Melanie A. Baldwin

Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1

Kimberly A. McAllister, K.M. Grogg, David W. Johnson et al. · Nature Genetics · 1994 · 1.5K citations · Full text

Endothelial Cell Pathobiology, Vascular Disease, Developmental Biology +10

Mutations in the activin receptor–like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2

David W. Johnson, Jonathan Berg, Melanie A. Baldwin et al. · Nature Genetics · 1996 · 1.1K citations

Activin Receptor–like, Developmental Biology, Signal Transduction +7

Six novel mutations in the endoglin gene in hereditary hemorrhagic telangiectasia type 1 suggest a dominant-negative effect of receptor function

Kimberly A. McAllister, Melanie A. Baldwin, Arun K. Thukkani et al. · Human Molecular Genetics · 1995 · 110 citations

Endoglin Gene, Genetics, Pathology +20

Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null alleles

Carol J. Gallione, Daniel J. Klaus, Eric Y. Yeh et al. · Human Mutation · 1998 · 100 citations

Expression Analysis, Hht Kindreds, Mendelian Disorder +12

Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null alleles

Carol J. Gallione, Daniel J. Klaus, Eric Y. Yeh et al. · Human Mutation · 1998 · 12 citations

Endoglin Gene, Genetics, Pathology +20