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Article

Impaired podosome formation and invasive migration of macrophages from patients with a PSTPIP1 mutation and PAPA syndrome.

Arthritis and rheumatism - 1 Aug 2010

Cortesio Christa L, Wernimont Sarah A, Kastner Daniel L, Cooper Kate M, Huttenlocher Anna

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 20506269
DOI: 10.1002/art.27521
PMCID: PMC2921034

Genes

PSTPIP1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Impaired podosome formation and invasive migration of macrophages from patients with a PSTPIP1 mutation and PAPA syndrome.PMID 20506269Read ↗

The expanding spectrum of clinical phenotypes associated with PSTPIP1 mutations: from PAPA to PAMI syndrome and beyond.Semantic proximity Read ↗

The F-BAR protein PSTPIP1 controls extracellular matrix degradation and filopodia formation in macrophages.Semantic proximity Read ↗

P02-006 - A novel PSTPIP1 mutation in PAPA syndromeSemantic proximity Read ↗

A novel mutatioin in the PSTPIP1 gene is associated with an autoinflammatory disease distinct from classical PAPA syndromeSemantic proximity Read ↗

A genome-wide CRISPR functional survey of the human phagocytosis molecular machinerySemantic proximity Read ↗

Abl-mediated PI3K activation regulates macrophage podosome formationSemantic proximity Read ↗

Alarming consequences - autoinflammatory disease spectrum due to mutations in proline-serine-threonine phosphatase-interacting protein 1.Semantic proximity Read ↗

Proline-serine-threonine phosphatase interacting protein 1 (PSTPIP1) controls immune synapse stability in human T cells.Semantic proximity Read ↗

Inflammation in mice ectopically expressing human Pyogenic Arthritis, Pyoderma Gangrenosum, and Acne (PAPA) Syndrome-associated PSTPIP1 A230T mutant proteins.Semantic proximity Read ↗

PW02-018 - Impact of PSTPIP1 mutaions on clinical phenotypeSemantic proximity Read ↗

Rare cases of PAMI syndrome in both father and son with the same missense mutation in PSTPIP1 gene and literature review.Semantic proximity Read ↗

Mutation of mouse Mayp/Pstpip2 causes a macrophage autoinflammatory diseaseSemantic proximity Read ↗

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