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    Adeno-associated Virus

    Adeno-associated virus (AAV) are small viruses from the parvovirus family, with a genome of single-stranded DNA. They are vectors that are most frequently used viral vectors for gene therapy. They mostly infect humans, but can also infect other members of the primate family.

    Trending News

    • AUG 24, 2020
      Genetics & Genomics
      Towards a Cure for Latent Herpes 1 Infections
      Towards a Cure for Latent Herpes 1 Infections
      Herpes simplex virus 1 (HSV-1) causes what's popularly known as cold sores, and is transmitted mostly through oral-t ...
      Written By: Carmen Leitch
      1
      JUL 20, 2020
      Genetics & Genomics
      A Tiny But Efficient Cas Protein is Discovered in a Bacteriophage
      A Tiny But Efficient Cas Protein is Discovered in a Bacteriophage
      The microbes of the world are locked in a struggle for survival and a battle for resources. They compete directly in dif ...
      Written By: Carmen Leitch
      1
      JUL 05, 2020
      Genetics & Genomics
      Two Deaths Occur During Gene Therapy Trial
      Two Deaths Occur During Gene Therapy Trial
      There is great promise, as well as serious risks in gene therapy. Many diseases can be traced back to an error or mutati ...
      Written By: Carmen Leitch
      1
      APR 20, 2020
      Genetics & Genomics
      Advances in Gene Therapy for Neurons
      Advances in Gene Therapy for Neurons
      New research may aid in the development of gene therapies for diseases like Alzheimer's and Parkinson's.
      Written By: Carmen Leitch
      1
      MAR 01, 2020
      Genetics & Genomics
      Treating Huntington's Disease With a Gene Therapy That Targets Brain Cells
      Treating Huntington's Disease With a Gene Therapy That Targets Brain Cells
      A new therapeutic approach for Huntington's disease may aid patients with other neurodegenerative disorders.
      Written By: Carmen Leitch
      1
      DEC 01, 2019
      Genetics & Genomics
      Engineering a Better Viral Delivery System for Gene Therapy
      Engineering a Better Viral Delivery System for Gene Therapy
      To send gene therapy to diseased cells, scientists have turned to adeno-associated viruses (AAVs) to act as a delivery s ...
      Written By: Carmen Leitch
      1
      OCT 03, 2019
      Genetics & Genomics
      A More Precise Version of CRISPR/Cas9 is Created
      A More Precise Version of CRISPR/Cas9 is Created
      A more accurate version of Cas9 has been created, reducing the number of off-target effects. It may be better suited for ...
      Written By: Carmen Leitch
      1
      AUG 25, 2018
      Genetics & Genomics
      Gene Therapy for Eye Disease is Getting Closer to the Clinic
      Gene Therapy for Eye Disease is Getting Closer to the Clinic
      About one of every 3,500 Americans suffers from a degenerative eye disease called retinitis pigmentosa
      Written By: Carmen Leitch
      1
      JUL 10, 2018
      Genetics & Genomics
      Reducing Cholesterol with Gene Editing
      Reducing Cholesterol with Gene Editing
      Patients with a severe kind of heart disease can't always take a drug that keep their cholesterol in check.
      Written By: Carmen Leitch
      2
      JUL 06, 2018
      Genetics & Genomics
      Progress in the Development of Gene Therapy for Diseased Kidneys
      Progress in the Development of Gene Therapy for Diseased Kidneys
      After early setbacks, genetic therapeutics are being developed again.
      Written By: Carmen Leitch
      1
      JAN 09, 2018
      Drug Discovery & Development
      Viruses could inspire nano drug-delivery device
      Viruses could inspire nano drug-delivery device
      Researchers have discovered a path toward virus-like, nanoscale devices that may be able to deliver drugs to cells by ch ...
      Written By: The Scripps Research Institute (TSRI)
      3
      DEC 10, 2017
      Drug Discovery & Development
      First Adeno-Associated Virus Gene Therapy to be FDA Approved for Rare Retinal Disease
      First Adeno-Associated Virus Gene Therapy to be FDA Approved for Rare Retinal Disease
      AAV viral vector gene delivery will soon be approved for FDA approval, and will likely just be the first of many proving ...
      Written By: Courtney Schaal
      2
      OCT 24, 2017
      Cell & Molecular Biology
      Editing Genes in the Brain with CRISPR/Cas9
      Editing Genes in the Brain with CRISPR/Cas9
      Relatively recent advancements in gene editing tools have completely revolutionized biomedical science, and now that tec ...
      Written By: Carmen Leitch
      2
      JAN 30, 2017
      Genetics & Genomics
      Gene Therapy Restores Partial Hearing and Balance
      Gene Therapy Restores Partial Hearing and Balance
      Our hearing ability depends on small sensory hair cells in the inner ear. These microscopic hair cells sense sound vibra ...
      Written By: Jennifer Ellis
      2
      APR 29, 2016
      Health & Medicine
      Gene Therapy For Treating Pulmonary Hypertension
      Gene Therapy For Treating Pulmonary Hypertension
      Whether spontaneous or due to genetic predisposition, occurrence of pulmonary hypertension is very detrimental to heart ...
      Written By: Kara Marker
      1
      JAN 22, 2016
      Cardiology
      Gene Therapy Successful in Treating Factor VII Deficiency
      Gene Therapy Successful in Treating Factor VII Deficiency
      Dogs and humans alike can suffer from a rare bleeding disorder called factor VII deficiency, where lacking a vital coagu ...
      Written By: Kara Marker
      2
      JAN 03, 2016
      Health & Medicine
      Gene Editing Stops Progression of Duchenne Muscular Dystrophy
      Gene Editing Stops Progression of Duchenne Muscular Dystrophy
      .body_content a{color: #175CA9;} .body_content a:hover{color: #1A4E75;text-decoration: underline;} .body_content{text-al ...
      Written By: Julianne Chiaet
      4
      AUG 29, 2015
      Cancer
      Virus Causes Liver Cancer
      Virus Causes Liver Cancer
      Viruses can be involved in the development of serious diseases. A case in point is liver cancer, which often develops in ...
      Written By: Ilene Schneider
      2 1
      APR 02, 2015
      Genetics & Genomics
      Team Identifies Efficient New Cas9 for In Vivo Genome Editing
      Team Identifies Efficient New Cas9 for In Vivo Genome Editing
      A collaborative study between researchers from the Broad Institute of MIT and Harvard, Massachusetts Institute of Techno ...
      Written By: Ilene Schneider
      6
    AUG 24, 2020
    Genetics & Genomics
    Towards a Cure for Latent Herpes 1 Infections
    Towards a Cure for Latent Herpes 1 Infections
    Herpes simplex virus 1 (HSV-1) causes what's popularly known as cold sores, and is transmitted mostly through oral-t ...
    Written By: Carmen Leitch
    1
    JUL 20, 2020
    Genetics & Genomics
    A Tiny But Efficient Cas Protein is Discovered in a Bacteriophage
    A Tiny But Efficient Cas Protein is Discovered in a Bacteriophage
    The microbes of the world are locked in a struggle for survival and a battle for resources. They compete directly in dif ...
    Written By: Carmen Leitch
    1
    JUL 05, 2020
    Genetics & Genomics
    Two Deaths Occur During Gene Therapy Trial
    Two Deaths Occur During Gene Therapy Trial
    There is great promise, as well as serious risks in gene therapy. Many diseases can be traced back to an error or mutati ...
    Written By: Carmen Leitch
    1
    APR 20, 2020
    Genetics & Genomics
    Advances in Gene Therapy for Neurons
    Advances in Gene Therapy for Neurons
    New research may aid in the development of gene therapies for diseases like Alzheimer's and Parkinson's.
    Written By: Carmen Leitch
    1
    MAR 01, 2020
    Genetics & Genomics
    Treating Huntington's Disease With a Gene Therapy That Targets Brain Cells
    Treating Huntington's Disease With a Gene Therapy That Targets Brain Cells
    A new therapeutic approach for Huntington's disease may aid patients with other neurodegenerative disorders.
    Written By: Carmen Leitch
    1
     
     
  • DEC 01, 2019
    Genetics & Genomics
    Engineering a Better Viral Delivery System for Gene Therapy
    Engineering a Better Viral Delivery System for Gene Therapy
    To send gene therapy to diseased cells, scientists have turned to adeno-associated viruses (AAVs) to act as a delivery s ...
    Written By: Carmen Leitch
    1
    OCT 03, 2019
    Genetics & Genomics
    A More Precise Version of CRISPR/Cas9 is Created
    A More Precise Version of CRISPR/Cas9 is Created
    A more accurate version of Cas9 has been created, reducing the number of off-target effects. It may be better suited for ...
    Written By: Carmen Leitch
    1
    AUG 25, 2018
    Genetics & Genomics
    Gene Therapy for Eye Disease is Getting Closer to the Clinic
    Gene Therapy for Eye Disease is Getting Closer to the Clinic
    About one of every 3,500 Americans suffers from a degenerative eye disease called retinitis pigmentosa
    Written By: Carmen Leitch
    1
    JUL 10, 2018
    Genetics & Genomics
    Reducing Cholesterol with Gene Editing
    Reducing Cholesterol with Gene Editing
    Patients with a severe kind of heart disease can't always take a drug that keep their cholesterol in check.
    Written By: Carmen Leitch
    2
    JUL 06, 2018
    Genetics & Genomics
    Progress in the Development of Gene Therapy for Diseased Kidneys
    Progress in the Development of Gene Therapy for Diseased Kidneys
    After early setbacks, genetic therapeutics are being developed again.
    Written By: Carmen Leitch
    1
     
     
  • JAN 09, 2018
    Drug Discovery & Development
    Viruses could inspire nano drug-delivery device
    Viruses could inspire nano drug-delivery device
    Researchers have discovered a path toward virus-like, nanoscale devices that may be able to deliver drugs to cells by ch ...
    Written By: The Scripps Research Institute (TSRI)
    3
    DEC 10, 2017
    Drug Discovery & Development
    First Adeno-Associated Virus Gene Therapy to be FDA Approved for Rare Retinal Disease
    First Adeno-Associated Virus Gene Therapy to be FDA Approved for Rare Retinal Disease
    AAV viral vector gene delivery will soon be approved for FDA approval, and will likely just be the first of many proving ...
    Written By: Courtney Schaal
    2
    OCT 24, 2017
    Cell & Molecular Biology
    Editing Genes in the Brain with CRISPR/Cas9
    Editing Genes in the Brain with CRISPR/Cas9
    Relatively recent advancements in gene editing tools have completely revolutionized biomedical science, and now that tec ...
    Written By: Carmen Leitch
    2
    JAN 30, 2017
    Genetics & Genomics
    Gene Therapy Restores Partial Hearing and Balance
    Gene Therapy Restores Partial Hearing and Balance
    Our hearing ability depends on small sensory hair cells in the inner ear. These microscopic hair cells sense sound vibra ...
    Written By: Jennifer Ellis
    2
    APR 29, 2016
    Health & Medicine
    Gene Therapy For Treating Pulmonary Hypertension
    Gene Therapy For Treating Pulmonary Hypertension
    Whether spontaneous or due to genetic predisposition, occurrence of pulmonary hypertension is very detrimental to heart ...
    Written By: Kara Marker
    1
     
     
  • JAN 22, 2016
    Cardiology
    Gene Therapy Successful in Treating Factor VII Deficiency
    Gene Therapy Successful in Treating Factor VII Deficiency
    Dogs and humans alike can suffer from a rare bleeding disorder called factor VII deficiency, where lacking a vital coagu ...
    Written By: Kara Marker
    2
    JAN 03, 2016
    Health & Medicine
    Gene Editing Stops Progression of Duchenne Muscular Dystrophy
    Gene Editing Stops Progression of Duchenne Muscular Dystrophy
    .body_content a{color: #175CA9;} .body_content a:hover{color: #1A4E75;text-decoration: underline;} .body_content{text-al ...
    Written By: Julianne Chiaet
    4
    AUG 29, 2015
    Cancer
    Virus Causes Liver Cancer
    Virus Causes Liver Cancer
    Viruses can be involved in the development of serious diseases. A case in point is liver cancer, which often develops in ...
    Written By: Ilene Schneider
    2 1
    APR 02, 2015
    Genetics & Genomics
    Team Identifies Efficient New Cas9 for In Vivo Genome Editing
    Team Identifies Efficient New Cas9 for In Vivo Genome Editing
    A collaborative study between researchers from the Broad Institute of MIT and Harvard, Massachusetts Institute of Techno ...
    Written By: Ilene Schneider
    6
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