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Nadja König

Showing results (1-10 of 4) with videos related to

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Pediatric Rheumatology Online Journal|August 24, 2017
Autoimmune phenotype with type I interferon signature in two brothers with ADA2 deficiency carrying a novel CECR1 mutationAndrea Skrabl-Baumgartner, Barbara Plecko, Wolfgang M Schmidt, et al.
Annals of the Rheumatic Diseases|August 28, 2016
Familial chilblain lupus due to a gain-of-function mutation in STINGNadja König, Christoph Fiehn, Christine Wolf, et al.
Nature Communications|May 28, 2016
RPA and Rad51 constitute a cell intrinsic mechanism to protect the cytosol from self DNAChristine Wolf, Alexander Rapp, Nicole Berndt, et al.
Annals of the Rheumatic Diseases|January 22, 2014
SAMHD1 prevents autoimmunity by maintaining genome stabilityStefanie Kretschmer, Christine Wolf, Nadja König, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Pediatric Rheumatology Online Journal|August 24, 2017
Autoimmune phenotype with type I interferon signature in two brothers with ADA2 deficiency carrying a novel CECR1 mutationAndrea Skrabl-Baumgartner, Barbara Plecko, Wolfgang M Schmidt, et al.
Annals of the Rheumatic Diseases|August 28, 2016
Familial chilblain lupus due to a gain-of-function mutation in STINGNadja König, Christoph Fiehn, Christine Wolf, et al.
Nature Communications|May 28, 2016
RPA and Rad51 constitute a cell intrinsic mechanism to protect the cytosol from self DNAChristine Wolf, Alexander Rapp, Nicole Berndt, et al.
Annals of the Rheumatic Diseases|January 22, 2014
SAMHD1 prevents autoimmunity by maintaining genome stabilityStefanie Kretschmer, Christine Wolf, Nadja König, et al.
Pageof 1