Nanoscintillator‐Mediated X‐Ray‐Triggered Boosting Transformation of Fe3+ into Fe2+ for Enhancing Tumor Ferroptosis/Immunotherapy

C Zhang, S Lu, K Deng, W Qian, Y Liu… - Advanced Functional …, 2023 - Wiley Online Library
Ferroptosis therapy induced by iron‐catalyzed Fenton reaction has offered enormous
opportunities for tumor therapy. Unfortunately, high catalytic activity ferrous (Fe2+)‐based …

Emerging role of SMILE in liver metabolism

N Sadasivam, K Radhakrishnan, HS Choi… - International Journal of …, 2023 - mdpi.com
Small heterodimer partner-interacting leucine zipper (SMILE) is a member of the CREB/ATF
family of basic leucine zipper (bZIP) transcription factors. SMILE has two isoforms, a small …

Exploration of novel clusters and prognostic value of immune‑related signatures and identify HAMP as hub gene in colorectal cancer

H Wu, H Dong, S Ren, J Chen, Y Zhang… - Oncology …, 2023 - spandidos-publications.com
Immune checkpoint inhibitors currently serve an important role in prolonging patients' overall
survival. However, the prognostic signatures of immune checkpoint inhibitors in colorectal …

Is the Role of Hepcidin and Erythroferrone in the Pathogenesis of Beta Thalassemia the Key to Developing Novel Treatment Strategies?

TY Au, S Benjamin, OW Wiśniewski - Thalassemia Reports, 2022 - mdpi.com
Thalassemia is a disease of erythrocytes that varies largely on its genetic composition and
associated clinical presentation. Though some patients may remain asymptomatic, those …

Relationships of vitamin d and vitamin b12 with malonaldehyde in patients with beta thalassemia major

AR Nama, WN Hussein… - Journal of Namibian …, 2023 - namibian-studies.com
Background: Beta thalassemia major (Cooley's anemia) is a congenital genetic blood
disorder resulting from a deficiency of β-globin chains due to severe anemia that depends …

[HTML][HTML] Thalassemia: Pathophysiology, Diagnosis, and Advances in Treatment

IZ Sadiq, FS Abubakar, HS Usman, AD Abdullahi… - Thalassemia …, 2024 - mdpi.com
Thalassemia represents a diverse group of inherited hematological disorders characterized
by defective globin chain synthesis, leading to chronic anemia and associated …

[HTML][HTML] Extracellular Vesicles in Thalassemia: Mechanisms, Implications, and Therapeutic Potential

SA Jiskani - Aspects of Molecular Medicine, 2024 - Elsevier
Thalassemia is one of the most common inherited disorders of erythrocytes, caused by
abnormalities in the production of globin chains. The clinical spectrum of thalassemia is …

[PDF][PDF] Profiling circulating microRNA and regulatory pathways in transfusion-dependent thalassemia and thalassemia trait compared to healthy controls: a preliminary …

L Rujito, T Wardana, J Mulyanto, IM Nainggolan… - ExRNA, 2024 - pdf.elspublishing.com
Background: Thalassemia is a genetic blood disorder characterized by abnormal
hemoglobin production. MicroRNAs (miRNAs) regulate gene expression and are implicated …

Understanding the influence of diabetes on wound healing and exploring effective management study.

DS Rautela, S Das, A Mazumder… - Current Science …, 2024 - search.ebscohost.com
Diabetes is a diverse metabolic disease that is caused by increased levels of blood glucose,
which also leads to the generation of several other complications. The formation of wounds …

Iron and Heart Failure: Current Concepts and Emerging Pharmacological Paradigms

MRD Pascale, MB Rondinelli… - World Journal of …, 2024 - publish.journalgazett.co.in
Background: Emerging evidence has recognized that anemia and iron deficiency are
recurrent comorbidities in chronic heart failure (HF) and several trials have established that …