Autoinflammatory gene mutations in Behçet's disease - Wikidata - awgldk - TriplyDB

Autoinflammatory gene mutations in Behçet's disease

Autoinflammatory gene mutations in Behçet's disease

http://www.wikidata.org/entity/Q24674998

about

Holding the inflammatory system in check: NLRs keep it cool Inflammasome-associated nucleotide-binding domain, leucine-rich repeat proteins and inflammatory diseases Behçet's Disease: an Insight from a Cardiologist's Point of View.Emerging role of antioxidants in the protection of uveitis complications.NOD2 is highly expressed in Behçet disease with pulmonary manifestations.The spectrum of autoinflammatory diseases: recent bench to bedside observations Inflammasomes in Myeloid Cells: Warriors Within.Inheritance of autoinflammatory diseases: shifting paradigms and nomenclature.Targeting inflammasomes in rheumatic diseases.Monogenic autoinflammatory diseases.Pathogenesis of Behçet's disease: autoinflammatory features and beyond.Hyperimmunoglobulinaemia D syndrome: a rare cause of prolonged fever and treatment with anti-interleukin 1 agent.A case report of a right ventricular mass in a patient with Behçet's disease: Myxoma or thrombus?[Autoinflammatory syndromes/fever syndromes].Evolution. Systematic humanization of yeast genes reveals conserved functions and genetic modularity.MDR1 C3435T polymorphism associated with the development of clinical features in Behçet's disease in Iranian Azeri Turkish patients.The association of NLRP3 and TNFRSF1A polymorphisms with risk of ankylosing spondylitis and treatment efficacy of etanercept.A novel single variant in the MEFV gene causing Mediterranean fever and Behçet's disease: a case report.Mevalonate kinase gene mutations and their clinical correlations in Behçet's disease.NLRP3gene polymorphisms in Iranian patients with recurrent aphthous stomatitis

P2860

Q28081065-2C175281-3D38-4E6D-8274-1539FD18E237 Q28267534-80EED4A4-D60E-41B2-A05F-BF2C10422527 Q33760174-E99EB7E0-625A-43D5-886F-99B7B6881613 Q34887046-82608154-9299-4E7C-A3E6-0A53D9B37E29 Q35847810-A6CF9D7C-7B2F-4E45-9627-BA18B4729E3A Q36048259-8658DD5D-49EA-4042-8F9A-8C6F39C2A79F Q37607695-7CBF39E3-8C6A-43B9-99C5-FC5CD04D8CB6 Q38093826-6ABC1C2A-FE79-4399-84FC-CF487F43300D Q38106621-D21A84D5-ABB6-4754-B91E-FAACEFC17087 Q38211947-BD708841-AA0E-4123-AAD8-E1A4277A7FC0 Q38525874-FE23183C-D45B-4378-A6C9-344B33D63250 Q40105382-E96689C4-81E5-44A8-B5D6-91E781BDF7E2 Q40229964-76E30A43-B49D-4D61-8747-AFA8485DED03 Q40326095-25616216-B8D8-4E4A-9FFA-C18BBFE6ED0A Q43079790-E598147C-66A7-4FB2-BE67-07907E3812A3 Q46884141-4557A2B5-E55F-4AB8-9B67-BC0CBB8A896C Q50936406-38203D7B-8FEE-4032-A8E0-9288CDE1914F Q52680970-60B0D2A7-2BE8-41B9-BAB6-E97EC21AF539 Q54385298-2712AABE-098D-4DB1-968B-B6A7929931C3 Q57578989-E900E4E5-ACDF-44E9-A7EB-03AE2BBE9463

P2860

Autoinflammatory gene mutations in Behçet's disease

http://www.wikidata.org/entity/Q24674998

description

2007 nî lūn-bûn

@nan

2007 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի հունիսին հրատարակված գիտական հոդված

@hy

2007年の論文

@ja

2007年論文

@yue

2007年論文

@zh-hant

2007年論文

@zh-hk

2007年論文

@zh-mo

2007年論文

@zh-tw

2007年论文

@wuu

name

Autoinflammatory gene mutations in Behçet's disease

@ast

Autoinflammatory gene mutations in Behçet's disease

@en

Autoinflammatory gene mutations in Behçet's disease

@nl

type

label

Autoinflammatory gene mutations in Behçet's disease

@ast

Autoinflammatory gene mutations in Behçet's disease

@en

Autoinflammatory gene mutations in Behçet's disease

@nl

prefLabel

Autoinflammatory gene mutations in Behçet's disease

@ast

Autoinflammatory gene mutations in Behçet's disease

@en

Autoinflammatory gene mutations in Behçet's disease

@nl

P1433

Q24674998-0B94CE20-BA93-4B2A-A0D2-F8EAA98BE62A

P1476

Q24674998-A94FF223-CC17-4694-8B37-BA2098694E76

P2093

Q24674998-9765AC7F-1E51-448F-848D-09E1BC145A32

Q24674998-A6173668-F908-4C43-8DFC-C4D0CF94E3AC

Q24674998-C2CDD4AE-1AB7-4B7F-B2CE-4EA5A249FA47

Q24674998-FCF6B6C3-E908-4FF9-96B8-92A81D85CD3F

P2860

Q24674998-0163FD23-686F-4818-AA5E-622E41AF7740

Q24674998-0869543E-FD3F-4DE1-B330-72A2944107B6

Q24674998-1A3BAADF-855B-4D3E-8155-79208F750504

Q24674998-1FE99E79-C1E6-4E9D-A80F-0504643C2AA9

Q24674998-38366225-2F42-48D7-9ED3-B9182929DA51

Q24674998-70743D9B-454E-47B9-96B6-B607E2DAE1A2

Q24674998-AB2BF0A6-5BDF-44A9-928C-7A42281AD6BB

Q24674998-B2DD552E-F0C1-4DC1-89AC-F838D891015B

Q24674998-B6E39506-0F84-407E-BA5B-668A3C1EA549

Q24674998-C48E6E35-4277-480D-B7BA-49025FB45A5C

P304

Q24674998-208B8121-FC78-46E8-9684-D32F73DE2FF5

P31

Q24674998-EBFB77A7-EC0C-4BD2-B808-4BD5D4AE76BC

Q24674998-f02fa809-2e56-4932-9a34-5ec60200e87c

P356

Q24674998-E663CF33-976A-4F43-8457-F0B49FBACBD9

P407

Q24674998-0DA0D257-24E6-462F-AE9A-4C22F1123270

P433

Q24674998-FBD93948-DCBD-435D-A820-FE9175970187

P478

Q24674998-3E955E25-09DA-4870-9EAF-736ED7BA2781

P50

Q24674998-87477070-2520-44D7-AF32-8213B44D9E02

P577

Q24674998-83397FD3-B239-4A98-9ABA-7CA94B06F00B

P5875

Q24674998-4ED1A4ED-0DDC-4EBD-B834-6BBE6302B390

P698

Q24674998-6738D24A-F3E0-49B3-88E2-9EDF80F7D0AF

P921

Q24674998-20479B1D-8F57-4BA1-9679-3B1FF58ACB68

P932

Q24674998-3F2A5852-A0B0-4862-987B-9F0CC7CAF924

P356

ARD.2006.068841

P1433

Annals of the Rheumatic Diseases

P1476

Autoinflammatory gene mutations in Behçet's disease

@en

P2093

A Le Quellec

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

E Sanchez

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

I Koné-Paut

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

I Touitou

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

P2860

Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome

Chronic infantile neurological cutaneous and articular syndrome is caused by mutations in CIAS1, a gene highly expressed in polymorphonuclear cells and chondrocytes

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

Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. International Hyper-IgD Study Group.

A decision tree for genetic diagnosis of hereditary periodic fever in unselected patients.

MEFV mutations in Behçet's disease.

Diagnostic challenge of hyper-IgD syndrome in four children with inflammatory gastrointestinal complaints.

Clinical and genetic heterogeneity among Spanish patients with recurrent autoinflammatory syndromes associated with the CIAS1/PYPAF1/NALP3 gene.

Infevers: an evolving mutation database for auto-inflammatory syndromes.

MEFV mutations are increased in Behçet's disease (BD) and are associated with vascular involvement.

P304

832-4

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

P31

scholarly article

P356

10.1136/ARD.2006.068841

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

P407

P433

6

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

P478

66

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

P50

P577

2007-06-01T00:00:00Z

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

P5875

6588648

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

P698

17213252

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

P921

Behcet's disease

P932

1954666

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