Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Down syndrome and mouse models

I Kola1, P J Hertzog

  • 1Molecular Genetics & Development Group, Institute of Reproduction & Development, Monash University, Clayton, Victoria, Australia. ismailko@silas.cc.monash.edu.au

Current Opinion in Genetics & Development
|August 5, 1998
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Evaluating Creatinine and Urea Levels as a Predictor of Renal Failure in Burn Patients.

Annals of burns and fire disasters·2026
Same author

Vitamin D status in patients with chronic obstructive pulmonary disease at Chris Hani Baragwanath Hospital, Johannesburg, South Africa.

African journal of thoracic and critical care medicine·2024
Same author

"Anterior interosseous nerve syndrome (Kiloh Nevin Syndrome) revealing Gantzer muscle and simultaneous myasthenia gravis".

Radiology case reports·2021
Same author

Biological and chemical studies on 8,9-dihydroxy-8,9-dihydro-aflatoxin B1 and some of its esters.

Carcinogenesis·2012
Same author

Influence of nucleotides flanking the ggaa core sequence on ets1 and ets2 DNA-binding activity and the mechanism of ets1 autoregulation.

International journal of oncology·2011
Same author

Activating point mutations of the Neu oncogene in schwannomas induced by ethylnitrosourea exposure to day-15 and day-18 fetal rats.

International journal of oncology·2011

Recent advancements characterize the Ts65Dn mouse model, a model for Down syndrome. New models trisomic for chromosome 21 regions show learning defects, implicating specific genes in Down syndrome pathologies.

Area of Science:

  • Genetics
  • Neuroscience
  • Developmental Biology

Background:

  • The Ts65Dn mouse model exhibits features relevant to Down syndrome.
  • Down syndrome is associated with behavioral and learning deficits.

Purpose of the Study:

  • To summarize recent advancements in Down syndrome mouse models.
  • To highlight the generation of new models and the investigation of genetic factors contributing to Down syndrome pathologies.

Main Methods:

  • Characterization of the Ts65Dn mouse model.
  • Generation of a new mouse model trisomic for the 21q22.2 region.
  • Investigating gene mutations (Minibrain, SOD1) implicated in learning defects.

Main Results:

  • The Ts65Dn mouse model displays many features of Down syndrome.

Related Experiment Videos

  • A new mouse model trisomic for the 21q22.2 region exhibits behavioral and learning defects.
  • Minibrain and SOD1 gene mutations are linked to learning impairments in Down syndrome.
  • Conclusions:

    • Advancements in mouse models are crucial for understanding Down syndrome.
    • New models and gene discoveries will facilitate the study of Down syndrome pathologies.
    • Further research into specific genes on chromosome 21 will aid in developing targeted therapies.