Associated Papers
Diagnostic Uptake of Targeted Sequencing in Adults With Steatotic Liver Disease and a Suspected Genetic Contribution.
Ronzoni L et al.
Liver International : Official Journal of the International Association for the Study of the Liver, 2025
The Role of Gene Variants in the Iron Metabolism of Anemic Adolescent Girls.
Varikuti SR et al.
Cureus, 2021
The <em>TMPRSS6</em> variant (SNP rs855791) affects iron metabolism and oral iron absorption - a stable iron isotope study in Taiwanese women.
Buerkli S et al.
Haematologica, 2021
Transferrin gene polymorphisms alter the transferrin focusing pattern, making congenital disorder of glycosylation diagnosis difficult.
Lipiński P et al.
Acta Biochimica Polonica, 2021
The impact of blood donation on blood counts and ferritin levels: A multi-center study from the Eastern Mediterranean region.
Hindawi S et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2021
Genetic and behavioral modification of hemoglobin and iron status among first-time and high-intensity blood donors.
Mast AE et al.
Transfusion, 2020
Differences in the frequency of genetic variants associated with iron imbalance among global populations.
Jallow MW et al.
Plos One, 2020
Mutant Proteomics of Lung Adenocarcinomas Harboring Different EGFR Mutations.
Nishimura T et al.
Frontiers in Oncology, 2020
Clonal Structures of Regionally Synchronous Gastric Adenomas and Carcinomas.
Jung SH et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2018
Transferrin variants: pitfalls in the diagnostics of Congenital disorders of glycosylation.
Zühlsdorf A et al.
Clinical Biochemistry, 2015
Identification of a novel quantitative trait nucleotype related to iron status in a calcium channel gene.
Baeza-Richer C et al.
Disease Markers, 2013
Iron deficiency in blood donors: the REDS-II Donor Iron Status Evaluation (RISE) study.
Cable RG et al.
Transfusion, 2012
The impact of HFE mutations on haemoglobin and iron status in individuals experiencing repeated iron loss through blood donation*.
Mast AE et al.
British Journal of Haematology, 2012
Four variants in transferrin and HFE genes as potential markers of iron deficiency anaemia risk: an association study in menstruating women.
Blanco-Rojo R et al.
Nutrition & Metabolism, 2011
A novel SNaPshot assay to detect genetic mutations related to iron metabolism.
Bertoncini S et al.
Genetic Testing and Molecular Biomarkers, 2011
The G277S transferrin mutation does not affect iron absorption in iron deficient women.
Sarria B et al.
European Journal of Nutrition, 2007
A new case of human atransferrinemia with a previously undescribed mutation in the transferrin gene.
Aslan D et al.
Acta Haematologica, 2007
Human transferrin G277S mutation and iron deficiency in pregnancy.
Delanghe J et al.
British Journal of Haematology, 2006
Of mice and men: genetic determinants of iron status.
McGregor J et al.
The Proceedings of the Nutrition Society, 2004
The G277S mutation in transferrin does not disturb function.
Aisen P
British Journal of Haematology, 2003
Human transferrin G277S mutation: a risk factor for iron deficiency anaemia.
Lee PL et al.
British Journal of Haematology, 2001