Genetic variation and sickle cell disease severity: a systematic review and meta-analysis
Importance Sickle cell disease (SCD) is a monogenic disorder, yet clinical outcomes are
influenced by additional genetic factors. Despite decades of research, the genetics of SCD …
influenced by additional genetic factors. Despite decades of research, the genetics of SCD …
Evaluation of antioxidants using electrochemical sensors: a bibliometric analysis
Y Zheng, H Karimi-Maleh, L Fu - Sensors, 2022 - mdpi.com
The imbalance of oxidation and antioxidant systems in the biological system can lead to
oxidative stress, which is closely related to the pathogenesis of many diseases. Substances …
oxidative stress, which is closely related to the pathogenesis of many diseases. Substances …
Toward a conversational agent to support the self-management of adults and young adults with sickle cell disease: usability and usefulness study
DZ Issom, MD Hardy-Dessources, M Romana… - Frontiers in Digital …, 2021 - frontiersin.org
Sickle cell disease (SCD) is the most common genetic blood disorder in the world and
affects millions of people. With aging, patients encounter an increasing number of …
affects millions of people. With aging, patients encounter an increasing number of …
Sickle cell in sickle cell disease in Latin America and the United States
A Huttle, GE Maestre, R Lantigua… - Pediatric blood & …, 2015 - Wiley Online Library
Latin Americans are an underappreciated population affected by sickle cell disease (SCD).
Sickle trait and SCD exist throughout Latin America and US Latino communities. We …
Sickle trait and SCD exist throughout Latin America and US Latino communities. We …
Oxidative profile of sickle cell patients in a Cameroonian urban hospital
VJ Ama Moor, CA Pieme, B Chetcha Chemegne… - BMC clinical …, 2016 - Springer
Background Sickle cell disease (SCD) is a class of hemoglobinopathy resulting from a
single mutation in the ß-globin chain inducing the substitution of valine for glutamic acid at …
single mutation in the ß-globin chain inducing the substitution of valine for glutamic acid at …
Inflammation in sickle cell disease: differential and down-expressed plasma levels of annexin A1 protein
LS Torres, JV Okumura, DGH Silva, KKO Mimura… - PloS one, 2016 - journals.plos.org
Sickle cell disease (SCD) is an inherited hemolytic anemia whose pathophysiology is driven
by polymerization of the hemoglobin S (Hb S), leading to hemolysis and vaso-occlusive …
by polymerization of the hemoglobin S (Hb S), leading to hemolysis and vaso-occlusive …
A sensing platform using Ag/Pt core‐shell nanostructures supported on multiwalled carbon nanotubes to detect hydroxyurea
M Haghshenas, M Mazloum‐Ardakani… - …, 2020 - Wiley Online Library
Developing anticancer sensing platforms has a significant impact on individual cancer
treatment. Monitoring of anticancer drugs in bodily fluid allows doctors to prescript the …
treatment. Monitoring of anticancer drugs in bodily fluid allows doctors to prescript the …
[HTML][HTML] Impact of Superoxide Dismutase genetic polymorphism (SOD2 Val16Ala) and Superoxide Dismutase level on disease severity in a cohort of Egyptian sickle …
MM Khorshied, IA Shaheen, YMM Selim… - … of Hematology and …, 2022 - ncbi.nlm.nih.gov
Background Oxidative stress plays a pivotal role in the pathophysiology of sickle cell
disease (SCD) and its associated disease complications. Superoxide Dismutases (SODs) …
disease (SCD) and its associated disease complications. Superoxide Dismutases (SODs) …
Exploring the antioxidant and antidiabetic potentials of Syzygium cumini L. landraces: phytochemicals, bioactive constituents and pathway enrichment analysis
HP Gajera, DG Hirpara, SN Gevariya… - … Journal of Food …, 2024 - Wiley Online Library
This study proposes an efficient antidiabetic strategy by identifying potential mechanisms of
antioxidant metabolism and α‐amylase inhibition in Syzygium cumini L. fruits. Six …
antioxidant metabolism and α‐amylase inhibition in Syzygium cumini L. fruits. Six …
[HTML][HTML] Ferroptosis as an emerging target in sickle cell disease
V Fortuna, J Lima, GF Oliveira, YS Oliveira… - Current Research in …, 2024 - Elsevier
Sickle cell disease (SCD) is an inherited hemoglobin disorder marked by red blood cell
sickling, resulting in severe anemia, painful episodes, extensive organ damage, and …
sickling, resulting in severe anemia, painful episodes, extensive organ damage, and …