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Survival Motor Neuron Protein

Known as: Component of Gems 1, Gemin-1 
Survival motor neuron protein (294 aa, ~32 kDa) is encoded by the human SMN1 and SMN2 genes. This protein plays a role in the assembly of small… 
National Institutes of Health

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CytoplasmGenes, RegulatorNucleoplasmProline-Rich Domain

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
The essential symbiosis of academic and clinical neurology
If you walk into the office of most paediatric neurologists – even in this time of the internet and Professor Google – it is… 
2017
2017
In the news: Clinical trials excite at AAN 2017
Over 13,000 neurologists from around the globe gathered for the 69th American Academy of Neurology (AAN) Annual Meeting in Boston… 
2014
2014
[Effect of valproic acid on SMN protein level in peripheral blood mononuclear cells of patients with spinal muscular atrophy and different SMN2 copy numbers].
OBJECTIVE Spinal muscular atrophy (SMA) is currently untreatable hereditary disorder caused by few types of mutations in the SMN1… 
2006
2006
SURVIVAL MOTOR NEURON PROTEIN (SMN) DEPLETION IN NEURONAL CELLS BY siRNA INHIBITION: AN IN VITRO MODEL FOR SMA
2003
2003
Erratum: Active transport of the survival motor neuron protein and the role of exon-7 in cytoplasmic localization (Journal of Neuroscience (July 23, 2003)) (6627-6637))
1998
1998
Corrigendum: The domain encoded by exon 2 of the survival motor neuron protein mediates nucleic acid binding (Human Molecular Genetics (1998) 7 (1269-1275))