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Laura J. Knoll

Researcher at University of Wisconsin-Madison

Publications -  59
Citations -  1240

Laura J. Knoll is an academic researcher from University of Wisconsin-Madison. The author has contributed to research in topics: Toxoplasma gondii & Mutant. The author has an hindex of 18, co-authored 52 publications receiving 1052 citations. Previous affiliations of Laura J. Knoll include University of Oregon.

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Dual transcriptional profiling of mice and Toxoplasma gondii during acute and chronic infection.

TL;DR: RNA-seq is a valuable tool to simultaneously analyze host and microbe transcriptomes and shows that T. gondii is metabolically active and synthesizing proteins at 28 days post-infection and that a distinct subset of host genes associated with the immune response are more abundant specifically during chronic infection.
Journal Article

Parasite Stage-Specific Recognition of Endogenous Toxoplasma gondii-Derived CD8+ T Cell Epitopes. Commentary

TL;DR: In this paper, the authors employed caged major histocompatibility complex molecules to generate ∼ 250 H-2L d tetramers and to distinguish T. gondii-specific CD8 + T cells in BALB/c mice.
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Parasite Stage-Specific Recognition of Endogenous Toxoplasma gondii-Derived CD8+ T Cell Epitopes

TL;DR: The authors' results shed light on the identity and the parasite stage-specificity of 2 CD8+ T cell epitopes recognized in the acute and chronic phase of infection with T. gondii.
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Long-Term Relationships: the Complicated Interplay between the Host and the Developmental Stages of Toxoplasma gondii during Acute and Chronic Infections

TL;DR: An overview of what is known and unknown about the complex relationship between the host and parasite during the progression of T. gondii infection is provided, with the ultimate goal of bridging these events.
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A HT/PEXEL motif in Toxoplasma dense granule proteins is a signal for protein cleavage but not export into the host cell.

TL;DR: Findings suggest that while Toxoplasma and Plasmodium share similar HT/PEXEL motifs, Txoplasma HT/ PEXEL containing proteins interact with but do not cross the PVM.