The Molecular Basis of Ferroportin-Linked Hemochromatosis

Proceedings of the National Academy of Sciences of the United States of America - United States
doi 10.1073/pnas.0503804102
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Proceedings of the National Academy of Sciences

Related search

Deciphering the Molecular Basis of Ferroportin Resistance to Hepcidin: Structure/Function Analysis of Rare SLC40A1 Missense Mutations Found in Suspected Hemochromatosis Type 4 Patients

Transfusion Clinique et Biologique
BiochemistryMedicineClinical BiochemistryHematology
2017English

Molecular Basis for the Kallmann Syndrome-Linked Fibroblast Growth Factor Receptor Mutation

Biochemical and Biophysical Research Communications
BiochemistryCell BiologyMolecular BiologyBiophysics
2012English

Evidence for Non-Hfe Linked Hemochromatosis in Asian Indians

Indian Journal of Medical Sciences
Medicine
2006English

The Molecular Basis of Hypopituitarism

Trends in Endocrinology and Metabolism
EndocrinologyMetabolismDiabetes
2009English

The Molecular Basis of Neoplasia

Postgraduate Medical Journal
Medicine
1963English

The Dynamics of Hepcidin-Ferroportin Internalization and Consequences of a Novel Ferroportin Disease Mutation

American Journal of Hematology
Hematology
2017English

The Molecular Basis of Allergenicity

Genome Biology
2001English

Exome Sequencing for Molecular Characterization of Non-Hfe Hereditary Hemochromatosis

Blood Cells, Molecules, and Diseases
Molecular MedicineHematologyMolecular BiologyCell Biology
2015English

Genetic Basis of Y-Linked Hearing Impairment

American Journal of Human Genetics
Genetics
2013English

Amanote Research

Note-taking for researchers

Follow Amanote

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

Privacy PolicyRefund Policy