL] [Abstract][Full Text] [Related]
38. The ubiquitin-like modifier FAT10 is degraded by the 20S proteasome in vitro but not in cellulo.
Oliveri F; Keller SJ; Goebel H; Alvarez Salinas GO; Basler M
Life Sci Alliance; 2023 Jun; 6(6):. PubMed ID: 37012049
[TBL] [Abstract][Full Text] [Related]
39. Identification of a novel binding protein of FAT10: eukaryotic translation elongation factor 1A1.
Yu X; Liu X; Liu T; Hong K; Lei J; Yuan R; Shao J
Dig Dis Sci; 2012 Sep; 57(9):2347-54. PubMed ID: 22569823
[TBL] [Abstract][Full Text] [Related]
40. Altered social behavior and neuronal development in mice lacking the Uba6-Use1 ubiquitin transfer system.
Lee PC; Dodart JC; Aron L; Finley LW; Bronson RT; Haigis MC; Yankner BA; Harper JW
Mol Cell; 2013 Apr; 50(2):172-84. PubMed ID: 23499007
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
