Literature DB >> 10575227

Interphase FISH for rapid identification of a down syndrome animal model.

J Strovel1, J Stamberg, P J Yarowsky.   

Abstract

Mouse models of Down syndrome (trisomy 21, DS) have been developed to study the consequences of triplication of regions syntenic to distal human chromosome 21. We report a technique for the identification of segmental trisomy 16 (Ts65Dn) and diploid progeny at any age using interphase fluorescence in situ hybridization (FISH) of uncultured tail fibroblasts. Our technique is faster and less expensive than blood karyotyping.

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Year:  1999        PMID: 10575227     DOI: 10.1159/000015320

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  3 in total

1.  Elevated expression of the G-protein-activated inwardly rectifying potassium channel 2 (GIRK2) in cerebellar unipolar brush cells of a Down syndrome mouse model.

Authors:  Chie Harashima; David M Jacobowitz; Markus Stoffel; Lina Chakrabarti; Tarik F Haydar; Richard J Siarey; Zygmunt Galdzicki
Journal:  Cell Mol Neurobiol       Date:  2006-06-17       Impact factor: 5.046

2.  Widespread impairment of cell proliferation in the neonate Ts65Dn mouse, a model for Down syndrome.

Authors:  A Contestabile; T Fila; A Cappellini; R Bartesaghi; E Ciani
Journal:  Cell Prolif       Date:  2009-04       Impact factor: 6.831

3.  Pharmacotherapy with fluoxetine restores functional connectivity from the dentate gyrus to field CA3 in the Ts65Dn mouse model of down syndrome.

Authors:  Fiorenza Stagni; Jacopo Magistretti; Sandra Guidi; Elisabetta Ciani; Chiara Mangano; Laura Calzà; Renata Bartesaghi
Journal:  PLoS One       Date:  2013-04-19       Impact factor: 3.240

  3 in total

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