Defective Pattern of Mitochondrial Respiratory Enzymes in Mitochondrial Myopathy

Overview

Journal J Inherit Metab Dis

Publisher Wiley

Date 1989 Jan 1

PMID 2559247

Citations 9

Authors

S Miyabayashi

K Haginoya

H Hanamizu

K Iinuma

K Narisawa

K Tada

Affiliations

Soon will be listed here.

Citing Articles

Mice deficient in the Shmt2 gene have mitochondrial respiration defects and are embryonic lethal.

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Mitochondrial DNA mutations regulate metastasis of human breast cancer cells.

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The innate immune system in host mice targets cells with allogenic mitochondrial DNA.

Ishikawa K, Toyama-Sorimachi N, Nakada K, Morimoto M, Imanishi H, Yoshizaki M J Exp Med. 2010; 207(11):2297-305.

PMID: 20937705 PMC: 2964578. DOI: 10.1084/jem.20092296.

Complete repopulation of mouse mitochondrial DNA-less cells with rat mitochondrial DNA restores mitochondrial translation but not mitochondrial respiratory function.

Yamaoka M, Isobe K, Shitara H, Yonekawa H, Miyabayashi S, Hayashi J Genetics. 2000; 155(1):301-7.

PMID: 10790404 PMC: 1461064. DOI: 10.1093/genetics/155.1.301.

Clinical and biochemical phenotype of the MELAS mutation.

Miyabayashi S, Hanamizu H, Nakamura R, Hayashi J, Tada K J Inherit Metab Dis. 1993; 16(5):886-92.

PMID: 8295406 DOI: 10.1007/BF00714284.

References

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Miyabayashi S, Ito T, Abukawa D, Narisawa K, Tada K, Tanaka M . Immunochemical study in three patients with cytochrome c oxidase deficiency presenting Leigh's encephalomyelopathy. J Inherit Metab Dis. 1987; 10(3):289-92. DOI: 10.1007/BF01800084. View

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