Results 111 to 120 of about 25,303 (208)

Molecular insights into the irreversible mechanical behavior of sickle hemoglobin. [PDF]

open access: yesJ Biomol Struct Dyn, 2019
Yesudasan S   +4 more
europepmc   +1 more source

Detection of the sickle hemoglobin allele using a surface plasmon resonance based biosensor. [PDF]

open access: yesSens Actuators B Chem, 2019
Breveglieri G   +7 more
europepmc   +1 more source

PATTERN OF THALASSEMIAS AND OTHER HEMOGLOBINOPATHIES: A STUDY IN DISTRICT DERA ISMAIL KHAN, PAKISTAN

open access: yesGomal Journal of Medical Sciences, 2014
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]

open access: yesJCI Insight
Wang X   +14 more
europepmc   +1 more source

Small-molecule inhibitor screen to identify mechanisms of sickle hemoglobin clearance by liver endothelium. [PDF]

open access: yesBlood Vessel Thromb Hemost
Kaminski TW   +6 more
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]

open access: yesMol Ther Methods Clin Dev, 2020
Demirci S   +10 more
europepmc   +1 more source

The Patient with Sickle Hemoglobin

open access: yesThe Journal of ExtraCorporeal Technology, 1973
Robert L. Richardson, Emily Taylor
openaire   +1 more source

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