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RED-CELL MEMBRANE-PROTEIN ABNORMALITIES IN HEREDITARY SPHEROCYTOSIS IN BRAZIL
(Blackwell Science LtdOxfordInglaterra, 1994)
Eryptosis is induced by hyperthermia in hereditary spherocytosis red blood cells
(De Gruyter, 2016-05)
In pediatric hereditary spherocytosis (HS) patients, anemiafrequently worsens throughout the course of infectiousdiseases, due either to increased hemolysis or to transitoryerythropoietic aplasia [1]. Hemolysis may be so ...
Effects of SPTA1 Gene Variants on the Hematological Phenotype of Mexican Patients with Hereditary Spherocytosis
(Mary Ann Liebert Inc., 2022)
Red blood cell aquaporin-1 expression is decreased in hereditary spherocytosis
(Springer, 2016-10)
Aquaporin-1 (AQP1) is the membrane water channel responsible for changes in erythrocyte volume in response to the tonicity of the medium. As the aberrant distribution of proteins in hereditary spherocytosis (HS) generates ...
beta-Spectrin S-ta Barbara: a novel frameshift mutation in hereditary spherocytosis associated with detectable levels of mRNA and a germ cell line mosaicism
(Blackwell Science LtdOxfordInglaterra, 2001)
Band 3(Tambau): a de novo mutation in the AE1 gene associated with hereditary spherocytosis. Implications for anion exchange and insertion into the red blood cell membrane
(Blackwell MunksgaardFrederiksberg CDinamarca, 2005)
ß-Spectrin São PauloII, a novel frameshift mutation of the ß-spectrin gene associated with hereditary spherocytosis and instability of the mutant mRNA
(Associação Brasileira de Divulgação Científica, 2002)
beta-Spectrin Sao Paulo(II), a novel frameshift mutation of the beta-spectrin gene associated with hereditary spherocytosis and instability of the mutant mRNA
(Assoc Bras Divulg CientificaSao PauloBrasil, 2002)