Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration.
Amyotrophic lateral sclerosis (ALS) is a spontaneous, relentlessly progressive motor neuron disease, usually resulting in death from respiratory failure within 3 years. Variation in the genes SOD1 and TARDBP accounts for a small percentage of cases, and other genes have shown association in both can...
Auteurs principaux: | Simpson, C, Lemmens, R, Miskiewicz, K, Broom, W, Hansen, V, van Vught, P, Landers, J, Sapp, P, Van Den Bosch, L, Knight, J, Neale, B, Turner, M, Veldink, J, Ophoff, R, Tripathi, V, Beleza, A, Shah, M, Proitsi, P, Van Hoecke, A, Carmeliet, P, Horvitz, H, Leigh, P, Shaw, C, van den Berg, L, Sham, P |
---|---|
Format: | Journal article |
Langue: | English |
Publié: |
2009
|
Documents similaires
-
Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration
par: Horvitz, Howard Robert
Publié: (2011) -
The Arabidopsis Elongator Subunit ELP3 and ELP4 Confer Resistance to Bacterial Speck in Tomato
par: Juliana A. Pereira, et autres
Publié: (2018-07-01) -
The Elongator subunit Elp3 is a non-canonical tRNA acetyltransferase
par: Ting-Yu Lin, et autres
Publié: (2019-02-01) -
The Arabidopsis ELP3/ELO3 and ELP4/ELO1 genes enhance disease resistance in Fragaria vesca L.
par: Katchen Julliany P. Silva, et autres
Publié: (2017-12-01) -
ELP: Tractable Rules for OWL 2.
par: Krötzsch, M, et autres
Publié: (2008)