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Tobias Brambrink

Researcher at Massachusetts Institute of Technology

Publications -  10
Citations -  8504

Tobias Brambrink is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: Embryonic stem cell & Induced pluripotent stem cell. The author has an hindex of 9, co-authored 10 publications receiving 8269 citations. Previous affiliations of Tobias Brambrink include University of Alabama at Birmingham.

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In vitro reprogramming of fibroblasts into a pluripotent ES-cell-like state

TL;DR: The results show that the biological potency and epigenetic state of in-vitro-reprogrammed induced pluripotent stem cells are indistinguishable from those of ES cells.
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Polycomb complexes repress developmental regulators in murine embryonic stem cells

TL;DR: It is shown that PcG proteins directly repress a large cohort of developmental regulators in murine ES cells, the expression of which would otherwise promote differentiation, and dynamic repression of developmental pathways by Polycomb complexes may be required for maintaining ES cell pluripotency and plasticity during embryonic development.
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Treatment of Sickle Cell Anemia Mouse Model with iPS Cells Generated from Autologous Skin

TL;DR: It is shown that mice can be rescued after transplantation with hematopoietic progenitors obtained in vitro from autologous iPS cells, providing proof of principle for using transcription factor–induced reprogramming combined with gene and cell therapy for disease treatment in mice.
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Sequential Expression of Pluripotency Markers during Direct Reprogramming of Mouse Somatic Cells

TL;DR: Using inducible constructs derived induced pluripotent stem (iPS) cells from mouse embryonic fibroblasts (MEFs) and found that transgene silencing is a prerequisite for normal cell differentiation, a step toward understanding some of the molecular events governing epigenetic reprogramming.
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Global loss of imprinting leads to widespread tumorigenesis in adult mice

TL;DR: It is demonstrated that LOI alone can predispose cells to tumorigenesis and a pathway through which immortality conferred by LOI lowers the threshold for transformation is identified.