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Publications by Jean-Jacques Brière

The Variability of the Harlequin Mouse Phenotype Resembles That of Human Mitochondrial-Complex I-Deficiency Syndromes

Multidisciplinary

English

The Warburg Effect Is Genetically Determined in Inherited Pheochromocytomas

Multidisciplinary

English

Related publications

Cell-Permeable Succinate Prodrugs Bypass Mitochondrial Complex I Deficiency

Nature Communications

Molecular Biology

English

Molecular Diagnosis in Mitochondrial Complex I Deficiency Using Exome Sequencing

Journal of Medical Genetics

English

Image Gallery: A Case of Harlequin and Horner Syndromes

British Journal of Dermatology

English

The Cortical Thickness Phenotype of Individuals With DISC1 Translocation Resembles Schizophrenia

Journal of Clinical Investigation

English

The Mutant Human ND4 Subunit of Complex I Induces Optic Neuropathy in the Mouse

Investigative Ophthalmology and Visual Science

Molecular Neuroscience

Sensory Systems

English

Chemomechanical Coupling of Mitochondrial Complex I

Biophysical Journal

English

NDUFB8 Mutations Cause Mitochondrial Complex I Deficiency in Individuals With Leigh-Like Encephalomyopathy

American Journal of Human Genetics

English

Modulation of Lupus Phenotype by Adiponectin Deficiency in Autoimmune Mouse Models

Journal of Clinical Immunology

English

Loss of Human Arylamine N-Acetyltransferase I Regulates Mitochondrial Function by Inhibition of the Pyruvate Dehydrogenase Complex

International Journal of Biochemistry and Cell Biology

English