Mutation of mouse Mayp/Pstpip2 causes a macrophage autoinflammatory disease. - Wikidata - wikimedia - TriplyDB

Mutation of mouse Mayp/Pstpip2 causes a macrophage autoinflammatory disease.

Mutation of mouse Mayp/Pstpip2 causes a macrophage autoinflammatory disease.

http://www.wikidata.org/entity/Q41839767

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FCHo proteins are nucleators of clathrin-mediated endocytosis.Horror autoinflammaticus: the molecular pathophysiology of autoinflammatory disease (*)An EF hand mutation in Stim1 causes premature platelet activation and bleeding in mice Interleukin-1 Family Cytokines in Liver Diseases Autoinflammatory bone diseases Advances in the genetically complex autoinflammatory diseases Dietary modulation of the microbiome affects autoinflammatory disease BAR Proteins PSTPIP1/2 Regulate Podosome Dynamics and the Resorption Activity of Osteoclasts The BAR Domain Superfamily Proteins from Subcellular Structures to Human Diseases The PCH family member proline-serine-threonine phosphatase-interacting protein 1 targets to the leukocyte uropod and regulates directed cell migration.PSTPIP2 deficiency in mice causes osteopenia and increased differentiation of multipotent myeloid precursors into osteoclasts.Pyrin Modulates the Intracellular Distribution of PSTPIP1.PSTPIP2 dysregulation contributes to aberrant terminal differentiation in GATA-1-deficient megakaryocytes by activating LYN Monogenic IL-1 mediated autoinflammatory and immunodeficiency syndromes: finding the right balance in response to danger signals New discoveries in CRMO: IL-1β, the neutrophil, and the microbiome implicated in disease pathogenesis in Pstpip2-deficient mice.Proline-serine-threonine phosphatase-interacting protein 2 (PSTPIP2), a host membrane-deforming protein, is critical for membranous web formation in hepatitis C virus replication Macrophage Migration and Its Regulation by CSF-1 BAR proteins in cancer and blood disorders Primary Chronic Osteomyelitis of the Jaws in Children: An Update on Pathophysiology, Radiological Findings, Treatment Strategies, and Prospective Analysis of Two Cases.Spontaneous inflammatory pain model from a mouse line with N-ethyl-N-nitrosourea mutagenesis.Recessive coding and regulatory mutations in FBLIM1 underlie the pathogenesis of chronic recurrent multifocal osteomyelitis (CRMO)Merck Ad5/HIV induces broad innate immune activation that predicts CD8⁺ T-cell responses but is attenuated by preexisting Ad5 immunity.NLRP3 inflammasome plays a redundant role with caspase 8 to promote IL-1β-mediated osteomyelitis.Current understanding of the pathogenesis and management of chronic recurrent multifocal osteomyelitis Analysis of gene expression profile identifies potential biomarkers for atherosclerosis.Primed innate immunity leads to autoinflammatory disease in PSTPIP2-deficient cmo mice.Critical role for inflammasome-independent IL-1β production in osteomyelitis.Inflammasome-independent IL-1β mediates autoinflammatory disease in Pstpip2-deficient mice Regulation of inflammasome activity.Genetics of monogenic autoinflammatory diseases: past successes, future challenges.Chronic recurrent multifocal osteomyelitis (CRMO): a longitudinal case series review.Autoinflammatory bone disorders: update on immunologic abnormalities and clues about possible triggers.Dynamic shaping of cellular membranes by phospholipids and membrane-deforming proteins.Chronic recurrent multifocal osteomyelitis in children and adults: current understanding and areas for development.Chronic Recurrent Multifocal Osteomyelitis and Related Diseases-Update on Pathogenesis.An Update on the Pathogenesis and Treatment of Chronic Recurrent Multifocal Osteomyelitis in Children.Microbiota and caspase-1/caspase-8 regulate IL-1β-mediated bone disease.Serum biomarkers for the diagnosis and monitoring of chronic recurrent multifocal osteomyelitis (CRMO).A large national cohort of French patients with chronic recurrent multifocal osteitis.Autoinflammatory bone disorders with special focus on chronic recurrent multifocal osteomyelitis (CRMO).

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P2860

Mutation of mouse Mayp/Pstpip2 causes a macrophage autoinflammatory disease.

http://www.wikidata.org/entity/Q41839767

description

2006 nî lūn-bûn

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2006年論文

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2006年论文

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2006年论文

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name

Mutation of mouse Mayp/Pstpip2 causes a macrophage autoinflammatory disease.

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Mutation of mouse Mayp/Pstpip2 causes a macrophage autoinflammatory disease.

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Mutation of mouse Mayp/Pstpip2 causes a macrophage autoinflammatory disease.

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Mutation of mouse Mayp/Pstpip2 causes a macrophage autoinflammatory disease

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Andreas Marquardt

http://www.w3.org/2001/XMLSchema#string

Bettina Barth

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Carolin Schmittwolf

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E Richard Stanley

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Gabriele Stumm

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Johannes Grosse

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Lutz Zeitlmann

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Michael Nehls

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Patricia Schropp

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Petra Hanke

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P2860

PYPAF1, a PYRIN-containing Apaf1-like protein that assembles with ASC and regulates activation of NF-kappa B

PYPAF7, a novel PYRIN-containing Apaf1-like protein that regulates activation of NF-kappa B and caspase-1-dependent cytokine processing

Identification of a novel polyproline recognition site in the cytoskeletal associated protein, proline serine threonine phosphatase interacting protein

Interferon-inducible T cell alpha chemoattractant (I-TAC): a novel non-ELR CXC chemokine with potent activity on activated T cells through selective high affinity binding to CXCR3

Pyrin binds the PSTPIP1/CD2BP1 protein, defining familial Mediterranean fever and PAPA syndrome as disorders in the same pathway

PSTPIP: a tyrosine phosphorylated cleavage furrow-associated protein that is a substrate for a PEST tyrosine phosphatase

Mutations in CD2BP1 disrupt binding to PTP PEST and are responsible for PAPA syndrome, an autoinflammatory disorder

Cdc42-interacting protein 4 mediates binding of the Wiskott-Aldrich syndrome protein to microtubules

The pyrin domain: a possible member of the death domain-fold family implicated in apoptosis and inflammation

The PYRIN domain: a novel motif found in apoptosis and inflammation proteins

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