Genetic analysis of MEFV gene pyrin domain in patients with Behçet's disease.

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Coexistence of vasculitides with familial Mediterranean fever.

P2860

Q37872631-80E755C2-0A32-44A2-8604-1BEFFADE0BC3

P2860

Genetic analysis of MEFV gene pyrin domain in patients with Behçet's disease.

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http://www.wikidata.org/entity/Q38402415

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2006 nî lūn-bûn

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2006年の論文

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@yue

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@zh-hk

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name

Genetic analysis of MEFV gene pyrin domain in patients with Behçet's disease.

@en

type

Item

label

Genetic analysis of MEFV gene pyrin domain in patients with Behçet's disease.

@en

prefLabel

Genetic analysis of MEFV gene pyrin domain in patients with Behçet's disease.

@en

P1476

Genetic analysis of MEFV gene pyrin domain in patients with Behçet's disease.

@en

P2093

Ahmet Dursun

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

Ayse Gul Zamani

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

Cengiz Yakicier

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

Hatice Gul Durakbasi-Dursun

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

Recep Dursun

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

Zerrin Gülin Gulbahar

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

P2860

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

Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome

ASC is an activating adaptor for NF-kappa B and caspase-8-dependent apoptosis

The PAAD/PYRIN-only protein POP1/ASC2 is a modulator of ASC-mediated nuclear-factor-kappa B and pro-caspase-1 regulation

A novel PAAD-containing protein that modulates NF-kappa B induction by cytokines tumor necrosis factor-alpha and interleukin-1beta

The inflammasome: a molecular platform triggering activation of inflammatory caspases and processing of proIL-beta

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

The death-domain fold of the ASC PYRIN domain, presenting a basis for PYRIN/PYRIN recognition

SCOP: a structural classification of proteins database for the investigation of sequences and structures

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

P304

41783

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P31

scholarly article

P356

10.1155/MI/2006/41783

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P433

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

P478

2006

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

P577

2006-01-01T00:00:00Z

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

P698

16951489

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

P921

Behcet's disease

P932

1592598

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

Genetic analysis of MEFV gene pyrin domain in patients with Behçet's disease.

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P2860

P2860

Genetic analysis of MEFV gene pyrin domain in patients with Behçet's disease.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921

P932