Results 11 to 20 of about 944,643 (357)

Two Rare Cases of Long Surviving Riboflavin Transporter Deficiency with Co-Existing Adenosine Monophosphate Deaminase (AMP) Deficiency

Brain Sciences, 2022
(1) Background: Riboflavin transporter deficiency (RTD), formerly known as Brown–Vialetto–Van Laere syndrome, is a rare condition that causes a progressive neurological syndrome in early life with features of auditory and optic neuropathy, weakness of ...
Lin Zhang, Dominic Thyagarajan
doaj   +2 more sources

Riboflavin deficiency induces a significant change in proteomic profiles in HepG2 cells. [PDF]

Sci Rep, 2017
Riboflavin deficiency is widespread in many regions over the world, especially in underdeveloped countries. In this study, we investigated the effects of riboflavin deficiency on protein expression profiles in HepG2 cells in order to provide molecular ...
Xin Z, Pu L, Gao W, Wang Y, Wei J, Shi T, Yao Z, Guo C.   +7 more
europepmc   +2 more sources

Riboflavin Attenuates Influenza Virus Through Cytokine-Mediated Effects on the Diversity of the Gut Microbiota in MAIT Cell Deficiency Mice

Frontiers in Microbiology, 2022
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, Ying Li, Ying Li, Ying Li, Chun-Wei Shi, Chun-Wei Shi, Chun-Wei Shi, Chun-Wei Shi, Yu-Ting Zhang, Yu-Ting Zhang, Yu-Ting Zhang, Yu-Ting Zhang, Hai-Bin Huang, Hai-Bin Huang, Hai-Bin Huang, Hai-Bin Huang, Yan-Long Jiang, Yan-Long Jiang, Yan-Long Jiang, Yan-Long Jiang, Jian-Zhong Wang, Jian-Zhong Wang, Jian-Zhong Wang, Jian-Zhong Wang, Xin Cao, Xin Cao, Xin Cao, Xin Cao, Nan Wang, Nan Wang, Nan Wang, Nan Wang, Yan Zeng, Yan Zeng, Yan Zeng, Yan Zeng, Gui-Lian Yang, Gui-Lian Yang, Gui-Lian Yang, Gui-Lian Yang, Wen-Tao Yang, Wen-Tao Yang, Wen-Tao Yang, Wen-Tao Yang, Chun-Feng Wang, Chun-Feng Wang, Chun-Feng Wang, Chun-Feng Wang   +47 more
doaj   +2 more sources

Role of riboflavin deficiency in malaria pathophysiology. [PDF]

PLoS Pathogens
The emergence of resistance against antimalarials and insecticides poses a significant threat to malaria elimination strategies. It is crucial to explore potential risk factors for malaria to identify new targets and alternative therapies.
Shweta Sharma, Arathy Ramachandran, Amit Sharma   +2 more
doaj   +2 more sources

Maternal riboflavin deficiency [PDF]

Definitions, 2020
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 ...
openaire   +2 more sources

Effect of riboflavin deficiency on intestinal morphology, jejunum mucosa proteomics, and cecal microbiota of Pekin ducks. [PDF]

Anim Nutr, 2023
Xu Y, Zhang B, Zhao R, Gao K, Liang S, Wu Y, Hao Y, Liu D, Guo Z, Hu J, Zhou Z, Xie M, Tang J.   +12 more
europepmc   +2 more sources

Effects of riboflavin deficiency on the lipid metabolism of duck breeders and duck embryos. [PDF]

Poult Sci, 2021
Zhang B, Tang J, Wu YB, Cao JT, Xing GN, Sun PX, Huang W, Xie M, Hou SS.   +8 more
europepmc   +2 more sources

Disruption of Slc52a3 gene causes neonatal lethality with riboflavin deficiency in mice. [PDF]

Sci Rep, 2016
Homeostasis of riboflavin should be maintained by transporters. Previous in vitro studies have elucidated basic information about riboflavin transporter RFVT3 encoded by SLC52A3 gene.
Yoshimatsu H, Yonezawa A, Yamanishi K, Yao Y, Sugano K, Nakagawa S, Imai S, Omura T, Nakagawa T, Yano I, Masuda S, Inui K, Matsubara K.   +12 more
europepmc   +2 more sources

Impact of natural mutations on the riboflavin transporter 2 and their relevance to human riboflavin transporter deficiency 2

IUBMB Life - A Journal of the International Union of Biochemistry and Molecular Biology, 2021
Riboflavin transporter deficiency 2 (RTD2) is a rare neurological disorder caused by mutations in the Solute carrier family 52 member 2 (Slc52a2) gene encoding human riboflavin transporter 2 (RFVT2).
Lara Console, Maria Tolomeo, Jessica Cosco, Keith Massey, Maria Barile, Cesare Indiveri   +5 more
openalex   +3 more sources

Riboflavin in neurological diseases: therapeutic advances, metabolic insights, and emerging genetic strategies [PDF]

Frontiers in Neurology
BackgroundRiboflavin (vitamin B2), a precursor of flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD), is essential for mitochondrial function, redox balance, and neuronal viability.
Zhiming Tao, Zhiming Tao, Zhiming Tao, Jinglu Huo, Jinglu Huo, Jinglu Huo, Xiaosheng Hao, Xiaosheng Hao, Xiaosheng Hao, Jianmin Liang, Jianmin Liang, Jianmin Liang   +11 more
doaj   +2 more sources