Video Experimental Relacionado

Updated: Jul 17, 2026

Generation of Human Nasal Epithelial Cell Spheroids for Individualized Cystic Fibrosis Transmembrane Conductance Regulator Study
08:00

Generation of Human Nasal Epithelial Cell Spheroids for Individualized Cystic Fibrosis Transmembrane Conductance Regulator Study

Published on: April 11, 2018

La fibrosis quística. también conocida como fibrosis quística. Un animal modelo bienvenido

F S Collins, J M Wilson

    Nature
    |August 27, 1992
    PubMed
    Resumen

    No abstract available in PubMed .

    Más Videos Relacionados

    Development of a Polymicrobial Colony Biofilm Model to Test Antimicrobials in Cystic Fibrosis
    07:16

    Development of a Polymicrobial Colony Biofilm Model to Test Antimicrobials in Cystic Fibrosis

    Published on: September 20, 2024

    Cystic Fibrosis Aggregate Biofilm Model to Study Infection-relevant Gene Expression
    08:58

    Cystic Fibrosis Aggregate Biofilm Model to Study Infection-relevant Gene Expression

    Published on: April 18, 2025

    Videos de Experimentos Relacionados

    Last Updated: Jul 17, 2026

    Generation of Human Nasal Epithelial Cell Spheroids for Individualized Cystic Fibrosis Transmembrane Conductance Regulator Study
    08:00

    Generation of Human Nasal Epithelial Cell Spheroids for Individualized Cystic Fibrosis Transmembrane Conductance Regulator Study

    Published on: April 11, 2018

    Development of a Polymicrobial Colony Biofilm Model to Test Antimicrobials in Cystic Fibrosis
    07:16

    Development of a Polymicrobial Colony Biofilm Model to Test Antimicrobials in Cystic Fibrosis

    Published on: September 20, 2024

    Cystic Fibrosis Aggregate Biofilm Model to Study Infection-relevant Gene Expression
    08:58

    Cystic Fibrosis Aggregate Biofilm Model to Study Infection-relevant Gene Expression

    Published on: April 18, 2025

    Videos de Conceptos Relacionados

    Cystic Fibrosis: Pathogenesis01:23

    Cystic Fibrosis: Pathogenesis

    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, but...
    Cystic Fibrosis: Management01:24

    Cystic Fibrosis: Management

    Cystic fibrosis (CF) is an autosomal recessive disorder that predominantly affects individuals of Northern European descent, occurring at a rate of 1 in 3500. It is caused by a genetic mutation in a gene on chromosome 7, most commonly the ΔF508 mutation, that codes for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. This results in thicker mucus secretions and obstruction pathologies in multiple organs, including the lungs and sinuses.
    Sinus disease and chronic sinusitis...
    JoVE
    x logofacebook logolinkedin logoyoutube logo
    ACERCA DE JoVE
    Visión GeneralLiderazgoBlogCentro de Ayuda JoVE
    AUTORES
    Proceso de PublicaciónConsejo EditorialAlcance y PolíticasRevisión por ParesPreguntas FrecuentesEnviar
    BIBLIOTECARIOS
    TestimoniosSuscripcionesAccesoRecursosConsejo Asesor de BibliotecasPreguntas Frecuentes
    INVESTIGACIÓN
    JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchivo
    EDUCACIÓN
    JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualCentro de Recursos para ProfesoresSitio de Profesores
    Términos y Condiciones de Uso
    Política de Privacidad
    Políticas
    Jove
    Visualize
    Contáctanos