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

Metastasis02:30

Metastasis

Metastasis is the spread of cancer cells from the original site to distant locations in the body. Cancer cells can spread via blood vessels (hematogenous) as well as lymph vessels in the body.
Epithelial-to-Mesenchymal Transition
The epithelial-to-mesenchymal transition or EMT is a developmental process commonly observed in wound healing, embryogenesis, and cancer metastasis. EMT is induced by transforming growth factor-beta (TGF-β) or receptor tyrosine kinase (RTK) ligands, which further...
Smooth Endoplasmic Reticulum01:21

Smooth Endoplasmic Reticulum

Smooth endoplasmic reticulum or smooth ER is a sub-organelle with specialized functions in animal cells and plant cells. It is often associated with the tubule morphology of the endoplasmic reticulum.
The ER provides optimal conditions for synthesizing steroid hormones and lipids, such as phospholipids and triglycerides. Traditionally, lipid metabolism was considered to be a smooth ER function. However, there is no direct evidence to prove that rough ER is completely excluded from lipid...
Inborn Errors of Metabolism01:20

Inborn Errors of Metabolism

Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...
Anorexia Nervosa01:28

Anorexia Nervosa

Anorexia nervosa is a complex and severe eating disorder characterized by an intense fear of weight gain, an unrelenting pursuit of thinness, and a distorted body image. It often leads to dangerously low body weight relative to an individual's age and height. This disorder is marked by significant physical and psychological consequences, making it one of the most life-threatening psychiatric illnesses.
Symptoms and Physical Effects
Individuals with anorexia nervosa commonly exhibit extreme...
Amebiasis01:28

Amebiasis

Entamoeba histolytica, a protozoan parasite, is responsible for intestinal and extraintestinal amebiasis. Though a significant proportion of infections remain asymptomatic, approximately 50 million individuals annually are estimated to present with clinical disease, resulting in up to 100,000 deaths globally. The disease burden is disproportionately high in regions with lower socioeconomic status, such as parts of India, Africa, Mexico, and Latin America.Etiology and TransmissionThe infective...
Alterations in Muscle Tone lll01:11

Alterations in Muscle Tone lll

Rigidity and myotonia are distinct abnormalities of muscle tone that affect resistance and relaxation during movement. Although both involve altered muscle contraction, they arise from different neurological and muscular mechanisms.CharacteristicsRigidity is characterized by uniform resistance to passive movement across the entire range, independent of speed, affecting flexors and extensors equally. It may appear as lead-pipe rigidity (smooth, constant resistance) or cogwheel rigidity...

You might also read

Related Articles

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

Sort by
Same author

Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral series.

Molecular psychiatry·2018
Same author

Cultural factors that affected the spatial and temporal epidemiology of kuru.

Royal Society open science·2017
Same author

Genome-wide association study of behavioural and psychiatric features in human prion disease.

Translational psychiatry·2015
Same author

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease.

Nature genetics·2013
Same author

Multiparameter MR imaging in the 6-OPRI variant of inherited prion disease.

AJNR. American journal of neuroradiology·2013
Same author

PRION-1 scales analysis supports use of functional outcome measures in prion disease.

Neurology·2011

Related Experiment Video

Updated: Jul 9, 2026

Detection of Alternative Splicing During Epithelial-Mesenchymal Transition
11:48

Detection of Alternative Splicing During Epithelial-Mesenchymal Transition

Published on: October 9, 2014

Variant Creutzfeldt-Jakob disease.

J Collinge1

  • 1Department of Neurogenetics, Imperial College School of Medicine at St Mary's, London, UK. J.Collinge@ic.ac.uk

Lancet (London, England)
|August 10, 1999
PubMed
Summary

Bovine spongiform encephalopathy (BSE) prions have caused a new human prion disease, variant Creutzfeldt-Jakob disease (vCJD). Public health risks from potential iatrogenic transmission and unquantified exposure require further investigation.

Area of Science:

  • Neuroscience
  • Epidemiology
  • Infectious Diseases

Background:

  • Bovine spongiform encephalopathy (BSE) has been linked to a novel human prion disease, variant Creutzfeldt-Jakob disease (vCJD).
  • Previous prion disease epidemics suggest exposure during the preclinical phase of the BSE epidemic may have caused early vCJD cases.
  • The long-term evolution of vCJD is anticipated, with potential for widespread future cases.

Purpose of the Study:

  • To analyze the transmission dynamics and public health implications of BSE prions in humans.
  • To highlight the urgent need for diagnostic tools and risk assessment strategies for vCJD.
  • To address concerns regarding potential iatrogenic transmission and interspecies prion transfer.

Main Methods:

  • Review of incubation periods from historical human prion disease epidemics.

More Related Videos

Normal and Malignant Muscle Cell Transplantation into Immune Compromised Adult Zebrafish
09:39

Normal and Malignant Muscle Cell Transplantation into Immune Compromised Adult Zebrafish

Published on: December 26, 2014

Comprehensive Autopsy Program for Individuals with Multiple Sclerosis
09:41

Comprehensive Autopsy Program for Individuals with Multiple Sclerosis

Published on: July 19, 2019

Related Experiment Videos

Last Updated: Jul 9, 2026

Detection of Alternative Splicing During Epithelial-Mesenchymal Transition
11:48

Detection of Alternative Splicing During Epithelial-Mesenchymal Transition

Published on: October 9, 2014

Normal and Malignant Muscle Cell Transplantation into Immune Compromised Adult Zebrafish
09:39

Normal and Malignant Muscle Cell Transplantation into Immune Compromised Adult Zebrafish

Published on: December 26, 2014

Comprehensive Autopsy Program for Individuals with Multiple Sclerosis
09:41

Comprehensive Autopsy Program for Individuals with Multiple Sclerosis

Published on: July 19, 2019

  • Analysis of species transmission barriers.
  • Assessment of potential iatrogenic transmission routes (blood, tissue, surgical instruments).
  • Main Results:

    • Early vCJD cases likely resulted from exposure during the BSE epidemic's preclinical phase.
    • The number of individuals incubating vCJD is unknown, posing a significant public health challenge.
    • Prions' resistance to sterilization raises concerns about surgical instrument contamination.
    • Iatrogenic transmission via blood transfusion and tissue donation is a potential risk.
    • Current diagnostic methods (tonsil biopsy) are limited; a prion-specific blood test is needed.

    Conclusions:

    • The emergence of vCJD from BSE represents a significant public health threat.
    • Further research is critical to quantify transmission risks and develop effective diagnostic and preventative measures.
    • The possibility of BSE prions infecting other species and posing ongoing human health risks remains.