(Q53378602)

13 May 2018

title

Humanin expression in skeletal muscles of patients with chronic progressive external ophthalmoplegia. (English)

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13 May 2018

chronic progressive external ophthalmoplegia

main subject

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author

Ichizo Nishino

5

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13 May 2018

author name string

Tesseki Kin

1

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13 May 2018

Kazuma Sugie

2

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13 May 2018

Makito Hirano

3

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13 May 2018

Yu-ichi Goto

4

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13 May 2018

Satoshi Ueno

6

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13 May 2018

publication date

26 April 2006

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13 May 2018

Journal of Human Genetics

published in

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13 May 2018

volume

51

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13 May 2018

page(s)

555-558

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13 May 2018

issue

6

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13 May 2018

https://scigraph.springernature.com/pub.10.1007/s10038-006-0397-2

exact match

0 references

cites work

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10038-006-0397-2

Clinical and genetic heterogeneity in progressive external ophthalmoplegia due to mutations in polymerase gamma

21 January 2018

1 reference

12 December 2020

Two pathogenic point mutations exist in the authentic mitochondrial genome, not in the nuclear pseudogene.

1 reference

12 December 2020

Humanin improves impaired metabolic activity and prolongs survival of serum-deprived human lymphocytes

1 reference

12 December 2020

Mitochondrial defects in cardiomyopathy and neuromuscular disease

1 reference

12 December 2020

Clinical features of MELAS and mitochondrial DNA mutations

1 reference

12 December 2020

Effect of humanin on decreased ATP levels of human lymphocytes harboring A3243G mutant mitochondrial DNA.

1 reference

12 December 2020

Humanin detected in skeletal muscles of MELAS patients: a possible new therapeutic agent.

1 reference

12 December 2020

Humanin peptide suppresses apoptosis by interfering with Bax activation

1 reference

12 December 2020

Chronic progressive external ophthalmoplegia

1 reference

12 December 2020

Molecular basis of mitochondrial DNA disease

1 reference

12 December 2020

Inefficient coupling between proton transport and ATP synthesis may be the pathogenic mechanism for NARP and Leigh syndrome resulting from the T8993G mutation in mtDNA.

1 reference

12 December 2020

A rescue factor abolishing neuronal cell death by a wide spectrum of familial Alzheimer's disease genes and Aβ

1 reference

12 December 2020

Mitochondrial disease associated with the T8993G mutation of the mitochondrial ATPase 6 gene: a clinical, biochemical, and molecular study in six families

1 reference

12 December 2020

Molecular analysis of the muscle pathology associated with mitochondrial DNA deletions

1 reference

12 December 2020

Chronic progressive external ophthalmoplegia: a correlative study of mitochondrial DNA deletions and their phenotypic expression in muscle biopsies

1 reference

12 December 2020

10.1007/S10038-006-0397-2

Identifiers

DOI

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13 May 2018

PubMed ID

16639504

1 reference

13 May 2018