Molecular analysis of the genetic defect in a large cohort of IP patients and identification of novel NEMO mutations interfering with NF-kappaB activation. [electronic resource]
Producer: 20050225Description: 1763-73 p. digitalISSN:- 0964-6906
- Animals
- Base Sequence
- Blotting, Western
- Carrier Proteins -- genetics
- Cells, Cultured
- Dosage Compensation, Genetic
- Exons -- genetics
- Gene Components
- Genetic Complementation Test
- Humans
- I-kappa B Kinase
- Immunoprecipitation
- Incontinentia Pigmenti -- genetics
- Lipopolysaccharides
- Mice
- Mutagenesis, Site-Directed
- Mutation -- genetics
- NF-kappa B -- metabolism
- Pedigree
- Phenotype
- Plasmids -- genetics
- Signal Transduction -- genetics
- Transfection
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Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
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