Metabolite accumulation inVLCADdeficiency markedly disrupts mitochondrial bioenergetics and Ca2+homeostasis in the heart-Reference-Cited by-同舟云学术

Metabolite accumulation inVLCADdeficiency markedly disrupts mitochondrial bioenergetics and Ca2+homeostasis in the heart

Published:2018-03-25 Issue:8 Volume:285 Page:1437-1455
ISSN:1742-464X
Container-title:The FEBS Journal
language:en
Short-container-title:FEBS J

Author:

Cecatto Cristiane¹,Amaral Alexandre Umpierrez¹²,Silva Janaína Camacho¹,Wajner Alessandro¹,Schimit Mariana de Oliveira Vargas¹,Silva Lucas Henrique Rodrigues¹,Wajner Simone Magagnin³,Zanatta Ângela¹,Castilho Roger Frigério⁴,Wajner Moacir¹⁵⁶

Affiliation:

1. Programa de Pós‐Graduação em Ciências Biológicas: Bioquímica Instituto de Ciências Básicas da Saúde Universidade Federal do Rio Grande do Sul Porto Alegre Brazil

2. Departamento de Ciências Biológicas Universidade Regional Integrada do Alto Uruguai e das Missões Erechim Brazil

3. Departamento de Medicina Interna Faculdade de Medicina Universidade Federal do Rio Grande do Sul Porto Alegre Brazil

4. Departamento de Patologia Clínica Faculdade de Ciências Médicas Universidade Estadual de Campinas Brazil

5. Departamento de Bioquímica Instituto de Ciências Básicas da Saúde Universidade Federal do Rio Grande do Sul Porto Alegre Brazil

6. Serviço de Genética Médica Hospital de Clínicas de Porto Alegre Brazil

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul

Pró-Reitoria de Pesquisa, Universidade Federal do Rio Grande do Sul

Instituto Nacional de Ciência e Tecnologia para Excitotoxicidade e Neuroproteção

Publisher

Wiley

Subject

Cell Biology,Molecular Biology,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/febs.14419

Reference102 articles.

1. A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency

2. Treatment recommendations in long-chain fatty acid oxidation defects: consensus from a workshop

3. Recognition and management of fatty acid oxidation defects: A series of 107 patients

4. Rhabdomyolysis in a neonate due to very long chain acyl CoA dehydrogenase deficiency

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