Christoph N. Berger
Children's Medical Research Institute
6 Papers
67 Citations
Christoph N. Berger is an academic researcher from Children's Medical Research Institute. The author has contributed to research in topics: Haematopoiesis & Embryonic stem cell. The author has an hindex of 6, co-authored 6 publications.
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Papers
Unrestricted lineage differentiation of parthenogenetic ES cells.
Karin S. Sturm,Christoph N. Berger,Sheila X. Zhou,Sally L. Dunwoodie,Seong-Seng Tan,Patrick P.L. Tam +5 more
TL;DR: It is suggested that, while P-ES cells display more extensive developmental potential than the cells of parthenogenetic embryos from which they were derived, they only retained properties related to the presence of the maternal genome.
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Simultaeous detection of β‐galactosidase activity and surface antigen expression in viable haematopoietic cells
TL;DR: Beta-galactosidase can be used as a marker in transplantation experiments to study the development of lymphoid and myeloid precursor cells and is readily combined with fluorescently labelled antibodies against cell surface antigens.
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The development of haematopoietic cells is biased in embryonic stem cell chimaeras.
TL;DR: Findings of uneven contribution to haematopoietic development by ES cells indicate that the commitment of ES cell descendants may be different from that of the host cells.
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Hematopoietic deficiencies and core binding factor expression in murine Ts16, an animal model for Down syndrome.
TL;DR: A disequilibrium of Cbfa2 expression and a dysregulation of the two CbFA2 mRNA species as a cause for the abnormalities in Ts16 fetuses in general and the deficient Ts16 thymocyte development in particular appears unlikely.
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Estimation of the number of hematopoietic precursor cells during fetal mouse development by covariance analysis
TL;DR: Determination of PC numbers can be used to assess the relative maturity and developmental potential of individual cell populations and find excellent correlations of the proportion of beta-galactosidase expressing cells for all hematopoietic lineages confirming that they share a common ancestry.
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