M.‐J. King

CASK and Protein 4.1 Support F-actin Nucleation on Neurexins

Mutations in the erythrocyte chemokine receptor (Duffy) gene: the molecular basis of the Fy^a/Fy^b antigens and identification of a deletion in the Duffy gene of an apparently healthy individual with the Fy(a – b–) phenotype

Homozygous Defect in HIV-1 Coreceptor Accounts for Resistance of Some Multiply-Exposed Individuals to HIV-1 Infection

Erythrocyte membrane protein destabilization versus clinical outcome in 160 Portuguese Hereditary Spherocytosis patients

Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels

The PDZ Domain of Human Erythrocyte p55 Mediates Its Binding to the Cytoplasmic Carboxyl Terminus of Glycophorin C

Red Cell Membrane Disorders

Homology requirements for unequal crossing over in humans.

A Pragmatic Guide to Enrichment Strategies for Mass Spectrometry–Based Glycoproteomics

Recurrent mutation in the human phenylalanine hydroxylase gene.

Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in Asian families with phenylketonuria (PKU).

Density Variant Glycan Microarray for Evaluating Cross-Linking of Mucin-like Glycoconjugates by Lectins

Chemokines

Microarrays with Varying Carbohydrate Density Reveal Distinct Subpopulations of Serum Antibodies

Identification of Tn Antigen O-GalNAc-expressing glycoproteins in human carcinomas using novel anti-Tn recombinant antibodies

International Union of Pharmacology. XXII. Nomenclature for Chemokine Receptors

The structure of the ankyrin-binding site of β-spectrin reveals how tandem spectrin-repeats generate unique ligand-binding properties

Identification of the Cystic Fibrosis Gene: Genetic Analysis

Reactivity with erythroid and non‐erythroid tissues of a murine monoclonal antibody to a synthetic peptide having amino acid sequence common to cytoplasmic domain of human glycophorins C and D

Guidelines for the diagnosis and management of hereditary spherocytosis

Immunochemical studies on the differential binding properties of two monoclonal antibodies reacting with Tn red cells

Point Mutation in the Glycophorin C Gene Results in the Expression of the Blood Group Antigen Dh^a

Haplotype distribution of the human phenylalanine hydroxylase locus in Scotland and Switzerland.