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Lunardi Joël
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http://hub.abes.fr/bmj/periodical/jmg/2001/volume_38/issue_1/B3598D6B5CD97CBEE053120B220A90C5/authorship/5
http://hub.abes.fr/acs/periodical/bichaw/1989/volume_28/issue_4/101021bi00430a003/authorship/5
http://hub.abes.fr/acs/periodical/bichaw/1979/volume_18/issue_24/101021bi00591a008/authorship/1
http://hub.abes.fr/acs/periodical/bichaw/1985/volume_24/issue_3/101021bi00324a029/authorship/3
http://hub.abes.fr/acs/periodical/bichaw/1985/volume_24/issue_3/101021bi00324a030/authorship/2
http://hub.abes.fr/acs/periodical/bichaw/1992/volume_31/issue_7/101021bi00122a028/authorship/3
http://hub.abes.fr/oup/periodical/hmg/2009/volume_18/issue_7/101093hmgddp029/authorship/24
http://hub.abes.fr/oup/periodical/hmg/2003/volume_12/issue_19/101093hmgddg250/authorship/4
http://hub.abes.fr/oup/periodical/hmg/2000/volume_9/issue_18/101093hmg9182599/authorship/8
http://hub.abes.fr/oup/periodical/brainj/2003/volume_126/issue_11/101093brainawg244/authorship/7
http://hub.abes.fr/oup/periodical/hmg/2005/volume_14/issue_11/101093hmgddi153/authorship/5
http://hub.abes.fr/oup/periodical/hmg/2001/volume_10/issue_22/101093hmg10222581/authorship/7
http://hub.abes.fr/oup/periodical/hmg/2003/volume_12/issue_10/101093hmgddg121/authorship/6
http://hub.abes.fr/acs/periodical/bichaw/2002/volume_41/issue_1/101021bi0114776/authorship/6
http://hub.abes.fr/bmj/periodical/jmg/2008/volume_45/issue_10/B3598D6B645B7CBEE053120B220A90C5/authorship/3
http://hub.abes.fr/acs/periodical/bichaw/1991/volume_30/issue_19/101021bi00233a013/authorship/3
http://hub.abes.fr/acs/periodical/bichaw/1981/volume_20/issue_3/101021bi00506a005/authorship/1
http://hub.abes.fr/acs/periodical/bichaw/1986/volume_25/issue_15/101021bi00363a039/authorship/4
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Reactivity of the .beta. subunit of Escherichia coli adenosine triphosphatase with 4-chloro-7-nitrobenzofurazan
Exploration of adenosine 5'-diphosphate-adenosine 5'-triphosphate binding sites of Escherichia coli adenosine 5'-triphosphatase with arylazido adenine nucleotides
Dominant and recessive central core disease associated with RYR1 mutations and fetal akinesia
Interactions between the oligomycin sensitivity conferring protein and beef heart mitochondrial F1-ATPase. 2. Identification of the interacting F1 subunits by crosslinking
An autosomal dominant congenital myopathy with cores and rods is associated with a neomutation in the RYR1 gene encoding the skeletal muscle ryanodine receptor
The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population
Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptor
Lowe syndrome protein Ocrl1 is translocated to membrane ruffles upon Rac GTPase activation: a new perspective on Lowe syndrome pathophysiology
Lowe syndrome protein OCRL1 interacts with Rac GTPase in the trans-Golgi network
A homozygous splicing mutation causing a depletion of skeletal muscle RYR1 is associated with multi-minicore disease congenital myopathy with ophthalmoplegia
Comparative Proteomics as a New Tool for Exploring Human Mitochondrial tRNADisorders
Does pyrophosphate bind to the catalytic sites of mitochondrial F1-ATPase?
Photolabeling of the phosphate binding site of mitochondrial F1-ATPase by [32P]azidonitrophenyl phosphate. Identification of the photolabeled amino acid residues
Fluoroaluminum and fluoroberyllium nucleoside diphosphate complexes as probes of the enzymic mechanism of the mitochondrial F1-ATPase
Identification of amino acid residues photolabeled with 2-azido[.alpha.-32P]adenosine diphosphate in the .beta. subunit of beef heart mitochondrial F1-ATPase
Interactions between the oligomycin sensitivity conferring protein (OSCP) and beef heart mitochondrial F1-ATPase. 1. Study of the binding parameters with a chemically radiolabeled OSCP
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