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The macrophage-specific V-ATPase subunit ATP6V0D2 restricts inflammasome activation and bacterial infection by facilitating autophagosome-lysosome fusion

Autophagy, 2019-06, Vol.15 (6), p.960-975

2019

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Control of the innate immune response by the mevalonate pathway

Nature immunology, 2016-08, Vol.17 (8), p.922-929

2016

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Targeted Disruption of Pyrin, the FMF Protein, Causes Heightened Sensitivity to Endotoxin and a Defect in Macrophage Apoptosis

Molecular cell, 2003-03, Vol.11 (3), p.591-604

2003

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The expanding spectrum of systemic autoinflammatory disorders and their rheumatic manifestations

Current opinion in rheumatology, 2003-01, Vol.15 (1), p.61-69

2003

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OP0193 Pyrin and PSTPIP1, Mutated in FMF, PAPA-, and PAMI Syndrome, are Involved in the Hypersecretion of Alarmins MRP8/14

Annals of the rheumatic diseases, 2015-06, Vol.74 (Suppl 2), p.144-144

2015

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The familial Mediterranean fever protein, pyrin, associates with microtubules and colocalizes with actin filaments

Blood, 2001-08, Vol.98 (3), p.851-859

2001

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OP0128 The Regulation of MRP8/14 in Pstpip1-Associated Myeloid-Related-Proteinaemia Inflammatory Syndrome (PAMI)

Annals of the rheumatic diseases, 2014-06, Vol.73 (Suppl 2), p.109-109

2014

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Mutation and Haplotype Studies of Familial Mediterranean Fever Reveal New Ancestral Relationships and Evidence for a High Carrier Frequency with Reduced Penetrance in the Ashkenazi Jewish Population

American journal of human genetics, 1999-04, Vol.64 (4), p.949-962

1999

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Activation of the pyrin inflammasome through the RhoA signaling pathway in FMF and HIDS

Pediatric rheumatology online journal, 2015-09, Vol.13 (Suppl 1), p.O11-O11, Article O11

2015

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Cofilin-1 is an essential redox sensor for NLRP3 inflammasome activation

Pediatric rheumatology online journal, 2015-09, Vol.13 (Suppl 1), p.O52-O52, Article O52

2015

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OP0260 The pathophysiology of S100A8/A9 in familial mediterranean fever (FMF)

Annals of the rheumatic diseases, 2013-06, Vol.71 (Suppl 3), p.144-144

2013

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Sexual dimorphism in immune response genes as a function of puberty

BMC immunology, 2006-02, Vol.7 (1), p.2-2, Article 2

2006

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OR11-003 - The NLRP3 inflammasome is regulated by CaSR

Pediatric rheumatology online journal, 2013-11, Vol.11 (S1), p.A192-A192, Article A192

2013

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A source and channel-coding framework for vector-based data hiding in video

IEEE transactions on circuits and systems for video technology, 2000-06, Vol.10 (4), p.630-645

2000

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Mice with mutations of TNFRSF1A may reveal insights into pathogenesis of TRAPS, a dominantly inherited autoinflammatory disease

Journal of allergy and clinical immunology, 2004-02, Vol.113 (2), p.S205-S205

2004

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Isolation, genomic organization, and expression analysis of the mouse and rat homologs of MEFV, the gene for familial Mediterranean fever

Mammalian genome, 2000-06, Vol.11 (6), p.428-435

2000

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Identification of mutations including de novo mutations in Korean patients with hypokalaemic periodic paralysis

Nephrology, dialysis, transplantation, 2001-05, Vol.16 (5), p.939-944

2001

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De novo CIAS1 mutations, cytokine activation, and evidence for genetic heterogeneity in patients with neonatal‐onset multisystem inflammatory disease (NOMID): A new member of the expanding family of pyrin‐associated autoinflammatory diseases

Arthritis and rheumatism, 2002-12, Vol.46 (12), p.3340-3348

2002

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Characterization of some silica-based reversed-phase liquid chromatographic columns based on linear solvation energy relationships

Journal of chromatography, 1994-04, Vol.664 (2), p.149-158

1994

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Long-Distance PCR-based Screening for Large Rearrangements of the LDL Receptor Gene in Korean Patients with Familial Hypercholesterolemia

Clinical chemistry (Baltimore, Md.), 1999-09, Vol.45 (9), p.1424-1430

1999

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Analysis of mitochondrial DNA deletions in four chambers of failing human heart: hemodynamic stress, age, and disease are important factors

Basic research in cardiology, 2000-04, Vol.95 (2), p.163-171

2000

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Two partial deletion mutations involving the same Alu sequence within intron 8 of the LDL receptor gene in Korean patients with familial hypercholesterolemia

Human genetics, 1997-02, Vol.99 (2), p.155-163

1997

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Identification of four novel mutations of the low-density lipoprotein receptor gene in Korean patients with familial hypercholesterolemia

Clinical genetics, 2000-03, Vol.57 (3), p.225-229

2000

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Dynamics of foams with and without wall rupture

Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics, 1997-01, Vol.55 (1), p.598-610

1997

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The effects of the cholesterol ester transfer protein gene and environmental factors on the plasma high density lipoprotein cholesterol levels the Korean population

Molecules and cells, 1997-10, Vol.7 (5), p.615-619

1997

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The macrophage-specific V-ATPase subunit ATP6V0D2 restricts inflammasome activation and bacterial infection by facilitating autophagosome-lysosome fusion

Control of the innate immune response by the mevalonate pathway

Targeted Disruption of Pyrin, the FMF Protein, Causes Heightened Sensitivity to Endotoxin and a Defect in Macrophage Apoptosis

The expanding spectrum of systemic autoinflammatory disorders and their rheumatic manifestations

OP0193 Pyrin and PSTPIP1, Mutated in FMF, PAPA-, and PAMI Syndrome, are Involved in the Hypersecretion of Alarmins MRP8/14

The familial Mediterranean fever protein, pyrin, associates with microtubules and colocalizes with actin filaments

OP0128 The Regulation of MRP8/14 in Pstpip1-Associated Myeloid-Related-Proteinaemia Inflammatory Syndrome (PAMI)

Mutation and Haplotype Studies of Familial Mediterranean Fever Reveal New Ancestral Relationships and Evidence for a High Carrier Frequency with Reduced Penetrance in the Ashkenazi Jewish Population

Activation of the pyrin inflammasome through the RhoA signaling pathway in FMF and HIDS

Cofilin-1 is an essential redox sensor for NLRP3 inflammasome activation

OP0260 The pathophysiology of S100A8/A9 in familial mediterranean fever (FMF)

Sexual dimorphism in immune response genes as a function of puberty

OR11-003 - The NLRP3 inflammasome is regulated by CaSR

A source and channel-coding framework for vector-based data hiding in video

Mice with mutations of TNFRSF1A may reveal insights into pathogenesis of TRAPS, a dominantly inherited autoinflammatory disease

Isolation, genomic organization, and expression analysis of the mouse and rat homologs of MEFV, the gene for familial Mediterranean fever

Identification of mutations including de novo mutations in Korean patients with hypokalaemic periodic paralysis

De novo CIAS1 mutations, cytokine activation, and evidence for genetic heterogeneity in patients with neonatal‐onset multisystem inflammatory disease (NOMID): A new member of the expanding family of pyrin‐associated autoinflammatory diseases

Characterization of some silica-based reversed-phase liquid chromatographic columns based on linear solvation energy relationships

Long-Distance PCR-based Screening for Large Rearrangements of the LDL Receptor Gene in Korean Patients with Familial Hypercholesterolemia

Analysis of mitochondrial DNA deletions in four chambers of failing human heart: hemodynamic stress, age, and disease are important factors

Two partial deletion mutations involving the same Alu sequence within intron 8 of the LDL receptor gene in Korean patients with familial hypercholesterolemia

Identification of four novel mutations of the low-density lipoprotein receptor gene in Korean patients with familial hypercholesterolemia

Dynamics of foams with and without wall rupture

The effects of the cholesterol ester transfer protein gene and environmental factors on the plasma high density lipoprotein cholesterol levels the Korean population

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