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Journal ArticleDOI

Derivation of embryonic stem-cell lines from human blastocysts.

TLDR
The procedures used to develop 17 lines of human embryonic stem cells from the inner cell masses of blastocysts are discussed.
Abstract
This report, first published online on March 3, 2004, discusses the procedures used to develop 17 lines of human embryonic stem cells from the inner cell masses of blastocysts. These cell lines are available to researchers under a Material Transfer Agreement; according to current regulations, the cells cannot be used for research supported by federal funds. These cells are expected to facilitate research on a variety of serious chronic diseases.

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Citations
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Journal ArticleDOI

Derivation of human embryonic stem cells from day-8 blastocysts recovered after three-step in vitro culture.

TL;DR: It is reported here that the novel three‐step culture conditions successfully support the development of day‐8 human blastocysts, which possess significantly (p <.01) more ICM cells than day‐6 Blastocysts.
Journal ArticleDOI

Enhanced efficiency of generating induced pluripotent stem (iPS) cells from human somatic cells by a combination of six transcription factors.

TL;DR: Enhanced efficiency of generating induced pluripotent stem cells from human somatic cells by a combination of six transcription factors is demonstrated.
Journal ArticleDOI

Generation of hypoimmunogenic human pluripotent stem cells

TL;DR: An approach is described that effectively targets adaptive as well as innate immune responses and may therefore enable cell therapy on a broader scale and informs future studies aiming to generate “off-the-shelf” universal cell products that may make cell therapy available to a larger pool of patients.
Journal ArticleDOI

Derivation, growth and applications of human embryonic stem cells

TL;DR: Recent progress in the derivation and growth of undifferentiated hES cells and their differentiated progeny, and the problems associated with these techniques are summarised.
Journal ArticleDOI

Derivation, characterization and differentiation of human embryonic stem cells: comparing serum-containing versus serum-free media and evidence of germ cell differentiation

TL;DR: The data support that hESC may be capable of differentiation into germ cells although further confirmation is needed, and it is suggested that strategies such as stepwise adaptation will be needed before implementing a serum-free culture condition for h ESC lines that have previously been derived in a medium containing serum.
References
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Journal ArticleDOI

Embryonic Stem Cell Lines Derived from Human Blastocysts

TL;DR: Human blastocyst-derived, pluripotent cell lines are described that have normal karyotypes, express high levels of telomerase activity, and express cell surface markers that characterize primate embryonic stem cells but do not characterize other early lineages.
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The serial cultivation of human diploid cell strains.

TL;DR: A consideration of the cause of the eventual degeneration of these strains leads to the hypothesis that non-cumulative external factors are excluded and that the phenomenon is attributable to intrinsic factors which are expressed as senescence at the cellular level.
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Formation of Pluripotent Stem Cells in the Mammalian Embryo Depends on the POU Transcription Factor Oct4

TL;DR: It is reported that the activity of Oct4 is essential for the identity of the pluripotential founder cell population in the mammalian embryo and also determines paracrine growth factor signaling from stem cells to the trophectoderm.
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Embryonic stem cell lines from human blastocysts: somatic differentiation in vitro.

TL;DR: The derivation of pluripotent embryonic stem (ES) cells from human blastocysts is described, providing a model to study early human embryology, an investigational tool for discovery of novel growth factors and medicines, and a potential source of cells for use in transplantation therapy.
Journal ArticleDOI

Differentiation of human embryonic stem cells into embryoid bodies compromising the three embryonic germ layers.

TL;DR: The ability to induce formation of human embryoid bodies that contain cells of neuronal, hematopoietic and cardiac origins will be useful in studying early human embryonic development as well as in transplantation medicine.
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