Cargando…
In utero adenine base editing corrects multi-organ pathology in a lethal lysosomal storage disease
In utero base editing has the potential to correct disease-causing mutations before the onset of pathology. Mucopolysaccharidosis type I (MPS-IH, Hurler syndrome) is a lysosomal storage disease (LSD) affecting multiple organs, often leading to early postnatal cardiopulmonary demise. We assessed in u...
Autores principales: | Bose, Sourav K., White, Brandon M., Kashyap, Meghana V., Dave, Apeksha, De Bie, Felix R., Li, Haiying, Singh, Kshitiz, Menon, Pallavi, Wang, Tiankun, Teerdhala, Shiva, Swaminathan, Vishal, Hartman, Heather A., Jayachandran, Sowmya, Chandrasekaran, Prashant, Musunuru, Kiran, Jain, Rajan, Frank, David B., Zoltick, Philip, Peranteau, William H. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8277817/ https://www.ncbi.nlm.nih.gov/pubmed/34257302 http://dx.doi.org/10.1038/s41467-021-24443-8 |
Ejemplares similares
-
In utero CRISPR-mediated therapeutic editing of metabolic genes
por: Rossidis, Avery C., et al.
Publicado: (2018) -
Ionizable lipid nanoparticles for in utero mRNA delivery
por: Riley, Rachel S., et al.
Publicado: (2021) -
In utero hematopoietic cell transplantation: induction of donor specific immune tolerance and postnatal transplants
por: Peranteau, William H.
Publicado: (2014) -
Adenine base editing to treat progeria syndrome and extend the lifespan
por: Musunuru, Kiran
Publicado: (2021) -
In utero pulse injection of isotopic amino acids quantifies protein turnover rates during murine fetal development
por: Baeza, Josue, et al.
Publicado: (2023)