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Details on Person Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita
| Class:Id | LiteratureReference:418255 |
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| _displayName | Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita |
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| _timestamp | 2009-04-17 20:42:49 |
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| author | [Person:418245] Vulliamy, T
[Person:418243] Beswick, R
[Person:418248] Kirwan, M
[Person:418251] Marrone, A
[Person:418238] Digweed, M
[Person:418252] Walne, A
[Person:418247] Dokal, I |
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| created | [InstanceEdit:418250] D'Eustachio, P, 2009-04-17 20:42:30 |
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| journal | Proc Natl Acad Sci U S A |
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| modified | [InstanceEdit:418257] D'Eustachio, P, 2009-04-17 20:42:47 |
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| pages | 8073-8 |
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| pubMedIdentifier | 18523010 |
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| title | Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita |
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| volume | 105 |
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| year | 2008 |
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| (literatureReference) | [Reaction:164616] Biogenesis and assembly of the telomerase RNP [Homo sapiens]
[Pathway:417076] Assembly of telomerase and telomere extension [Gallus gallus]
[Reaction:417114] Assembly of telomerase RNP [Gallus gallus]
[RegulationReference:9642970] Positive regulation by 'NHP2 [nucleoplasm]' Human H/ACA small nucleolar RNPs and telomerase share evolutionarily conserved proteins NHP2 and NOP10 |
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