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Aicardi-Goutières syndrome: a model disease for systemic autoimmunity.
Lee-Kirsch MA, Wolf C, Günther C. Lee-Kirsch MA, et al. Among authors: wolf 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.
SAMHD1 prevents autoimmunity by maintaining genome stability.
Kretschmer S, Wolf C, König N, Staroske W, Guck J, Häusler M, Luksch H, Nguyen LA, Kim B, Alexopoulou D, Dahl A, Rapp A, Cardoso MC, Shevchenko A, Lee-Kirsch MA. Kretschmer S, et al. Among authors: wolf c. Ann Rheum Dis. 2015 Mar;74(3):e17. doi: 10.1136/annrheumdis-2013-204845. Epub 2014 Jan 20. Ann Rheum Dis. 2015. PMID: 24445253 Free PMC article.
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. Among authors: wolf c. JAMA Dermatol. 2015 Apr;151(4):426-31. doi: 10.1001/jamadermatol.2014.3438. JAMA Dermatol. 2015. PMID: 25517357
OBSERVATIONS: We report on a family with dominant chilblain lupus segregating a novel TREX1 mutation (c.585C>G; H195Q) within the highly conserved exonuclease (Exo) III domain. ...
OBSERVATIONS: We report on a family with dominant chilblain lupus segregating a novel TREX1 mutation (c.585C>G; H195Q) within the …
Type I interferonopathies--an expanding disease spectrum of immunodysregulation.
Lee-Kirsch MA, Wolf C, Kretschmer S, Roers A. Lee-Kirsch MA, et al. Among authors: wolf c. Semin Immunopathol. 2015 Jul;37(4):349-57. doi: 10.1007/s00281-015-0500-x. Epub 2015 May 22. Semin Immunopathol. 2015. PMID: 25998914 Review.
Severe immune dysregulation with neurological impairment and minor bone changes in a child with spondyloenchondrodysplasia due to two novel mutations in the ACP5 gene.
Girschick H, Wolf C, Morbach H, Hertzberg C, Lee-Kirsch MA. Girschick H, et al. Among authors: wolf c. Pediatr Rheumatol Online J. 2015 Sep 7;13(1):37. doi: 10.1186/s12969-015-0035-7. Pediatr Rheumatol Online J. 2015. PMID: 26346816 Free PMC article.
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. Nat Commun. 2016 May 27;7:11752. doi: 10.1038/ncomms11752. Nat Commun. 2016. PMID: 27230542 Free PMC article.
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: wolf 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
Variable clinical phenotype in two siblings with Aicardi-Goutières syndrome type 6 and a novel mutation in the ADAR gene.
Schmelzer L, Smitka M, Wolf C, Lucas N, Tüngler V, Hahn G, Tzschach A, Di Donato N, Lee-Kirsch MA, von der Hagen M. Schmelzer L, et al. Among authors: wolf c. Eur J Paediatr Neurol. 2018 Jan;22(1):186-189. doi: 10.1016/j.ejpn.2017.11.003. Epub 2017 Nov 22. Eur J Paediatr Neurol. 2018. PMID: 29221912
Therapeutic Approaches to Type I Interferonopathies.
Bienias M, Brück N, Griep C, Wolf C, Kretschmer S, Kind B, Tüngler V, Berner R, Lee-Kirsch MA. Bienias M, et al. Among authors: wolf c. Curr Rheumatol Rep. 2018 Apr 20;20(6):32. doi: 10.1007/s11926-018-0743-3. Curr Rheumatol Rep. 2018. PMID: 29679241 Review.
Assessment of Clinical Response to Janus Kinase Inhibition in Patients With Familial Chilblain Lupus and TREX1 Mutation.
Zimmermann N, Wolf C, Schwenke R, Lüth A, Schmidt F, Engel K, Lee-Kirsch MA, Günther C. Zimmermann N, et al. Among authors: wolf c. JAMA Dermatol. 2019 Mar 1;155(3):342-346. doi: 10.1001/jamadermatol.2018.5077. JAMA Dermatol. 2019. PMID: 30673078 Free PMC article.
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