Academic Journal

Interpreting Iron Homeostasis in Congenital and Acquired Disorders

التفاصيل البيبلوغرافية
العنوان: Interpreting Iron Homeostasis in Congenital and Acquired Disorders
المؤلفون: Scaramellini N., Fischer D., Agarvas A. R., Motta I., Muckenthaler M. U., Mertens C.
المساهمون: N. Scaramellini, D. Fischer, A.R. Agarva, I. Motta, M.U. Muckenthaler, C. Mertens
بيانات النشر: MDPI
سنة النشر: 2023
المجموعة: The University of Milan: Archivio Istituzionale della Ricerca (AIR)
مصطلحات موضوعية: anemia, hematology, hemochromatosi, iron, iron deficiency, iron metabolism, iron overload, rare disease, Settore MED/09 - Medicina Interna
الوصف: Mammalian cells require iron to satisfy their metabolic needs and to accomplish specialized functions, such as hematopoiesis, mitochondrial biogenesis, energy metabolism, or oxygen transport. Iron homeostasis is balanced by the interplay of proteins responsible for iron import, storage, and export. A misbalance of iron homeostasis may cause either iron deficiencies or iron overload diseases. The clinical work-up of iron dysregulation is highly important, as severe symptoms and pathologies may arise. Treating iron overload or iron deficiency is important to avoid cellular damage and severe symptoms and improve patient outcomes. The impressive progress made in the past years in understanding mechanisms that maintain iron homeostasis has already changed clinical practice for treating iron-related diseases and is expected to improve patient management even further in the future.
نوع الوثيقة: article in journal/newspaper
اللغة: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/36986429; info:eu-repo/semantics/altIdentifier/wos/WOS:000958875000001; volume:16; issue:3; firstpage:1; lastpage:19; numberofpages:19; journal:PHARMACEUTICALS; https://hdl.handle.net/2434/968073; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85152434553
DOI: 10.3390/ph16030329
الاتاحة: https://hdl.handle.net/2434/968073
https://doi.org/10.3390/ph16030329
Rights: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.AE01EE86
قاعدة البيانات: BASE