Günther C - Search Results

1

SMARCAD1 Haploinsufficiency Underlies Huriez Syndrome and Associated Skin Cancer Susceptibility.

Günther C, Lee-Kirsch MA, Eckhard J, Matanovic A, Kerscher T, Rüschendorf F, Klein B, Berndt N, Zimmermann N, Flachmeier C, Thuß T, Lucas N, Marenholz I, Esparza-Gordillo J, Hübner N, Traupe H, Delaporte E, Lee YA. Günther C, et al. J Invest Dermatol. 2018 Jun;138(6):1428-1431. doi: 10.1016/j.jid.2018.01.015. Epub 2018 Feb 1. J Invest Dermatol. 2018. PMID: 29409814 Free article. No abstract available.

2

Familial chilblain lupus--a monogenic form of cutaneous lupus erythematosus due to a heterozygous mutation in TREX1.

Günther C, Meurer M, Stein A, Viehweg A, Lee-Kirsch MA. Günther C, et al. Dermatology. 2009;219(2):162-6. doi: 10.1159/000222430. Epub 2009 May 28. Dermatology. 2009. PMID: 19478477

3

Up-regulation of the chemokine CCL18 by macrophages is a potential immunomodulatory pathway in cutaneous T-cell lymphoma.

Günther C, Zimmermann N, Berndt N, Grosser M, Stein A, Koch A, Meurer M. Günther C, et al. Am J Pathol. 2011 Sep;179(3):1434-42. doi: 10.1016/j.ajpath.2011.05.040. Epub 2011 Jul 8. Am J Pathol. 2011. PMID: 21741937 Free PMC article.

4

Human 6-sulfo LacNAc (slan) dendritic cells are a major population of dermal dendritic cells in steady state and inflammation.

Günther C, Starke J, Zimmermann N, Schäkel K. Günther C, et al. Clin Exp Dermatol. 2012 Mar;37(2):169-76. doi: 10.1111/j.1365-2230.2011.04213.x. Epub 2011 Dec 20. Clin Exp Dermatol. 2012. PMID: 22188261

5

Inherited or de novo mutation affecting aspartate 18 of TREX1 results in either familial chilblain lupus or Aicardi-Goutières syndrome.

Tüngler V, Silver RM, Walkenhorst H, Günther C, Lee-Kirsch MA. Tüngler V, et al. Among authors: gunther c. Br J Dermatol. 2012 Jul;167(1):212-4. doi: 10.1111/j.1365-2133.2012.10813.x. Br J Dermatol. 2012. PMID: 22356656 No abstract available.

6

Innate immune processes in lupus erythematosus.

Aringer M, Günther C, Lee-Kirsch MA. Aringer M, et al. Among authors: gunther c. Clin Immunol. 2013 Jun;147(3):216-22. doi: 10.1016/j.clim.2012.11.012. Epub 2012 Dec 12. Clin Immunol. 2013. PMID: 23290784 Review.

7

Aicardi-Goutières syndrome: a model disease for systemic autoimmunity.

Lee-Kirsch MA, Wolf C, Günther C. Lee-Kirsch MA, et al. Among authors: gunther c. Clin Exp Immunol. 2014 Jan;175(1):17-24. doi: 10.1111/cei.12160. Clin Exp Immunol. 2014. PMID: 23786362 Free PMC article. Review.

8

Systemic involvement in TREX1-associated familial chilblain lupus.

Günther C, Hillebrand M, Brunk J, Lee-Kirsch MA. Günther C, et al. J Am Acad Dermatol. 2013 Oct;69(4):e179-81. doi: 10.1016/j.jaad.2013.04.020. J Am Acad Dermatol. 2013. PMID: 24034389 No abstract available.

9

Deregulated type I IFN response in TREX1-associated familial chilblain lupus.

Peschke K, Friebe F, Zimmermann N, Wahlicht T, Schumann T, Achleitner M, Berndt N, Luksch H, Behrendt R, Lee-Kirsch MA, Roers A, Günther C. Peschke K, et al. Among authors: gunther c. J Invest Dermatol. 2014 May;134(5):1456-1459. doi: 10.1038/jid.2013.496. Epub 2013 Nov 22. J Invest Dermatol. 2014. PMID: 24270665 Free article. No abstract available.

10

Familial chilblain lupus due to a novel mutation in the exonuclease III domain of 3' repair exonuclease 1 (TREX1).

Günther C, Berndt N, Wolf C, Lee-Kirsch MA. Günther C, et al. JAMA Dermatol. 2015 Apr;151(4):426-31. doi: 10.1001/jamadermatol.2014.3438. JAMA Dermatol. 2015. PMID: 25517357

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

513 results

Search Page