Found: 12
Select item for more details and to access through your institution.
Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 271, doi. 10.1038/15452
- By:
- Publication type:
- Article
Correction: Distinct Mechanisms of Inadequate Erythropoiesis Induced by Tumor Necrosis Factor Alpha or Malarial Pigment.
- Published in:
- PLoS ONE, 2015, v. 10, n. 4, p. 1, doi. 10.1371/journal.pone.0127124
- By:
- Publication type:
- Article
Distinct Mechanisms of Inadequate Erythropoiesis Induced by Tumor Necrosis Factor Alpha or Malarial Pigment.
- Published in:
- PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0119836
- By:
- Publication type:
- Article
Distinct gene expression program dynamics during erythropoiesis from human induced npluripotent stem cells compared with adult and cord blood progenitors.
- Published in:
- BMC Genomics, 2016, v. 17, p. 1, doi. 10.1186/s12864-016-3134-z
- By:
- Publication type:
- Article
A targeted approach significantly increases the identification rate of patients with undiagnosed haemochromatosis.
- Published in:
- 2003
- By:
- Publication type:
- journal article
Prevalence of HFE mutations among the Thai population and correlation with iron loading in haemoglobin E disorder.
- Published in:
- European Journal of Haematology, 2004, v. 73, n. 1, p. 43, doi. 10.1111/j.1600-0609.2004.00246.x
- By:
- Publication type:
- Article
Does osteogenic potential of clonal human bone marrow mesenchymal stem/stromal cells correlate with their vascular supportive ability?
- Published in:
- Stem Cell Research & Therapy, 2018, v. 9, n. 1, p. 1, doi. 10.1186/s13287-018-1095-7
- By:
- Publication type:
- Article
The haemochromatosis gene: A global perspective and implications for the Asia–Pacific region.
- Published in:
- Journal of Gastroenterology & Hepatology, 1999, v. 14, n. 9, p. 838, doi. 10.1046/j.1440-1746.1999.01980.x
- By:
- Publication type:
- Article
Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 17, p. 2241, doi. 10.1093/hmg/ddg225
- By:
- Publication type:
- Article
A retrospective anonymous pilot study in screening newborns for HFE mutations in Scandinavian populations.
- Published in:
- Human Mutation, 1999, v. 13, n. 2, p. 154, doi. 10.1002/(SICI)1098-1004(1999)13:2<154::AID-HUMU8>3.0.CO;2-E
- By:
- Publication type:
- Article
The effect of HFE mutations on serum ferritin and transferrin saturation in the Jersey population.
- Published in:
- British Journal of Haematology, 1998, v. 101, n. 2, p. 369, doi. 10.1046/j.1365-2141.1998.00736.x
- By:
- Publication type:
- Article
A rapid non-invasive method for the detection of the haemochromatosis C282Y mutation.
- Published in:
- British Journal of Haematology, 1997, v. 99, n. 2, p. 460, doi. 10.1046/j.1365-2141.1997.4193224.x
- By:
- Publication type:
- Article