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Quantifying glucose uptake at the single cell level with confocal microscopy reveals significant variability within and across individuals.

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January 2025

Applied Research and Technology, Abbott Diagnostics Division, Abbott Laboratories, Abbott Park, IL, 60064, USA.

Measurement of glycated hemoglobin (HbA1c) in human red blood cells plays a critical role in the diagnosis and treatment of diabetes mellitus. However, recent studies have suggested large variation in the relationship between average glucose levels and HbA1c, creating the need to understand glucose variability at the cellular level. Here, we devised a fluorescence-based method to quantitatively observe GLUT1-mediated intracellular glucose analog tracer uptake in individual RBCs utilizing microfluidics and confocal microscopy.

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Background: The antigen Na-GST-1, expressed by the hookworm Necator americanus, plays crucial biochemical roles in parasite survival. This study explores the development of mRNA vaccine candidates based on Na-GST-1, building on the success of recombinant Na-GST-1 (rNa-GST-1) protein, currently assessed as a subunit vaccine candidate, which has shown promise in preclinical and clinical studies.

Methodology/findings: By leveraging the flexible design of RNA vaccines and protein intracellular trafficking signal sequences, we developed three variants of Na-GST-1 as native (cytosolic), secretory, and plasma membrane-anchored (PM) antigens.

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Streptomycetes are bacteria of significant biotechnological interest due to their production of bioactive specialised metabolites used in medicine and agriculture. In these bacteria, specialised metabolism and morphological differentiation are linked and typically repressed under high phosphate conditions. This study characterises a DeoR-like transcriptional regulator, SCO1897, in Streptomyces coelicolor, whose expression increases during sporulation.

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From heart to gut: Exploring the gut microbiome in congenital heart disease.

Imeta

November 2023

Pediatric Cardiac Surgery Centre, Fuwai Hospital, National Centre for Cardiovascular Diseases, State Key Laboratory of Cardiovascular Disease, Chinese Academy of Medical Sciences Peking Union Medical College Beijing China.

Congenital heart disease (CHD) is a prevalent birth defect and a significant contributor to childhood mortality. The major characteristics of CHD include cardiovascular malformations and hemodynamical disorders. However, the impact of CHD extends beyond the circulatory system.

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Mitochondrial dysfunction in brain tissues and Extracellular Vesicles Fragile X-associated tremor/ataxia syndrome.

Ann Clin Transl Neurol

June 2024

Laboratory of Clinical Investigation, Intramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, USA.

Article Synopsis
  • - The study investigates mitochondrial dysfunction in patients with Fragile X-associated tremor/ataxia syndrome (FXTAS) by comparing postmortem brain tissues and plasma neuron-derived extracellular vesicles (NDEVs) from living carriers of the FMR1 gene premutations.
  • - Results showed that FXTAS patients had lower activity and quantity of specific mitochondrial proteins (Complex IV and V) in the cerebellum compared to controls, while NDEVs from premutation carriers also exhibited abnormalities despite higher Complex V quantity.
  • - The findings suggest that mitochondrial impairments in FXTAS may be detectable in plasma NDEVs, offering potential for developing biomarkers for early symptom prediction and monitoring the disease's progression.
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