Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2. [electronic resource]
Producer: 19970203Description: 1181-90 p. digitalISSN:- 0092-8674
- Amino Acid Sequence
- Chromosome Mapping
- Chromosomes, Human, Pair 9
- Endothelium, Vascular -- physiology
- Enzyme Activation
- Female
- Haplotypes
- Humans
- Ligands
- Male
- Molecular Sequence Data
- Muscle, Smooth, Vascular -- physiology
- Neovascularization, Pathologic -- genetics
- Pedigree
- Phosphorylation
- Point Mutation
- Polymorphism, Genetic
- Protein-Tyrosine Kinases -- physiology
- Proteins -- physiology
- Receptor, TIE-2
- Recombinant Proteins
- Sequence Alignment
- Signal Transduction
- Veins -- abnormalities
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.
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