Related Experiment Video

Updated: Oct 22, 2025

In Vivo Modeling of the Morbid Human Genome using Danio rerio
12:31

In Vivo Modeling of the Morbid Human Genome using Danio rerio

Published on: August 24, 2013

20.9K

Correction: Molecular basis for a new bovine model of Niemann-Pick type C disease

Shernae A Woolley, Emily R Tsimnadis, Cor Lenghaus

    Plos One
    |August 31, 2021
    PubMed

    Abstract:

    [This corrects the article DOI: 10.1371/journal.pone.0238697.].

    More Related Videos

    Modeling Charcot-Marie-Tooth Disease In Vitro by Transfecting Mouse Primary Motoneurons
    07:43

    Modeling Charcot-Marie-Tooth Disease In Vitro by Transfecting Mouse Primary Motoneurons

    Published on: January 7, 2019

    7.1K
    An In Vitro Model for the Study of Cellular Pathophysiology in Globoid Cell Leukodystrophy
    07:45

    An In Vitro Model for the Study of Cellular Pathophysiology in Globoid Cell Leukodystrophy

    Published on: October 21, 2014

    8.1K

    Related Experiment Videos

    Last Updated: Oct 22, 2025

    In Vivo Modeling of the Morbid Human Genome using Danio rerio
    12:31

    In Vivo Modeling of the Morbid Human Genome using Danio rerio

    Published on: August 24, 2013

    20.9K
    Modeling Charcot-Marie-Tooth Disease In Vitro by Transfecting Mouse Primary Motoneurons
    07:43

    Modeling Charcot-Marie-Tooth Disease In Vitro by Transfecting Mouse Primary Motoneurons

    Published on: January 7, 2019

    7.1K
    An In Vitro Model for the Study of Cellular Pathophysiology in Globoid Cell Leukodystrophy
    07:45

    An In Vitro Model for the Study of Cellular Pathophysiology in Globoid Cell Leukodystrophy

    Published on: October 21, 2014

    8.1K

    Related Concept Videos

    Cystic Fibrosis: Pathogenesis01:23

    Cystic Fibrosis: Pathogenesis

    434
    Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
    CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
    434

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

    Mice with the mono-allelic p.R37H Dhdds variant show aberrant glycosylation and interneuron deficits.

    Brain : a journal of neurology·2026

    A novel pipeline for the validation of manganese chelators for the treatment of manganese overload.

    Biochemical pharmacology·2026

    The Animal Variant Classification Guidelines v2: An Update With New Criteria and Improved Clarifications.

    Animal genetics·2026

    A Contemporary Pathomechanistic Nosology of Inherited Lysosomal Disorders.

    Journal of inherited metabolic disease·2026

    Prediction, pain, and the power of context: toward a contemporary identity for the chiropractic profession.

    Chiropractic & manual therapies·2026

    Morphometric Brain Changes in a Merino Sheep (Ovis aries) CLN6 Neuronal Ceroid Lipofuscinosis Model.

    Biology·2026
    See all related articles
    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
    Jove
    Visualize
    Contact Us