(Q64094610)

2

0 references

Ming Xue

3

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Zhanbao Guo

4

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Ming Xie

5

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Bo Zhang

6

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Zhengkui Zhou

7

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Wei Huang

8

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Shuisheng Hou

Creative Commons Attribution 4.0 International

9

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language of work or name

English

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publication date

2019

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published in

Nutrition and Metabolism

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volume

16

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issue

1

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page(s)

19

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copyright license

start time

14 March 2019

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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exact match

https://scigraph.springernature.com/pub.10.1186/s12986-019-0345-8

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cites work

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Riboflavin deficiency and beta-oxidation systems in rat liver

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Riboflavin-deficient chicken embryos: hypoglycemia without dicarboxylic aciduria

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Vitamin profiles of eggs as indicators of nutritional status in the laying hen: riboflavin study

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Sudden death of chicken embryos with hereditary riboflavin deficiency

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Molecular cloning and characterization of the human mitochondrial 2,4-dienoyl-CoA reductase gene (DECR)

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Peroxisomal Delta3-cis-Delta2-trans-enoyl-CoA isomerase encoded by ECI1 is required for growth of the yeast Saccharomyces cerevisiae on unsaturated fatty acids

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Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndrome

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Gene ontology: tool for the unification of biology

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The molecular mechanism of ATP synthesis by F1F0-ATP synthase

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Structural and functional genomics of the CPT1B gene for muscle-type carnitine palmitoyltransferase I in mammals.

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Succinate dehydrogenase and human diseases: new insights into a well-known enzyme

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Clear relationship between ETF/ETFDH genotype and phenotype in patients with multiple acyl-CoA dehydrogenation deficiency

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The alpha-ketoglutarate-dehydrogenase complex: a mediator between mitochondria and oxidative stress in neurodegeneration

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Riboflavin enhances the assembly of mitochondrial cytochrome c oxidase in C. elegans NADH-ubiquinone oxidoreductase mutants

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Coordinated and reversible reduction of enzymes involved in terminal oxidative metabolism in skeletal muscle mitochondria from a riboflavin-responsive, multiple acyl-CoA dehydrogenase deficiency patient

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Analysis of the assembly profiles for mitochondrial- and nuclear-DNA-encoded subunits into complex I

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alpha-Ketoglutarate dehydrogenase contributes to production of reactive oxygen species in glutamate-stimulated hippocampal neurons in situ

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Genetic variation in ATP5O is associated with skeletal muscle ATP50 mRNA expression and glucose uptake in young twins

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Regulation of the human SLC25A20 expression by peroxisome proliferator-activated receptor alpha in human hepatoblastoma cells

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Rapid determination of vitamin B₂ (riboflavin) in plasma by HPLC

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Mitochondrial carnitine palmitoyltransferase 1a (CPT1a) is part of an outer membrane fatty acid transfer complex

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Complex I assembly function and fatty acid oxidation enzyme activity of ACAD9 both contribute to disease severity in ACAD9 deficiency.

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Riboflavin deficiency induces a significant change in proteomic profiles in HepG2 cells

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Severe riboflavin deficiency induces alterations in the hepatic proteome of starter Pekin ducks

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Transcriptional profiling of liver in riboflavin-deficient chicken embryos explains impaired lipid utilization, energy depletion, massive hemorrhaging, and delayed feathering.

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