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Haematologica|June 3, 2017
CRISPR-Cas9-induced t(11;19)/MLL-ENL translocations initiate leukemia in human hematopoietic progenitor cells in vivoJana Reimer, Sabine Knöß, Maurice Labuhn, et al.
Annals of Hematology|October 27, 2009
Patients with del(5q) MDS who fail to achieve sustained erythroid or cytogenetic remission after treatment with lenalidomide have an increased risk for clonal evolution and AML progressionGudrun Göhring, Aristoteles Giagounidis, Guntram Büsche, et al.
European Journal of Haematology|December 17, 2009
Epigenetic inactivation of tumour suppressor gene KLF11 in myelodysplastic syndromes*Anna Potapova, Britta Hasemeier, Daniel Römermann, et al.
Stem Cell Research|May 31, 2022
Generation of an induced pluripotent stem cell line (DHMCi008-A) from an individual with TUBA1A tubulinopathyJulian Schröter, Hanna Syring, Gudrun Göhring, et al.
Stem Cell Research|September 26, 2022
Generation of two TMEM16A knockout iPSC clones each from a healthy human iPSC line, from a Cystic Fibrosis patient specific line with p.Phe508del mutation and from the gene corrected iPSC lineMark-Christian Jaboreck, Jonathan Lukas Lühmann, Mia Mielenz, et al.
Stem Cell Research|August 5, 2022
Generation of an induced pluripotent stem cell line (DHMCi009-A) from an individual with TUBB2A tubulinopathyJulian Schröter, Hanna Syring, Gudrun Göhring, et al.
Cancers|May 14, 2022
Optical Genome Mapping as a Diagnostic Tool in Pediatric Acute Myeloid LeukemiaJulia Suttorp, Jonathan Lukas Lühmann, Yvonne Lisa Behrens, et al.
Genes, Chromosomes & Cancer|January 8, 2019
Jumping translocations: Short telomeres or pathogenic TP53 variants as underlying mechanism in acute myeloid leukemia and myelodysplastic syndrome?Yvonne Lisa Behrens, Kathrin Thomay, Maike Hagedorn, et al.
Cytogenetic and Genome Research|March 3, 2017
Identification of a Cryptic Insertion ins(11;X)(q23;q28q12) Resulting in a KMT2A-FLNA Fusion in a 13-Month-Old Child with Acute Myelomonocytic LeukemiaJana Lentes, Kathrin Thomay, Dominik T Schneider, et al.
Blood|August 29, 2012
Loss of p53 accelerates the complications of myelodysplastic syndrome in a NUP98-HOXD13-driven mouse modelHaiming Xu, Silvia Menendez, Brigitte Schlegelberger, et al.
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