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 - United States
doi 10.1172/jci116203
Full Text
Abstract

Available in full text

Categories
Medicine
Date
Authors
Publisher

American Society for Clinical Investigation

Related search

Hereditary Elliptocytosis With Protein Band 4.1 Deficiency in the Dog

Blood
BiochemistryImmunologyCell BiologyHematology
1983English

Deficiency of Skeletal Membrane Protein Band 4.1 in Homozygous Hereditary Elliptocytosis. Implications for Erythrocyte Membrane Stability.

Journal of Clinical Investigation
Medicine
1981English

Structural Protein 4.1 Is Located in Mammalian Centrosomes

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
1997English

Identification of a Third Protein 4.1 Tumor Suppressor, Protein 4.1R, in Meningioma Pathogenesis

Neurobiology of Disease
Neurology
2003English

Protein 4.1 Is a Component of the Nuclear Matrix of Mammalian Cells

Biochemical Journal
BiochemistryCell BiologyMolecular Biology
1995English

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
GeneticsMolecular BiologyPharmacologyBiochemistryNeuroscienceMedicineToxicologyPharmaceutics
2009English

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
BiochemistryCell BiologyMolecular Biology
2010English

Credits 4.1 // Créditos 4.1

Ecozon@: European Journal of Literature, Culture and Environment
2013English

4.1 Geschlechtergerechtigkeit

2015English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy