170 related articles for article (PubMed ID: 21899701)
1. Stage-specific depletion of myosin A supports an essential role in motility of malarial ookinetes.
Siden-Kiamos I; Ganter M; Kunze A; Hliscs M; Steinbüchel M; Mendoza J; Sinden RE; Louis C; Matuschewski K
Cell Microbiol; 2011 Dec; 13(12):1996-2006. PubMed ID: 21899701
[TBL] [Abstract][Full Text] [Related]
2. TREP, a novel protein necessary for gliding motility of the malaria sporozoite.
Combe A; Moreira C; Ackerman S; Thiberge S; Templeton TJ; Ménard R
Int J Parasitol; 2009 Mar; 39(4):489-96. PubMed ID: 19000911
[TBL] [Abstract][Full Text] [Related]
3. Compositional and expression analyses of the glideosome during the
Green JL; Wall RJ; Vahokoski J; Yusuf NA; Ridzuan MAM; Stanway RR; Stock J; Knuepfer E; Brady D; Martin SR; Howell SA; Pires IP; Moon RW; Molloy JE; Kursula I; Tewari R; Holder AA
J Biol Chem; 2017 Oct; 292(43):17857-17875. PubMed ID: 28893907
[TBL] [Abstract][Full Text] [Related]
4. Independent roles of apical membrane antigen 1 and rhoptry neck proteins during host cell invasion by apicomplexa.
Giovannini D; Späth S; Lacroix C; Perazzi A; Bargieri D; Lagal V; Lebugle C; Combe A; Thiberge S; Baldacci P; Tardieux I; Ménard R
Cell Host Microbe; 2011 Dec; 10(6):591-602. PubMed ID: 22177563
[TBL] [Abstract][Full Text] [Related]
5. Polarization of MTIP is a signature of gliding locomotion in Plasmodium ookinetes and sporozoites.
Siden-Kiamos I; Goosmann C; Buscaglia CA; Brinkmann V; Matuschewski K; Montagna GN
Mol Biochem Parasitol; 2020 Jan; 235():111247. PubMed ID: 31874192
[TBL] [Abstract][Full Text] [Related]
6. Motility and infectivity of Plasmodium berghei sporozoites expressing avian Plasmodium gallinaceum circumsporozoite protein.
Tewari R; Rathore D; Crisanti A
Cell Microbiol; 2005 May; 7(5):699-707. PubMed ID: 15839899
[TBL] [Abstract][Full Text] [Related]
7. A novel genetic technique in Plasmodium berghei allows liver stage analysis of genes required for mosquito stage development and demonstrates that de novo heme synthesis is essential for liver stage development in the malaria parasite.
Rathnapala UL; Goodman CD; McFadden GI
PLoS Pathog; 2017 Jun; 13(6):e1006396. PubMed ID: 28617870
[TBL] [Abstract][Full Text] [Related]
8. A malarial cysteine protease is necessary for Plasmodium sporozoite egress from oocysts.
Aly AS; Matuschewski K
J Exp Med; 2005 Jul; 202(2):225-30. PubMed ID: 16027235
[TBL] [Abstract][Full Text] [Related]
9. Plasticity and redundancy among AMA-RON pairs ensure host cell entry of Toxoplasma parasites.
Lamarque MH; Roques M; Kong-Hap M; Tonkin ML; Rugarabamu G; Marq JB; Penarete-Vargas DM; Boulanger MJ; Soldati-Favre D; Lebrun M
Nat Commun; 2014 Jun; 5():4098. PubMed ID: 24934579
[TBL] [Abstract][Full Text] [Related]
10. Apical membrane antigen 1 mediates apicomplexan parasite attachment but is dispensable for host cell invasion.
Bargieri DY; Andenmatten N; Lagal V; Thiberge S; Whitelaw JA; Tardieux I; Meissner M; Ménard R
Nat Commun; 2013; 4():2552. PubMed ID: 24108241
[TBL] [Abstract][Full Text] [Related]
11. Plasticity between MyoC- and MyoA-glideosomes: an example of functional compensation in Toxoplasma gondii invasion.
Frénal K; Marq JB; Jacot D; Polonais V; Soldati-Favre D
PLoS Pathog; 2014 Oct; 10(10):e1004504. PubMed ID: 25393004
[TBL] [Abstract][Full Text] [Related]
12. Arp1, an actin-related protein, in Plasmodium berghei.
Siden-Kiamos I; Schüler H; Liakopoulos D; Louis C
Mol Biochem Parasitol; 2010 Oct; 173(2):88-96. PubMed ID: 20580650
[TBL] [Abstract][Full Text] [Related]
13. Toxoplasma gondii myosins B/C: one gene, two tails, two localizations, and a role in parasite division.
Delbac F; Sänger A; Neuhaus EM; Stratmann R; Ajioka JW; Toursel C; Herm-Götz A; Tomavo S; Soldati T; Soldati D
J Cell Biol; 2001 Nov; 155(4):613-23. PubMed ID: 11706051
[TBL] [Abstract][Full Text] [Related]
14. Inhibitor of cysteine proteases is critical for motility and infectivity of Plasmodium sporozoites.
Boysen KE; Matuschewski K
mBio; 2013 Nov; 4(6):e00874-13. PubMed ID: 24281719
[TBL] [Abstract][Full Text] [Related]
15. ADF2 is required for transformation of the ookinete and sporozoite in malaria parasite development.
Doi Y; Shinzawa N; Fukumoto S; Okano H; Kanuka H
Biochem Biophys Res Commun; 2010 Jul; 397(4):668-72. PubMed ID: 20529666
[TBL] [Abstract][Full Text] [Related]
16. Depletion of the Plasmodium berghei thrombospondin-related sporozoite protein reveals a role in host cell entry by sporozoites.
Labaied M; Camargo N; Kappe SH
Mol Biochem Parasitol; 2007 Jun; 153(2):158-66. PubMed ID: 17418435
[TBL] [Abstract][Full Text] [Related]
17. PbGEST mediates malaria transmission to both mosquito and vertebrate host.
Talman AM; Lacroix C; Marques SR; Blagborough AM; Carzaniga R; Ménard R; Sinden RE
Mol Microbiol; 2011 Oct; 82(2):462-74. PubMed ID: 21958024
[TBL] [Abstract][Full Text] [Related]
18. CTRP is essential for mosquito infection by malaria ookinetes.
Dessens JT; Beetsma AL; Dimopoulos G; Wengelnik K; Crisanti A; Kafatos FC; Sinden RE
EMBO J; 1999 Nov; 18(22):6221-7. PubMed ID: 10562534
[TBL] [Abstract][Full Text] [Related]
19. Plasmodium berghei ookinetes glide and release Pbs25 and circumsporozoite thrombospondin-related protein on solid surface substrata.
Lecona AN; Rodríguez MH; Argotte RS; Alvarado A; Rodríguez MC
J Parasitol; 2010 Feb; 96(1):216-8. PubMed ID: 19747017
[TBL] [Abstract][Full Text] [Related]
20. Systematic analysis of Plasmodium myosins reveals differential expression, localisation, and function in invasive and proliferative parasite stages.
Wall RJ; Zeeshan M; Katris NJ; Limenitakis R; Rea E; Stock J; Brady D; Waller RF; Holder AA; Tewari R
Cell Microbiol; 2019 Oct; 21(10):e13082. PubMed ID: 31283102
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
