Publications by authors named "Kerstin Engel"

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UNC93B1 variants underlie TLR7-dependent autoimmunity.
Christine Wolf, Ee Lyn Lim, Mohammad Mokhtari, Barbara Kind, Alexandru Odainic, Kerstin Engel

Sci Immunol· February 2024

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Generation of induced pluripotent stem cell lines from two patients with Aicardi-Goutières syndrome type 1 due to biallelic TREX1 mutations.
Vanessa Hänchen, Stefanie Kretschmer, Christine Wolf, Kerstin Engel, Shahryar Khattak

Stem Cell Res· October 2022

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Generation of induced pluripotent stem cell lines from three patients with Aicardi-Goutières syndrome type 5 due to biallelic SAMDH1 mutations.
Vanessa Hänchen, Stefanie Kretschmer, Christine Wolf, Kerstin Engel, Shahryar Khattak

Stem Cell Res· October 2022

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Assessment of Clinical Response to Janus Kinase Inhibition in Patients With Familial Chilblain Lupus and TREX1 Mutation.
Nick Zimmermann, Christine Wolf, Reiner Schwenke, Anne Lüth, Franziska Schmidt, Kerstin Engel

JAMA Dermatol· March 2019

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Single Cell Gel Electrophoresis for the Detection of Genomic Ribonucleotides.
Barbara Kind, Christine Wolf, Kerstin Engel, Alexander Rapp, M Cristina Cardoso

Methods Mol Biol· June 2018

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Familial chilblain lupus due to a gain-of-function mutation in STING.
Nadja König, Christoph Fiehn, Christine Wolf, Max Schuster, Emanuel Cura Costa, Kerstin Engel

Ann Rheum Dis· February 2017

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Response to: 'JAK inhibition in STING-associated interferonopathy' by Crow et al.
Victoria Tüngler, Nadja König, Claudia Günther, Kerstin Engel, Christoph Fiehn

Ann Rheum Dis· December 2016

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Expanding the phenotypic spectrum of lupus erythematosus in Aicardi-Goutières syndrome.
Georgia Ramantani, Jürgen Kohlhase, Christoph Hertzberg, A Micheil Innes, Kerstin Engel

Arthritis Rheum· May 2010

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Correspondence (letter to the editor): Interdisciplinary Diagnostic System.
Kerstin Engel, Wolfram Seidel

Dtsch Arztebl Int· November 2008

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Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosus.
Min Ae Lee-Kirsch, Maolian Gong, Dipanjan Chowdhury, Lydia Senenko, Kerstin Engel

Nat Genet· September 2007

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A mutation in TREX1 that impairs susceptibility to granzyme A-mediated cell death underlies familial chilblain lupus.
Min Ae Lee-Kirsch, Dipanjan Chowdhury, Scott Harvey, Maoliang Gong, Lydia Senenko, Kerstin Engel

J Mol Med (Berl)· May 2007

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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, Kirsten Praedicow, Julia Rohayem, Kerstin Engel

Hum Mutat· May 2005

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