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Methods in Molecular Biology (Clifton, N.J.)|October 19, 2017
Single Cell Gel Electrophoresis for the Detection of Genomic RibonucleotidesBarbara Kind, Christine Wolf, Kerstin Engel, et al.Stem Cell Research|August 26, 2022
Generation of induced pluripotent stem cell lines from two patients with Aicardi-Goutières syndrome type 1 due to biallelic TREX1 mutationsVanessa Hänchen, Stefanie Kretschmer, Christine Wolf, et al.Stem Cell Research|September 17, 2022
Generation of induced pluripotent stem cell lines from three patients with Aicardi-Goutières syndrome type 5 due to biallelic SAMDH1 mutationsVanessa Hänchen, Stefanie Kretschmer, Christine Wolf, et al.JAMA Dermatology|January 24, 2019
Assessment of Clinical Response to Janus Kinase Inhibition in Patients With Familial Chilblain Lupus and TREX1 MutationNick Zimmermann, Christine Wolf, Reiner Schwenke, et al.Human Mutation|April 21, 2005
Identification of novel GCK and HNF1A/TCF1 mutations and polymorphisms in German families with maturity-onset diabetes of the young (MODY)Dalia Toaima, Andrea Näke, Jutta Wendenburg, et al.Journal of Molecular Medicine (Berlin, Germany)|April 19, 2007
A mutation in TREX1 that impairs susceptibility to granzyme A-mediated cell death underlies familial chilblain lupusMin Ae Lee-Kirsch, Dipanjan Chowdhury, Scott Harvey, 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.Arthritis and Rheumatism|February 5, 2010
Expanding the phenotypic spectrum of lupus erythematosus in Aicardi-Goutières syndromeGeorgia Ramantani, Jürgen Kohlhase, Christoph Hertzberg, et al.Nature Genetics|July 31, 2007
Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosusMin Ae Lee-Kirsch, Maolian Gong, Dipanjan Chowdhury, et al.Science Immunology|January 11, 2024
UNC93B1 variants underlie TLR7-dependent autoimmunityChristine Wolf, Ee Lyn Lim, Mohammad Mokhtari, et al.Pageof 1