Results 161 to 170 of about 1,051,766 (308)

A Novel Alpha1‐Variant (HBA1:c.‐35T>C) Complexed With the First Reported Hb M‐Saskatoon in the Chinese Population

open access: yesMolecular Genetics &Genomic Medicine, Volume 14, Issue 1, January 2026.
The research subjects were diagnosed with two distinct types of abnormal hemoglobin. Our study reports the first case of a complex hemoglobinopathy in China, characterized by the presence of the globally first‐reported alpha1 variant (HBA1:c.‐35T>C) and the initial identification of Hb M‐Saskatoon (HBB:c.190C>T) in China.
Yujing Yang   +5 more
wiley   +1 more source

Pre-Natal Diagnosis of beta – Thalassemia by Chorionic Villous Sampling

open access: yesJournal of Rawalpindi Medical College, 2009
Background: To promote the utility of Chorionic Villous Sampling (CVS) for pre-natal diagnosis of beta thalassemia in at risk population and to highlight its demographic area distribution and effect of consanguinity.
Shazia Syed,
doaj  

Is there an association of giardiasis with beta-thalassemia minor? [PDF]

open access: yes, 2010
Beta–thalassemia minor is a symptomless carrier state of a hemoglobinopathy which predisposes to bacterial infections. We report three cases presenting with giardiasis, a parasitic infection of gastrointestinal tract caused by Giardia lamblia.
Jafri, Wasim   +2 more
core   +1 more source

Targeted Carrier Screening for Thalassemia, Hereditary Deafness, and Spinal Muscular Atrophy: A Feasible Approach for Preventing Birth Defects in China's Community Healthcare System

open access: yesMolecular Genetics &Genomic Medicine, Volume 14, Issue 1, January 2026.
Current carrier screening primarily focuses on high detection rates and broad testing ranges. We approach the issue from the perspective of a community physician, evaluating the suitability of carrier screening based on factors such as cost, ease of report interpretation, and compliance issues.
Zhihui Wang   +6 more
wiley   +1 more source

FREQUENCY OF BETA THALASSEMIA TRAIT AMONG THE HEALTHY INDIVIDUALS - A SINGLE CENTRE STUDY

open access: yesPakistan Armed Forces Medical Journal, 2018
Objective: To determine the frequency of beta thalassemia trait among the asymptomatic healthy individuals. Study Design: Cross sectional study. Place and Duration of Study: This was carried out at Pakistan Air Force (PAF) Hospital Lahore from ...
Muhammad Arif Sadiq   +3 more
doaj  

Protein Target Highlights in CASP16: Insights From the Structure Providers

open access: yesProteins: Structure, Function, and Bioinformatics, Volume 94, Issue 1, Page 25-50, January 2026.
ABSTRACT This article presents an in‐depth analysis of selected CASP16 targets, with a focus on their biological and functional significance. The authors highlight the most relevant features of the target proteins and discuss how well these were reproduced in the submitted predictions.
Leila T. Alexander   +34 more
wiley   +1 more source

Study of vascular endothelial dysfunction in children with beta-thalassemia major before and after quercetin therapy [PDF]

open access: diamond
Fatma Al Zahraa Sherai   +4 more
openalex   +1 more source

Insulin-like growth factor-1 levels in children with Beta-thalassemia minor [PDF]

open access: yes, 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  

Lipid Nanoparticles for Delivery of CRISPR Gene Editing Components

open access: yesSmall Methods, Volume 10, Issue 2, 22 January 2026.
The review presents a comprehensive overview of each component of lipid nanoparticles(LNPs)and their effects on editing efficiency. It specifically highlights strategies for achieving non‐liver delivery, aiming for broader applications in gene editing. Furthermore, this review summarizes the applications of LNPs in gene editing and offers insights for ...
Fan Wu   +6 more
wiley   +1 more source

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