By Heinz Lother, Rudolf Dernick, Wolfram Ostertag
Utilizing the most recent ideas of molecular genetics it truly is now attainable to review the mechanisms of cellphone progress and differentiation on the molecular point. in particular the applying of viral vectors to imagine and learn gene expression, the ideas of stem mobilephone manipulation in addition to quite a few effects in regards to the functionality of oncogenes or the function of cytokines and development elements are mentioned resulting in new interpretations of the mechanisms which result in basic or irregular mobile differentiation.
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Additional resources for Vectors as Tools for the Study of Normal and Abnormal Growth and Differentiation
1988, and this article) gives access to a number of unresolved questions. Using this approach, a complete picture of the expression throughout development of an engineered construct can be obtained. Other applications lLaboratoire de Biochimie Genetique, H6pital Necker, 149 rue de Sevres, 75743 Paris Cedex 15, France NATO AS! Series, Vol. H 34 Vectors as Tools for the Study of Nonnal and Abnormal Growth and Differentiation. Edited by H. Lather et al. © Springer-Verlag Berlin Heidelberg 1989 34 of in situ detectable genetic markers include clonal analysis and the description of lineages.
Cell 37:179 183 45 Monk M (1988) Genomic imprinting. Genes & Development 2:921 925 Nicolas JF, Rubenstein JLR (1987) Retroviral vectors. In: Rodriguez RL, Denhardt DT (eds) Vectors: a survey of molecular cloning vectors and their uses. Butterworth, Stoneham, MA, USA, P 493 Nicolas JF, Bonnerot C (1988) Recombinant retrovirus, cell lineage and gene expression in the mouse embryo. In: Cellular factors in development and differentiation Embryos, teratocarcinomas and differentiated tissues. Alan R Liss, New York, p 125 Nolan GP, Fiering S, Nicolas JF, Herzenberg LA (1988) Fluorescence activated cell analysis and sorting of viable mammalian cells based on B-D-galactosidase activity after transduction of E.
The reaction product of B-galactosidase associates with Fe++/Fe+++ and therefore can be detected by electron microscopy. With nlsLacZ the labelling mainly appears as patches in the outer nuclear membrane and is probably associated with the nuclear pores (see Fig. , 1987). These intense patches are evident even after silver staining. 36 c A JGlO on -' 8 'J ~ ~ ~ z 10 I 5(;3 10 2 FlUJRESCElN 10) 1("" . 1 B o , . ,. FIG. 2. Purification of heterogenous B-galactosidase cell population by FACS. 1