SUMO4 C438T polymorphism is associated with papulopustular skin lesion in Korean patients with Behçet's disease. (Q53407382)

14 May 2018

title

SUMO4 C438T polymorphism is associated with papulopustular skin lesion in Korean patients with Behçet's disease. (English)

1 reference

14 May 2018

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Geon Park

1

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14 May 2018

Hyun-Sook Kim

series ordinal

2

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14 May 2018

Jung-Yoon Choe

series ordinal

3

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14 May 2018

Seong-Kyu Kim

series ordinal

4

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14 May 2018

publication date

8 September 2011

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14 May 2018

Rheumatology International

published in

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14 May 2018

volume

32

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14 May 2018

issue

10

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14 May 2018

page(s)

3031-3037

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14 May 2018

https://scigraph.springernature.com/pub.10.1007/s00296-011-2086-5

exact match

0 references

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2086-5

Pathogenesis of Adamantiades-Behçet's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2086-5

A functional variant of SUMO4, a new I kappa B alpha modifier, is associated with type 1 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2086-5

A M55V polymorphism in a novel SUMO gene (SUMO-4) differentially activates heat shock transcription factors and is associated with susceptibility to type I diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2086-5

Evidence for the role of small ubiquitin-like modifier 4 as a general autoimmunity locus in the Japanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2086-5

Study of the role of functional variants of SLC22A4, RUNX1 and SUMO4 in systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2086-5

SUMO4 gene polymorphisms in Chinese Han patients with Behcet's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2086-5

The NF-kappa B and I kappa B proteins: new discoveries and insights

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2086-5

Vascular endothelial growth factor expression of intercellular adhesion molecule 1 (ICAM-1), vascular cell adhesion molecule 1 (VCAM-1), and E-selectin through nuclear factor-kappa B activation in endothelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2086-5

NF-kappaB protects Behçet's disease T cells against CD95-induced apoptosis up-regulating antiapoptotic proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2086-5

SLC11A1 gene polymorphisms in Korean patients with Behçet's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2086-5

TNF and TNF receptor polymorphisms in Korean Behcet's disease patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2086-5

The functional role of nuclear factor kappa-kappaB1 -94 ins/del ATTG promotor gene polymorphism in Behçet's disease: an exploratory study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2086-5

IkappaBalpha promoter polymorphisms in patients with Behçet's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2086-5

Sumoylation regulates diverse biological processes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2086-5

SUMO-1 modification of IkappaBalpha inhibits NF-kappaB activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2086-5

Characteristics of T cell lines established from skin lesions of Behçet's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-011-2086-5

Criteria for diagnosis of Behçet's disease. International Study Group for Behçet's Disease

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21901353

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Small ubiquitin-like modifier 4 (SUMO4) polymorphisms and Vogt-Koyanagi-Harada (VKH) syndrome in the Chinese Han population.

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21901353

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00296-011-2086-5

1 reference

14 May 2018

PubMed ID

21901353

1 reference

14 May 2018