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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

Genetic recombination pathways and their application for genome modification of human embryonic stem cells.

TL;DR: Human embryonic stem cells are pluripotent cells derived from early human embryo and retain a potential to differentiate into all adult cell types and are expected to become significant tools in drug discovery as well as in the studies of cellular and developmental functions of human genes.
Journal ArticleDOI

Two fillips for human embryonic stem cells.

TL;DR: The derivation of human embryonic stem cells obtained from a cloned blastocyst represents a significant step toward the cure of diseases that involve the loss of a particular cell type — diseases such as type 1 diabetes and Parkinson's disease.
Book ChapterDOI

Single Cell Enzymatic Dissociation of Human Embryonic Stem Cells: A Straightforward, Robust, and Standardized Culture Method

TL;DR: This chapter shows how hES cells, which have been derived and passaged by traditional mechanical dissection, can be rapidly adjusted to propagation by enzymatic dissociation to single cells.
Patent

Methods and platforms for drug discovery using induced pluripotent stem cells

TL;DR: In this paper, the authors present methods for identifying an agent that corrects a phenotype associated with a health condition or a predisposition for a health conditions, and also reveal human induced pluripotent stem cell lines.
Journal ArticleDOI

Generation of multidrug resistant human tissues by overexpression of the ABCG2 multidrug transporter in embryonic stem cells.

TL;DR: The stable overexpression of GFP-ABCG2, driven by a constitutive (CAG) promoter, in HUES9 human embryonic stem cells provided increased toxin resistance in the stem cells, and protected the derived cardiomyocytes against doxorubicin toxicity.
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.
Journal ArticleDOI

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.
Journal ArticleDOI

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.
Journal ArticleDOI

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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