Pathogenesis of proximal autosomal recessive spinal muscular atrophy.
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Spinal muscular atrophyHistone deacetylase inhibitors as potential treatment for spinal muscular atrophyGemin5 Binds to the Survival Motor Neuron mRNA to Regulate SMN ExpressionProlactin increases SMN expression and survival in a mouse model of severe spinal muscular atrophy via the STAT5 pathway.SMN is required for sensory-motor circuit function in Drosophila.Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick?Conserved requirement for DEAD-box RNA helicase Gemin3 in Drosophila oogenesisSpinal Muscular Atrophy Therapeutics: Where do we Stand?p38 Mitogen-activated protein kinase stabilizes SMN mRNA through RNA binding protein HuR.Using General Anesthesia plus Muscle Relaxant in a Patient with Spinal Muscular Atrophy Type IV: A Case Report.Spinal muscular atrophy and a model for survival of motor neuron protein function in axonal ribonucleoprotein complexesVariant U1 snRNAs are implicated in human pluripotent stem cell maintenance and neuromuscular disease.U1A regulates 3' processing of the survival motor neuron mRNA.The Zagreb Collection of human brains: a unique, versatile, but underexploited resource for the neuroscience community.Spliceosomal small nuclear ribonucleoprotein biogenesis defects and motor neuron selectivity in spinal muscular atrophy.Spinal muscular atrophy and the antiapoptotic role of survival of motor neuron (SMN) protein.Genotype-phenotype correlation of survival motor neuron and neuronal apoptosis inhibitory protein genes in spinal muscular atrophy patients from Iran.Chatting with the neighbors: crosstalk between Rho-kinase (ROCK) and other signaling pathways for treatment of neurological disorders.Effects of flavonoid quercetin on survival of motor neuron gene expression.Linking amyotrophic lateral sclerosis and spinal muscular atrophy through RNA-transcriptome homeostasis: a genomics perspective.SMN deficiency disrupts brain development in a mouse model of severe spinal muscular atrophy.Weakness and fatigue in diverse neuromuscular diseases.Gem formation upon constitutive Gemin3 overexpression in Drosophila.
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Pathogenesis of proximal autosomal recessive spinal muscular atrophy.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 16 July 2008
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Pathogenesis of proximal autosomal recessive spinal muscular atrophy.
@en
Pathogenesis of proximal autosomal recessive spinal muscular atrophy.
@nl
type
label
Pathogenesis of proximal autosomal recessive spinal muscular atrophy.
@en
Pathogenesis of proximal autosomal recessive spinal muscular atrophy.
@nl
prefLabel
Pathogenesis of proximal autosomal recessive spinal muscular atrophy.
@en
Pathogenesis of proximal autosomal recessive spinal muscular atrophy.
@nl
P2860
P1476
Pathogenesis of proximal autosomal recessive spinal muscular atrophy.
@en
P2093
Goran Simic
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P2888
P304
P356
10.1007/S00401-008-0411-1
P577
2008-07-16T00:00:00Z