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Publications by Amanda P. Cline

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

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
2001English

Related publications

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

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2010English

Erythrocyte Sodium Flux in Hereditary Spherocytosis: Its Significance

Pediatric Research
Child HealthPediatricsPerinatology
1970English

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

Molecular and Cellular Biology
Cell BiologyMolecular Biology
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

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
1995English

Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability

American Journal of Human Genetics
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2012English

Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts

American Journal of Human Genetics
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2011English

Recombinant Erythropoietin in Infants With Hereditary Spherocytosis

Pediatric Research
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1999English

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

Molecular Brain
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2019English

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