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Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Genetic alterations in lymphoblastic leukaemia<b> / lymphoma - a practical guide to WHO HAEM5</b>Doris Steinemann, Małgorzata Dawidowska, Lisa J Russell, et al.
Annals of Hematology|September 16, 2010
Expression of myelopoiesis-associated microRNA in bone marrow cells of atypical chronic myeloid leukaemia and chronic myelomonocytic leukaemiaKais Hussein, Guntram Büsche, Michaela Muth, et al.
Stem Cell Research|July 13, 2019
Generation of a NKX2.1 knock-in reporter cell line from human induced pluripotent stem cells (MHHi006-A-2)Ruth Olmer, Julia Dahlmann, Sylvia Merkert, et al.
Anticancer Research|February 26, 2004
P-glycoprotein modulation improves in vitro chemosensitivity in malignant pediatric liver tumorsSteven Warmann, Gudrun Göhring, Birgit Teichmann, et al.
Stem Cell Research|March 23, 2019
Generation of 2 iPSC clones from a patient with DNAJC12 deficiency: DHMCi003-A and DHMCi003-BSabine Jung-Klawitter, Selina Wächter, Maike Hagedorn, et al.
Stem Cell Research|December 10, 2016
Generation of an iPSC line from a patient with tyrosine hydroxylase (TH) deficiency: TH-1 iPSCSabine Jung-Klawitter, Nenad Blau, Attila Sebe, et al.
Stem Cell Research|June 1, 2018
Generation of a human CDX2 knock-in reporter iPSC line (MHHi007-A-1) to model human trophoblast differentiationSvitlana V Malysheva, Stephanie Wunderlich, Alexandra Haase, et al.
Stem Cell Research|February 18, 2019
GMP-compatible manufacturing of three iPS cell lines from human peripheral bloodAlexandra Haase, Wolfgang Glienke, Lena Engels, et al.
British Journal of Haematology|March 10, 2021
Paediatric chronic myeloid leukaemia presenting in de novo or secondary blast phase - a comparison of clinical and genetic characteristicsStephanie Sembill, Gudrun Göhring, Elke Schirmer, et al.
Stem Cell Research|October 25, 2021
Generation of an induced pluripotent stem cell line (DHMCi006-A) from a patient with autosomal recessive polycystic kidney disease (ARPKD) carrying a compound heterozygous missense mutation in the fibrocystin encoding PKHD1 geneTheresa Leonie Fluhr, Mansoureh Tabatabaeifar, Hanna Syring, et al.
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