Results 11 to 20 of about 908,771 (315)
Influenza is a serious respiratory disease that continues to threaten global health. Mucosa-associated invariant T (MAIT) cells use T-cell receptors (TCRs) that recognize microbial riboflavin derived intermediates presented by the major ...
Ying Li +47 more
doaj +2 more sources
Riboflavin transporter deficiency (RTD) is a rare genetic disorder characterized by motor, sensory and cranial neuropathy. This childhood-onset neurodegenerative disease is caused by biallelic pathogenic variants in either SLC52A2 or SLC52A3 genes ...
Fiorella Colasuonno +5 more
doaj +2 more sources
Effects of riboflavin deficiency on the lipid metabolism of duck breeders and duck embryos. [PDF]
Zhang B +8 more
europepmc +2 more sources
Circumcorneal Injection in Riboflavin Deficiency [PDF]
Harold Scarborough
openalex +4 more sources
Riboflavin improves meat quality, antioxidant capacity, muscle development, and lipids composition of breast muscle in pigeon [PDF]
This study investigated the effects of different dietary riboflavin supplementation levels on riboflavin status, meat quality, antioxidant capacity, breast muscle development, and lipid composition in pigeons.
Bo Zhang +8 more
doaj +2 more sources
Problems in Riboflavin and Allied Deficiencies--II [PDF]
Hugh S. Stannus
openalex +7 more sources
Riboflavin Deficiency-Implications for General Human Health and Inborn Errors of Metabolism. [PDF]
As an essential vitamin, the role of riboflavin in human diet and health is increasingly being highlighted. Insufficient dietary intake of riboflavin is often reported in nutritional surveys and population studies, even in non-developing countries with ...
Mosegaard S +5 more
europepmc +2 more sources
Effect of riboflavin deficiency on development of the cerebral cortex in Slc52a3 knockout mice. [PDF]
Riboflavin transporter 3 (RFVT3), encoded by the SLC52A3 gene, is important for riboflavin homeostasis in the small intestine, kidney, and placenta. Our previous study demonstrated that Slc52a3 knockout (Slc52a3−/−) mice exhibited neonatal lethality and ...
Jin C +11 more
europepmc +2 more sources
Maternal riboflavin deficiency [PDF]
Maternal riboflavin deficiency is a rare, genetic disorder of metabolite absorption or transport characterized by persistently decreased riboflavin serum levels due to a primary genetic defect in the mother and which leads to clinical and biochemical ...
openalex +2 more sources

