Related Experiment Video

Updated: Dec 30, 2025

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
08:22

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on: December 1, 2017

8.9K

Corrigendum: Single-nucleotide polymorphism screening and RNA sequencing of key messenger RNAs associated with

    Neural Regeneration Research
    |January 22, 2020
    PubMed

    Abstract:

    [This corrects the article DOI: 10.4103/1673-5374.264469].

    More Related Videos

    Modeling Encephalopathy of Prematurity Using Prenatal Hypoxia-ischemia with Intra-amniotic Lipopolysaccharide in Rats
    07:36

    Modeling Encephalopathy of Prematurity Using Prenatal Hypoxia-ischemia with Intra-amniotic Lipopolysaccharide in Rats

    Published on: November 20, 2015

    11.7K
    Early Pathological and Magnetic Resonance Detection of Cerebral Injury Using a Rat Model of Neonatal Hypoxic Ischemic Encephalopathy
    05:52

    Early Pathological and Magnetic Resonance Detection of Cerebral Injury Using a Rat Model of Neonatal Hypoxic Ischemic Encephalopathy

    Published on: October 28, 2022

    976

    Related Experiment Videos

    Last Updated: Dec 30, 2025

    A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
    08:22

    A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

    Published on: December 1, 2017

    8.9K
    Modeling Encephalopathy of Prematurity Using Prenatal Hypoxia-ischemia with Intra-amniotic Lipopolysaccharide in Rats
    07:36

    Modeling Encephalopathy of Prematurity Using Prenatal Hypoxia-ischemia with Intra-amniotic Lipopolysaccharide in Rats

    Published on: November 20, 2015

    11.7K
    Early Pathological and Magnetic Resonance Detection of Cerebral Injury Using a Rat Model of Neonatal Hypoxic Ischemic Encephalopathy
    05:52

    Early Pathological and Magnetic Resonance Detection of Cerebral Injury Using a Rat Model of Neonatal Hypoxic Ischemic Encephalopathy

    Published on: October 28, 2022

    976

    Related Concept Videos

    RNA-seq03:21

    RNA-seq

    11.6K
    RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
    Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
    11.6K

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

    Cuproptosis-associated retinal degeneration in a mouse model of retinitis pigmentosa and neuroprotection by copper chelation.

    Neural regeneration research·2026

    Multi-target molecular mechanisms underlying the protective effects of cannabidiol against methamphetamine-induced neurotoxicity.

    Neural regeneration research·2026

    Neurodegeneration epicenters: Distinct network mechanisms of dopaminergic treatment in Parkinson's disease.

    Neural regeneration research·2026

    Microglial Ring1 enhances post-phagocytic myelin debris processing: Attenuation of cognitive dysfunction after hemorrhagic shock and reperfusion.

    Neural regeneration research·2026

    Invasive vagus nerve stimulation paired with upper limb motor rehabilitation after intracerebral hemorrhage: A single-arm pilot cohort study.

    Neural regeneration research·2026

    Mechanisms of ubiquitination in central nervous system injury and potential therapeutic targets.

    Neural regeneration research·2026

    A new noninvasive prenatal paternity test based on double nucleotide polymorphisms abates sequencing uncertainties and improves sensitivity.

    Genome research·2026

    Conserved SINE and lineage-variable LINE-1 depletion at neurodevelopmental disorder promoters.

    Mammalian genome : official journal of the International Mammalian Genome Society·2026

    Familial Risk of Biliary Tract Cancers among Offspring and Its Interaction with Gallstones: A Population-Based Cohort Study.

    Cancer research and treatment·2026

    The impact of nationwide folic acid fortification on genetic variants associated with conotruncal heart defects.

    Human genetics·2026

    Generation and Validation of a GnRH-iCreERT2-tdTomato Mouse Line for Genetic Manipulation in GnRH Neurons.

    Genesis (New York, N.Y. : 2000)·2026

    A homozygous variant in the GJB2 gene as a potential phenocopy of Waardenburg syndrome: case report.

    Frontiers in medicine·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