Dissociation of disease onset, progression and sex differences from androgen receptor levels in a mouse model of amyotrophic lateral sclerosis
Abstract Amyotrophic lateral sclerosis (ALS) is an adult-onset neurodegenerative disorder caused by loss of motor neurons. ALS incidence is skewed towards males with typically earlier age of onset and limb site of onset. The androgen receptor (AR) is the major mediator of androgen effects in the bod...
Guardado en:
Autores principales: | Doris Tomas, Victoria M. McLeod, Mathew D. F. Chiam, Nayomi Wanniarachchillage, Wah C. Boon, Bradley J. Turner |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/d568045e10774a8ab9a42419d98dbd32 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Amyotrophic lateral sclerosis and frontotemporal degeneration
Publicado: (2000) -
The cortical signature of amyotrophic lateral sclerosis.
por: Federica Agosta, et al.
Publicado: (2012) -
Abnormal RNA stability in amyotrophic lateral sclerosis
por: E. M. Tank, et al.
Publicado: (2018) -
Current and emerging treatments for amyotrophic lateral sclerosis
por: Stefano Zoccolella, et al.
Publicado: (2009) -
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia
por: Russell L. McLaughlin, et al.
Publicado: (2017)