(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

0 references

Geon Park

1

1 reference

14 May 2018

Hyun-Sook Kim

series ordinal

2

1 reference

14 May 2018

Jung-Yoon Choe

series ordinal

3

1 reference

14 May 2018

Seong-Kyu Kim

series ordinal

4

1 reference

14 May 2018

publication date

8 September 2011

1 reference

14 May 2018

Rheumatology International

published in

1 reference

14 May 2018

volume

32

1 reference

14 May 2018

issue

10

1 reference

14 May 2018

page(s)

3031-3037

1 reference

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