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Publications by J G Conboy
An Isoform-Specific Mutation in the Protein 4.1 Gene Results in Hereditary Elliptocytosis and Complete Deficiency of Protein 4.1 in Erythrocytes but Not in Nonerythroid Cells.
Journal of Clinical Investigation
Medicine
Related publications
Hereditary Elliptocytosis With Protein Band 4.1 Deficiency in the Dog
Blood
Biochemistry
Immunology
Cell Biology
Hematology
Deficiency of Skeletal Membrane Protein Band 4.1 in Homozygous Hereditary Elliptocytosis. Implications for Erythrocyte Membrane Stability.
Journal of Clinical Investigation
Medicine
Structural Protein 4.1 Is Located in Mammalian Centrosomes
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Identification of a Third Protein 4.1 Tumor Suppressor, Protein 4.1R, in Meningioma Pathogenesis
Neurobiology of Disease
Neurology
Protein 4.1 Is a Component of the Nuclear Matrix of Mammalian Cells
Biochemical Journal
Biochemistry
Cell Biology
Molecular Biology
Inhibition of Protein 4.1 R and NuMA Interaction by Mutagenization of Their Binding-Sites Abrogates Nuclear Localization of 4.1 R
Clinical and Translational Science
Genetics
Molecular Biology
Pharmacology
Biochemistry
Neuroscience
Medicine
Toxicology
Pharmaceutics
Similarities and Differences in the Structure and Function of 4.1G and 4.1R135, Two Protein 4.1 Paralogues Expressed in Erythroid Cells
Biochemical Journal
Biochemistry
Cell Biology
Molecular Biology
Credits 4.1 // Créditos 4.1
Ecozon@: European Journal of Literature, Culture and Environment
4.1 Geschlechtergerechtigkeit
