Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration.

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...

Disgrifiad llawn

Manylion Llyfryddiaeth
Prif Awduron:	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
Fformat:	Journal article
Iaith:	English
Cyhoeddwyd:	2009

Eitemau Tebyg

Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration
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hElp3 directly modulates the expression of HSP70 gene in HeLa cells via HAT activity.
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The European language portfolio (ELP) in Slovenian primary education: the teachers’ perspective
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Elp1 is required for development of visceral sensory peripheral and central circuitry
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Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner
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Comparative studies of genome-wide maps of nucleosomes between deletion mutants of elp3 and hos2 genes of Saccharomyces cerevisiae.
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