Cargando…
Animal models of β-hemoglobinopathies: utility and limitations
The structural and functional conservation of hemoglobin throughout mammals has made the laboratory mouse an exceptionally useful organism in which to study both the protein and the individual globin genes. Early researchers looked to the globin genes as an excellent model in which to examine gene r...
Autores principales: | McColl, Bradley, Vadolas, Jim |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5104300/ https://www.ncbi.nlm.nih.gov/pubmed/27853395 http://dx.doi.org/10.2147/JBM.S87955 |
Ejemplares similares
-
The therapeutic potential of genome editing for β-thalassemia
por: Glaser, Astrid, et al.
Publicado: (2015) -
GFP to BFP Conversion: A Versatile Assay for the Quantification of CRISPR/Cas9-mediated Genome Editing
por: Glaser, Astrid, et al.
Publicado: (2016) -
Prenatal Diagnosis of β-Thalassemias and Hemoglobinopathies.
por: Rosatelli, Maria Cristina, et al.
Publicado: (2009) -
Genome Editing for β-Hemoglobinopathies: Advances and Challenges
por: Frati, Giacomo, et al.
Publicado: (2021) -
Genomic approaches to identifying targets for treating β hemoglobinopathies
por: Ngo, Duyen A., et al.
Publicado: (2015)