Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy’s disease

This publication has 7 references indexed in Scilit:

• Nonsense-mediated decay approaches the clinic
  Nature Genetics, 2004
• Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedema
  Journal of Medical Genetics, 2003
• Vascular endothelial growth factor receptors in the regulation of angiogenesis and lymphangiogenesis
  Oncogene, 2000
• Congenital Hereditary Lymphedema Caused by a Mutation That Inactivates VEGFR3 Tyrosine Kinase
  American Journal of Human Genetics, 2000
• Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema
  Nature Genetics, 2000
• Characterization of the Extracellular Domain in Vascular Endothelial Growth Factor Receptor‐1 (Flt‐1 Tyrosine Kinase)
  Japanese Journal of Cancer Research, 1997
• Chromosomal localization of FLT4, a novel receptor-type tyrosine kinase gene
  Genomics, 1992