(Q46084447)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19294884%20AND%20SRC:MED&resulttype=core&format=json

23 January 2020

title

Complex I and ATP content deficiency in lymphocytes from Friedreich's ataxia (English)

1 reference

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23 January 2020

1 reference

Mohammad Mehdi Heidari

1

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23 January 2020

author name string

Massoud Houshmand

2

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23 January 2020

Saman Hosseinkhani

3

1 reference

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23 January 2020

Shahriar Nafissi

4

1 reference

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23 January 2020

Mehri Khatami

5

1 reference

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23 January 2020

publication date

1 January 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19294884%20AND%20SRC:MED&resulttype=core&format=json

Canadian Journal of Neurological Sciences

23 January 2020

published in

1 reference

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23 January 2020

volume

36

1 reference

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23 January 2020

issue

1

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23 January 2020

page(s)

26-31

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Cardiomyopathy in children with mitochondrial disease; clinical course and cardiological findings

23 January 2020

cites work

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7 January 2021

Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA

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Respiratory deficiency due to loss of mitochondrial DNA in yeast lacking the frataxin homologue

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Mitochondrial functional interactions between frataxin and Isu1p, the iron-sulfur cluster scaffold protein, in Saccharomyces cerevisiae

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7 January 2021

Iron-sulfur protein maturation in human cells: evidence for a function of frataxin

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7 January 2021

Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranes

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7 January 2021

Real time PCR quantification of frataxin mRNA in the peripheral blood leucocytes of Friedreich ataxia patients and carriers.

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7 January 2021

Aconitase and mitochondrial iron–sulphur protein deficiency in Friedreich ataxia

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7 January 2021

Brain Cytochrome Oxidase in Alzheimer's Disease

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7 January 2021

Clinical Description and Roentgenologic Evaluation of Patients with Friedreich's Ataxia

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7 January 2021

3-Nitropropionic acid increases frataxin expression in human lymphoblasts and in transgenic rat PC12 cells

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7 January 2021

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

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7 January 2021

Identification and sizing of GAA trinucleotide repeat expansion, investigation for D-loop variations and mitochondrial deletions in Iranian patients with Friedreich's ataxia

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7 January 2021

Use of the liquid scintillation spectrometer for determining adenosine triphosphate by the luciferase enzyme

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7 January 2021

Evolution of the Friedreich's ataxia trinucleotide repeat expansion: founder effect and premutations

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7 January 2021

Friedreich's ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features

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7 January 2021

Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin

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7 January 2021

Properties of DNA fragmentation activity generated by ATP depletion

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7 January 2021

Interactions of reduced and oxidized triphosphopyridine nucleotides with the electron-transport system of bovine heart mitochondria

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7 January 2021

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

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7 January 2021

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

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7 January 2021

Steady-state kinetics of high molecular weight (type-I) NADH dehydrogenase

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7 January 2021

Clinical, biochemical and molecular genetic correlations in Friedreich's ataxia

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7 January 2021

Frataxin interacts functionally with mitochondrial electron transport chain proteins

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7 January 2021

Deletion of the yeast homologue of the human gene associated with Friedreich's ataxia elicits iron accumulation in mitochondria

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7 January 2021

Deficit of in vivo mitochondrial ATP production in patients with Friedreich ataxia

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7 January 2021

Ageing-associated 5 kb deletion in human liver mitochondrial DNA.

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7 January 2021

Human mitochondrial complex I dysfunction

1 reference

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7 January 2021

Mitochondrial complex I deficiency in Parkinson's disease

1 reference

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7 January 2021

10.1017/S0317167100006260

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19294884%20AND%20SRC:MED&resulttype=core&format=json

23 January 2020

1 reference