Fatal Propionic Acidemia in Mice Lacking Propionyl-CoA Carboxylase and Its Rescue by Postnatal, Liver-specific Supplementation via a Transgene-Reference-Cited by-同舟云学术

Fatal Propionic Acidemia in Mice Lacking Propionyl-CoA Carboxylase and Its Rescue by Postnatal, Liver-specific Supplementation via a Transgene

Published:2001-09 Issue:38 Volume:276 Page:35995-35999
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Miyazaki Toru,Ohura Toshihiro,Kobayashi Makio,Shigematsu Yosuke,Yamaguchi Seiji,Suzuki Yoichi,Hata Ikue,Aoki Yoko,Yang Xue,Minjares Christina,Haruta Ikuko,Uto Hirofumi,Ito Yuriko,Müller Urs

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference36 articles.

1. The Metabolic and Molecular Bases of Inherited Disease;Fenton,1995

2. Potential relationship between genotype and clinical outcome in propionic acidaemia patients

3. Overview of mutations in thePCCA andPCCB genes causing propionic acidemia

4. Propionicacidemia (Ketotic Hyperglycinemia): Dietary Treatment Resulting in Normal Growth and Development

5. Liver transplantation in propionic acidaemia

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2. Disrupted propionate metabolism evokes transcriptional changes in the heart by increasing histone acetylation and propionylation;Nature Cardiovascular Research;2023-11-23

3. Systemic gene therapy using an AAV44.9 vector rescues a neonatal lethal mouse model of propionic acidemia;Molecular Therapy - Methods & Clinical Development;2023-09

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