Cargando…
Introducing an expanded CAG tract into the huntingtin gene causes a wide spectrum of ultrastructural defects in cultured human cells
Modeling of neurodegenerative diseases in vitro holds great promise for biomedical research. Human cell lines harboring a mutations in disease-causing genes are thought to recapitulate early stages of the development an inherited disease. Modern genome-editing tools allow researchers to create isoge...
Autores principales: | Morozova, Ksenia N., Suldina, Lyubov A., Malankhanova, Tuyana B., Grigor’eva, Elena V., Zakian, Suren M., Kiseleva, Elena, Malakhova, Anastasia A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192588/ https://www.ncbi.nlm.nih.gov/pubmed/30332437 http://dx.doi.org/10.1371/journal.pone.0204735 |
Ejemplares similares
-
A Human Induced Pluripotent Stem Cell-Derived Isogenic Model of Huntington’s Disease Based on Neuronal Cells Has Several Relevant Phenotypic Abnormalities
por: Malankhanova, Tuyana, et al.
Publicado: (2020) -
Modern Genome Editing Technologies in Huntington’s Disease Research
por: Malankhanova, Tuyana B., et al.
Publicado: (2017) -
Biochemical Characteristics of iPSC-Derived Dopaminergic Neurons from N370S GBA Variant Carriers with and without Parkinson’s Disease
por: Grigor’eva, Elena V., et al.
Publicado: (2023) -
The Cutting Edge of Disease Modeling: Synergy of Induced Pluripotent Stem Cell Technology and Genetically Encoded Biosensors
por: Valetdinova, Kamila R., et al.
Publicado: (2021) -
The Effect of Dietary Phospholipids on the Ultrastructure and Function of Intestinal Epithelial Cells
por: Saydakova, Snezhanna, et al.
Publicado: (2023)