H. Seznec

发表

Week in The Journal F Cellular / Molecular cAMP and a Retinal Clock

D. Hommer, D. Storm, M. Koenig, 2004 .

Friedreich ataxia: the oxidative stress paradox.

M. Koenig, P. Golik, V. Procaccio, 2005, Human molecular genetics.

Transgenic mice carrying large human genomic sequences with expanded CTG repeat mimic closely the DM CTG repeat intergenerational and somatic instability.

C. Junien, G. Gourdon, H. Hofmann-Radvanyi, 2000, Human molecular genetics.

New nomenclature and DNA testing guidelines for myotonic dystrophy type 1 (DM1)

T. Cooper, A. Roses, S. Tapscott, 2000, Neurology.

Somatic instability of the CTG repeat in mice transgenic for the myotonic dystrophy region is age dependent but not correlated to the relative intertissue transcription levels and proliferative capacities.

C. Junien, F. Radvanyi, G. Gourdon, 1998, Human molecular genetics.

Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities.

A. Delacourte, C. Junien, A. Ghestem, 2001, Human molecular genetics.

Limitations in a frataxin knockdown cell model for Friedreich ataxia in a high-throughput drug screen

M. Koenig, P. Rustin, J. Haiech, 2009, BMC neurology.

2003 International Friedreich's Ataxia Research Conference, 14–16 February 2003, Bethesda, MD, USA

Robert B. Wilson, H. Puccio, H. Seznec, 2004, Neuromuscular Disorders.

Idebenone delays the onset of cardiac functional alteration without correction of Fe-S enzymes deficit in a mouse model for Friedreich ataxia.

M. Koenig, P. Rustin, A. Gansmuller, 2004, Human molecular genetics.

Friedreich Ataxia Mouse Models with Progressive Cerebellar and Sensory Ataxia Reveal Autophagic Neurodegeneration in Dorsal Root Ganglia

M. Koenig, P. Rustin, A. Gansmuller, 2004, The Journal of Neuroscience.