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 Concept Videos

Trichomoniasis01:18

Trichomoniasis

Trichomonas vaginalis is a flagellated protozoan parasite and the causative agent of trichomoniasis, one of the most prevalent non-viral sexually transmitted infections in the United States. This extracellular parasite primarily colonizes the lower genitourinary tract in women—particularly the vagina—and in men, the urethra and prostate. Its structural and functional adaptations enable its survival, motility, and pathogenicity within the host environment.Structural Features and Host EntryT.
X-Inactivation01:58

X-Inactivation

The human X chromosome contains over ten times the number of genes as in the Y chromosome. Since males have only one X chromosome, and females have two, one might expect females to produce twice as many of the proteins, with undesirable results.
Meiosis I01:49

Meiosis I

Meiosis is a carefully orchestrated set of cell divisions, the goal of which—in humans—is to produce haploid sperm or eggs, each containing half the number of chromosomes present in somatic cells elsewhere in the body. Meiosis I is the first such division, and involves several key steps, among them: condensation of replicated chromosomes in diploid cells; the pairing of homologous chromosomes and their exchange of information; and finally, the separation of homologous chromosomes by a...
Nondisjunction01:21

Nondisjunction

Nondisjunction is the failure of homologous chromosomes or sister chromatids to separate correctly and move to the opposite poles of the cells. This produces daughter cells with abnormal chromosome numbers.  Nondisjunction is common during anaphase I or anaphase II of meiosis.  Mutations in synaptonemal complex proteins that attach homologous chromosomes increase the chances of nondisjunction in anaphase I of meiosis I. In contrast, mutations in topoisomerases and condensins that hold sister...

You might also read

Related Articles

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

Sort by
Same author

Impact of donor mare and stallion identity on the likelihood of pregnancy after transfer of in vitro produced embryos.

Equine veterinary journal·2026
Same author

From reviews to real-time: dynamic evidence in dentistry.

Evidence-based dentistry·2026
Same author

Morphospace engineering: Morphological computation in scaffold design.

Bio Systems·2025
Same author

Threshold of understanding: disease as the interface of lifeworld and science.

Medicine, health care, and philosophy·2025
Same author

Seeing to learn and learning to see: histology teaching between new technologies, old paradigms and natural cyborgs.

Advances in health sciences education : theory and practice·2025
Same author

Marked blastomere herniation is the only post-thaw morphological characteristic associated with a reduced pregnancy rate for in vitro produced equine blastocysts.

Theriogenology·2025

Related Experiment Video

Updated: Jun 10, 2026

Analysis of Chromosome Segregation, Histone Acetylation, and Spindle Morphology in Horse Oocytes
12:11

Analysis of Chromosome Segregation, Histone Acetylation, and Spindle Morphology in Horse Oocytes

Published on: May 11, 2017

X trisomy in a sterile mare.

L de Lorenzi1, L Molteni, M Zannotti

  • 1Department of Animal Science, Milan University, Italy.

Equine Veterinary Journal
|July 20, 2010
PubMed
Summary
This summary is machine-generated.

This study analyzed a sterile mare using cytogenetic techniques, revealing a rare XXX condition. This finding suggests that X trisomy in horses can cause infertility without obvious physical traits.

More Related Videos

Monitoring Blood Glucose in Mouse Offspring After Intracytoplasmic Sperm Injection
06:11

Monitoring Blood Glucose in Mouse Offspring After Intracytoplasmic Sperm Injection

Published on: May 17, 2024

Embryo Transfer Surgery via Laparotomy in Gilts
05:41

Embryo Transfer Surgery via Laparotomy in Gilts

Published on: October 18, 2024

Related Experiment Videos

Last Updated: Jun 10, 2026

Analysis of Chromosome Segregation, Histone Acetylation, and Spindle Morphology in Horse Oocytes
12:11

Analysis of Chromosome Segregation, Histone Acetylation, and Spindle Morphology in Horse Oocytes

Published on: May 11, 2017

Monitoring Blood Glucose in Mouse Offspring After Intracytoplasmic Sperm Injection
06:11

Monitoring Blood Glucose in Mouse Offspring After Intracytoplasmic Sperm Injection

Published on: May 17, 2024

Embryo Transfer Surgery via Laparotomy in Gilts
05:41

Embryo Transfer Surgery via Laparotomy in Gilts

Published on: October 18, 2024

Area of Science:

  • Animal genetics
  • Reproductive biology
  • Cytogenetics

Background:

  • Infertility in mares can have various causes, including genetic factors.
  • Cytogenetic abnormalities, though rare, are potential contributors to reproductive failure in horses.
  • Understanding the genetic basis of infertility is crucial for equine breeding programs.

Purpose of the Study:

  • To investigate the cytogenetic profile of a reproductively unsuccessful mare.
  • To determine if chromosomal abnormalities are associated with infertility in this specific case.
  • To contribute to the understanding of genetic causes of equine infertility.

Main Methods:

  • The study employed C-banding and fluorescence in situ hybridisation (FISH) for detailed chromosomal analysis.
  • These techniques allowed for precise identification of chromosomal number and structure.
  • The mare's cells were analyzed to detect any signs of mosaicism.

Main Results:

  • The sterile mare was found to have a 2n = 65, XXX chromosomal condition.
  • No evidence of chromosomal mosaicism was detected in the analyzed cells.
  • The identified XXX condition represents a rare occurrence in the horse population.

Conclusions:

  • The XXX condition, or X trisomy, is implicated as a cause of infertility in mares.
  • This chromosomal abnormality does not appear to be linked to other discernible phenotypic characteristics.
  • The findings support the hypothesis that X trisomy is a significant factor in equine infertility.