Molecular insights into the irreversible mechanical behavior of sickle hemoglobin. [PDF]
Yesudasan S +4 more
europepmc +1 more source
Detection of the sickle hemoglobin allele using a surface plasmon resonance based biosensor. [PDF]
Breveglieri G +7 more
europepmc +1 more source
PATTERN OF THALASSEMIAS AND OTHER HEMOGLOBINOPATHIES: A STUDY IN DISTRICT DERA ISMAIL KHAN, PAKISTAN
Background: Thalassemia is used to describe disorders with a significant decrease in the rate of synthesis of a globin chain. The term hemoglobinopathy is used to indicate those disorders with structurally abnormal hemoglobin.
Javaid Hussain +4 more
doaj
Pyruvate kinase deficiency modifies sickle hemoglobin carrier and sickle cell disease phenotypes in mice. [PDF]
Wang X +14 more
europepmc +1 more source
Small-molecule inhibitor screen to identify mechanisms of sickle hemoglobin clearance by liver endothelium. [PDF]
Kaminski TW +6 more
europepmc +1 more source
Sticking together: Polymerization of sickle hemoglobin drives the multiscale pathophysiology of sickle cell disease. [PDF]
Williams DC, Szafraniec HM, Wood DK.
europepmc +1 more source
βT87Q-Globin Gene Therapy Reduces Sickle Hemoglobin Production, Allowing for <i>Ex Vivo</i> Anti-sickling Activity in Human Erythroid Cells. [PDF]
Demirci S +10 more
europepmc +1 more source
International flight-associated splenic infarction in a 33-year-old man with sickle cell trait. [PDF]
Chadelat A, Tassart M, Bachmeyer C.
europepmc +1 more source
The Patient with Sickle Hemoglobin
Robert L. Richardson, Emily Taylor
openaire +1 more source

