Identification of the interactors of human nibrin (NBN) and of its 26 kDa and 70 kDa fragments arising from the NBN 657del5 founder mutation. [electronic resource]
Producer: 20160112Description: e114651 p. digitalISSN:- 1932-6203
- Blotting, Western
- Cell Cycle Proteins -- genetics
- Cell Nucleus -- genetics
- DNA Breaks, Double-Stranded
- Electrophoresis, Polyacrylamide Gel
- Fluorescent Antibody Technique
- Gene Regulatory Networks
- HEK293 Cells
- Heterozygote
- Homozygote
- Humans
- Mutation -- genetics
- Nijmegen Breakage Syndrome -- genetics
- Nuclear Proteins -- genetics
- Protein Interaction Domains and Motifs
- Sequence Deletion
- Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
- Tandem Mass Spectrometry
- X-Rays
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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