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Peter J. Donovan

Researcher at Royal Brisbane and Women's Hospital

Publications -  167
Citations -  14129

Peter J. Donovan is an academic researcher from Royal Brisbane and Women's Hospital. The author has contributed to research in topics: Stem cell & Embryonic stem cell. The author has an hindex of 52, co-authored 154 publications receiving 13508 citations. Previous affiliations of Peter J. Donovan include Johns Hopkins University & National Institutes of Health.

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Derivation of pluripotent stem cells from cultured human primordial germ cells

TL;DR: In this article, a set of primordial germ cells (PGCs, 5-9 weeks postfertilization) were cultured on mouse STO fibroblast feeder layers in the presence of human recombinant leukemia inhibitory factor (HILI) and forskolin.

Derivation of pluripotent stem cells from cultured human primordial germ cells (alkaline phosphataseyembryoid bodyyembryonic stem cellyembryonic germ cell)

TL;DR: Based on their origin and demonstrated properties, these human PGC-derived cultures meet the criteria for pluripotent stem cells and most closely resemble EG cells.
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Long-term proliferation of mouse primordial germ cells in culture.

TL;DR: This work reports a further factor that stimulates PGC proliferation in vitro, basic fibroblast growth factor (bFGF), which, in the presence of steel factor and leukaemia inhibitory factor, stimulates long-term proliferation of PGCs, leading to the derivation of large colonies of cells.
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Mast cell growth factor maps near the steel locus on mouse chromosome 10 and is deleted in a number of steel alleles.

TL;DR: The cloning of sequences encoding MGF, a c-kit ligand, is described and it is shown that Mgf maps near Sl in the distal region of mouse chromosome 10 and is deleted in a number of Sl alleles, strongly support the notion that Sl encodes the mast cell growth factor.
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Requirement for mast cell growth factor for primordial germ cell survival in culture

TL;DR: It is reported that MGF is essential for PGC survival in culture, but does not stimulate PGC proliferation, thus explaining the sterility in mice carrying the steel-dickie (Sld) mutation.