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Altered Erythropoiesis in Mouse Models of Type 3 Hemochromatosis.
- Published in:
- BioMed Research International, 2017, v. 2017, p. 1, doi. 10.1155/2017/2408941
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- Publication type:
- Article
Activation of the Hepcidin-Ferroportin1 pathway in the brain and astrocytic–neuronal crosstalk to counteract iron dyshomeostasis during aging.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-15812-4
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- Publication type:
- Article
The Functional Versatility of Transferrin Receptor 2 and Its Therapeutic Value.
- Published in:
- Pharmaceuticals (14248247), 2018, v. 11, n. 4, p. 115, doi. 10.3390/ph11040115
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- Publication type:
- Article
Detection of a rare mutation in the ferroportin gene through targeted next generation sequencing.
- Published in:
- 2016
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- Publication type:
- Case Study
β-Myosin Mutations in Hypertrophic Cardiomyopathies<sup>a</sup>.
- Published in:
- Annals of the New York Academy of Sciences, 1995, v. 752, n. 1, p. 227, doi. 10.1111/j.1749-6632.1995.tb17429.x
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- Publication type:
- Article
Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis.
- Published in:
- Nature Genetics, 2003, v. 33, n. 1, p. 21, doi. 10.1038/ng1053
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- Publication type:
- Article
The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22.
- Published in:
- Nature Genetics, 2000, v. 25, n. 1, p. 14, doi. 10.1038/75534
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- Publication type:
- Article
Characterization of human mitochondrial ferritin promoter: identification of transcription factors and evidences of epigenetic control.
- Published in:
- Scientific Reports, 2016, p. 33432, doi. 10.1038/srep33432
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- Publication type:
- Article
Transferrin Receptor 2 Dependent Alterations of Brain Iron Metabolism Affect Anxiety Circuits in the Mouse.
- Published in:
- Scientific Reports, 2016, p. 30725, doi. 10.1038/srep30725
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- Publication type:
- Article
Iron supplementation is sufficient to rescue skeletal muscle mass and function in cancer cachexia.
- Published in:
- EMBO Reports, 2022, v. 23, n. 4, p. 1, doi. 10.15252/embr.202153746
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- Publication type:
- Article
Juvenile hemochromatosis locus maps to chromosome 1q in a French Canadian population.
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- European Journal of Human Genetics, 2003, v. 11, n. 8, p. 585, doi. 10.1038/sj.ejhg.5201009
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- Publication type:
- Article
Generation of a transcription map of a 1 Mbase region containing the HFE gene (6p22).
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- European Journal of Human Genetics, 1998, v. 6, n. 2, p. 105, doi. 10.1038/sj.ejhg.5200162
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- Publication type:
- Article
Comprehensive analysis of mitochondrial and nuclear DNA variations in patients affected by hemoglobinopathies: A pilot study.
- Published in:
- PLoS ONE, 2020, v. 15, n. 10, p. 1, doi. 10.1371/journal.pone.0240632
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- Publication type:
- Article
Genetic interactions in thalassemia intermedia: Analysis of β-Mutations, α-Genotype, γ-Promoters, and β-LCR hypersensitive sites 2 and 4 in Italian patients.
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- American Journal of Hematology, 1995, v. 48, n. 2, p. 82, doi. 10.1002/ajh.2830480203
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- Publication type:
- Article
Nrf2 as a Therapeutic Target in the Resistance to Targeted Therapies in Melanoma.
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- Antioxidants, 2023, v. 12, n. 6, p. 1313, doi. 10.3390/antiox12061313
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- Publication type:
- Article
Iron Overload, Oxidative Stress, and Ferroptosis in the Failing Heart and Liver.
- Published in:
- Antioxidants, 2021, v. 10, n. 12, p. 1864, doi. 10.3390/antiox10121864
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- Publication type:
- Article
Identification of new BMP6 pro-peptide mutations in patients with iron overload.
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- American Journal of Hematology, 2017, v. 92, n. 6, p. 562, doi. 10.1002/ajh.24730
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- Publication type:
- Article
Development of cellular and humoral response against WT1 protein vaccination in mice.
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- American Journal of Hematology, 2015, v. 90, n. 9, p. E193, doi. 10.1002/ajh.24092
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- Publication type:
- Article
Different hematological phenotypes caused by the interaction of triplicated α-globin genes and heterozygous β-thalassemia.
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- American Journal of Hematology, 1997, v. 55, n. 2, p. 83, doi. 10.1002/(SICI)1096-8652(199706)55:2<83::AID-AJH6>3.0.CO;2-Z
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- Publication type:
- Article
Iron: An Essential Element of Cancer Metabolism.
- Published in:
- Cells (2073-4409), 2020, v. 9, n. 12, p. 2591, doi. 10.3390/cells9122591
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- Publication type:
- Article
A novel mutation in the CUB sequence of matriptase-2 ( TMPRSS6) is implicated in iron-resistant iron deficiency anaemia - response to Jaspers et al.
- Published in:
- British Journal of Haematology, 2013, v. 160, n. 4, p. 566, doi. 10.1111/bjh.12145
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- Publication type:
- Article
Two novel mutations in the tmprss6 gene associated with iron-refractory iron-deficiency anaemia (irida) and partial expression in the heterozygous form.
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- British Journal of Haematology, 2012, v. 158, n. 5, p. 668, doi. 10.1111/j.1365-2141.2012.09198.x
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- Publication type:
- Article
Natural history of juvenile haemochromatosis.
- Published in:
- British Journal of Haematology, 2002, v. 117, n. 4, p. 973, doi. 10.1046/j.1365-2141.2002.03509.x
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- Publication type:
- Article
Identification of a Novel Mutation in the L Ferritin Iron-Responsive Element Causing Hereditary Hyperferritinemia-Cataract Syndrome.
- Published in:
- Acta Haematologica, 2009, v. 122, n. 4, p. 223, doi. 10.1159/000253031
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- Publication type:
- Article
Detection of Humoral Immune Responses against WT1 Antigen in Patients Affected by Different Hematological Malignancies.
- Published in:
- Acta Haematologica, 2008, v. 120, n. 1, p. 47, doi. 10.1159/000158576
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- Publication type:
- Article
Deferasirox Treatment Improved the Hemoglobin Level and Decreased Transfusion Requirements in Four Patients with the Myelodysplastic Syndrome and Primary Myelofibrosis.
- Published in:
- Acta Haematologica, 2008, v. 120, n. 2, p. 70, doi. 10.1159/000158631
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- Publication type:
- Article
Lack of Hfe and TfR2 in Macrophages Impairs Iron Metabolism in the Spleen and the Bone Marrow.
- Published in:
- International Journal of Molecular Sciences, 2024, v. 25, n. 17, p. 9142, doi. 10.3390/ijms25179142
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- Publication type:
- Article
Chlorinated benzenes as physioloical markers for coyotes.
- Published in:
- Journal of Wildlife Management, 1998, v. 62, n. 1, p. 410, doi. 10.2307/3802307
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- Publication type:
- Article
Growth hormone (GH)-induced reconstitution of CD8+ CD28+ T lymphocytes in a rare case of severe lymphopenia associated with Juvenile Haemochromatosis and Turner's syndrome.
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- Clinical Endocrinology, 2004, v. 61, n. 4, p. 437, doi. 10.1111/j.1365-2265.2004.02069.x
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- Publication type:
- Article
Linkage analysis of 6p21 polymorphic markers and the hereditary hemochromatosis: localization of the gene centromeric to HLA-F.
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- Human Molecular Genetics, 1993, v. 2, n. 5, p. 571
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- Publication type:
- Article
A comparative study of myocardial molecular phenotypes of two tfr2β null mice: Role in ischemia/reperfusion.
- Published in:
- Biofactors, 2015, v. 41, n. 5, p. 360, doi. 10.1002/biof.1237
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- Publication type:
- Article
A new mutation (G51C) in the iron-responsive element (IRE) of l-ferritin associated with hyperferritinaemia–cataract syndrome decreases the binding affinity of the mutated IRE for iron-regulatory proteins.
- Published in:
- British Journal of Haematology, 2000, v. 108, n. 3, p. 480, doi. 10.1046/j.1365-2141.2000.01920.x
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- Publication type:
- Article
DIAGNOSIS AND MANAGEMENT OF HAEMOCHROMATOSIS SINCE THE DISCOVERY OF THE HFE GENE: A EUROPEAN EXPERIENCE.
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- British Journal of Haematology, 2000, v. 108, n. 1, p. 31, doi. 10.1046/j.1365-2141.2000.01687.x
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- Publication type:
- Article