Incubating green synthesized iron oxide nanorods for proteomics-derived motif exploration: A fusion to deep learning oncogenesis

Y Manzoor, M Hasan, A Zafar, M Dilshad… - ACS …, 2022 - ACS Publications
The nanotechnological arena has revolutionized the diagnostic efficacies by investigating
the protein corona. This displays provoking proficiencies in determining biomarkers and …

Pharmacogenomics of Drugs Used in β-Thalassemia and Sickle-Cell Disease: From Basic Research to Clinical Applications

R Gambari, AD Waziri, H Goonasekera… - International journal of …, 2024 - mdpi.com
In this short review we have presented and discussed studies on pharmacogenomics (also
termed pharmacogenetics) of the drugs employed in the treatment of β-thalassemia or Sickle …

Activating transcription factor 4 in erythroid development and -thalassemia: a powerful regulator with therapeutic potential

J Li, A Lv, M Chen, L Xu, H Huang - Annals of hematology, 2024 - Springer
Abstract Activating transcription factor 4 (ATF4) is a fundamental basic region/leucine zipper
transcription factor, responds to various stress signals, and plays crucial roles in normal …

Human cellular model systems of β-thalassemia enable in-depth analysis of disease phenotype

DE Daniels, I Ferrer-Vicens, J Hawksworth… - Nature …, 2023 - nature.com
Abstract β-thalassemia is a prevalent genetic disorder causing severe anemia due to
defective erythropoiesis, with few treatment options. Studying the underlying molecular …

Prime Editor 3 Mediated Beta-Thalassemia Mutations of the HBB Gene in Human Erythroid Progenitor Cells

H Zhang, Q Zhou, H Chen, D Lu - International Journal of Molecular …, 2022 - mdpi.com
Recently developed Prime Editor 3 (PE3) has been implemented to induce genome editing
in various cell types but has not been proven in human hematopoietic stem and progenitor …

[HTML][HTML] Erythropoiesis and Gene Expression Analysis in Erythroid Progenitor Cells Derived from Patients with Hemoglobin H/Constant Spring Disease

N Wongkhammul, P Khamphikham, S Tongjai… - International Journal of …, 2024 - mdpi.com
Hemoglobin H/Constant Spring (Hb H/CS) disease represents a form of non-deletional Hb H
disease characterized by chronic hemolytic anemia that ranges from moderate to severe …

A Review of CRISPR Cas9 for SCA: Treatment Strategies and Could Target β-globin Gene and BCL11A Gene using CRISPR Cas9 Prevent the Patient from Sickle …

BE Suwito, AS Adji, JS Widjaja… - … Journal of Medical …, 2023 - repository.unusa.ac.id
BACKGROUND: Sickle cell anemia is a hereditary globin chain condition that leads to
hemolysis and persistent organ damage. Chronic hemolytic anemia, severe acute and …

[PDF][PDF] Choirotussanijjah. A Review of CRISPR Cas9 for SCA: Treatment Strategies and Could Target β-globin Gene and BCL11A Gene using CRISPR Cas9 Prevent …

BE Suwito, AS Adji, JS Widjaja, SCS Angel… - 2023 - researchgate.net
BACKGROUND: Sickle cell anemia is a hereditary globin chain condition that leads to
hemolysis and persistent organ damage. Chronic hemolytic anemia, severe acute and …

Tissue-specific variations in transcription factors elucidate complex immune system regulation

H Lu, YC Tang, A Gottlieb - Genes, 2022 - mdpi.com
Gene expression plays a key role in health and disease. Estimating the genetic components
underlying gene expression can thus help understand disease etiology. Polygenic models …

Ferroptosis, un mecanismo de muerte celular presente en β-talasemia menor

MM Terán, ME Mónaco, C Haro… - Revista Bioquímica y …, 2025 - revistabypc.org.ar
La ferroptosis es un tipo de muerte celular programada, dependiente de hierro, impulsada
por una severa peroxidación lipídica, la cual es consecuencia del metabolismo celular y de …