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Literature DB >> 7474906

Glutaric aciduria mediated by gut bacteria.

U Wendel¹, J Bakkeren, J de Jong, G Bongaerts.

Abstract

Entities: Chemical

Mesh：

Substances：

Year: 1995 PMID： 7474906 DOI： 10.1007/bf00710431

Source DB: PubMed Journal: J Inherit Metab Dis ISSN： 0141-8955 Impact factor: 4.982

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4 in total

1. Glutaryl-coenzyme A dehydrogenase deficiency: a distinct encephalopathy.

Authors: G F Hoffmann; F K Trefz; P G Barth; H J Böhles; B Biggemann; H J Bremer; E Christensen; M Frosch; F Hanefeld; D H Hunneman
Journal: Pediatrics Date: 1991-12 Impact factor: 7.124

2. Implication of a peroxisomal enzyme in the catabolism of glutaryl-CoA.

Authors: J Vamecq; F Van Hoof
Journal: Biochem J Date: 1984-07-01 Impact factor: 3.857

3. Atypical riboflavin-responsive glutaric aciduria, and deficient peroxisomal glutaryl-CoA oxidase activity: a new peroxisomal disorder.

Authors: M J Bennett; R J Pollitt; S I Goodman; D E Hale; J Vamecq
Journal: J Inherit Metab Dis Date: 1991 Impact factor: 4.982

4. Glutaric, 3-hydroxypropionic, and lactic aciduria with metabolic acidemia, following extensive small bowel resection.

Authors: E R McCabe; S I Goodman; P V Fennessey; B S Miles; M Wall; A Silverman
Journal: Biochem Med Date: 1982-10

4 in total

7 in total

1. Glutaric aciduria type III: a distinctive non-disease?

Authors: I Knerr; J Zschocke; U Trautmann; L Dorland; T J de Koning; P Müller; E Christensen; F K Trefz; G F Wündisch; W Rascher; G F Hoffmann
Journal: J Inherit Metab Dis Date: 2002-10 Impact factor: 4.982

2. C7orf10 encodes succinate-hydroxymethylglutarate CoA-transferase, the enzyme that converts glutarate to glutaryl-CoA.

Authors: Simon Marlaire; Emile Van Schaftingen; Maria Veiga-da-Cunha
Journal: J Inherit Metab Dis Date: 2013-07-27 Impact factor: 4.982

3. Glutaric Aciduria Type 3: Three Unrelated Canadian Cases, with Different Routes of Ascertainment.

Authors: Paula J Waters; Thomas M Kitzler; Annette Feigenbaum; Michael T Geraghty; Osama Al-Dirbashi; Patrick Bherer; Christiane Auray-Blais; Serge Gravel; Nathan McIntosh; Komudi Siriwardena; Yannis Trakadis; Catherine Brunel-Guitton; Walla Al-Hertani
Journal: JIMD Rep Date: 2017-08-02

Glutaric aciduria mediated by gut bacteria.

1. Glutaryl-coenzyme A dehydrogenase deficiency: a distinct encephalopathy.

2. Implication of a peroxisomal enzyme in the catabolism of glutaryl-CoA.

3. Atypical riboflavin-responsive glutaric aciduria, and deficient peroxisomal glutaryl-CoA oxidase activity: a new peroxisomal disorder.

4. Glutaric, 3-hydroxypropionic, and lactic aciduria with metabolic acidemia, following extensive small bowel resection.

1. Glutaric aciduria type III: a distinctive non-disease?

2. C7orf10 encodes succinate-hydroxymethylglutarate CoA-transferase, the enzyme that converts glutarate to glutaryl-CoA.

3. Glutaric Aciduria Type 3: Three Unrelated Canadian Cases, with Different Routes of Ascertainment.

4. False-positive newborn screening mimicking glutaric aciduria type I in infants with renal insufficiency.

5. Towards the fecal metabolome derived from moderate red wine intake.

6. Widespread bacterial lysine degradation proceeding via glutarate and L-2-hydroxyglutarate.

7. Small intestinal bacterial overgrowth in children with intestinal failure on home parenteral nutrition.