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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
2010
Review
2010
Beta-thalassemias are a group of hereditary blood disorders characterized by anomalies in the synthesis of the beta chains of… Expand
Review
2010
Review
2010
Summary Background Gram-negative Enterobacteriaceae with resistance to carbapenem conferred by New Delhi metallo-β-lactamase 1… 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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Review
1998
Review
1998
Increased use of titanium alloys as biomaterials is occurring due to their lower modulus, superior biocompatibility and enhanced… Expand
Highly Cited
1997
Highly Cited
1997
Human bone marrow contains a population of cells capable of differentiating along multiple mesenchymal cell lineages. Recently… Expand
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
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
Highly Cited
1987
Highly Cited
1987
  • R. A. Jefferson, T. A. Kavanagh, M. W. Bevan
  • The EMBO journal
  • 1987
  • Corpus ID: 27705523
We have used the Escherichia coli beta‐glucuronidase gene (GUS) as a gene fusion marker for analysis of gene expression in… Expand
Highly Cited
1986
Highly Cited
1986
Transforming growth factor type beta (TGF-beta), when injected subcutaneously in newborn mice, causes formation of granulation… Expand
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Review
1985
Review
1985
Long-term beta blockade for perhaps a year or so following discharge after an MI is now of proven value, and for many such… Expand