A Gene for Inherited Cutaneous Venous Anomalies (“Glomangiomas”) Localizes to Chromosome 1p21-22

This publication has 31 references indexed in Scilit:

• Endothelial receptor tyrosine kinases activate the STAT signaling pathway: mutant Tie-2 causing venous malformations signals a distinct STAT activation response
  Oncogene, 1999
• The Tek/Tie2 receptor signals through a novel Dok-related docking protein, Dok-R
  Oncogene, 1998
• Endothelial Tie2/Tek Ligands Angiopoietin-1 (ANGPT1) and Angiopoietin-2 (ANGPT2): Regional Localization of the Human Genes to 8q22.3–q23 and 8p23
  Genomics, 1998
• Mutation of the Stargardt Disease Gene ( ABCR ) in Age-Related Macular Degeneration
  Science, 1997
• Mutations in the activin receptor–like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2
  Nature Genetics, 1996
• Distinct roles of the receptor tyrosine kinases Tie-1 and Tie-2 in blood vessel formation
  Nature, 1995
• Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus
  Cell, 1995
• Assignment of a locus for dominantly inherited venous malformations to chromosome 9p
  Human Molecular Genetics, 1994
• Familial Multiple Glomangiomas
  Annals of Plastic Surgery, 1993
• Multiple glomus tumors. A clinical and electron microscopic study
  Archives of Dermatology, 1971