BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 20086045)

  • 1. Membrane protein SMP-1 is required for normal flagellum function in Leishmania.
    Tull D; Naderer T; Spurck T; Mertens HD; Heng J; McFadden GI; Gooley PR; McConville MJ
    J Cell Sci; 2010 Feb; 123(Pt 4):544-54. PubMed ID: 20086045
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Flagellum elongation is required for correct structure, orientation and function of the flagellar pocket in Trypanosoma brucei.
    Absalon S; Blisnick T; Bonhivers M; Kohl L; Cayet N; Toutirais G; Buisson J; Robinson D; Bastin P
    J Cell Sci; 2008 Nov; 121(Pt 22):3704-16. PubMed ID: 18940910
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Acylation-dependent and-independent membrane targeting and distinct functions of small myristoylated proteins (SMPs) in Leishmania major.
    Tull D; Heng J; Gooley PR; Naderer T; McConville MJ
    Int J Parasitol; 2012; 42(3):239-47. PubMed ID: 22281304
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Membrane targeting of the small myristoylated protein 2 (SMP-2) in Leishmania major.
    Heng J; Saunders EC; Gooley PR; McConville MJ; Naderer T; Tull D
    Mol Biochem Parasitol; 2013 Jul; 190(1):1-5. PubMed ID: 23727225
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Stuck in reverse: loss of LC1 in Trypanosoma brucei disrupts outer dynein arms and leads to reverse flagellar beat and backward movement.
    Baron DM; Kabututu ZP; Hill KL
    J Cell Sci; 2007 May; 120(Pt 9):1513-20. PubMed ID: 17405810
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Actin-depolymerizing factor, ADF/cofilin, is essentially required in assembly of Leishmania flagellum.
    Tammana TV; Sahasrabuddhe AA; Mitra K; Bajpai VK; Gupta CM
    Mol Microbiol; 2008 Nov; 70(4):837-52. PubMed ID: 18793337
    [TBL] [Abstract][Full Text] [Related]  

  • 7. SMP-1, a member of a new family of small myristoylated proteins in kinetoplastid parasites, is targeted to the flagellum membrane in Leishmania.
    Tull D; Vince JE; Callaghan JM; Naderer T; Spurck T; McFadden GI; Currie G; Ferguson K; Bacic A; McConville MJ
    Mol Biol Cell; 2004 Nov; 15(11):4775-86. PubMed ID: 15342784
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Two flagellar genes, AGG2 and AGG3, mediate orientation to light in Chlamydomonas.
    Iomini C; Li L; Mo W; Dutcher SK; Piperno G
    Curr Biol; 2006 Jun; 16(11):1147-53. PubMed ID: 16753570
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Functional genomics in Trypanosoma brucei identifies evolutionarily conserved components of motile flagella.
    Baron DM; Ralston KS; Kabututu ZP; Hill KL
    J Cell Sci; 2007 Feb; 120(Pt 3):478-91. PubMed ID: 17227795
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The two cytoplasmic dynein-2 isoforms in Leishmania mexicana perform separate functions.
    Adhiambo C; Forney JD; Asai DJ; LeBowitz JH
    Mol Biochem Parasitol; 2005 Oct; 143(2):216-25. PubMed ID: 16054709
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Flagellar localization of a novel isoform of myosin, myosin XXI, in Leishmania.
    Katta SS; Sahasrabuddhe AA; Gupta CM
    Mol Biochem Parasitol; 2009 Apr; 164(2):105-10. PubMed ID: 19121339
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The Chlamydomonas MBO2 locus encodes a conserved coiled-coil protein important for flagellar waveform conversion.
    Tam LW; Lefebvre PA
    Cell Motil Cytoskeleton; 2002 Apr; 51(4):197-212. PubMed ID: 11977094
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evidence for a sliding-resistance at the tip of the trypanosome flagellum.
    Woolley D; Gadelha C; Gull K
    Cell Motil Cytoskeleton; 2006 Dec; 63(12):741-6. PubMed ID: 17009329
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The Parkin co-regulated gene product, PACRG, is an evolutionarily conserved axonemal protein that functions in outer-doublet microtubule morphogenesis.
    Dawe HR; Farr H; Portman N; Shaw MK; Gull K
    J Cell Sci; 2005 Dec; 118(Pt 23):5421-30. PubMed ID: 16278296
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Trypanosomatid flagellum biogenesis: ARL-3A is involved in several species.
    Sahin A; Lemercier G; Tetaud E; Espiau B; Myler P; Stuart K; Bakalara N; Merlin G
    Exp Parasitol; 2004; 108(3-4):126-33. PubMed ID: 15582509
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Intraflagellar transport complex in Leishmania spp. In silico genome-wide screening and annotation of gene function.
    Gouveia JJ; Vasconcelos EJ; Pacheco AC; Araújo-Filho R; Maia AR; Kamimura MT; Costa MP; Viana DA; Costa RB; Maggioni R; Oliveira DM
    Genet Mol Res; 2007 Oct; 6(4):766-98. PubMed ID: 18058704
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Two novel flagellar components and H-NS are involved in the motor function of Escherichia coli.
    Ko M; Park C
    J Mol Biol; 2000 Oct; 303(3):371-82. PubMed ID: 11031114
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Flagellar and ciliary beating in trypanosome motility.
    Gadelha C; Wickstead B; Gull K
    Cell Motil Cytoskeleton; 2007 Aug; 64(8):629-43. PubMed ID: 17549738
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Involvement of a Leishmania thymidine kinase in flagellum formation, promastigote shape and growth as well as virulence.
    Thiel M; Harder S; Wiese M; Kroemer M; Bruchhaus I
    Mol Biochem Parasitol; 2008 Apr; 158(2):152-62. PubMed ID: 18222009
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Assembly of the Leishmania amazonensis flagellum during cell differentiation.
    Gadelha AP; Cunha-e-Silva NL; de Souza W
    J Struct Biol; 2013 Nov; 184(2):280-92. PubMed ID: 24041804
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.