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

Trisomy 13 in the mouse

K Hongell, A Gropp

    Teratology
    |August 1, 1982
    PubMed
    Summary
    This summary is machine-generated.

    Trisomy 13 (Ts 13) in fetal mice causes significant growth retardation, developmental delays, and malformations like cleft palate. Impaired cell proliferation is suggested as the underlying cause of these developmental issues.

    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

    Chromosome survey of seals in the Baltic Sea in 1988-1992.

    Archives of environmental contamination and toxicology·1996
    Same author

    Cholinesterase activity in the chondrocranium of normal and exencephalic mouse fetus with trisomy 12.

    Journal of the Medical Association of Thailand = Chotmaihet thangphaet·1992
    Same author

    Restriction fragment polymorphism in the sex-determining region of the Y chromosomal DNA of European wild mice.

    Molecular & general genetics : MGG·1988
    Same author

    Drug-induced liver injury in liver biopsies of the years 1981 and 1983, their prevalence and type of presentation.

    Pathology, research and practice·1985
    Same author

    Quantitative histology of human fetal testes in chromosomal disease.

    Pediatric pathology·1985
    Same author

    Cytogenetics of pregnancy wastage.

    Advances in human genetics·1985
    Same journal

    Statement of the Public Affairs Committee of the Teratology Society on the fetal alcohol syndrome.

    Teratology·2002
    Same journal

    Quantification and localization of expression of the retinoic acid receptor-beta and -gamma mRNA isoforms during neurulation in mouse embryos with or without spina bifida.

    Teratology·2002
    Same journal

    Timing of prenatal care initiation and risk of congenital malformations.

    Teratology·2002
    Same journal

    A new rapid radiological procedure for routine teratological use in bone ossification assessment: a supplement for staining methods.

    Teratology·2002
    Same journal

    Dose and litter allocations in the design of teratological studies for detecting hormesis.

    Teratology·2002
    Same journal

    Effect of sera from women with systemic lupus erythematosus or antiphospholipid syndrome and recurrent abortions on human placental explants in culture.

    Teratology·2002
    See all related articles

    Area of Science:

    • Developmental Biology
    • Genetics
    • Teratology

    Background:

    • Trisomy 13 (Ts 13) is a chromosomal abnormality.
    • Understanding its impact on fetal development is crucial.

    Purpose of the Study:

    • Investigate fetal development in mice with trisomy 13.
    • Identify key developmental abnormalities and their potential causes.

    Main Methods:

    • Produced Ts 13 mouse fetuses using Robertsonian translocation.
    • Monitored fetal development from day 12 to 19 of gestation.
    • Analyzed fetal size, weight, ossification, and malformations.

    Main Results:

    • Ts 13 fetuses exhibited significant growth retardation and hypoplasia.

    Related Experiment Videos

  • A 1-1.5 day delay in general development and ossification was observed.
  • 86% of Ts 13 fetuses presented with cleft palate; edema was also noted.
  • Conclusions:

    • Ts 13 leads to severe fetal growth retardation and developmental delays.
    • Impaired trisomic cell proliferation may underlie hypoplasia and malformations.
    • This cellular mechanism could also impact placental development.