Found: 15
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Gender effect on production and enrichment of F cell numbers in sickle cell disease patients in Tanzania.
- Published in:
- American Journal of Hematology, 2023, v. 98, n. 6, p. E139, doi. 10.1002/ajh.26914
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- Article
A survey of genetic fetal-haemoglobin modifiers in Nigerian patients with sickle cell anaemia.
- Published in:
- PLoS ONE, 2018, v. 13, n. 6, p. 1, doi. 10.1371/journal.pone.0197927
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- Article
Two candidate genes for low platelet count identified in an Asian Indian kindred by genome-wide linkage analysis: glycoprotein IX and thrombopoietin.
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- European Journal of Human Genetics, 2006, v. 14, n. 1, p. 101, doi. 10.1038/sj.ejhg.5201499
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- Article
A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.
- Published in:
- Nature Genetics, 2007, v. 39, n. 10, p. 1197, doi. 10.1038/ng2108
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- Article
Global Genetic Architecture of an Erythroid Quantitative Trait Locus, HMIP-2.
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- Annals of Human Genetics, 2014, v. 78, n. 6, p. 434, doi. 10.1111/ahg.12077
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- Article
Genetic determinants of haemolysis in sickle cell anaemia.
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- British Journal of Haematology, 2013, v. 161, n. 2, p. 270, doi. 10.1111/bjh.12245
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- Article
Hb A<sub>2</sub> levels in normal adults are influenced by two distinct genetic mechanisms.
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- British Journal of Haematology, 2013, v. 160, n. 1, p. 101, doi. 10.1111/bjh.12084
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- Article
Heterogeneity of theℇ γ δ β-thalassaemias: characterization of three novel English deletions.
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- British Journal of Haematology, 2005, v. 128, n. 5, p. 722, doi. 10.1111/j.1365-2141.2005.05368.x
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- Article
Genome Wide Association Study of Fetal Hemoglobin in Sickle Cell Anemia in Tanzania.
- Published in:
- PLoS ONE, 2014, v. 9, n. 11, p. 1, doi. 10.1371/journal.pone.0111464
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- Article
F cell numbers are associated with an X‐linked genetic polymorphism and correlate with haematological parameters in patients with sickle cell disease.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 888, doi. 10.1111/bjh.17102
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- Article
Beta thalassaemia intermedia due to co-inheritance of three unique alpha globin cluster duplications characterised by next generation sequencing analysis.
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- British Journal of Haematology, 2018, v. 180, n. 1, p. 160, doi. 10.1111/bjh.14294
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- Article
HBS1L-MYB intergenic variants modulate fetal hemoglobin via long-range MYB enhancers.
- Published in:
- Journal of Clinical Investigation, 2014, v. 124, n. 4, p. 1699, doi. 10.1172/JCI71520
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- Article
Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer.
- Published in:
- BMC Medical Genetics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12881-015-0148-3
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- Article
Next Generation Sequencing Identifies a Novel Rearrangement in the HBB Cluster Permitting to-the-Base Characterization.
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- Human Mutation, 2015, v. 36, n. 1, p. 142, doi. 10.1002/humu.22707
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- Article
The genetic dissection of fetal haemoglobin persistence in sickle cell disease in Nigeria.
- Published in:
- Human Molecular Genetics, 2024, v. 33, n. 10, p. 919, doi. 10.1093/hmg/ddae014
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- Article