Cyrill Schipp

STAT3 gain-of-function mutations associated with autoimmune lymphoproliferative syndrome like disease deregulate lymphocyte apoptosis and can be targeted by BH3 mimetic compounds.

A. Borkhardt, S. Postovsky, U. Fischer, 2017, Clinical immunology.

EBV Negative Lymphoma and Autoimmune Lymphoproliferative Syndrome Like Phenotype Extend the Clinical Spectrum of Primary Immunodeficiency Caused by STK4 Deficiency

A. Borkhardt, U. Fischer, B. Fleckenstein, 2018, Front. Immunol..

Hematopoietic Stem Cell Transplantation in an Infant with Immunodeficiency, Centromeric Instability, and Facial Anomaly Syndrome

A. Borkhardt, D. Wieczorek, M. Kuhlen, 2017, Front. Immunol..

Specific antibody deficiency and autoinflammatory disease extend the clinical and immunological spectrum of heterozygous NFKB1 loss-of-function mutations in humans

A. Borkhardt, U. Fischer, E. Yefenof, 2016, Haematologica.