Tunable substrates unveil chemical complementation of a genetic cell migration defect.
about
The Actin Filament-Binding Protein Coronin Regulates Motility in Plasmodium Sporozoites.The toxoplasma Acto-MyoA motor complex is important but not essential for gliding motility and host cell invasionSurface attachment, promoted by the actomyosin system of Toxoplasma gondii is important for efficient gliding motility and invasionParasites lacking the micronemal protein MIC2 are deficient in surface attachment and host cell egress, but remain virulent in vivoMalaria parasite LIMP protein regulates sporozoite gliding motility and infectivity in mosquito and mammalian hosts.A unique profilin-actin interface is important for malaria parasite motilityHost cell invasion by apicomplexan parasites: the junction conundrumLocalisation-based imaging of malarial antigens during erythrocyte entry reaffirms a role for AMA1 but not MTRAP in invasionMicrostructured Blood Vessel Surrogates Reveal Structural Tropism of Motile Malaria Parasites.Orthogonally engineering matrix topography and rigidity to regulate multicellular morphology.Unraveling the Plasmodium vivax sporozoite transcriptional journey from mosquito vector to human host
P2860
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P2860
Tunable substrates unveil chemical complementation of a genetic cell migration defect.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
Tunable substrates unveil chemical complementation of a genetic cell migration defect.
@en
Tunable substrates unveil chemical complementation of a genetic cell migration defect.
@nl
type
label
Tunable substrates unveil chemical complementation of a genetic cell migration defect.
@en
Tunable substrates unveil chemical complementation of a genetic cell migration defect.
@nl
prefLabel
Tunable substrates unveil chemical complementation of a genetic cell migration defect.
@en
Tunable substrates unveil chemical complementation of a genetic cell migration defect.
@nl
P2093
P2860
P356
P1476
Tunable substrates unveil chemical complementation of a genetic cell migration defect.
@en
P2093
Friedrich Frischknecht
Janina Kristin Hellmann
Joachim P Spatz
Nadine Perschmann
P2860
P304
P356
10.1002/ADHM.201200426
P577
2013-01-25T00:00:00Z