Results 111 to 120 of about 821,341 (299)

EHMT1 and EHMT2 inhibition induces fetal hemoglobin expression.

open access: yesBlood, 2015
Fetal hemoglobin (HbF, α2γ2) induction is a well-validated strategy for sickle cell disease (SCD) treatment. Using a small-molecule screen, we found that UNC0638, a selective inhibitor of EHMT1 and EHMT2 histone methyltransferases, induces γ-globin ...
Aline Renneville   +10 more
semanticscholar   +1 more source

Single-nucleotide-level mapping of DNA regulatory elements that control fetal hemoglobin expression

open access: yesNature Genetics, 2021
Li Cheng   +14 more
semanticscholar   +1 more source

Blessing in disguise; a case of Hereditary Persistence of Fetal Hemoglobin

open access: yesJournal of Community Hospital Internal Medicine Perspectives, 2018
Fetal Hemoglobin (HbF, α2γ2) is produced from the eighth week of gestation, constitutes 60 – 80 % of total hemoglobin by birth, which is then replaced with adult Hemoglobin A1 (HbA1: α2β2) by 6–12 months. Hereditary Persistence of Fetal Hemoglobin (HPFH)
Irfan Shaukat   +4 more
doaj   +1 more source

Rapid point-of-care Hemoglobin measurement through low-cost optics and Convolutional Neural Network based validation [PDF]

open access: yesarXiv, 2017
A low-cost, robust, and simple mechanism to measure hemoglobin would play a critical role in the modern health infrastructure. Consistent sample acquisition has been a long-standing technical hurdle for photometer-based portable hemoglobin detectors which rely on micro cuvettes and dry chemistry. Any particulates (e.g.
arxiv  

Inhibition of G9a methyltransferase stimulates fetal hemoglobin production by facilitating LCR/γ-globin looping.

open access: yesBlood, 2015
Induction of fetal hemoglobin (HbF) production in adult erythrocytes can reduce the severity of sickle cell disease and β-thalassemia. Transcription of β-globin genes is regulated by the distant locus control region (LCR), which is brought into direct ...
I. Krivega   +6 more
semanticscholar   +1 more source

Magnetic mechanism for the biological functioning of hemoglobin [PDF]

open access: yesarXiv, 2019
The role of magnetism in the biological functioning of hemoglobin has been debated since its discovery by Pauling and Coryell in 1936. The hemoglobin molecule contains four heme groups each having a porphyrin layer with a Fe ion at the center. Here, we present combined density-functional theory and quantum Monte Carlo calculations for an effective ...
arxiv  

Failure of Microchromatographic Measurement of Fetal Hemoglobin in β0 Thalassemia-Hereditary Persistence of Fetal Hemoglobin

open access: yesClinical Chemistry, 1992
Abstract We report microchromatographic measurement of fetal hemoglobin (HbF) proportions in a 36-year-old African-American multigravida woman. At 34 weeks she delivered a 630-g male infant who subsequently did well. Hemoglobin electrophoresis of the hemolysate revealed nearly 100% HbF without HbA, an extremely unusual naturally ...
C. G. Pantazis   +3 more
openaire   +3 more sources

The LSD1 inhibitor RN-1 induces fetal hemoglobin synthesis and reduces disease pathology in sickle cell mice.

open access: yesBlood, 2015
Inhibition of lysine-specific demethylase 1 (LSD1) has been shown to induce fetal hemoglobin (HbF) levels in cultured human erythroid cells in vitro. Here we report the in vivo effects of LSD1 inactivation by a selective and more potent inhibitor, RN-1 ...
Shuaiying Cui   +14 more
semanticscholar   +1 more source

HSCB, a co-chaperone in mitochondrial iron-sulfur cluster biogenesis, is a novel candidate gene for congenital sideroblastic anemia [PDF]

open access: yes, 2017
Congenital sideroblastic anemias (CSA) are inherited diseases resulting from defects in heme biosynthesis, mitochondrial iron-sulfur cluster (ISC) assembly, or mitochondrial translation.
Crispin, Andrew
core  

Epigenetic modulations on the fetal hemoglobin induction [PDF]

open access: yesInternational Journal of Hematology-Oncology and Stem Cell Research, 2012
In recent years of experience fetal hemoglobin (HbF) induction considers as novel therapeutic approach for β-thalassemia and sickle cell in therapeutic approaches.
Najmaldin Saki   +4 more
doaj   +2 more sources

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