Joël Lunardi

Overview

Best Publications

• Improvement of the solubilization of proteins in two-dimensional electrophoresis with immobilized pH gradients.

  Thierry Rabilloud;Céline Adessi;Anne Giraudel;Joël Lunardi

  754
  Citations

• Incidence and Risk Factors of Arrhythmic Events in Catecholaminergic Polymorphic Ventricular Tachycardia

  Meiso Hayashi;Isabelle Denjoy;Fabrice Extramiana;Alice Maltret

  681
  Citations

• Malignant-Hyperthermia Susceptibility Is Associated with a Mutation of the a1-Subunit of the Human Dihydropyridine-Sensitive L-Type Voltage-Dependent Calcium-Channel Receptor in Skeletal Muscle

  Nicole Monnier;Vincent Procaccio;Paul Stieglitz;Joël. Lunardi

  553
  Citations

• New zwitterionic detergents improve the analysis of membrane proteins by two-dimensional electrophoresis.

  Mireille Chevallet;Véronique Santoni;Alexandra Poinas;David Rouquié

  467
  Citations

• A comparison between Sypro Ruby and ruthenium II tris (bathophenanthroline disulfonate) as fluorescent stains for protein detection in gels.

  Thierry Rabilloud;Jean-Marc Strub;Sylvie Luche;Alain van Dorsselaer

  427
  Citations

• Homozygous mutation of AURKC yields large-headed polyploid spermatozoa and causes male infertility.

  Klaus Dieterich;Ricardo Soto Rifo;Ricardo Soto Rifo;Anne Karen Faure;Anne Karen Faure;Sylviane Hennebicq;Sylviane Hennebicq

  321
  Citations

• Absence of Triadin, a Protein of the Calcium Release Complex, is Responsible for Cardiac Arrhythmia with Sudden Death in Human

  Nathalie Roux-Buisson;Marine Cacheux;Marine Cacheux;Anne Fourest-Lieuvin;Anne Fourest-Lieuvin;Jeremy Fauconnier

  291
  Citations

• Two‐dimensional electrophoresis of human placental mitochondria and protein identification by mass spectrometry: Toward a human mitochondrial proteome

  Thierry Rabilloud;Sylvie Kieffer;Vincent Procaccio;Mathilde Louwagie

  266
  Citations

• Development and implementation of standardized respiratory chain spectrophotometric assays for clinical diagnosis.

  Fadia Medja;S. Allouche;Paule Frachon;Claude Jardel;Claude Jardel

  263
  Citations

• A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene.

  Ana Ferreiro;Nicole Monnier;Norma B. Romero;Jean-Paul Leroy

  256
  Citations

• A Recurrent Deletion of DPY19L2 Causes Infertility in Man by Blocking Sperm Head Elongation and Acrosome Formation

  Radu Harbuz;Radu Harbuz;Raoudha Zouari;Virginie Pierre;Virginie Pierre;Mariem Ben Khelifa;Mariem Ben Khelifa

  221
  Citations

• Dominant and recessive central core disease associated with RYR1 mutations and fetal akinesia

  Norma Beatriz Romero;Nicole Monnier;Louis Viollet;Anne Cortey

  208
  Citations

• Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptor

  Nicole Monnier;Norma Beatriz Romero;Joëlle Lerale;Pierre Landrieu

  203
  Citations

• Analysis of membrane proteins by two-dimensional electrophoresis: comparison of the proteins extracted from normal or Plasmodium falciparum-infected erythrocyte ghosts.

  Thierry Rabilloud;Thierry Blisnick;Manfred Heller;Sylvie Luche

  202
  Citations

• A homozygous splicing mutation causing a depletion of skeletal muscle RYR1 is associated with multi-minicore disease congenital myopathy with ophthalmoplegia

  Nicole Monnier;Ana Ferreiro;Isabelle Marty;Annick Labarre-Vila

  190
  Citations

• Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion

  Nigel F. Clarke;Leigh B. Waddell;Leigh B. Waddell;Sandra T. Cooper;Sandra T. Cooper;Margaret Perry;Margaret Perry

  185
  Citations

• An appraisal of the functional significance of the inhibitory effect of long chain acyl-CoAs on mitochondrial transports

  F. Morel;G. Lauquin;J. Lunardi;J. Duszynski

  179
  Citations

• From Lowe syndrome to Dent disease: correlations between mutations of the OCRL1 gene and clinical and biochemical phenotypes.

  Haifa Hichri;John Rendu;Nicole Monnier;Charles Coutton

  172
  Citations

• The 49‐kDa subunit of NADH‐ubiquinone oxidoreductase (Complex I) is involved in the binding of piericidin and rotenone, two quinone‐related inhibitors

  Elisabeth Darrouzet;Jean-Paul Issartel;Joël Lunardi;Alain Dupuis

  169
  Citations

• Chemical probes of the mitochondrial ATP synthesis and translocation

  Pierre V. Vignais;Joël Lunardi

  145
  Citations