Co-Induction of ULK-1 and AHSP mRNAs in Erythroid Precursor Cells Isolated From a Sirolimus-Treated β-Thalassemia Patient: A Case Report Study
IntroductionThe β-thalassemias are inherited genetic disorders affecting the hematopoietic system and caused by mutations of the adult β-globin gene, leading to low or absent production of adult hemoglobin. In addition, an excess of free α-globin is associated with ineffective erythropoiesis. In fac...
Saved in:
Main Authors: | Matteo Zurlo, Alessia Finotti, Maria Rita Gamberini, Roberto Gambari |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2025-06-01
|
Series: | British Journal of Biomedical Science |
Subjects: | |
Online Access: | https://www.frontierspartnerships.org/articles/10.3389/bjbs.2025.14311/full |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
The triad interaction of ULK1, ATG13, and FIP200 is required for ULK complex formation and autophagy
by: Yutaro Hama, et al.
Published: (2025-06-01) -
Comparative acute toxicity of intravenous paclitaxel and sirolimus in rats
by: Jing Xie, et al.
Published: (2025-01-01) -
Human Metabolism of Sirolimus Revisited
by: Baharak Davari, et al.
Published: (2025-07-01) -
Additive Therapeutic Effects of Topical Sirolimus Following Oral Propranolol Therapy for Kaposiform Hemangioendothelioma
by: Xiu B, et al.
Published: (2025-05-01) -
Effect of sex class on the levels of some biochemical variables in thalassemia patients
by: Khalaf N. Mohammed, et al.
Published: (2019-11-01)