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Showing: 1 - 20 of 36 results
  1. BeHeard Award 2018: Diseases of Glycosylation, Arginine Mutagenesis, & Neural Development

    Type
    Blog Post
    ...neural development. Paula Videira: Congenital disorders of glycosylation Paula Videira is an Assistant...with the Portuguese Association for Congenital Disorders of Glycosylation (APCDG) and an international ...International Network (CDG&Allies-PPAIN).  Congenital disorders of glycosylation (CDG) are a group of rare inherited...Videira, P. A. Immunological aspects of congenital disorders of glycosylation (CDG): a review. J. Inherit. ...are developed for specific NFI-related genetic disorders, these will also allow better treatment of these...
  2. CRISPR in the Clinic

    Type
    Blog Post
    ...classes of edits in cancer therapy. Blood disorders Two blood disorders are promising CRISPR targets — Sickle...therapeutic potential in mice with a dominant cataract disorder caused by a single copy of a gene known as Crygc...of the targeted treatment strategies for these disorders have involved turning on fetal hemoglobin to compensate...experiencing sustained and substantial relief from both disorders. As of publication, submissions to the UK, EU,...
  3. Supporting Rare Disease Research with the 2020 BeHEARD Awards

    Type
    Blog Post
    ...global developmental delays or autism spectrum disorder. It is estimated that CTD is the second cause ...syndrome Turner syndrome (TS) is a developmental disorder where one of the X chromosomes is partially or...variants identified from 58 individuals with GNB1 disorder since the identification of this disease in 2016... The lab aims to “expand our knowledge of GNB1 disorder by understanding affected signaling pathways and...
  4. Neurodegeneration Research Collection

    Type
    Collection
    ...Resources Neurodegenerative Disorders Neurodegenerative diseases are a group of disorders characterized by the...therapies to prevent, treat, or cure most of these disorders. An integrated study of the overlapping biology...genetics associated with some of the most common disorders followed by a list of some of the relevant collections...disease (HD) is a fatal autosomal dominant genetic disorder that causes the progressive degeneration of nerve...(PD) is a chronic and progressive neurological disorder that primarily affects movement. More than ten...and gRNAs for genes linked to neurodegenerative disorders. Find plasmids expressing HTT, C9ORF72, LRRK2,...treatments for Alzheimer’s disease and related disorders. The site curates information on useful resources...
  5. Rett Syndrome: A History of Research and Therapeutic Outlooks

    Type
    Blog Post
    ... rare, progressive, neurodevelopmental genetic disorder that affects primarily girls. After a period of... Clinical Course of Rett Syndrome and Related Disorders. Cell 152:984–996 . https://doi.org/10.1016/j.... Repair of a Protein Underlying a Neurological Disorder by Programmable RNA Editing. Cell Reports 32:107878...
  6. Zebrafish Plasmid Collection

    Type
    Collection
    ...and infection, regeneration, human neurological disorders, microbiota studies, and drug discovery and development... Gateway-compatible Kit for Neurodegenerative Disorders - Nicholas Cole Lab. A kit consisting of plasmids...transgenic zebrafish for studying neurodegenerative disorders. Fluorescent Protein Fusion Construct Set - Amro...
  7. Lentiviral Vector Uses and Overview

    Type
    Blog Post
    ... diseases, including the common hematopoietic disorders sickle cell anemia and beta-thalassemia. Lentiviral... 23322669. 6. Genetic treatment of a molecular disorder: gene therapy approaches to sickle cell disease...
  8. Treating Muscular Dystrophy with CRISPR Gene Editing

    Type
    Blog Post
    ...muscular dystrophy (DMD), an X-linked recessive disorder affecting approximately 1 in 5000 males. DMD is...defects, including ataxia telangiectasia, congenital disorder of glycosylation, and Niemann-Pick disease type...
  9. Rett Syndrome

    Type
    Collection
    ...and cures for Rett Syndrome and related MECP2 disorders. The RSRT has a comprehensive, strategic and aggressive...Syndrome Rett syndrome is a neurodevelopmental disorder that presents in early toddlerhood primarily affecting... ( MECP2 ). MECP2 Rett syndrome is an X-linked disorder caused from loss-of-function mutations in the ...
  10. Science Communication for Everyone

    Type
    Blog Post
    ...disease related topics. Neurodegenerative and brain disorders are frequently overshadowed by other medical conditions...
Showing: 1 - 20 of 36 results