(Q80586649)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17619138%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

title

Investigation on mitochondrial tRNA(Leu/Lys), NDI and ATPase 6/8 in Iranian multiple sclerosis patients (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17619138%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

1 reference

Solmaz Etemad Ahari

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17619138%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

Massoud Houshmand

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17619138%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

Mehdi Shafa Shariat Panahi

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17619138%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

Sadaf Kasraie

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17619138%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

Mostafa Moin

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17619138%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

Mohammad Ali Bahar

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17619138%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

publication date

6 July 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17619138%20AND%20SRC:MED&resulttype=core&format=json

Cellular and Molecular Neurobiology

1 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17619138%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

volume

27

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17619138%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17619138%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

page(s)

695-700

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17619138%20AND%20SRC:MED&resulttype=core&format=json

Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia

1 January 2020

cites work

1 reference

12 December 2020

Suppression of complex I gene expression induces optic neuropathy

1 reference

12 December 2020

Human mitochondrial complex I in health and disease

1 reference

12 December 2020

Clinical mitochondrial genetics

1 reference

12 December 2020

Phylogenetic analysis of mitochondrial DNA in patients with an occipital stroke. Evaluation of mutations by using sequence data on the entire coding region

1 reference

12 December 2020

Parent-child concordance in multiple sclerosis

1 reference

12 December 2020

Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harbouring the mitochondrial DNA 11778 mutation

1 reference

12 December 2020

Is the mitochondrial DNA involved in determining susceptibility to multiple sclerosis?

1 reference

12 December 2020

Evolutional analysis in determining pathogenic versus nonpathogenic mutations of ATPase 6 in human mitochondriopathy.

1 reference

12 December 2020

MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNA(Lys) and premature translation termination

1 reference

12 December 2020

Brain Cytochrome Oxidase in Alzheimer's Disease

1 reference

12 December 2020

Oxidative damage to mitochondrial DNA and activity of mitochondrial enzymes in chronic active lesions of multiple sclerosis

1 reference

12 December 2020

Detection of mitochondrial DNA mutations in pancreatic cancer offers a "mass"-ive advantage over detection of nuclear DNA mutations.

1 reference

12 December 2020

Genetic variants of Complex I in multiple sclerosis

1 reference

12 December 2020

Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees

1 reference

12 December 2020

The mitochondrial electron transport and oxidative phosphorylation system

1 reference

12 December 2020

Complex I deficiency in Persian multiple sclerosis patients

1 reference

12 December 2020

Mitochondrial complex I deficiency in Parkinson's disease

1 reference

12 December 2020

Genes and susceptibility to multiple sclerosis

1 reference

12 December 2020

Leber's hereditary optic neuropathy: the etiological role of a mutation in the mitochondrial cytochrome b gene.

1 reference

12 December 2020

Nitric oxide, mitochondria and neurological disease

1 reference

12 December 2020

The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation

1 reference

12 December 2020

Molecular scanning of candidate mitochondrial tRNA genes in type 2 (non-insulin dependent) diabetes mellitus.

1 reference

12 December 2020

New diagnostic criteria for multiple sclerosis: guidelines for research protocols

1 reference

12 December 2020

Restoration of mitochondrial function in cells with complex I deficiency

1 reference

12 December 2020

Increased oxidative damage is correlated to altered mitochondrial function in heterozygous manganese superoxide dismutase knockout mice

1 reference

12 December 2020

Mitochondrial encephalomyopathies

1 reference

12 December 2020

Maternally transmitted histocompatibility antigen of mice: a hydrophobic peptide of a mitochondrially encoded protein

1 reference

12 December 2020

In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria

1 reference

12 December 2020

Genetic features of mitochondrial respiratory chain disorders

1 reference

12 December 2020