Results 191 to 200 of about 219,391 (317)
Evaluation of cardiac and hepatic iron overload in thalassemia major patients with T2* magnetic resonance imaging [PDF]
Pustika Amalia Wahidiyat +5 more
openalex +1 more source
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
Background: Beta thalassemia is a common health problem in Iran especially in Northern provinces. Premarital screening for thalassemia is compulsory in Iran and identification of the carriers is based on primary CBC (Cell Blood Count) and hemoglobin ...
Hossein Karami +3 more
doaj
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
ABSTRACT Necrotizing fasciitis (NF) is a rare but serious life‐threatening condition in children that can be easily overlooked due to its atypical presentation and absence of common risk factors. This case involves a 10‐year‐old girl with a history of non‐transfusion‐dependent thalassemia and epilepsy who developed cervicofacial NF without any prior ...
Anza Muhammad Mohsin +3 more
wiley +1 more source
ATRX: From Chromatin Remodeling to Disease
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
Background: Beta thalassemia is the most common genetic disorder in Pakistan. Thalassemia is a preventive disease a fact well demonstrated by countries such as Italy, Greece and Cyprus.
Muhammad Usman
doaj
Interscanner reproducibility of cardiovascular magnetic resonance T2* measurements of tissue iron in thalassemia [PDF]
Mark A. Westwood +6 more
openalex +1 more source
Antenatal dexamethasone for late preterm delivery: Rate of complete course and neonatal outcomes
Abstract Objective This retrospective cohort study aimed to assess the rate of complete dexamethasone administration among late preterm deliveries and its impact on neonatal outcomes. Methods We reviewed medical records of 1500 late preterm deliveries (gestational age 34–36 + 6 weeks) between January 2018 and December 2020, analyzing baseline ...
Piyamon Srisakulpanich +3 more
wiley +1 more source
Identification of maternal <sup>G</sup>γ(<sup>A</sup>γδβ)<sup>0</sup> thalassemia through retrospective reanalysis of prenatal cfDNA sequencing data. [PDF]
Zhu X +9 more
europepmc +1 more source

