F. Pons

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Fiber Types and Myosin Types in Human Atrial and Ventricular Myocardium An Anatomical Description

J. Léger, C. Dechesne, P. Bouvagnet, 1984, Circulation research.

Probing functional regions in cardiac isomyosins with monoclonal antibodies.

J. Léger, D. Mornet, P. Eldin, 1993, Biochemistry.

Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IkappaB alpha/NF-kappaB pathway in limb-girdle muscular dystrophy type 2A.

J. Beckmann, J. Loiselet, G. Lefranc, 1999, Nature medicine.

Anti-myosin heavy chain monoclonal antibodies reveal two IIB (fast) fiber subtypes.

J. Léger, J. Marini, J. Léger, 1989, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Cytoskeletal protein contents before and after hindlimb suspension in a fast and slow rat skeletal muscle.

J. Marini, F. Pons, A. Chopard, 2001, American journal of physiology. Regulatory, integrative and comparative physiology.

Comparison of the foetal development of fibre types in four bovine muscles

B. Picard, J. Robelin, Y. Geay, 1994, Journal of Muscle Research & Cell Motility.

A homologue of dystrophin is expressed at the neuromuscular junctions of normal individuals and DMD patients, and of normal and mdx mice Immunological evidence

J. Léger, T. Voit, M. Fardeau, 1991, FEBS letters.

Vinculin and meta-vinculin in fast and slow rat skeletal muscle before and after hindlimb suspension

J. Marini, F. Pons, A. Chopard, 2002, Pflügers Archiv.

Myosin light chains in normal and pathological human skeletal muscles

F. Bonnel, J. Léger, J. Léger, 1983, Muscle & nerve.

Purification and characterization of myosins from human and rabbit skeletal muscles by using specific monoclonal antibodies.

J. Léger, J. Léger, F. Pons, 1986, Comparative biochemistry and physiology. B, Comparative biochemistry.

Does utrophin expression in muscles of mdx mice during postnatal development functionally compensate for dystrophin deficiency?

J. Léger, J. Marini, A. Robert, 1994, Journal of the Neurological Sciences.

Mdx transgenic mouse: restoration of recombinant dystrophin to the dystrophic muscle.

J. Léger, C. Caskey, F. Pons, 1993, Human gene therapy.

Expression of myosin heavy chain isoforms in Duchenne muscular dystrophy patients and carriers

J. Léger, J. Marini, M. Chevallay, 1991, Neuromuscular Disorders.

Dystrophin and dystrophin-related protein (utrophin) distribution in normal and dystrophin-deficient skeletal muscles

J. Léger, T. Voit, A. Robert, 1993, Neuromuscular Disorders.

Xp21 dystrophin and 6q dystrophin-related protein. Comparative immunolocalization using multiple antibodies.

J. Léger, T. Voit, J. Léger, 1991, The American journal of pathology.

Myosin expression in semitendinosus muscle during fetal development of cattle: immunocytochemical and electrophoretic analyses.

B. Picard, C. Jurie, J. Robelin, 1993, Reproduction, nutrition, development.

Presence of an unidentified myosin isoform in certain bovine foetal muscles.

B. Picard, J. Robelin, Y. Geay, 1995, Meat science.

Probing myosin light chain 1 structure with monoclonal antibodies

J. Léger, J. Liautard, D. Mornet, 1992, Journal of Muscle Research & Cell Motility.

Exclusion of muscle specific actinin-associated LIM protein (ALP) gene from 4q35 facioscapulohumeral muscular dystrophy (FSHD) candidate genes

C. Auffray, C. Dechesne, F. Pons, 1999, Neuromuscular Disorders.

Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IκBα/NF-κB pathway in limb-girdle muscular dystrophy type 2A

J. Beckmann, J. Loiselet, G. Lefranc, 1999, Nature Medicine.

Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IkBa/NF-kB pathway in limb-girdle muscular dystrophy type 2A

J. Beckmann, J. Loiselet, G. Lefranc, 1999, Nature Medicine.

The dystrophin superfamily: variability and complexity

E. Fabbrizio, G. Hugon, A. Robert, 1994, Journal of Muscle Research & Cell Motility.

Quantitative analysis of relative protein contents by Western blotting: Comparison of three members of the dystrophin‐glycoprotein complex in slow and fast rat skeletal muscle

J. Marini, F. Pons, P. Charpiot, 2000, Electrophoresis.

Properties of chicken cardiac dystrophin

E. Fabbrizio, D. Mornet, J. Léger, 1992, Biology of the cell.

Utrophin Localization in Normal and Dystrophin‐Deficient Heart

E. Fabbrizio, Jean Martinez, J. Fehrentz, 1994, Circulation.

Proteolytic susceptibility of the central domain in chicken gizzard and skeletal muscle dystrophins.

J. Léger, A. Robert, D. Mornet, 1992, Biochimica et biophysica acta.

Dystrophin in central nervous system: a developmental, regional distribution and subcellular localization study

J. Léger, D. Aunis, F. Pons, 1991, Neuroscience Letters.

Comparative Studies on Chicken Skeletal and Smooth Muscle Dystrophins

R. Heilig, J. Léger, A. Robert, 1991 .

Early postnatal muscle contractile activity regulates the carbonic anhydrase phenotype of proprioceptive neurons in young and mature mice: Evidence for a critical period in development

J. Valmier, F. Pons, M. Baldy‐Moulinier, 1996, Neuroscience.

Identification and Immunocytochemical Localization of Utrophin and Dystrophin Products in the Rat Peripheral Vestibular System

F. Pons, C. Dechesne, J. Griffoin, 2012 .

[Presence of dystrophine-like protein at the neuromuscular junction in Duchenne muscular dystrophy and in "mdx" mutant mice].

J. Léger, M. Fardeau, F. Tomé, 1990, Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie.

Mosaic expression of two dystrophins in a boy with progressive muscular dystrophy

F. Pons, Sylvie Tuffery, Dominique Mornet, 1998, Muscle & nerve.

Expression of Various NCAM Isoforms in Human Embryonic Muscles: Correlation with Myosin Heavy Chain Phenotypes

J. Léger, D. Figarella-Branger, G. Rougon, 1992, Journal of neuropathology and experimental neurology.

Immunocytochemical analysis of myosin heavy chains in human fetal skeletal muscles

J. Léger, M. Chevallay, M. Fardeau, 1986, Journal of the Neurological Sciences.

Myosin heavy chains in fibers of TTX-paralyzed rat soleus and medial gastrocnemius muscles.

P. Gardiner, J. Marini, F. Pons, 2000, Journal of applied physiology.

Isolated dystrophin molecules as seen by electron microscopy.

R. Heilig, J. Léger, F. Pons, 1990, Proceedings of the National Academy of Sciences of the United States of America.

Congenital muscular dystrophy and cerebellar atrophy

F. Rivier, B. Echenne, M. Tardieu, 1998, Neurology.

Merosin positive congenital muscular dystrophy with mental deficiency, epilepsy and MRI changes in the cerebral white matter

F. Rivier, B. Echenne, D. Mornet, 1997, Neuromuscular Disorders.

Comparative evolution of muscular dystrophy in diaphragm, gastrocnemius and masseter muscles from old male mdx mice

N. Vayssiere, M. Royuela, M. Leger, 2004, Journal of Muscle Research & Cell Motility.

Utrophin Localization in Normal and Dystrophin‐Deficient Heart

E. Fabbrizio, Jean Martinez, J. Fehrentz, 1994, Circulation.

Characterization and distribution of myosin variants in normal and pathological human hearts.

J. Léger, C. Dechesne, P. Bouvagnet, 1984, European Heart Journal.