Results 141 to 150 of about 429,758 (251)

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

Gomal 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, Sara Arif, Sher Zamir, Mohammad Amin Jan Mahsud, Shah Jahan   +4 more
doaj  

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

Sens Actuators B Chem, 2019
Breveglieri G, D'Aversa E, Cosenza LC, Boutou E, Balassopoulou A, Voskaridou E, Gambari R, Borgatti M.   +7 more
europepmc   +1 more source

Lost in the Vaso‐Occlusion: A Patient's Abdominal Pain Returns With a Vengeance

Pediatric Blood &Cancer, Volume 73, Issue 11, November 2026.
Dunia Hatabah, Martha E. Stewart, Nathan Maassel, James P. Stevens, Claudia R. Morris, Chris A. Rees   +5 more
wiley   +1 more source

Pyruvate kinase deficiency modifies sickle hemoglobin carrier and sickle cell disease phenotypes in mice. [PDF]

JCI Insight
Wang X, Smith M, Kamimura S, Li Q, Shah N, Quezado M, Almeida LE, Vogel S, Tegegn MB, Sun KY, Villasmil R, Liu C, Eaton WA, Thein SL, Quezado ZM.   +14 more
europepmc   +1 more source

Discovery of Osivelotor (GBT021601): A Potent, Next-Generation Sickle Hemoglobin Polymerization Inhibitor. [PDF]

ACS Med Chem Lett
Li Z, Alt C, Dufu K, Hutchaleelaha A, Xu Q, Zhang X, Li CM, Rademacher P, Bosmajian C, Pochron MP, Partridge JR, Oksenberg D, Cathers BE.   +12 more
europepmc   +1 more source

Detecting sickle hemoglobin. [PDF]

BMJ, 1972
openaire   +2 more sources

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

Blood Vessel Thromb Hemost
Kaminski TW, Zhang H, Katoch O, Shi Q, Kato GJ, Sundd P, Pradhan-Sundd T.   +6 more
europepmc   +1 more source

Forced chromatin looping raises fetal hemoglobin in adult sickle cells to higher levels than pharmacologic inducers.

Blood, 2016
L. Breda, I. Motta, S. Lourenço, Chiara Gemmo, Wu-Lan Deng, J. Rupon, O. Abdulmalik, D. Manwani, G. Blobel, S. Rivella   +9 more
semanticscholar   +1 more source

Sticking together: Polymerization of sickle hemoglobin drives the multiscale pathophysiology of sickle cell disease. [PDF]

Biophys Rev (Melville)
Williams DC, Szafraniec HM, Wood DK.
europepmc   +1 more source

The Patient with Sickle Hemoglobin

The Journal of ExtraCorporeal Technology, 1973
Robert L. Richardson, Emily Taylor
openaire   +1 more source