Pamela M. Thomas

Mutations in the Sulfonylurea Receptor Gene in Familial Persistent Hyperinsulinemic Hypoglycemia of Infancy

Pamela M. Thomas, Gilbert J. Cote, Nelson Wohllk et al. · Science · 1995 · 815 citations

Increased bone mass is an unexpected phenotype associated with deletion of the calcitonin gene

Ana O. Hoff, Philip Catalá-Lehnen, Pamela M. Thomas et al. · Journal of Clinical Investigation · 2002 · 209 citations · Full text

The glycophosphatidylinositol-anchored Thy-1 molecule interacts with the p60fyn protein tyrosine kinase in T cells.

Pamela M. Thomas, Lawrence E. Samelson · Journal of Biological Chemistry · 1992 · 190 citations · Full text

T-regulatory Cell, Immunology, Immune Regulation +20

A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland.

Timo Otonkoski, Carina Ämmälä, Hanna Huopio et al. · Diabetes · 1999 · 154 citations

Sulfonylurea Receptor, Insulin Signaling, Persistent Hyperinsulinemic Hypoglycemia +15

Homozygosity mapping, to chromosome 11p, of the gene for familial persistent hyperinsulinemic hypoglycemia of infancy.

Pamela M. Thomas, Gilbert J. Cote, David Hallman et al. · PubMed · 1995 · 82 citations