A novel Werner Syndrome mutation: pharmacological treatment by read-through of nonsense mutations and epigenetic therapies
about
Hallmarks of progeroid syndromes: lessons from mice and reprogrammed cellsMetabolic and Phenotypic Differences between Mice Producing a Werner Syndrome Helicase Mutant Protein and Wrn Null MiceWRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational ProspectsTargeting Nonsense Mutations in Diseases with Translational Read-Through-Inducing Drugs (TRIDs).Human RECQ Helicase Pathogenic Variants, Population Variation and "Missing" Diseases.Aminoglycoside interactions and impacts on the eukaryotic ribosome.Bloom syndrome: research and data priorities for the development of precision medicine as identified by some affected families.
P2860
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P2860
A novel Werner Syndrome mutation: pharmacological treatment by read-through of nonsense mutations and epigenetic therapies
description
2015 nî lūn-bûn
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2015年の論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年论文
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2015年论文
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name
A novel Werner Syndrome mutati ...... tions and epigenetic therapies
@ast
A novel Werner Syndrome mutati ...... tions and epigenetic therapies
@en
type
label
A novel Werner Syndrome mutati ...... tions and epigenetic therapies
@ast
A novel Werner Syndrome mutati ...... tions and epigenetic therapies
@en
prefLabel
A novel Werner Syndrome mutati ...... tions and epigenetic therapies
@ast
A novel Werner Syndrome mutati ...... tions and epigenetic therapies
@en
P2093
P2860
P1433
P1476
A novel Werner Syndrome mutati ...... tions and epigenetic therapies
@en
P2093
Fabian Aldunate
Fernando Setien
Miguel Arocena Sutz
Ricardo Achenbach
Ruben Agrelo
Valeria Da Costa
P2860
P304
P356
10.1080/15592294.2015.1027853
P577
2015-01-01T00:00:00Z