Results 71 to 80 of about 8,693 (164)
Abstract Fish vaccination has been practiced globally for several decades and is increasingly recognized as a cornerstone of sustainable disease management in aquaculture, offering an effective alternative to antibiotic and chemotherapeutic use. This PRISMA‐ScR guided Scoping Review synthesized evidence from 173 peer‐reviewed studies and reports to ...
Fredrick Juma Syanya +6 more
wiley +1 more source
Classical galactosaemia is an inborn error of metabolism due to the deficiency of the enzyme galactose-1-phosphate uridylyltransferase (GALT). The aim of the study was to identify the underlying mutations in Greek patients with GALT deficiency and evaluate their psychomotor and speech development.
Schulpis, K.H. +7 more
openaire +3 more sources
Glycosylation of arabinogalactan-proteins essential for development in Arabidopsis
Arabinogalactan-proteins (AGPs) are ubiquitous cell wall components present throughout the plant kingdom. They are extensively post translationally modified by conversion of proline to hydroxyproline (Hyp) and by addition of arabinogalactan (AG ...
Allan M. Showalter, Debarati Basu
doaj +1 more source
The aim of this study was to determine the role of an exopolysaccharide produced by natural dairy isolate Lactobacillus paracasei subsp. paracasei BGSJ2-8, in the adhesion to intestinal epithelial cells and a decrease in E. coli’s association with Caco-2
Milica eZivkovic +8 more
doaj +1 more source
The gastrointestinal tract is an ideal habitat for diverse bacterial species that reside in a homeostatic balance with local tissue and significantly contribute to host health.
Anshu Babbar +7 more
doaj +1 more source
The unfolded protein response has a protective role in yeast models of classic galactosemia
Classic galactosemia is a human autosomal recessive disorder caused by mutations in the GALT gene (GAL7 in yeast), which encodes the enzyme galactose-1-phosphate uridyltransferase.
Evandro A. De-Souza +6 more
doaj +1 more source
Molecular characterization of Galactosemia and identification of GALT gene mutations
S. N. Mammadova, L. S. Huseynova
openaire +1 more source
Biochemical Diagnosis of Common Gene Mutations in Galactosemia
Objective: Galactosemia is an inborn error of galactose metabolism that is inherited in an autosomal recessive trait. Classical galactosemia is caused by deficient activity of the galactose-1-phosphate uridyltransferase (GALT) enzyme that can result in ...
Farzaneh Mirzajani +6 more
doaj
Background The objective of this study was to document the clinical, laboratory and genetic features of galactosemia in patients from the Cape Town metropolitan region.
Brown Ruth +3 more
doaj +1 more source
Galactosemia, caused by mutations in the GALT gene, leads to multi-organ damage. This study investigates the impact of Galt c.847 + 1G > T mutation on lung tissue using single-cell transcriptomics. We employed CRISPR/Cas9 to generate a Galt gene-edited mouse model with the Galt c.
Zhihao, Li +8 more
openaire +2 more sources

