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Published in 2020 at "Journal of Clinical Laboratory Analysis"
DOI: 10.1002/jcla.23243
Abstract: Increased levels of fetal hemoglobin (HbF) can improve the clinical course of the patients with sickle cell anemia (SCA) or β‐thalassemia. The HBG1‐HBD intergenic region plays an important role in this process. However, very few…
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Keywords:
hbf;
association polymorphisms;
intergenic region;
hbg1 hbd ... See more keywords
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Published in 2021 at "American journal of human genetics"
DOI: 10.1016/j.ajhg.2021.03.005
Abstract: The fetal-to-adult hemoglobin switch is regulated in a developmental stage-specific manner and reactivation of fetal hemoglobin (HbF) has therapeutic implications for treatment of β-thalassemia and sickle cell anemia, two major global health problems. Although significant…
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Keywords:
hbf;
erf;
epigenetic inactivation;
thalassemia ... See more keywords
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Published in 2021 at "Biological Control"
DOI: 10.1016/j.biocontrol.2020.104469
Abstract: Abstract The larvae of Holotrichia parallela Motschulsky (Coleoptera: Scarabaeidae) are notorious soil insect pests that cause severe damage to crop production in China. However, the long-term use of insecticides seriously pollutes the environment and threatens…
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Keywords:
larvae;
beicherriana strain;
hbf;
holotrichia parallela ... See more keywords
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Published in 2021 at "Journal of pediatric surgery"
DOI: 10.1016/j.jpedsurg.2021.04.018
Abstract: PURPOSE The aim of this study was to assess the percent decrease in fetal hemoglobin (HbF) after transfusion of adult-derived donor packed red blood cell (pRBC) units in extremely low gestational age newborns (ELGANs). METHODS…
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Keywords:
hbf;
hemoglobin;
blood;
fetal hemoglobin ... See more keywords
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Published in 2017 at "Transfusion Clinique Et Biologique"
DOI: 10.1016/j.tracli.2017.06.189
Abstract: Objectif Evaluer un kit de detection et quantification de l’hemorragie fœto-maternelle par cytometrie en flux utilisant un double marquage antihemoglobine fœtale (anti-HbF) et anti-anhydrase carbonique (anti-AC). Materiel & methode Vingt-neuf prelevements de femmes enceintes, dont…
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Keywords:
double marquage;
hbf;
anti;
avec reactif ... See more keywords
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Published in 2020 at "Eye"
DOI: 10.1038/s41433-020-0938-5
Abstract: Background/objectives Previous studies have suggested that lower mean foetal haemoglobin (HbF) levels is associated with an increased risk for developing retinopathy of prematurity (ROP). Lower HbF levels may lead to high oxygen exposure to the…
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Keywords:
hbf;
age;
rop;
hbf levels ... See more keywords
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Published in 2019 at "Lab Animal"
DOI: 10.1038/s41684-019-0406-7
Abstract: β-hemoglobinopathies are inherited disorders caused by mutations in the β-globin gene. Sickle cell disease, for example, is the result of deficient hemoglobin (Hb); patients with β-thalassemia produce insufficient amounts of the oxygen-carrying protein. To date,…
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Keywords:
hbf;
crispr cas9;
cas9 edited;
gene ... See more keywords
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Published in 2018 at "Journal of Biomolecular Structure and Dynamics"
DOI: 10.1080/07391102.2018.1532320
Abstract: Abstract Quasi-palindromic sequences (AT)XN12(AT)Y present in HS2 (hypersensitive site 2) of the human β-globin locus are known to be significantly associated with increased fetal hemoglobin (HbF) levels. High HbF levels in some adults arise due…
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Keywords:
xn12;
hbf;
fetal hemoglobin;
unusual stability ... See more keywords
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Published in 2022 at "Expert Opinion on Therapeutic Targets"
DOI: 10.1080/14728222.2022.2066519
Abstract: ABSTRACT Introduction Sickle cell disease and β thalassemia are the principal β hemoglobinopathies. The complex pathophysiology of sickle cell disease is initiated by sickle hemoglobin polymerization. In β thalassemia, insufficient β-globin synthesis results in excessive…
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Keywords:
thalassemia;
hbf;
cell disease;
sickle cell ... See more keywords
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Published in 2022 at "Expert Opinion on Drug Discovery"
DOI: 10.1080/17460441.2022.2141708
Abstract: ABSTRACT Introduction Sickle cell anemia (SCA) is a hematological genetic disorder caused by a mutation in the gene of the β-globin. Pharmacological treatments will continue to be an important approach, including the strategy to induce…
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Keywords:
new drugs;
art fetal;
hbf;
state art ... See more keywords
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Published in 2018 at "Journal of Pediatric Hematology/Oncology"
DOI: 10.1097/mph.0000000000001093
Abstract: Background: Any mutation in the Krüppel-like factor 1 (KLF1) gene may interfere with its proper related function in the erythropoiesis process and lead to alterations in proper activation of its downstream protein through globin switching,…
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Keywords:
hbf;
individuals increased;
fetal hemoglobin;
gene ... See more keywords