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Selective inhibition of NLRP3 inflammasome by designed peptide originating from ASC

The FASEB journal, 2020-08, Vol.34 (8), p.11068-11086

2020

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Shikonin Suppresses NLRP3 and AIM2 Inflammasomes by Direct Inhibition of Caspase-1

PloS one, 2016-07, Vol.11 (7), p.e0159826

2016

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Prions, prionoid complexes and amyloids: the bad, the good and something in between

Swiss medical weekly, 2017-04, Vol.147, p.w14424

Hafner Bratkovič, Iva

2017

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Differential Effect of Extracellular Acidic Environment on IL-1β Released from Human and Mouse Phagocytes

International journal of molecular sciences, 2020-09, Vol.21 (19), p.7229

2020

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NLRP3 is its own gatekeeper: a group hug of NLRP3 monomers controls inflammation

Trends in biochemical sciences (Amsterdam. Regular ed.), 2022-08, Vol.47 (8), p.635-637

Hafner-Bratkovič, Iva

2022

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Ion homeostasis and ion channels in NLRP3 inflammasome activation and regulation

Current opinion in immunology, 2018-06, Vol.52, p.8-17

2018

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Delivery of an Artificial Transcription Regulator dCas9-VPR by Extracellular Vesicles for Therapeutic Gene Activation

ACS synthetic biology, 2018-12, Vol.7 (12), p.2715-2725

2018

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Pathological mutations H187R and E196K facilitate subdomain separation and prion protein conversion by destabilization of the native structure

The FASEB journal, 2015-03, Vol.29 (3), p.882-893

2015

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Correction: Shikonin Suppresses NLRP3 and AIM2 Inflammasomes by Direct Inhibition of Caspase-1

PloS one, 2016-09, Vol.11 (9), p.e0163887-e0163887

2016

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Curcumin binds to the α-helical intermediate and to the amyloid form of prion protein - a new mechanism for the inhibition of PrPSc accumulation

Journal of neurochemistry, 2008-03, Vol.104 (6), p.1553-1564

2008

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NLRP3 inflammasome activation in macrophage cell lines by prion protein fibrils as the source of IL-1β and neuronal toxicity

Cellular and molecular life sciences : CMLS, 2012-12, Vol.69 (24), p.4215-4228

2012

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The mechanism of NLRP3 inflammasome initiation: Trimerization but not dimerization of the NLRP3 pyrin domain induces robust activation of IL-1β

Biochemical and biophysical research communications, 2017-02, Vol.483 (2), p.823-828

2017

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Increased gene translation stringency in mammalian cells by nonsense suppression at multiple permissive sites with a single noncanonical amino acid

FEBS letters, 2020-08, Vol.594 (15), p.2452-2461

2020

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Tetracysteine-tagged prion protein allows discrimination between the native and converted forms

The FEBS journal, 2010-05, Vol.277 (9), p.2038-2050

2010

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Control of gasdermin D oligomerization and pyroptosis by the Ragulator-Rag-mTORC1 pathway

Cell, 2021-08, Vol.184 (17), p.4495-4511.e19

2021

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Curcumin binds to the alpha-helical intermediate and to the amyloid form of prion protein - a new mechanism for the inhibition of PrP(Sc) accumulation

Journal of neurochemistry, 2008-03, Vol.104 (6), p.1553

2008

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Disruption of disulfides within RBD of SARS‐CoV‐2 spike protein prevents fusion and represents a target for viral entry inhibition by registered drugs

The FASEB journal, 2021-06, Vol.35 (6), p.e21651-n/a

2021

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Disulfide mapping reveals the domain swapping as the crucial process of the structural conversion of prion protein

Prion, 2011-04, Vol.5 (2), p.56-59

2011

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NLRP3 lacking the leucine-rich repeat domain can be fully activated via the canonical inflammasome pathway

Nature communications, 2018-12, Vol.9 (1), p.5182-18, Article 5182

2018

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Development of an Acrylate Derivative Targeting the NLRP3 Inflammasome for the Treatment of Inflammatory Bowel Disease

Journal of medicinal chemistry, 2017-05, Vol.60 (9), p.3656-3671

2017

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Expression, purification and structural studies of a short antimicrobial peptide

Biochimica et biophysica acta, 2009-02, Vol.1788 (2), p.314-323

2009

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Gasdermin D pore-forming activity is redox-sensitive

Cell reports (Cambridge), 2023-01, Vol.42 (1), p.112008-112008, Article 112008

2023

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Anchorless forms of prion protein – Impact of truncation on structure destabilization and prion protein conversion

Biochemical and biophysical research communications, 2016-12, Vol.481 (1-2), p.1-6

2016

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Cell stress response to two different types of polymer coated cobalt ferrite nanoparticles

Toxicology letters, 2017-03, Vol.270, p.108-118

2017

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The POM monoclonals: a comprehensive set of antibodies to non-overlapping prion protein epitopes

PloS one, 2008-12, Vol.3 (12), p.e3872-e3872

2008

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Selective inhibition of NLRP3 inflammasome by designed peptide originating from ASC

Shikonin Suppresses NLRP3 and AIM2 Inflammasomes by Direct Inhibition of Caspase-1

Prions, prionoid complexes and amyloids: the bad, the good and something in between

Differential Effect of Extracellular Acidic Environment on IL-1β Released from Human and Mouse Phagocytes

NLRP3 is its own gatekeeper: a group hug of NLRP3 monomers controls inflammation

Ion homeostasis and ion channels in NLRP3 inflammasome activation and regulation

Delivery of an Artificial Transcription Regulator dCas9-VPR by Extracellular Vesicles for Therapeutic Gene Activation

Pathological mutations H187R and E196K facilitate subdomain separation and prion protein conversion by destabilization of the native structure

Correction: Shikonin Suppresses NLRP3 and AIM2 Inflammasomes by Direct Inhibition of Caspase-1

Curcumin binds to the α-helical intermediate and to the amyloid form of prion protein - a new mechanism for the inhibition of PrPSc accumulation

NLRP3 inflammasome activation in macrophage cell lines by prion protein fibrils as the source of IL-1β and neuronal toxicity

The mechanism of NLRP3 inflammasome initiation: Trimerization but not dimerization of the NLRP3 pyrin domain induces robust activation of IL-1β

Increased gene translation stringency in mammalian cells by nonsense suppression at multiple permissive sites with a single noncanonical amino acid

Tetracysteine-tagged prion protein allows discrimination between the native and converted forms

Control of gasdermin D oligomerization and pyroptosis by the Ragulator-Rag-mTORC1 pathway

Curcumin binds to the alpha-helical intermediate and to the amyloid form of prion protein - a new mechanism for the inhibition of PrP(Sc) accumulation

Disruption of disulfides within RBD of SARS‐CoV‐2 spike protein prevents fusion and represents a target for viral entry inhibition by registered drugs

Disulfide mapping reveals the domain swapping as the crucial process of the structural conversion of prion protein

NLRP3 lacking the leucine-rich repeat domain can be fully activated via the canonical inflammasome pathway

Development of an Acrylate Derivative Targeting the NLRP3 Inflammasome for the Treatment of Inflammatory Bowel Disease

Expression, purification and structural studies of a short antimicrobial peptide

Gasdermin D pore-forming activity is redox-sensitive

Anchorless forms of prion protein – Impact of truncation on structure destabilization and prion protein conversion

Cell stress response to two different types of polymer coated cobalt ferrite nanoparticles

The POM monoclonals: a comprehensive set of antibodies to non-overlapping prion protein epitopes

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