List of works by J M Cooper

A 31P magnetic resonance spectroscopy study of mitochondrial function in skeletal muscle of patients with Parkinson's disease

scientific article published on 01 August 1994

A missense mutation of cytochrome oxidase subunit II causes defective assembly and myopathy

scientific journal article

A novel α-synuclein missense mutation in Parkinson disease

scientific article published on 20 February 2013

Ambroxol improves lysosomal biochemistry in glucocerebrosidase mutation-linked Parkinson disease cells

scientific article

Analyses of mitochondrial respiratory chain function and mitochondrial DNA deletion in human skeletal muscle: effect of ageing

scientific article published on 01 November 1992

Analysis of the factors influencing the cardiac phenotype in Friedreich's ataxia

scientific article published on 13 April 2010

Antibodies to human optic nerve in Leber's hereditary optic neuropathy

scientific article published on 01 June 1995

Antioxidant treatment of patients with Friedreich ataxia: four-year follow-up

scientific article

Assessment of the significance of mitochondrial DNA damage by chemotherapeutic agents.

scientific article published on August 2005

Biochemical abnormalities and excitotoxicity in Huntington's disease brain.

scientific article published in January 1999

Biochemical and molecular aspects of human mitochondrial respiratory chain disorders

scientific article published on 01 August 1990

Brain, skeletal muscle and platelet homogenate mitochondrial function in Parkinson's disease ⬇️

scientific article published on April 1, 1992

Cardiac bioenergetics in Friedreich's ataxia

scientific article published on 01 October 2003

Cardiac energetics are abnormal in Friedreich ataxia patients in the absence of cardiac dysfunction and hypertrophy: an in vivo 31P magnetic resonance spectroscopy study.

scientific article

Central role and mechanisms of β-cell dysfunction and death in friedreich ataxia-associated diabetes

scientific article published on December 2012

Chaperone-mediated autophagy markers in Parkinson disease brains

scientific journal article

Clinical correlates of mitochondrial function in Huntington's disease muscle

scientific article

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

scientific article published on 01 January 2000

Coenzyme Q10 and vitamin E deficiency in Friedreich's ataxia: predictor of efficacy of vitamin E and coenzyme Q10 therapy.

scientific article published in December 2008

Complex I inhibitors induce dose-dependent apoptosis in PC12 cells: relevance to Parkinson's disease

scientific article published on November 1994

Complex I, iron, and ferritin in Parkinson's disease substantia nigra

scientific article published on December 1994

Coordinating outcomes measurement in ataxia research: do some widely used generic rating scales tick the boxes?

scientific article published in September 2006

Cyclosporin inhibition of apoptosis induced by mitochondrial complex I toxins

scientific article published in October 1998

Cytochrome oxidase immunohistochemistry: clues for genetic mechanisms

scientific article published on 01 March 2000

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

scientific article published on September 1999

Detection of nitrosyl complexes in human substantia nigra, in relation to Parkinson's disease

scientific article

Differences in toxicity of the catechol-O-methyl transferase inhibitors, tolcapone and entacapone to cultured human neuroblastoma cells

scientific article published in March 2004

Free radical scavengers protect dopaminergic cell lines from apoptosis induced by complex I inhibitors

scientific article published in November 1997

Friedreich's ataxia impact scale: a new measure striving to provide the flexibility required by today's studies

scientific article published in May 2009

Functional consequences of the 3460-bp mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

scientific article published on 01 May 1999

G2019S leucine-rich repeat kinase 2 causes uncoupling protein-mediated mitochondrial depolarization

scientific article

Glucocerebrosidase deficiency in substantia nigra of parkinson disease brains

scientific article published on September 2012

Human mitochondrial complex I dysfunction ⬇️

scientific article published on July 17, 1992

Influence of microRNA deregulation on chaperone-mediated autophagy and α-synuclein pathology in Parkinson's disease.

scientific article published on 14 March 2013

International Cooperative Ataxia Rating Scale (ICARS): appropriate for studies of Friedreich's ataxia?

scientific article published on 01 December 2005

Iron induced oxidative stress and mitochondrial dysfunction: relevance to Parkinson's disease

scientific article published on 01 November 1993

Irreversible inhibition of mitochondrial complex I by 1-methyl-4-phenylpyridinium: evidence for free radical involvement

scientific article published on 01 February 1992

Liver failure associated with mitochondrial DNA depletion

scientific article published on 01 April 1998

Lysosomal dysfunction increases exosome-mediated alpha-synuclein release and transmission.

scientific article published on 18 February 2011

MitBASE : a comprehensive and integrated mitochondrial DNA database. The present status

scientific article published on January 2000

Mitochondria in the etiology and pathogenesis of Parkinson's disease

scholarly article by A H Schapira et al published September 1998 in Annals of Neurology

Mitochondria in the etiology and pathogenesis of parkinson's disease

scientific article published in September 1998

Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotype.

scientific article published in May 1995

Mitochondrial DNA depletion syndrome is expressed in amniotic fluid cell cultures.

scientific article published on July 1999

Mitochondrial complex I deficiency in Parkinson's disease

scientific article published on 01 June 1989

Mitochondrial defect in Huntington's disease caudate nucleus

scientific article published in March 1996

Mitochondrial dysfunction and free radical damage in the Huntington R6/2 transgenic mouse

scientific article published in January 2000

Mitochondrial function and parental sex effect in Huntington's disease

scientific article published in September 1990

Mitochondrial function in Alzheimer's disease

scientific article

Mitochondrial myopathies: clinical defects

scientific article published on 01 August 1990

Mitofusin 1 and mitofusin 2 are ubiquitinated in a PINK1/parkin-dependent manner upon induction of mitophagy

scientific article

Molecular basis of mitochondrial myopathies: polypeptide analysis in complex-I deficiency

scientific article published on 01 March 1988

Molecular defects of NADH-ubiquinone oxidoreductase (complex I) in mitochondrial diseases

scientific article published on June 1988

Molecular mechanisms in mitochondrial DNA depletion syndrome

scientific article published on 01 June 1997

Nuclear complementation restores mtDNA levels in cultured cells from a patient with mtDNA depletion.

scientific article published on September 1993

Oxidative-phosphorylation defects in liver of patients with Wilson's disease

scientific article published on 01 August 2000

Platelet mitochondrial function in Leber's hereditary optic neuropathy

scientific article published on 01 March 1994

Platelet mitochondrial function in Parkinson's disease. The Royal Kings and Queens Parkinson Disease Research Group

scientific article published on 01 December 1992

Pramipexole protects against MPTP toxicity in non-human primates

scientific article published on 8 February 2006

Pramipexole protects against apoptotic cell death by non-dopaminergic mechanisms

scientific article

Proteasomal inhibition causes loss of nigral tyrosine hydroxylase neurons

scientific article published in August 2006

Protection against paraquat and A53T alpha-synuclein toxicity by cabergoline is partially mediated by dopamine receptors

scientific article

Quantitation of a mitochondrial DNA deletion in Parkinson's disease

scientific article published on March 16, 1992

Rasagiline protects against alpha-synuclein induced sensitivity to oxidative stress in dopaminergic cells

scientific article published on 17 July 2010

Relationship between alpha synuclein phosphorylation, proteasomal inhibition and cell death: relevance to Parkinson's disease pathogenesis

scientific article

Reversible inhibition of cytochrome c oxidase, the terminal enzyme of the mitochondrial respiratory chain, by nitric oxide. Implications for neurodegenerative diseases

scientific article published on 01 May 1994

Role of oxidative damage in Friedreich's ataxia

scientific article published in March 2004

Sensitivity of respiratory chain activities to lipid peroxidation: effect of vitamin E deficiency

scientific article

Silencing of PINK1 expression affects mitochondrial DNA and oxidative phosphorylation in dopaminergic cells

scientific article

Systemic exosomal siRNA delivery reduced alpha-synuclein aggregates in brains of transgenic mice

scientific article

The molecular pathology of respiratory-chain dysfunction in human mitochondrial myopathies

scientific article published on 01 July 1990

Update of the Human MitBASE database.

scientific article published on January 1999

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