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beta Thalassemia

Known as: Type Thalassemia, beta, beta thalassemias, beta Type Microcytemias 
A disorder characterized by reduced synthesis of the beta chains of hemoglobin. There is retardation of hemoglobin A synthesis in the heterozygous… Expand
National Institutes of Health

Papers overview

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Review
2018
Review
2018
An online survey of mycology laboratories in seven Asian countries was conducted to assess the status, competence, and services… Expand
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Review
2010
Review
2010
Beta-thalassemias are a group of hereditary blood disorders characterized by anomalies in the synthesis of the beta chains of… Expand
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Highly Cited
2009
Highly Cited
2009
ABSTRACT A Swedish patient of Indian origin traveled to New Delhi, India, and acquired a urinary tract infection caused by a… Expand
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Highly Cited
2006
Highly Cited
2006
Deferasirox (ICL670) is a once-daily oral iron chelator developed for the treatment of chronic iron overload from blood… Expand
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Highly Cited
2001
Highly Cited
2001
The synthesis and photophysical study of a family of cyclometalated iridium(III) complexes are reported. The iridium complexes… Expand
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Highly Cited
1999
Highly Cited
1999
BACKGROUND In patients with heart failure, beta-blockade has improved morbidity and left-ventricular function, but the impact on… Expand
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Highly Cited
1997
Highly Cited
1997
Human bone marrow contains a population of cells capable of differentiating along multiple mesenchymal cell lineages. Recently… Expand
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Highly Cited
1995
Highly Cited
1995
Hypoxia-inducible factor 1 (HIF-1) is found in mammalian cells cultured under reduced O2 tension and is necessary for… Expand
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Highly Cited
1988
Highly Cited
1988
The capacity of 12 cytokines to induce NO2- or H2O2 release from murine peritoneal macrophages was tested by using resident… Expand
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Highly Cited
1987
Highly Cited
1987
We have used the Escherichia coli beta‐glucuronidase gene (GUS) as a gene fusion marker for analysis of gene expression in… Expand
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