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Bone Marrow Transplantation|May 4, 2018
Diagnostic value of highly-sensitive chimerism analysis after allogeneic stem cell transplantationLea Sellmann, Kim Rabe, Ivonne Bünting, et al.
Stem Cell Research|February 18, 2019
Generation of an iPSC line from a patient with infantile liver failure syndrome 2 due to mutations in NBAS: DHMCi004-ADominic Lenz, Christian Staufner, Selina Wächter, et al.
Haematologica|October 3, 2009
Clonal heterogeneity in the 5q- syndrome: p53 expressing progenitors prevail during lenalidomide treatment and expand at disease progressionMartin Jädersten, Leonie Saft, Andrea Pellagatti, et al.
American Journal of Medical Genetics. Part A|February 9, 2012
Occurrence of acute lymphoblastic leukemia and juvenile myelomonocytic leukemia in a patient with Noonan syndrome carrying the germline PTPN11 mutation p.E139DSilke Pauli, Doris Steinemann, Kai Dittmann, et al.
Stem Cell Research|April 9, 2019
Generation of an induced pluripotent stem cell (iPSC) line, DHMCi005-A, from a patient with CALFAN syndrome due to mutations in SCYL1Dominic Lenz, Christian Staufner, Selina Wächter, et al.
Oncotarget|July 26, 2018
Effect of TP53 contact and conformational mutations on cell survival and erythropoiesis of human hematopoietic stem cells in a long term culture modelAzam Salari, Kathrin Thomay, Jana Lentes, et al.
Stem Cell Research|February 13, 2022
Generation of human induced pluripotent stem cell lines encoding for genetically encoded calcium indicators RCaMP1h and GCaMP6fMaria Elena Ricci Signorini, Monika Szepes, Anna Melchert, et al.
Stem Cell Research|December 4, 2022
Generation of human induced pluripotent stem cell line encoding for a genetically encoded voltage indicator Arclight A242Rajesh Vivekanandan, Monika Szepes, Maria Elena Ricci Signorini, et al.
International Journal of Molecular Sciences|October 24, 2018
Routes of Clonal Evolution into Complex Karyotypes in Myelodysplastic Syndrome Patients with 5q DeletionSimone Feurstein, Kathrin Thomay, Winfried Hofmann, et al.
Stem Cell Research|May 30, 2020
Generation of two human induced pluripotent stem cell lines (MHHi017-A, MHHi017-B) from a patient with primary ciliary dyskinesia carrying a homozygous mutation (c.7915C > T [p.Arg2639*]) in the DNAH5 geneNora Drick, Julia Dahlmann, Anais Sahabian, et al.
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