Reduced cell size, chromosomal aberration and altered proliferation rates are characteristics and confounding factors in the STHdh cell model of Huntington disease
Abstract Huntington disease is a fatal neurodegenerative disorder caused by a CAG repeat expansion in the gene encoding the huntingtin protein. Expression of the mutant protein disrupts various intracellular pathways and impairs overall cell function. In particular striatal neurons seem to be most v...
Guardado en:
Autores principales: | Elisabeth Singer, Carolin Walter, Jonasz J. Weber, Ann-Christin Krahl, Ulrike A. Mau-Holzmann, Nadine Rischert, Olaf Riess, Laura E. Clemensson, Huu P. Nguyen |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2017
|
Materias: | |
Acceso en línea: | https://doaj.org/article/baca3f0edb594d1fb92d80a01ad67420 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Reduced motivation in the BACHD rat model of Huntington disease is dependent on the choice of food deprivation strategy.
por: Erik Karl Håkan Jansson, et al.
Publicado: (2014) -
Prophages and Growth Dynamics Confound Experimental Results with Antibiotic-Tolerant Persister Cells
por: Alexander Harms, et al.
Publicado: (2017) -
Non-Cell Autonomous and Epigenetic Mechanisms of Huntington’s Disease
por: Chaebin Kim, et al.
Publicado: (2021) -
Relaxation of Some Confusions about Confounders
por: Ádám Zlatniczki, et al.
Publicado: (2021) -
Heterogeneity Confounds Establishment of “a” Model Microbial Strain
por: Nancy P. Keller
Publicado: (2017)