about
Functional and clinical impact of novel TMPRSS6 variants in iron-refractory iron-deficiency anemia patients and genotype-phenotype studiesThe role of Matriptase-2 during the early postnatal development in humans.How I Diagnose Non-thalassemic Microcytic Anemias.Trasferrin receptor 2 gene regulation by microRNA 221 in SH-SY5Y cells treated with MPP⁺ as Parkinson's disease cellular model.Is the acronym IRIDA acceptable for slow responders to iron in the presence of TMPRSS6 mutations?Identification and characterization of the first SLC11A2 isoform 1a mutation causing a defect in splicing process and an hypomorphic allele expression of the SLC11A2 geneIron-refractory iron deficiency anemia (IRIDA) cases with 2 novel TMPRSS6 mutations
P50
Q24302484-58758A8B-0DEC-4FC3-BB8C-AE6C810F6FD0Q37216264-CD0786FF-9AE5-4682-86A7-6C62E980928FQ38592556-4D33D6B6-9986-46E3-9144-814C97466D92Q39093505-AD4F2E07-7D69-4FAE-BC7B-C539D7DB2411Q54379906-3E9359EC-580B-4620-95C9-0B3F7ECA57A3Q87386240-31132817-AE57-45C3-8327-1AAFEF8D122AQ89307695-247F2493-0169-4F67-804F-84463F518C53
P50
description
researcher ORCID ID = 0000-0003-1218-1745
@en
name
Mariasole Bruno
@ast
Mariasole Bruno
@en
Mariasole Bruno
@es
Mariasole Bruno
@nl
type
label
Mariasole Bruno
@ast
Mariasole Bruno
@en
Mariasole Bruno
@es
Mariasole Bruno
@nl
prefLabel
Mariasole Bruno
@ast
Mariasole Bruno
@en
Mariasole Bruno
@es
Mariasole Bruno
@nl
P31
P496
0000-0003-1218-1745