The loss of the snoRNP chaperone Nopp140 from Cajal bodies of patient fibroblasts correlates with the severity of spinal muscular atrophy.
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A systematic RNAi synthetic interaction screen reveals a link between p53 and snoRNP assembly.The role of nuclear bodies in gene expression and disease.Towards an understanding of regulating Cajal body activity by protein modification.Diverse role of survival motor neuron protein.Cajal body surveillance of U snRNA export complex assembly.Small-molecule flunarizine increases SMN protein in nuclear Cajal bodies and motor function in a mouse model of spinal muscular atrophy.
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The loss of the snoRNP chaperone Nopp140 from Cajal bodies of patient fibroblasts correlates with the severity of spinal muscular atrophy.
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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 07 January 2009
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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
The loss of the snoRNP chapero ...... ty of spinal muscular atrophy.
@en
The loss of the snoRNP chapero ...... ty of spinal muscular atrophy.
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type
label
The loss of the snoRNP chapero ...... ty of spinal muscular atrophy.
@en
The loss of the snoRNP chapero ...... ty of spinal muscular atrophy.
@nl
prefLabel
The loss of the snoRNP chapero ...... ty of spinal muscular atrophy.
@en
The loss of the snoRNP chapero ...... ty of spinal muscular atrophy.
@nl
P2093
P2860
P921
P356
P1476
The loss of the snoRNP chapero ...... ty of spinal muscular atrophy.
@en
P2093
Benoît Renvoisé
Louis Viollet
Philippe Burlet
Sabrina Colasse
Suzie Lefebvre
U Thomas Meier
P2860
P304
P356
10.1093/HMG/DDP009
P577
2009-01-07T00:00:00Z