These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

343 related articles for article (PubMed ID: 20855502)

  • 1. Cdc48/p97 and Shp1/p47 regulate autophagosome biogenesis in concert with ubiquitin-like Atg8.
    Krick R; Bremer S; Welter E; Schlotterhose P; Muehe Y; Eskelinen EL; Thumm M
    J Cell Biol; 2010 Sep; 190(6):965-73. PubMed ID: 20855502
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cheating on ubiquitin with Atg8.
    Krick R; Bremer S; Welter E; Eskelinen EL; Thumm M
    Autophagy; 2011 Feb; 7(2):250-1. PubMed ID: 21150310
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Shp1 and Ubx2 are adaptors of Cdc48 involved in ubiquitin-dependent protein degradation.
    Schuberth C; Richly H; Rumpf S; Buchberger A
    EMBO Rep; 2004 Aug; 5(8):818-24. PubMed ID: 15258615
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Atg4 recycles inappropriately lipidated Atg8 to promote autophagosome biogenesis.
    Nakatogawa H; Ishii J; Asai E; Ohsumi Y
    Autophagy; 2012 Feb; 8(2):177-86. PubMed ID: 22240591
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The budding yeast Cdc48(Shp1) complex promotes cell cycle progression by positive regulation of protein phosphatase 1 (Glc7).
    Böhm S; Buchberger A
    PLoS One; 2013; 8(2):e56486. PubMed ID: 23418575
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Atg8, a ubiquitin-like protein required for autophagosome formation, mediates membrane tethering and hemifusion.
    Nakatogawa H; Ichimura Y; Ohsumi Y
    Cell; 2007 Jul; 130(1):165-78. PubMed ID: 17632063
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Atg4 plays an important role in efficient expansion of autophagic isolation membranes by cleaving lipidated Atg8 in Saccharomyces cerevisiae.
    Hirata E; Ohya Y; Suzuki K
    PLoS One; 2017; 12(7):e0181047. PubMed ID: 28704456
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A role for Atg8-PE deconjugation in autophagosome biogenesis.
    Nair U; Yen WL; Mari M; Cao Y; Xie Z; Baba M; Reggiori F; Klionsky DJ
    Autophagy; 2012 May; 8(5):780-93. PubMed ID: 22622160
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cdc48/Shp1 participates in dissociation of protein complexes to regulate their activity.
    Lauinger L; Flick K; Kaiser P
    Curr Genet; 2021 Apr; 67(2):263-265. PubMed ID: 33388824
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Bidirectional substrate shuttling between the 26S proteasome and the Cdc48 ATPase promotes protein degradation.
    Li H; Ji Z; Paulo JA; Gygi SP; Rapoport TA
    Mol Cell; 2024 Apr; 84(7):1290-1303.e7. PubMed ID: 38401542
    [TBL] [Abstract][Full Text] [Related]  

  • 11. New thoughts regarding Atg8 and ubiquitination.
    Thumm M; Klionsky DJ
    Autophagy; 2011 Feb; 7(2):125-6. PubMed ID: 21160277
    [No Abstract]   [Full Text] [Related]  

  • 12. Dual roles of Atg8-PE deconjugation by Atg4 in autophagy.
    Yu ZQ; Ni T; Hong B; Wang HY; Jiang FJ; Zou S; Chen Y; Zheng XL; Klionsky DJ; Liang Y; Xie Z
    Autophagy; 2012 Jun; 8(6):883-92. PubMed ID: 22652539
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The autophagy-related protein kinase Atg1 interacts with the ubiquitin-like protein Atg8 via the Atg8 family interacting motif to facilitate autophagosome formation.
    Nakatogawa H; Ohbayashi S; Sakoh-Nakatogawa M; Kakuta S; Suzuki SW; Kirisako H; Kondo-Kakuta C; Noda NN; Yamamoto H; Ohsumi Y
    J Biol Chem; 2012 Aug; 287(34):28503-7. PubMed ID: 22778255
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The AAA-ATPase Cdc48 and cofactor Shp1 promote chromosome bi-orientation by balancing Aurora B activity.
    Cheng YL; Chen RH
    J Cell Sci; 2010 Jun; 123(Pt 12):2025-34. PubMed ID: 20483956
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A conserved protein with AN1 zinc finger and ubiquitin-like domains modulates Cdc48 (p97) function in the ubiquitin-proteasome pathway.
    Sá-Moura B; Funakoshi M; Tomko RJ; Dohmen RJ; Wu Z; Peng J; Hochstrasser M
    J Biol Chem; 2013 Nov; 288(47):33682-33696. PubMed ID: 24121501
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The amino-terminal region of Atg3 is essential for association with phosphatidylethanolamine in Atg8 lipidation.
    Hanada T; Satomi Y; Takao T; Ohsumi Y
    FEBS Lett; 2009 Apr; 583(7):1078-83. PubMed ID: 19285500
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cellular functions of Ufd2 and Ufd3 in proteasomal protein degradation depend on Cdc48 binding.
    Böhm S; Lamberti G; Fernández-Sáiz V; Stapf C; Buchberger A
    Mol Cell Biol; 2011 Apr; 31(7):1528-39. PubMed ID: 21282470
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cdc48/p97, a key actor in the interplay between autophagy and ubiquitin/proteasome catabolic pathways.
    Dargemont C; Ossareh-Nazari B
    Biochim Biophys Acta; 2012 Jan; 1823(1):138-44. PubMed ID: 21807033
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Doa1 is a Cdc48 adapter that possesses a novel ubiquitin binding domain.
    Mullally JE; Chernova T; Wilkinson KD
    Mol Cell Biol; 2006 Feb; 26(3):822-30. PubMed ID: 16428438
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Visualization of Atg3 during autophagosome formation in Saccharomyces cerevisiae.
    Ngu M; Hirata E; Suzuki K
    J Biol Chem; 2015 Mar; 290(13):8146-53. PubMed ID: 25645919
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.