✦ LIBER ✦

Analysis of Different Promoter Systems for Efficient Transgene Expression in Mouse Embryonic Stem Cell Lines

✍ Scribed by Sangmi Chung; Therese Andersson; Kai-C. Sonntag; Lars Björklund; Ole Isacson; Kwang-Soo Kim

Book ID: 111843328
Publisher: AlphaMed Press
Year: 2002
Tongue: English
Weight: 252 KB
Volume: 20
Category: Article
ISSN: 1066-5099
DOI: 10.1634/stemcells.20-2-139

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Analysis of expression of genes specific

Analysis of expression of genes specific for pluripotent and primordial germ cells in human and mouse embryonic stem cell lines

✍ O. F. Gordeeva; N. Yu. Krasnikova; A. V. Larionova; T. A. Krylova; G. G. Polyans 📂 Article 📅 2006 🏛 Springer 🌐 English ⚖ 197 KB

Stable suppression of gene expression by

Stable suppression of gene expression by short interfering RNAs targeted to promoter in a mouse embryonal carcinoma stem cell line

✍ Fariba Esmaeili; Taravat Bamdad; Sorayya Ghasemi 📂 Article 📅 2010 🏛 Society for In Vitro Biology 🌐 English ⚖ 356 KB

Other transgenic mutation assays: Develo

Other transgenic mutation assays: Development of a novel mouse tk+/− embryonic stem cell line for use in mutagenicity studies

✍ Vasily N. Dobrovolsky; Daniel A. Casciano; Robert H. Heflich 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 663 KB

A tk+/mouse embryonic stem (ES) cell line, designated 1G2, has been created in which one allele of the thymidine kinase (tk) gene was inactivated by targeted homologous recombination. This line is an analog of the mouse lymphoma tk+/-L5 178Y cell line, which is used widely to assess the mutagenicity

The influence of the cell-adhesive prote

The influence of the cell-adhesive proteins E-cadherin and fibronectin embedded in carbonate-apatite DNA carrier on transgene delivery and expression in a mouse embryonic stem cell line

✍ K. Kutsuzawa; T. Akaike; Ezharul H. Chowdhury 📂 Article 📅 2008 🏛 Elsevier Science 🌐 English ⚖ 956 KB

Stem cells have the potential to be differentiated to a specific cell type through genetic manipulation and therefore, represent a new and versatile source of cell replacement in regenerative medicine. However, conventional ways of gene transfer to these progenitor cells, suffer from a number of dis