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Keyword [Werner syndrome]
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1. Clinical And Basic Studies Of Werner Syndrome With Newly Identified Phenotypes
2. Reserch Of P21 Function Deficiency Effects On Gastric And MEFs Of Werner Syndrome Mouse
3. Molecular Mechanisim Of The Expression Of DNA Replication Key Protein MCM Regulated By P53N236S
4. The Impact Of P21Waf1/Cip1 Or P16Ink4a Dysfunction In The Aging Process Of Werner Syndrome Mice And Its Molecualr Mechanism
5. The Impact Of P21 Dysfunction In The Aging Processof Werner Syndrome Mice And Its Molecualr Mechanism
6. The Molecular Mechanism Of P16INK4a In Regulating The Aging Progress Of Werner Syndrome Mice By Modulating DNA Damage Repair And Mitochondria Biosynthesis
7. The Molecular Mechanism Of P53N236S In Elongating The Life Span Of Werner Syndrome Mice
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