... the association between RANTES (regulated upon activation, normal T cell expressed and secreted) polymorphisms and clinical outcomes in patients treated with allogeneic hematopoietic stem cell transplantation (allo-HSCT). Three RANTES gene polymorphisms, i.e. –403G/A (rs2107538), –28C/G (rs2280788) and In1.1T/C...

... in the intensive care unit (ICU). Plasminogen activator inhibitor (PAI)-1 is the chief inhibitor of fibrinolysis. We investigated the influence of the 4G/5G polymorphism (rs1799768) of the PAI-1 gene on the plasma PAI-1 level and the outcome of critically ill patients. Methods: In 41 consecutive patients admitted...

...S. Galimberti; B. Nagy; G.A. Palumbo; E. Ciancia; G. Buda; E. Orciuolo; A. Melosi; P. Lambelet; F. Ronca; M. Petrini In this study, we determined the allele and genotype frequencies of vascular endothelial growth factor (VEGF) G+405C, C–460T , C+936T and C–2578A single nucleotide polymorphisms...

...). Polymorphisms of the DNMT3B gene may influence DNMT3B activity on DNA methylation and increase the susceptibility to several diseases. The current study investigated the association between DNMT3B 579G>T and the risk for idiopathic thrombocytopenic purpura (ITP). The DNMT3B 579G>T polymorphisms were...

... to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. γ-Globin Hb F Hb F Sardinia Polymorphism Thalassaemia intermedia β + -Thalassaemia Acta haemat. 76: 208-211 (1986) © I986S. Karger AG, Basel 0001-5792/86/0764-0208...

..., instructions or products referred to in the content or advertisements. Cyclic 3´,5´-adenosine monophosphate Erythrocytes Rat Polymorphism Acta Haematol 1991;85:195-198 © 1991 S. Karger AG, Basel 0001-5792/91/0854-0195 S 2.75/0 Polymorphism of Cyclic 3',5'-Adenosine Monophosphate Stimulation in Rat...

... variants differ with respect to the 1311 polymorphism, suggesting that they may have arisen independently. Enzyme from a child with chronic hemolytic anemia, designated G6PD ‘LeJeune’, proved to be due to a G→T substitution at nt 637, a change identical with that in 3 unrelated patients who had been...

.... Amniocentesis Deficiency G6PD PCR Polymorphism Prenatal diagnosis Restriction endonuclease Short Communication Acta Haematol 1992;87:103-104 Ernest Beutler* Wanda Kuhla Michelle Foxb Khalil Tabshh Barbara F. CrandalP Department of Molecular and Experimental Medicine, Scripps Clinic and Research...

...Mohsen A.F. El-Hazmi; Hassan M. Bahakim; Arjumad S. Warsy Significant DNA polymorphisms have been reported in the β-globin gene cluster of ε-Gγ -Aγ – ψβ-δ-β-gene region, in normal (Hb AA) individuals and in patients with sickle cell anaemia (SCA). Investigations of the extent of the DNA...

... segregation analysis using the polymorphic markers of the factor IX gene, as none of her other family members were found to be deficient in factor IX. However, the Dde I polymorphic marker of the factor IX gene for which the mother was informative showed the inheritance of a ‘369-bp’ allele in the mother...