Disruption of snRNP biogenesis factors Tgs1 and pICln induces phenotypes that mirror aspects of SMN-Gemins complex perturbation in Drosophila, providing new insights into spinal muscular atrophy.
about
Spinal Muscular Atrophy: From Defective Chaperoning of snRNP Assembly to Neuromuscular Dysfunction.Linking amyotrophic lateral sclerosis and spinal muscular atrophy through RNA-transcriptome homeostasis: a genomics perspective.Diverse role of survival motor neuron protein.Novel interactors of the Drosophila Survival Motor Neuron (SMN) Complex suggest its full conservation.Genetic screen identifies a requirement for SMN in mRNA localisation within the Drosophila oocyte.
P2860
Disruption of snRNP biogenesis factors Tgs1 and pICln induces phenotypes that mirror aspects of SMN-Gemins complex perturbation in Drosophila, providing new insights into spinal muscular atrophy.
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2016 nî lūn-bûn
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2016年の論文
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2016年学术文章
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2016年学术文章
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2016年学术文章
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2016年学术文章
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2016年学术文章
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2016年学术文章
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2016年學術文章
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2016年學術文章
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name
Disruption of snRNP biogenesis ...... into spinal muscular atrophy.
@en
Disruption of snRNP biogenesis ...... into spinal muscular atrophy.
@nl
type
label
Disruption of snRNP biogenesis ...... into spinal muscular atrophy.
@en
Disruption of snRNP biogenesis ...... into spinal muscular atrophy.
@nl
prefLabel
Disruption of snRNP biogenesis ...... into spinal muscular atrophy.
@en
Disruption of snRNP biogenesis ...... into spinal muscular atrophy.
@nl
P2093
P1476
Disruption of snRNP biogenesis ...... into spinal muscular atrophy.
@en
P2093
Benji Fenech Salerno
Neville Vassallo
Rebecca M Borg
Rémy Bordonne
P304
P356
10.1016/J.NBD.2016.06.015
P577
2016-07-04T00:00:00Z