A missense mutation in pstpip2 is associated with the murine autoinflammatory disorder chronic multifocal osteomyelitis - Wikidata - wikimedia - TriplyDB

A missense mutation in pstpip2 is associated with the murine autoinflammatory disorder chronic multifocal osteomyelitis

A missense mutation in pstpip2 is associated with the murine autoinflammatory disorder chronic multifocal osteomyelitis

http://www.wikidata.org/entity/Q37053052

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A proposed classification of the immunological diseases Efficacy of antibiotic therapy for SAPHO syndrome is lost after its discontinuation: an interventional study An autoinflammatory disease with deficiency of the interleukin-1-receptor antagonist Horror autoinflammaticus: the molecular pathophysiology of autoinflammatory disease (*)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 F-BAR family proteins, emerging regulators for cell membrane dynamic changes-from structure to human diseases.The BAR Domain Superfamily Proteins from Subcellular Structures to Human Diseases PSTPIP2 deficiency in mice causes osteopenia and increased differentiation of multipotent myeloid precursors into osteoclasts.Pyrin Modulates the Intracellular Distribution of PSTPIP1.Monogenic IL-1 mediated autoinflammatory and immunodeficiency syndromes: finding the right balance in response to danger signals Monogenic autoinflammatory diseases: new insights into clinical aspects and pathogenesis.Sclerosing osteomyelitis of Garré: management of femoral pain by intramedullary nailing.New discoveries in CRMO: IL-1β, the neutrophil, and the microbiome implicated in disease pathogenesis in Pstpip2-deficient mice.The spectrum of autoinflammatory diseases: recent bench to bedside observations 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)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 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.Immunology in clinic review series; focus on autoinflammatory diseases: update on monogenic autoinflammatory diseases: the role of interleukin (IL)-1 and an emerging role for cytokines beyond IL-1.Chronic recurrent multifocal osteomyelitis (CRMO): a longitudinal case series review.A systematic review of SAPHO syndrome and inflammatory bowel disease association.Autoinflammatory bone disorders: update on immunologic abnormalities and clues about possible triggers.A clinical and pathomechanistic profile of chronic nonbacterial osteomyelitis/chronic recurrent multifocal osteomyelitis and challenges facing the field.Dynamic shaping of cellular membranes by phospholipids and membrane-deforming proteins.The SAPHO syndrome revisited with an emphasis on spinal manifestations.A Review and Proposed Approach to the Neutrophilic Dermatoses of Childhood.Chronic recurrent multifocal osteomyelitis in children and adults: current understanding and areas for development.SAPHO Syndrome: Current Developments and Approaches to Clinical Treatment.Clinical and genetic association, radiological findings and response to biological therapy in seven children from Qatar with non-bacterial osteomyelitis.Chronic Recurrent Multifocal Osteomyelitis and Related Diseases-Update on Pathogenesis.

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A missense mutation in pstpip2 is associated with the murine autoinflammatory disorder chronic multifocal osteomyelitis

http://www.wikidata.org/entity/Q37053052

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 24 August 2005

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

@da

vědecký článek

@cs

name

A missense mutation in pstpip2 ...... ronic multifocal osteomyelitis

@en

A missense mutation in pstpip2 ...... onic multifocal osteomyelitis.

@nl

type

label

A missense mutation in pstpip2 ...... ronic multifocal osteomyelitis

@en

A missense mutation in pstpip2 ...... onic multifocal osteomyelitis.

@nl

prefLabel

A missense mutation in pstpip2 ...... ronic multifocal osteomyelitis

@en

A missense mutation in pstpip2 ...... onic multifocal osteomyelitis.

@nl

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J.BONE.2005.07.009

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A missense mutation in pstpip2 ...... ronic multifocal osteomyelitis

@en

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Amar Mahgoub

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Lorraine T Tygrett

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Luis A Ochoa

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Mohammed A Vasef

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Polly J Ferguson

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Xinyu Bing

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P2860

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

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

PSTPIP 2, a second tyrosine phosphorylated, cytoskeletal-associated protein that binds a PEST-type protein-tyrosine phosphatase

A novel macrophage actin-associated protein (MAYP) is tyrosine-phosphorylated following colony stimulating factor-1 stimulation

The PCH family member MAYP/PSTPIP2 directly regulates F-actin bundling and enhances filopodia formation and motility in macrophages.

The syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia. Report of a new family and a review.

Neutrophilic dermatosis-associated sterile chronic multifocal osteomyelitis in pediatric patients: case report and review.

Homozygous mutations in LPIN2 are responsible for the syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia (Majeed syndrome).

Chronic recurrent multifocal osteomyelitis and psoriasis--a report of a new association and review of related disorders.

Chronic multifocal osteomyelitis.

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10.1016/J.BONE.2005.07.009

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1

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38

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Hatem El-shanti

Thomas J Waldschmidt

Annette J Schlueter

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2005-08-24T00:00:00Z

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16122996

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3726202

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