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Publications by Douglas M. Nilson

Erythrocyte Ankyrin Promoter Mutations Associated With Recessive Hereditary Spherocytosis Cause Significant Abnormalities in Ankyrin Expression

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
2001English

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A New Ankyrin Mutation (ANK1 EXON E9X) Causing Severe Hereditary Spherocytosis in the Neonatal Period

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Erythrocyte Sodium Flux in Hereditary Spherocytosis: Its Significance

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Ankyrin-Bound Fatty Acid Turns Over Rapidly at the Erythrocyte Plasma Membrane.

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1987English

Ankyrin-B Regulates Kir6.2 Membrane Expression and Function in Heart

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The ANK Repeats of Erythrocyte Ankyrin Form Two Distinct but Cooperative Binding Sites for the Erythrocyte Anion Exchanger

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Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability

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Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts

American Journal of Human Genetics
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Recombinant Erythropoietin in Infants With Hereditary Spherocytosis

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Ankyrin B and Ankyrin B Variants Differentially Modulate Intracellular and Surface Cav2.1 Levels

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