Sentence examples for mouse embryonic skin from inspiring English sources

To investigate the role of HIP/RPL29 normal expression during cartilage formation, we designed a ribozyme-mediated knock-down approach to partially down-regulate HIP/RPL29 expression in the multipotent mouse embryonic skin fibroblast cell line C3H/10T ½.

We have now thoroughly evaluated the expression of TAp63 and ΔNp63 in mouse embryonic skin using antibodies generated in our laboratory that are specific to each isoform.

However, the fact that undisputed identification of TAp63 mRNA and protein in mouse embryonic skin remains elusive and that the TAp63 isoform-specific knockout mice have no discernible skin phenotype warrants a re-evaluation of this observation [22].

None of the other candidates indicated biallelic expression in any of the examined cells, suggesting that they are X-inactivated in mouse embryonic skin fibroblasts.

They designed a ribozyme-mediated knock-down approach to partially down-regulate HIP/RPL29 expression in the multipotent mouse embryonic skin fibroblast cell line C3H/10T To investigate the role of HIP/RPL29 normal expression during cartilage formation [ 51].

However, recent analysis of E18.5 mouse embryonic skin in which the β-galactosidase gene is knocked into the Dll1 locus has provided evidence that Dll1 is not only expressed in the dermal papilla but also in the epithelial cells at the base of the hair follicle and in clusters of cells in the basal layer of the IFE [ 16 ].

Taken together, these data indicate that p63 directly activates Fgfr2 expression in primary mouse keratinocytes and in embryonic skin.

As a first step, to identify novel escapee genes, we here investigated possible biallelic expression of five candidate genes in primary female mouse embryonic fibroblasts derived from skin.

Binding to this region of the genome was observed by ChIP in primary human and mouse keratinocytes and in E14.5 embryonic skin (Fig 4D and E Supporting Information Figg S8B).

The creation of mouse embryonic stem cells from mouse skin cells was carried out by Dr. Teruhiko Wakayama and colleagues in the Rockefeller University laboratory of Dr. Peter Mombaerts.

Mouse embryonic fibroblasts (MEFs) derived from skin were cultured in Minimum Essential Medium Eagle (Sigma) supplemented with 2% L-glutamine, 10% fetal bovine serum and 1.5% penicillin/streptomycin (Invitrogen).