M.J.Bernadette Jean-François

Neuroradiological features of six kindreds with MELAS tRNALeu A3243G point mutation: implications for pathogenesis

Carolyn M. Sue, Denis Crimmins, Young Soo et al. · Journal of Neurology Neurosurgery & Psychiatry · 1998 · 141 citations · Full text

A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex I.

Patcharee Lertrit, A.S. Noer, M.J.Bernadette Jean-François et al. · PubMed · 1992 · 76 citations

The definition of mitochondrial H+ ATPase assembly defects in mit− mutants of Saccharomyces cerevisiae with a monoclonal antibody to the enzyme complex as an assembly probe

Richard G. Hadikusumo, Sybella Meltzer, Wan Mee Choo et al. · Biochimica et Biophysica Acta (BBA) - Bioenergetics · 1988 · 76 citations

Assembly Probe, Cellular Enzymology, Biochemistry +12

Presymptomatic motor neuron loss and reactive astrocytosis in the SOD1 mouse model of amyotrophic lateral sclerosis

Sandra J. Feeney, Penelope McKelvie, Lawrence Austin et al. · Muscle & Nerve · 2001 · 50 citations

The effect of leukaemia inhibitory factor on SOD1 G93A murine amyotrophic lateral sclerosis

Sandra J. Feeney, Lawrence Austin, Timothy M. Bennett et al. · Cytokine · 2003 · 29 citations

Amyotrophic Lateral Sclerosis, Medicine, Immunology +5