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 | 11 | 17 | |||
| Cytokinetic abscission in Toxoplasma gondii is governed by protein phosphatase 2A and the daughter cell scaffold complex | EMBO journal | 2024 | 148 | 80 | |||
| ATM1, an essential conserved transporter in Apicomplexa, bridges mitochondrial and cytosolic [Fe-S] biogenesis | PLOS pathogens | 2024 | 163 | 121 | |||
| Toxoplasma gondii HOOK-FTS-HIP Complex is Critical for Secretory Organelle Discharge during Motility, Invasion, and Egress | MBio | 2023 | 180 | 170 | |||
| Ceramide biosynthesis is critical for establishment of the intracellular niche of Toxoplasma gondii | Cell reports | 2022 | 313 | 232 | |||
| Importance of Aspartyl Protease 5 in the establishment of the intracellular niche during acute and chronic infection of Toxoplasma gondii | Molecular microbiology | 2022 | 329 | 148 | |||
| Toxoplasma gondii phosphatidylserine flippase complex ATP2B-CDC50.4 critically participates in microneme exocytosis | PLOS pathogens | 2022 | 354 | 230 | |||
| The ZIP code of vesicle trafficking in apicomplexa: SEC1/Munc18 and SNARE proteins | mBio | 2020 | 368 | 173 | |||
| Toxoplasma gondii GRA60 is an effector protein that modulates host cell autonomous immunity and contributes to virulence | Cellular Microbiology | 2020 | 387 | 284 | |||
| CRISPR/cas9-based knockout of GNAQ reveals differences in host cell signaling necessary for egress of apicomplexan parasites | mSphere | 2020 | 334 | 173 | |||
| Modeling and resistant alleles explain the selectivity of antimalarial compound 49c towards apicomplexan aspartyl proteases | EMBO Journal | 2018 | 680 | 15 | |||
| Crosstalk between PKA and PKG controls pH‐dependent host cell egress of Toxoplasma gondii | EMBO Journal | 2017 | 620 | 263 | |||
| Phosphatidic Acid-Mediated Signaling Regulates Microneme Secretion in Toxoplasma | Cell host & microbe | 2016 | 737 | 417 | |||
| The Conoid Associated Motor MyoH Is Indispensable for Toxoplasma gondii Entry and Exit from Host Cells | PLOS pathogens | 2016 | 688 | 310 | |||
| Fundamental Roles of the Golgi-Associated Toxoplasma Aspartyl Protease, ASP5, at the Host-Parasite Interface | PLOS pathogens | 2015 | 723 | 305 | |||
| Distinct contribution of Toxoplasma gondii rhomboid proteases 4 and 5 to micronemal protein protease 1 activity during invasion | Molecular microbiology | 2015 | 620 | 5 | |||
| Plasticity and redundancy among AMA-RON pairs ensure host cell entry of Toxoplasma parasites | Nature communications | 2014 | 729 | 270 | |||
| Plasticity between MyoC- and MyoA-Glideosomes: An Example of Functional Compensation in Toxoplasma gondii Invasion | PLOS pathogens | 2014 | 704 | 367 | |||
| Assessment of phosphorylation in Toxoplasma glideosome assembly and function | Cellular microbiology | 2014 | 727 | 295 | |||
| Galactose recognition by the apicomplexan parasite Toxoplasma gondii | The Journal of biological chemistry | 2012 | 766 | 0 | |||
| Unusual Anchor of a Motor Complex (MyoD-MLC2) to the Plasma Membrane of Toxoplasma gondii | Traffic | 2011 | 731 | 525 | |||
| 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 | 643 | 0 | |||
| Functional dissection of the apicomplexan glideosome molecular architecture | Cell host & microbe | 2010 | 864 | 947 | |||
| 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 | 688 | 0 | |||
| RIG-I and dsRNA-induced IFNbeta activation | PloS one | 2008 | 668 | 317 | |||
| 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 | 653 | 365 | |||
| Sendai virus budding in the course of an infection does not require Alix and VPS4A host factors | Virology | 2007 | 605 | 368 | |||
| Targeting of the Sendai virus C protein to the plasma membrane via a peptide-only membrane anchor | Journal of virology | 2007 | 568 | 302 | |||
| 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 | 632 | 306 | |||
| 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 | 620 | 1,190 | |||
| Chemical modification of nucleotide bases and mRNA editing depend on hexamer or nucleoprotein phase in Sendai virus nucleocapsids | RNA | 2002 | 577 | 528 | |||
| All four Sendai Virus C proteins bind Stat1, but only the larger forms also induce its mono-ubiquitination and degradation | Virology | 2002 | 725 | 596 |
