Günther C - Search Results

1

C-terminal variants in CDC42 drive type I interferon-dependent autoinflammation in NOCARH syndrome reversible by ruxolitinib.

Kapp FG, Kretschmer S, Beckmann CCA, Wäsch L, Molitor A, Carapito R, Schubert M, Lucas N, Conrad S, Poignant S, Isidor B, Rohlfs M, Kisaarslan AP, Schanze D, Zenker M, Schmitt-Graeff A, Strahm B, Peters A, Yoshimi A, Driever W, Zillinger T, Günther C, Maharana S, Guan K, Klein C, Ehl S, Niemeyer CM, Unal E, Bahram S, Hauck F, Lee-Kirsch MA, Speckmann C. Kapp FG, et al. Among authors: gunther c. Clin Immunol. 2023 Nov;256:109777. doi: 10.1016/j.clim.2023.109777. Epub 2023 Sep 22. Clin Immunol. 2023. PMID: 37741518

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

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.

4

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.

5

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.

6

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

7

[Type I interferonopathies. Systemic inflammatory diseases triggered by type I interferons].

Günther C, Schmidt F, König N, Lee-Kirsch MA. Günther C, et al. Z Rheumatol. 2016 Mar;75(2):134-40. doi: 10.1007/s00393-015-0027-5. Z Rheumatol. 2016. PMID: 26744186 Review. German.

8

RPA and Rad51 constitute a cell intrinsic mechanism to protect the cytosol from self DNA.

Wolf C, Rapp A, Berndt N, Staroske W, Schuster M, Dobrick-Mattheuer M, Kretschmer S, König N, Kurth T, Wieczorek D, Kast K, Cardoso MC, Günther C, Lee-Kirsch MA. Wolf C, et al. Among authors: gunther c. Nat Commun. 2016 May 27;7:11752. doi: 10.1038/ncomms11752. Nat Commun. 2016. PMID: 27230542 Free PMC article.

9

Familial chilblain lupus due to a gain-of-function mutation in STING.

König N, Fiehn C, Wolf C, Schuster M, Cura Costa E, Tüngler V, Alvarez HA, Chara O, Engel K, Goldbach-Mansky R, Günther C, Lee-Kirsch MA. König N, et al. Among authors: gunther c. Ann Rheum Dis. 2017 Feb;76(2):468-472. doi: 10.1136/annrheumdis-2016-209841. Epub 2016 Aug 26. Ann Rheum Dis. 2017. PMID: 27566796

10

Nucleic acid-mediated autoinflammation and autoimmunity-type I interferonopathies.

Lee-Kirsch MA, Günther C, Roers A. Lee-Kirsch MA, et al. Among authors: gunther c. J Mol Med (Berl). 2016 Oct;94(10):1081-1084. doi: 10.1007/s00109-016-1467-3. J Mol Med (Berl). 2016. PMID: 27638338 No abstract available.

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