Pyruvate therapy for Leigh syndrome due to cytochrome c oxidase deficiency-Reference-Cited by-同舟云学术

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Pyruvate therapy for Leigh syndrome due to cytochrome c oxidase deficiency

Published:2010-03 Issue:3 Volume:1800 Page:313-315
ISSN:0304-4165
Container-title:Biochimica et Biophysica Acta (BBA) - General Subjects
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - General Subjects

Author:

Komaki Hirofumi,Nishigaki Yutaka,Fuku Noriyuki,Hosoya Hiroko,Murayama Kei,Ohtake Akira,Goto Yu-ichi,Wakamoto Hiroyuki,Koga Yasutoshi,Tanaka Masashi

Publisher

Elsevier BV

Subject

Molecular Biology,Biochemistry,Biophysics

Reference14 articles.

1. Gene therapy for mitochondrial disease by delivering restriction endonuclease SmaI into mitochondria;Tanaka;J. Biomed. Sci.,2002

2. Diagnosis and molecular analysis of three male patients with thiamine-responsive pyruvate dehydrogenase complex deficiency;Naito;J. Neurol. Sci.,2002

3. Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutations;Lopez;Am. J. Hum. Genet.,2006

4. A mutation in para-hydroxybenzoate-polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiency;Quinzii;Am. J. Hum. Genet.,2006

5. Therapeutic potential of pyruvate therapy for mitochondrial diseases;Tanaka;Mitochondrion,2007

Cited by 24 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Pyruvate and uridine rescue the metabolic profile of OXPHOS dysfunction;Molecular Metabolism;2022-09

2. Defective metabolic programming impairs early neuronal morphogenesis in neural cultures and an organoid model of Leigh syndrome;Nature Communications;2021-03-26

3. Pioglitazone and Deoxyribonucleoside Combination Treatment Increases Mitochondrial Respiratory Capacity in m.3243A>G MELAS Cybrid Cells;International Journal of Molecular Sciences;2020-03-20

4. Understanding the role of OXPHOS dysfunction in the pathogenesis of ECHS1 deficiency;FEBS Letters;2020-01-29

5. Therapeutic potential of pyruvate therapy for patients with mitochondrial diseases: a systematic review;Therapeutic Advances in Endocrinology and Metabolism;2020-01

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