JM
| Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
|---|---|---|---|---|---|---|---|
| RNG2 tethers the conoid to the apical polar ring in Toxoplasma gondii to enable parasite motility and invasion | PLoS biology | 2025 | 21 | 24 | |||
| Cytokinetic abscission in Toxoplasma gondii is governed by protein phosphatase 2A and the daughter cell scaffold complex | EMBO journal | 2024 | 149 | 84 | |||
| ATM1, an essential conserved transporter in Apicomplexa, bridges mitochondrial and cytosolic [Fe-S] biogenesis | PLOS pathogens | 2024 | 164 | 128 | |||
| Toxoplasma gondii HOOK-FTS-HIP Complex is Critical for Secretory Organelle Discharge during Motility, Invasion, and Egress | MBio | 2023 | 182 | 195 | |||
| Ceramide biosynthesis is critical for establishment of the intracellular niche of Toxoplasma gondii | Cell reports | 2022 | 315 | 255 | |||
| Importance of Aspartyl Protease 5 in the establishment of the intracellular niche during acute and chronic infection of Toxoplasma gondii | Molecular microbiology | 2022 | 331 | 158 | |||
| Toxoplasma gondii phosphatidylserine flippase complex ATP2B-CDC50.4 critically participates in microneme exocytosis | PLOS pathogens | 2022 | 355 | 234 | |||
| The ZIP code of vesicle trafficking in apicomplexa: SEC1/Munc18 and SNARE proteins | mBio | 2020 | 369 | 186 | |||
| Toxoplasma gondii GRA60 is an effector protein that modulates host cell autonomous immunity and contributes to virulence | Cellular Microbiology | 2020 | 390 | 383 | |||
| CRISPR/cas9-based knockout of GNAQ reveals differences in host cell signaling necessary for egress of apicomplexan parasites | mSphere | 2020 | 335 | 192 | |||
| Modeling and resistant alleles explain the selectivity of antimalarial compound 49c towards apicomplexan aspartyl proteases | EMBO Journal | 2018 | 681 | 15 | |||
| Crosstalk between PKA and PKG controls pH‐dependent host cell egress of Toxoplasma gondii | EMBO Journal | 2017 | 621 | 274 | |||
| Phosphatidic Acid-Mediated Signaling Regulates Microneme Secretion in Toxoplasma | Cell host & microbe | 2016 | 740 | 437 | |||
| The Conoid Associated Motor MyoH Is Indispensable for Toxoplasma gondii Entry and Exit from Host Cells | PLOS pathogens | 2016 | 691 | 345 | |||
| Fundamental Roles of the Golgi-Associated Toxoplasma Aspartyl Protease, ASP5, at the Host-Parasite Interface | PLOS pathogens | 2015 | 726 | 336 | |||
| Distinct contribution of Toxoplasma gondii rhomboid proteases 4 and 5 to micronemal protein protease 1 activity during invasion | Molecular microbiology | 2015 | 625 | 5 | |||
| Plasticity and redundancy among AMA-RON pairs ensure host cell entry of Toxoplasma parasites | Nature communications | 2014 | 732 | 276 | |||
| Plasticity between MyoC- and MyoA-Glideosomes: An Example of Functional Compensation in Toxoplasma gondii Invasion | PLOS pathogens | 2014 | 706 | 377 | |||
| Assessment of phosphorylation in Toxoplasma glideosome assembly and function | Cellular microbiology | 2014 | 731 | 305 | |||
| Galactose recognition by the apicomplexan parasite Toxoplasma gondii | The Journal of biological chemistry | 2012 | 768 | 0 | |||
| Unusual Anchor of a Motor Complex (MyoD-MLC2) to the Plasma Membrane of Toxoplasma gondii | Traffic | 2011 | 734 | 539 | |||
| Short double-stranded RNAs with an overhanging 5' ppp-nucleotide, as found in arenavirus genomes, act as RIG-I decoys | The Journal of biological chemistry | 2011 | 646 | 0 | |||
| Functional dissection of the apicomplexan glideosome molecular architecture | Cell host & microbe | 2010 | 867 | 975 | |||
| Unpaired 5' ppp-nucleotides, as found in arenavirus double-stranded RNA panhandles, are not recognized by RIG-I | The Journal of biological chemistry | 2010 | 634 | 0 | |||
| The double-stranded RNA binding domain of the vaccinia virus E3L protein inhibits both RNA- and DNA-induced activation of interferon beta | The Journal of biological chemistry | 2009 | 689 | 0 | |||
| RIG-I and dsRNA-induced IFNbeta activation | PloS one | 2008 | 672 | 339 | |||
| Activation of the beta interferon promoter by unnatural Sendai virus infection requires RIG-I and is inhibited by viral C proteins | Journal of virology | 2007 | 657 | 396 | |||
| Sendai virus budding in the course of an infection does not require Alix and VPS4A host factors | Virology | 2007 | 610 | 390 | |||
| Targeting of the Sendai virus C protein to the plasma membrane via a peptide-only membrane anchor | Journal of virology | 2007 | 571 | 329 | |||
| A short peptide at the amino terminus of the Sendai virus C protein acts as an independent element that induces STAT1 instability | Journal of virology | 2004 | 636 | 335 | |||
| The amino-terminal extensions of the longer Sendai virus C proteins modulate pY701-Stat1 and bulk Stat1 levels independently of interferon signaling | Journal of virology | 2003 | 622 | 1,228 | |||
| Chemical modification of nucleotide bases and mRNA editing depend on hexamer or nucleoprotein phase in Sendai virus nucleocapsids | RNA | 2002 | 580 | 532 | |||
| All four Sendai Virus C proteins bind Stat1, but only the larger forms also induce its mono-ubiquitination and degradation | Virology | 2002 | 726 | 843 |
