Zobrazeno 1 - 10
of 2 487
pro vyhledávání: '"tdt"'
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract Perceptual learning, known to improve visual perception, demonstrates the plasticity of brain processes underlying vision. Early studies, using the backward-masked texture discrimination task (TDT), focused on the lack of generalizing learni
Externí odkaz:
https://doaj.org/article/a985d8e3a3574306865b4cf2ea18e781
Publikováno v:
eJHaem, Vol 5, Iss 6, Pp 1351-1353 (2024)
Externí odkaz:
https://doaj.org/article/154d76e4dab9415cb4aec8cc6c3afc40
Autor:
Nigar Omar, Rawand P. Shamoon
Publikováno v:
Zanco Journal of Medical Sciences, Vol 28, Iss 2, Pp 129-138 (2024)
Background and objective: β-Thalassemia is a common inherited disease in this region. A considerable number of transfusion-dependent β-thalassemia (TDT) patients suffer bone problems. The objective of this study was to evaluate bone mineral density
Externí odkaz:
https://doaj.org/article/c5f6e8ff506c4f88b9eaee5c281f641e
Autor:
Mei YU, Yang CHEN, Xian LI, Qiuhong MO, Linbin HUANG, Xipeng YAN, Baoren HE, Bin LI, Limin CHEN
Publikováno v:
Zhongguo shuxue zazhi, Vol 37, Iss 5, Pp 567-574 (2024)
Objective To retrospectively analyze the blood use of transfusion-dependent thalassemia (TDT) patients in 9 designated transfusion medical institutions from 2018 to 2023 in Nanning, and to evaluate the effect of " three designated " blood transfusion
Externí odkaz:
https://doaj.org/article/d60fe23fe7fe4ed2b92e51afb02e17ea
Publikováno v:
In Heliyon 15 January 2025 11(1)
Publikováno v:
Global Journal of Medicine and Public Health, Vol 13, Iss 1 (2024)
Background Interaction of Hb E with beta-thalassemia results in red cell phenotypes with weakened alpha -beta interface causing decreased red cell survival. Severe forms of Hb E/beta-thalassemia on regular blood transfusion are exposed to multi
Externí odkaz:
https://doaj.org/article/9f7d7258a916487babcb2a464900328f
Publikováno v:
Biomolecules, Vol 14, Iss 8, p 961 (2024)
Human terminal deoxynucleotidyl transferase (TdT) can catalyze template-independent DNA synthesis during the V(D)J recombination and DNA repair through nonhomologous end joining. The capacity for template-independent random addition of nucleotides to
Externí odkaz:
https://doaj.org/article/7de0eb4adcee41ecb55624fd8cc8d8e1
Understanding the Intricacies of Iron Overload Associated with β-Thalassemia: A Comprehensive Review
Autor:
Subhangi Basu, Motiur Rahaman, Tuphan Kanti Dolai, Praphulla Chandra Shukla, Nishant Chakravorty
Publikováno v:
Thalassemia Reports, Vol 13, Iss 3, Pp 179-194 (2023)
β-thalassemia, a congenital genetic hematological disorder characterized by the decrease or absence of β-globin chains, leads to a decrease in levels of Hemoglobin A. The affected individuals can be categorized into two cohorts based on transfusion
Externí odkaz:
https://doaj.org/article/798f97d3697b45a8973ffb6bfe5197f7
Publikováno v:
Uluslararası Ekonomi, İşletme ve Politika Dergisi, Vol 7, Iss 1, Pp 132-151 (2023)
Çalışmanın amacı Türkiye’nin Türk Devletleri Teşkilatı (TDT) asıl üye ülkeleri ve gözlemci üye ülkeleri ile olan ticaretinde hangi mal gruplarında karşılaştırmalı üstünlüğe sahip olduğunu, hangi mal gruplarında ise karş
Externí odkaz:
https://doaj.org/article/c5d73ec62f73449d9e2188ff9f06ffca
Publikováno v:
工程科学学报, Vol 45, Iss 3, Pp 369-379 (2023)
The composition of nonmetallic inclusions in the steel varied continuously during the solidification and cooling process of the molten steel and the heating process of the solid steel. To quantitatively evaluate this evolution of inclusion compositio
Externí odkaz:
https://doaj.org/article/a1bd1f8cd6d14135abb80ba392f099f6