| 1 |
34454814 | Infant with early onset bilateral facial and bulbar weakness: Successful treatment of riboflavin in multiple acyl-CoA dehydrogenase deficiency caused by biallelic nonsense FLAD1 variants. | 2021 Nov |
1 |
| 2 |
34558787 | Mimicking human riboflavin responsive neuromuscular disorders by silencing flad-1 gene in C. elegans: Alteration of vitamin transport and cholinergic transmission. | 2021 Sep 24 |
1 |
| 3 |
30311138 | A Novel Truncating FLAD1 Variant, Causing Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) in an 8-Year-Old Boy. | 2019 |
3 |
| 4 |
31351152 | The hidden side of the human FAD synthase 2. | 2019 Oct 1 |
1 |
| 5 |
31835305 | Mutation of Aspartate 238 in FAD Synthase Isoform 6 Increases the Specific Activity by Weakening the FAD Binding. | 2019 Dec 9 |
1 |
| 6 |
29316637 | Bacterial Production, Characterization and Protein Modeling of a Novel Monofuctional Isoform of FAD Synthase in Humans: An Emergency Protein? | 2018 Jan 6 |
2 |
| 7 |
30061063 | Post-mortem detection of FLAD1 mutations in 2 Turkish siblings with hypotonia in early infancy. | 2018 Sep |
1 |
| 8 |
28433476 | Patient with multiple acyl-CoA dehydrogenation deficiency disease and FLAD1 mutations benefits from riboflavin therapy. | 2017 Jun |
4 |
| 9 |
26277395 | Human FAD synthase is a bi-functional enzyme with a FAD hydrolase activity in the molybdopterin binding domain. | 2015 Sep 25 |
1 |
| 10 |
25135855 | Significance of redox-active cysteines in human FAD synthase isoform 2. | 2014 Dec |
2 |
| 11 |
23443125 | Bacterial over-expression and purification of the 3'phosphoadenosine 5'phosphosulfate (PAPS) reductase domain of human FAD synthase: functional characterization and homology modeling. | 2012 Dec 11 |
2 |
| 12 |
21308351 | Involvement of riboflavin kinase expression in cellular sensitivity against cisplatin. | 2011 Apr |
1 |
| 13 |
20060505 | Mitochondrial localization of human FAD synthetase isoform 1. | 2010 Apr |
2 |
| 14 |
17049878 | Over-expression in Escherichia coli, purification and characterization of isoform 2 of human FAD synthetase. | 2007 Mar |
2 |
| 15 |
17689999 | Transient multiple acyl-CoA dehydrogenation deficiency in a newborn female caused by maternal riboflavin deficiency. | 2007 Sep-Oct |
1 |
| 16 |
16643857 | Over-expression in Escherichia coli and characterization of two recombinant isoforms of human FAD synthetase. | 2006 Jun 9 |
2 |