Propionyl-CoA carboxylase pcca-1 and pccb-1 gene deletions in Caenorhabditis elegans globally impair mitochondrial energy metabolism-Reference-Cited by-同舟云学术

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Propionyl-CoA carboxylase pcca-1 and pccb-1 gene deletions in Caenorhabditis elegans globally impair mitochondrial energy metabolism

Published:2017-11-20 Issue:2 Volume:41 Page:157-168
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Chapman Kimberly A.,Ostrovsky Julian,Rao Meera,Dingley Stephen D.,Polyak Erzsebet,Yudkoff Marc,Xiao Rui,Bennett Michael J.,Falk Marni J.

Funder

National Institutes of Health

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/article/10.1007/s10545-017-0111-x/fulltext.html

Reference38 articles.

1. Baumgartner MR, Horster F, Dionisi-Vici C et al (2014) Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia. Orphanet J Rare Dis 9:130

2. Chandler RJ, Aswani V, Tsai MS et al (2006) Propionyl-CoA and adenosylcobalamin metabolism in Caenorhabditis elegans: evidence for a role of methylmalonyl-CoA epimerase in intermediary metabolism. Mol Genet Metab 89:64–73

3. Chemelli AP, Schocke M, Sperl W, Trieb T, Aichner F, Felber S (2000) Magnetic resonance spectroscopy (MRS) in five patients with treated propionic acidemia. J Magn Reson Imaging 11:596–600

4. Clarke C, Xiao R, Place E et al (2013) Mitochondrial respiratory chain disease discrimination by retrospective cohort analysis of blood metabolites. Mol Genet Metab 110:145–152

5. de Keyzer Y, Valayannopoulos V, Benoist JF et al (2009) Multiple OXPHOS deficiency in the liver, kidney, heart, and skeletal muscle of patients with methylmalonic aciduria and propionic aciduria. Pediatr Res 66:91–95

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