Beate Schwinzer

HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)

Christoph Klein, Magda Grudzien, Giridharan Appaswamy et al. · Nature Genetics · 2006 · 501 citations

Hax1 Deficiency, Mendelian Disorder, Genetic Disorder +7

The Severe Chronic Neutropenia International Registry: 10-Year Follow-up Report

David C. Dale, Audrey Anna Bolyard, Beate Schwinzer et al. · Supportive Cancer Therapy · 2006 · 165 citations

10-Year Follow-up Report, Hematology, International Health +5

Gangliosides of murine T lymphocyte subpopulations

Johannes Müthing, Beate Schwinzer · Biochemistry · 1989 · 46 citations

Activation of autoreactive T-lymphocytes by cultured syngeneic glomerular mesangial cells

Heinfried H. Radeke, Andreas Emmendörffer, Peter Uciechowski et al. · Kidney International · 1994 · 27 citations · Full text

Glomerulonephritis, Autoimmune Disease, T-regulatory Cell +7

Expression and regulation of c-kit receptor and response to stem cell factor in childhood malignant T-lymphoblastic cells

Jörg Tomeczkowski, D Frick, Beate Schwinzer et al. · Leukemia · 1998 · 20 citations

Lineage Plasticity, C-kit Receptor, Cell Therapy +8