Literature DB >> 6895440

Organic aciduria in the riboflavin-deficient rat.

S I Goodman.   

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Year:  1981        PMID： 6895440     DOI： 10.1093/ajcn/34.11.2434

Source DB:  PubMed          Journal:  Am J Clin Nutr        ISSN： 0002-9165            Impact factor:   7.045


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  7 in total

1.  Hepatic peroxisomal and mitochondrial fatty acid oxidation in the riboflavin-deficient rat.

Authors:  P S Brady; C L Hoppel
Journal:  Biochem J       Date:  1985-08-01       Impact factor: 3.857

2.  Effects of riboflavin deficiency and clofibrate treatment on the five acyl-CoA dehydrogenases in rat liver mitochondria.

Authors:  K Veitch; J P Draye; F Van Hoof; H S Sherratt
Journal:  Biochem J       Date:  1988-09-01       Impact factor: 3.857

3.  Acyl-CoA dehydrogenase activity in the riboflavin-deficient rat. Effects of starvation.

Authors:  N S Ross; C L Hoppel
Journal:  Biochem J       Date:  1987-06-01       Impact factor: 3.857

4.  Products and intermediates of the beta-oxidation of [U-14C]hexadecanedionoyl-mono-CoA by rat liver peroxisomes and mitochondria.

Authors:  M Pourfarzam; K Bartlett
Journal:  Biochem J       Date:  1991-01-01       Impact factor: 3.857

5.  Brown-Vialetto-Van Laere and Fazio Londe syndrome is associated with a riboflavin transporter defect mimicking mild MADD: a new inborn error of metabolism with potential treatment.

Authors:  Annet M Bosch; Nico G G M Abeling; Lodewijk Ijlst; Hennie Knoester; W Ludo van der Pol; Alida E M Stroomer; Ronald J Wanders; Gepke Visser; Frits A Wijburg; Marinus Duran; Hans R Waterham
Journal:  J Inherit Metab Dis       Date:  2010-11-26       Impact factor: 4.982

6.  First report of paternal uniparental disomy of chromosome 8 with SLC52A2 mutation in Brown-vialetto-van laere syndrome type 2 and an analysis of genotype-phenotype correlations.

Authors:  Siyu Zhao; Fengyu Che; Le Yang; Yanyan Zheng; Dong Wang; Ying Yang; Yan Wang
Journal:  Front Genet       Date:  2022-09-15       Impact factor: 4.772

7.  Impaired riboflavin transport due to missense mutations in SLC52A2 causes Brown-Vialetto-Van Laere syndrome.

Authors:  Tobias B Haack; Christine Makowski; Yoshiaki Yao; Elisabeth Graf; Maja Hempel; Thomas Wieland; Ulrike Tauer; Uwe Ahting; Johannes A Mayr; Peter Freisinger; Hiroki Yoshimatsu; Ken Inui; Tim M Strom; Thomas Meitinger; Atsushi Yonezawa; Holger Prokisch
Journal:  J Inherit Metab Dis       Date:  2012-08-03       Impact factor: 4.982
  7 in total

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