Log in to save to my catalogue

Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for...

Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3224224

Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling down syndrome

About this item

Full title

Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling down syndrome

Publisher

New York: Springer-Verlag

Journal title

Mammalian genome, 2011-12, Vol.22 (11-12), p.674-684

Language

English

Formats

Publication information

Publisher

New York: Springer-Verlag

More information

Scope and Contents

Contents

Down syndrome (DS) is the most frequent genetic disorder leading to intellectual disabilities and is caused by three copies of human chromosome 21. Mouse models are widely used to better understand the physiopathology in DS or to test new therapeutic approaches. The older and the most widely used mouse models are the trisomic Ts65Dn and the Ts1Cje...

Alternative Titles

Full title

Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling down syndrome

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3224224

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3224224

Other Identifiers

ISSN

0938-8990

E-ISSN

1432-1777

DOI

10.1007/s00335-011-9356-0

How to access this item