Literature DB >> 3530382

Autosomal aneuploidy in mice: generation and developmental consequences.

J D Gearhart, M T Davisson, M L Oster-Granite.   

Abstract

Spontaneous aneuploidy in the mouse is uncommon, but specific mating schemes have been developed that produce aneuploid conceptuses at high frequencies. The most commonly reported aneuploid condition in the mouse is autosomal trisomy, in which there is an extra copy (in whole or in part) of a chromosome. In this review, we present several of the schemes used in producing trisomic, partially (tertiary) trisomic, and monosomic conceptuses and summarize the developmental consequences that are associated with each of the autosomal trisomies of the mouse.

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Year:  1986        PMID: 3530382     DOI: 10.1016/0361-9230(86)90075-4

Source DB:  PubMed          Journal:  Brain Res Bull        ISSN: 0361-9230            Impact factor:   4.077


  15 in total

1.  Nerve growth factor corrects developmental impairments of basal forebrain cholinergic neurons in the trisomy 16 mouse.

Authors:  P Corsi; J T Coyle
Journal:  Proc Natl Acad Sci U S A       Date:  1991-03-01       Impact factor: 11.205

2.  c-ets-2 protooncogene has mitogenic and oncogenic activity.

Authors:  A Seth; D K Watson; D G Blair; T S Papas
Journal:  Proc Natl Acad Sci U S A       Date:  1989-10       Impact factor: 11.205

3.  Use of cross-species in-situ hybridization (ZOO-FISH) to assess chromosome abnormalities in day-6 in-vivo- or in-vitro-produced sheep embryos.

Authors:  Gianfranco Coppola; Basil Alexander; Dino Di Berardino; Elizabeth St John; Parvathi K Basrur; W Allan King
Journal:  Chromosome Res       Date:  2007-05-10       Impact factor: 5.239

4.  A unique downregulation of h2-calponin gene expression in Down syndrome: a possible attenuation mechanism for fetal survival by methylation at the CpG island in the trisomic chromosome 21.

Authors:  J Kuromitsu; H Yamashita; H Kataoka; T Takahara; M Muramatsu; T Sekine; N Okamoto; Y Furuichi; Y Hayashizaki
Journal:  Mol Cell Biol       Date:  1997-02       Impact factor: 4.272

5.  Blastomere karyotyping and transfer of chromosomally selected embryos. Implications for the production of specific animal models and human prenatal diagnosis.

Authors:  C Bacchus; W Buselmaier
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

6.  Genesis and systematization of cardiovascular anomalies and analysis of skeletal malformations in murine trisomy 16 and 19. Two animal models for human trisomies.

Authors:  C Bacchus; H Sterz; W Buselmaier; S Sahai; H Winking
Journal:  Hum Genet       Date:  1987-09       Impact factor: 4.132

7.  Consequences of trisomy 16 for mouse brain development: corticogenesis in a model of Down syndrome.

Authors:  T F Haydar; M E Blue; M E Molliver; B K Krueger; P J Yarowsky
Journal:  J Neurosci       Date:  1996-10-01       Impact factor: 6.167

8.  Gene network disruptions and neurogenesis defects in the adult Ts1Cje mouse model of Down syndrome.

Authors:  Chelsee A Hewitt; King-Hwa Ling; Tobias D Merson; Ken M Simpson; Matthew E Ritchie; Sarah L King; Melanie A Pritchard; Gordon K Smyth; Tim Thomas; Hamish S Scott; Anne K Voss
Journal:  PLoS One       Date:  2010-07-16       Impact factor: 3.240

9.  Somatostatin expression in TS16 mouse brain cultures.

Authors:  P Corsi; G Forloni; M Troia; T Lettini; J T Coyle
Journal:  J Mol Neurosci       Date:  1998-04       Impact factor: 3.444

10.  [Corneal anomalies in murine trisomy 16].

Authors:  F Tost; J Wolfinger; J Giebel; W Buselmaier
Journal:  Ophthalmologe       Date:  2005-01       Impact factor: 1.059

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