C. Halloran

Integrin alpha IIb beta 3 (platelet GPIIb-IIIa) recognizes multiple sites in fibronectin.

S. Aota, M. Obara, K. Yamada, 1991, The Journal of biological chemistry.

Polymorphisms in the transferrin 5' flanking region associated with differences in total iron binding capacity: possible implications in iron homeostasis.

E. Beutler, Pauline L. Lee, P. Lee, 2001, Blood cells, molecules & diseases.

Mutation analysis of the transferrin receptor-2 gene in patients with iron overload.

E. Beutler, C. West, P. Lee, 2001, Blood cells, molecules & diseases.

A study of genes that may modulate the expression of hereditary hemochromatosis: transferrin receptor-1, ferroportin, ceruloplasmin, ferritin light and heavy chains, iron regulatory proteins (IRP)-1 and -2, and hepcidin.

V. Felitti, E. Beutler, Pauline L. Lee, 2001, Blood cells, molecules & diseases.

Seeking candidate mutations that affect iron homeostasis.

E. Beutler, Pauline L. Lee, C. West, 2002, Blood cells, molecules & diseases.

Localization of a PlA1 epitope to the amino terminal 66 residues of platelet glycoprotein IIIa.

A. Frelinger, M. Ginsberg, P. Tani, 1992, Blood.

The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphisms.

E. Beutler, Pauline L. Lee, C. West, 1998, Blood cells, molecules & diseases.

The Amino-terminal One-third of Defines the Ligand Recognition Specificity of Integrin (*)

Jeffrey W. Smith, J. Zablocki, J. Loftus, 1996, The Journal of Biological Chemistry.

Polymorphisms in iron‐responsive binding protein 2 and lack of association with sporadic Parkinson's disease

E. Beutler, Pauline L. Lee, C. West, 2002, Movement disorders : official journal of the Movement Disorder Society.

Human transferrin G277S mutation: a risk factor for iron deficiency anaemia

V. Felitti, E. Beutler, Pauline L. Lee, 2001, British journal of haematology.