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High Foetal Haemoglobin In Sickle Cell Disease: Not So Protective?
(ELSEVIER SCIENCE BVAMSTERDAM, 2015)
Mutagenicity of New Lead Compounds to Treat Sickle Cell Disease Symptoms in a Salmonella/Microsome Assay
(Mdpi Ag, 2010-02-01)
A series of phthalimide derivatives planned as drugs candidates to treat the symptoms of sickle cell anemia were evaluated in a mutagenicity test using strains of Salmonella typhimurium TA100 and TA102, without and with ...
Mutagenicity of New Lead Compounds to Treat Sickle Cell Disease Symptoms in a Salmonella/Microsome Assay
(Mdpi Ag, 2010-02-01)
A series of phthalimide derivatives planned as drugs candidates to treat the symptoms of sickle cell anemia were evaluated in a mutagenicity test using strains of Salmonella typhimurium TA100 and TA102, without and with ...
Sickle cell disease: Only one road, but different pathways for inflammation
(Scientific Research Publishing, 2016)
Effect of cytokines and chemokines on sickle neutrophil adhesion to fibronectin
(KargerBaselSuíça, 2005)
Participation of Mac-1, LFA-1 and VLA-4 integrins in the in vitro adhesion of sickle cell disease neutrophils to endothelial layers, and reversal of adhesion by simvastatin
(Ferrata Storti FoundationPaviaItália, 2011)
Transcranial Doppler in hemoglobin SC disease
(Wiley, 2017)
Anemia falciforme: desafios e avanços na busca de novos fármacos
(Sociedade Brasileira de Química, 2012-01-01)
Sickle Cell Disease (SCD) is a disease characterized by a punctual mutation (GTG - GAG) in the sixth codon of the gamma globin gene leading to a substitution of glutamic acid by a valine in the β chain of hemoglobin. Despite ...
Anemia falciforme: desafios e avanços na busca de novos fármacos
(Sociedade Brasileira de Química, 2012-01-01)
Sickle Cell Disease (SCD) is a disease characterized by a punctual mutation (GTG - GAG) in the sixth codon of the gamma globin gene leading to a substitution of glutamic acid by a valine in the β chain of hemoglobin. Despite ...