BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

215 related articles for article (PubMed ID: 26596346)

  • 1. ESCRT-Dependent Cell Death in a Caenorhabditis elegans Model of the Lysosomal Storage Disorder Mucolipidosis Type IV.
    Huynh JM; Dang H; Munoz-Tucker IA; O'Ketch M; Liu IT; Perno S; Bhuyan N; Crain A; Borbon I; Fares H
    Genetics; 2016 Feb; 202(2):619-38. PubMed ID: 26596346
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Suppression of the cup-5 mucolipidosis type IV-related lysosomal dysfunction by the inactivation of an ABC transporter in C. elegans.
    Schaheen L; Patton G; Fares H
    Development; 2006 Oct; 133(19):3939-48. PubMed ID: 16943270
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Roles of CUP-5, the Caenorhabditis elegans orthologue of human TRPML1, in lysosome and gut granule biogenesis.
    Campbell EM; Fares H
    BMC Cell Biol; 2010 Jun; 11():40. PubMed ID: 20540742
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Basis of lethality in C. elegans lacking CUP-5, the Mucolipidosis Type IV orthologue.
    Schaheen L; Dang H; Fares H
    Dev Biol; 2006 May; 293(2):382-91. PubMed ID: 16530747
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Caenorhabditis elegans functional orthologue of human protein h-mucolipin-1 is required for lysosome biogenesis.
    Treusch S; Knuth S; Slaugenhaupt SA; Goldin E; Grant BD; Fares H
    Proc Natl Acad Sci U S A; 2004 Mar; 101(13):4483-8. PubMed ID: 15070744
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Caenorhabditis elegans as a model for lysosomal storage disorders.
    de Voer G; Peters D; Taschner PE
    Biochim Biophys Acta; 2008; 1782(7-8):433-46. PubMed ID: 18501720
    [TBL] [Abstract][Full Text] [Related]  

  • 7. CUP-5, the C. elegans ortholog of the mammalian lysosomal channel protein MLN1/TRPML1, is required for proteolytic degradation in autolysosomes.
    Sun T; Wang X; Lu Q; Ren H; Zhang H
    Autophagy; 2011 Nov; 7(11):1308-15. PubMed ID: 21997367
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Induction of autophagy in ESCRT mutants is an adaptive response for cell survival in C. elegans.
    Djeddi A; Michelet X; Culetto E; Alberti A; Barois N; Legouis R
    J Cell Sci; 2012 Feb; 125(Pt 3):685-94. PubMed ID: 22389403
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Interactions between endosomal maturation and autophagy: analysis of ESCRT machinery during Caenorhabditis elegans development.
    Manil-Ségalen M; Culetto E; Legouis R; Lefebvre C
    Methods Enzymol; 2014; 534():93-118. PubMed ID: 24359950
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The Caenorhabditis elegans mucolipin-like gene cup-5 is essential for viability and regulates lysosomes in multiple cell types.
    Hersh BM; Hartwieg E; Horvitz HR
    Proc Natl Acad Sci U S A; 2002 Apr; 99(7):4355-60. PubMed ID: 11904372
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The type IV mucolipidosis-associated protein TRPML1 is an endolysosomal iron release channel.
    Dong XP; Cheng X; Mills E; Delling M; Wang F; Kurz T; Xu H
    Nature; 2008 Oct; 455(7215):992-6. PubMed ID: 18794901
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Chaperone-mediated autophagy is defective in mucolipidosis type IV.
    Venugopal B; Mesires NT; Kennedy JC; Curcio-Morelli C; Laplante JM; Dice JF; Slaugenhaupt SA
    J Cell Physiol; 2009 May; 219(2):344-53. PubMed ID: 19117012
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Regulation of endocytosis by CUP-5, the Caenorhabditis elegans mucolipin-1 homolog.
    Fares H; Greenwald I
    Nat Genet; 2001 May; 28(1):64-8. PubMed ID: 11326278
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Differential physiological roles of ESCRT complexes in Caenorhabditis elegans.
    Kim DW; Sung H; Shin D; Shen H; Ahnn J; Lee SK; Lee S
    Mol Cells; 2011 Jun; 31(6):585-92. PubMed ID: 21688204
    [TBL] [Abstract][Full Text] [Related]  

  • 15. CUPpling calcium to lysosomal biogenesis.
    Piper RC; Luzio JP
    Trends Cell Biol; 2004 Sep; 14(9):471-3. PubMed ID: 15350973
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mucolipidosis type IV and the mucolipins.
    Bach G; Zeevi DA; Frumkin A; Kogot-Levin A
    Biochem Soc Trans; 2010 Dec; 38(6):1432-5. PubMed ID: 21118102
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Loss of LIN-35, the Caenorhabditis elegans ortholog of the tumor suppressor p105Rb, results in enhanced RNA interference.
    Lehner B; Calixto A; Crombie C; Tischler J; Fortunato A; Chalfie M; Fraser AG
    Genome Biol; 2006; 7(1):R4. PubMed ID: 16507136
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Biochemical Approaches to Studying Caenorhabditis elegans ESCRT Functions In Vitro.
    Block S; Schuh AL; Audhya A
    Methods Mol Biol; 2019; 1998():189-202. PubMed ID: 31250303
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Lysosomal exocytosis is impaired in mucolipidosis type IV.
    LaPlante JM; Sun M; Falardeau J; Dai D; Brown EM; Slaugenhaupt SA; Vassilev PM
    Mol Genet Metab; 2006 Dec; 89(4):339-48. PubMed ID: 16914343
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The ESCRT-III protein CeVPS-32 is enriched in domains distinct from CeVPS-27 and CeVPS-23 at the endosomal membrane of epithelial cells.
    Michelet X; Alberti A; Benkemoun L; Roudier N; Lefebvre C; Legouis R
    Biol Cell; 2009 Jul; 101(10):599-615. PubMed ID: 19432559
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.