Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

20 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
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: tungler v. Curr Rheumatol Rep. 2018 Apr 20;20(6):32. doi: 10.1007/s11926-018-0743-3. Curr Rheumatol Rep. 2018. PMID: 29679241 Review.
[Genetic methods for analysis of autoinflammatory diseases].
Bienias M, König N, Wolf C, Kretschmer S, Rösen-Wolff A, Berner R, Tüngler V, Lee-Kirsch MA. Bienias M, et al. Among authors: tungler v. Z Rheumatol. 2017 May;76(4):295-302. doi: 10.1007/s00393-017-0300-x. Z Rheumatol. 2017. PMID: 28378116 Review. German.
Single-stranded nucleic acids promote SAMHD1 complex formation.
Tüngler V, Staroske W, Kind B, Dobrick M, Kretschmer S, Schmidt F, Krug C, Lorenz M, Chara O, Schwille P, Lee-Kirsch MA. Tüngler V, et al. J Mol Med (Berl). 2013 Jun;91(6):759-70. doi: 10.1007/s00109-013-0995-3. Epub 2013 Jan 31. J Mol Med (Berl). 2013. PMID: 23371319
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: tungler v. 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
Defective removal of ribonucleotides from DNA promotes systemic autoimmunity.
Günther C, Kind B, Reijns MA, Berndt N, Martinez-Bueno M, Wolf C, Tüngler V, Chara O, Lee YA, Hübner N, Bicknell L, Blum S, Krug C, Schmidt F, Kretschmer S, Koss S, Astell KR, Ramantani G, Bauerfeind A, Morris DL, Cunninghame Graham DS, Bubeck D, Leitch A, Ralston SH, Blackburn EA, Gahr M, Witte T, Vyse TJ, Melchers I, Mangold E, Nöthen MM, Aringer M, Kuhn A, Lüthke K, Unger L, Bley A, Lorenzi A, Isaacs JD, Alexopoulou D, Conrad K, Dahl A, Roers A, Alarcon-Riquelme ME, Jackson AP, Lee-Kirsch MA. Günther C, et al. Among authors: tungler v. J Clin Invest. 2015 Jan;125(1):413-24. doi: 10.1172/JCI78001. Epub 2014 Dec 15. J Clin Invest. 2015. PMID: 25500883 Free PMC article.
Aicardi-Goutières syndrome due to a paternal mosaic IFIH1 mutation.
Tüngler V, Doebler-Neumann M, Salandin M, Kaufmann P, Wolf C, Lucas N, Harmuth F, Reichbauer J, Krägeloh-Mann I, Schüle R, Lee-Kirsch MA. Tüngler V, et al. Neurol Genet. 2019 Dec 19;6(1):e384. doi: 10.1212/NXG.0000000000000384. eCollection 2020 Feb. Neurol Genet. 2019. PMID: 32042913 Free PMC article. No abstract available.
20 results