Combination of a triple alpha-globin gene with beta-thalassemia in a gypsy family: importance of the genetic testing in the diagnosis and search for a donor for bone marrow transplantation for one of their children [PDF]
, 2016 Flor Yus Cebrian +4 more
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Advanced Science, Volume 12, Issue 45, December 4, 2025.This study employed tRNASUAG, an anticodon‐engineered tRNA (ACE‐tRNA), to introduce a phosphorylatable serine into the C‐terminal domain of HBc by reading through its stop codon, thereby potentially promoting the ubiquitin‐proteasome degradation of HBc, and subsequently inhibiting HBV replication. Through a tRNASUAG‐gHBV1‐tRNASUAG‐gHBV2‐tRNASUAG tandem
Xingwen Yang +7 more
wiley +1 more source
Serum erythropoietin and erythropoiesis in high- and low-fetal hemoglobin beta-thalassemia intermedia patients [PDF]
, 1994 R. Galanello +8 more
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Analytical Science Advances, Volume 6, Issue 2, December 2025.ABSTRACT In this work, we developed a matrix‐assisted laser desorption ionization time‐of‐flight mass spectrometry (MALDI‐TOF‐MS) method to directly analyze human whole blood samples. 1.0 µL of whole blood samples and 1.0 µL of optimized organic matrix were directly loaded onto the sample plates for MALDI‐TOF‐MS detection.
Dan‐ping Liu +11 more
wiley +1 more source
The levels of nitric oxide in beta-thalassemia minor
Turkish Journal of Hematology, 2008 OBJECTIVE: The aim of this study was to investigate the relationship between NO (nitric oxide) and beta-thalassemia minor. METHODS: A total of 60 patients with beta-thalassemia minor (30 M, 30 F) were included in the study. The control group consisted of
Yalçın Başaran +3 more
doaj
Quality of life among patients with beta-thalassemia major in Shahrekord city, Iran [PDF]
, 2016 Background and aims: Nowadays introduction of regular blood transfusion therapy has obviously improved the life expectancy of patients with thalassemia. However, these patients face with newer challenges which influence their quality of life (QoL).
Emadi Dehaghi, B. +2 more
core
ATRX: From Chromatin Remodeling to Disease
genesis, Volume 63, Issue 6, December 2025.ABSTRACT Chromatin remodeling proteins are evolutionarily conserved factors involved in a wide range of biological processes. In this review, we describe ATRX, a chromatin remodeling protein belonging to the SWI/SNF2 family. Its association with different protein complexes, and its roles in embryonic development, sexual differentiation, as well as ...
Mauro Magaña‐Acosta +1 more
wiley +1 more source
Anemia, 2012 Beta thalassemia major is an inherited disease resulting from reduction or total lack of beta globin chains. Patients with this disease need repeated blood transfusion for survival.
Q. Shazia +3 more
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Insulin-like growth factor-1 levels in children with Beta-thalassemia minor [PDF]
, 2008 Objective: Growth retardation in children with b-thalassemia major is multifactorial. Some etiologies described for this condition are hemochromatosis, disturbed growth hormone (GH) / insulin growth factor-1 (IGF-1) axis, undernutrition and ...
Hamdollah Karamifar +2 more
core
Controversies surrounding the effects of beta S-haplotype and alpha- thalassemia-2 on the clinical severity of sickle cell anemia [letter] [PDF]
, 1994 LS Chan, DR Powars
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