Characterization of SH2D1A missense mutations identified in X-linked lymphoproliferative disease patients. [electronic resource]
Producer: 20011101Description: 36809-16 p. digitalISSN:- 0021-9258
- Amino Acid Sequence
- Amino Acids -- chemistry
- Animals
- Blotting, Western
- COS Cells
- Carrier Proteins -- chemistry
- Cloning, Molecular
- Dose-Response Relationship, Drug
- Humans
- Intracellular Signaling Peptides and Proteins
- Jurkat Cells
- Lymphoproliferative Disorders -- genetics
- Models, Molecular
- Molecular Sequence Data
- Mutation
- Mutation, Missense
- Phenotype
- Phosphorylation
- Plasmids -- metabolism
- Precipitin Tests
- Protein Binding
- Protein Structure, Tertiary
- Signal Transduction
- Signaling Lymphocytic Activation Molecule Associated Protein
- Transfection
- src Homology Domains
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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