Umbilical vein and placental vessels from newborns with hereditary haemorrhagic telangiectasia type 1 genotype are normal despite reduced expression of endoglin.

Chan, N L M; Bourdeau, A; Vera, S; Abdalla, S; Gross, M; Wong, J; Cymerman, U; Paterson, A D; Mullen, B; Letarte, M

Chan, N L M; Bourdeau, A; Vera, S; Abdalla, S; Gross, M; Wong, J; Cymerman, U; Paterson, A D; Mullen, B; Letarte, M.

Affiliation

Chan NL; Cancer Research Program, The Hospital for Sick Children, 555 University Avenue, Toronto M5G 1X8, Canada.

Placenta ; 25(2-3): 208-17, 2004.

Article in En | MEDLINE | ID: mdl-14972453

Subject(s)

Endothelium, Vascular/metabolism; Hyperbilirubinemia, Hereditary/metabolism; Placenta/blood supply; Umbilical Veins/metabolism; Vascular Cell Adhesion Molecule-1/metabolism; Antigens, CD; Cells, Cultured; DNA Mutational Analysis; Endoglin; Endothelium, Vascular/cytology; Humans; Hyperbilirubinemia, Hereditary/genetics; Hyperbilirubinemia, Hereditary/pathology; Image Processing, Computer-Assisted; Infant, Newborn; Mutation; Platelet Endothelial Cell Adhesion Molecule-1/metabolism; Receptors, Cell Surface; Umbilical Veins/cytology; Vascular Cell Adhesion Molecule-1/genetics

Search on Google

Add to My VHL

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Placenta / Umbilical Veins / Endothelium, Vascular / Vascular Cell Adhesion Molecule-1 / Hyperbilirubinemia, Hereditary Limits: Humans / Newborn Language: En Journal: Placenta Year: 2004 Document type: Article Affiliation country: Canada Country of publication: Netherlands

Search on Google

Add to My VHL

XML

PubMed Links