M. Muriel

发表

Cellular distribution and subcellular localization of spatacsin and spastizin, two proteins involved in hereditary spastic paraplegia

C. Duyckaerts, A. Brice, G. Stevanin, 2011, Molecular and Cellular Neuroscience.

Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia.

A. Durr, C. Depienne, A. Brice, 2014, American journal of human genetics.

Nondopaminergic neurons in Parkinson's disease.

E. Hirsch, C. François, J. Féger, 2003, Advances in neurology.

Deregulation of autophagy in postmortem brains of Machado‐Joseph disease patients

A. Brice, W. D. den Dunnen, M. Muriel, 2018, Neuropathology : official journal of the Japanese Society of Neuropathology.

The endoplasmic reticulum-mitochondria interface is perturbed in PARK2 knockout mice and patients with PARK2 mutations.

A. Brice, J. Corvol, D. Bohl, 2016, Human molecular genetics.

PML clastosomes prevent nuclear accumulation of mutant ataxin-7 and other polyglutamine proteins

M. Ruberg, A. Brice, A. Janer, 2006, The Journal of cell biology.

Annonacin, a Natural Mitochondrial Complex I Inhibitor, Causes Tau Pathology in Cultured Neurons

E. Hirsch, W. Oertel, M. Ruberg, 2007, The Journal of Neuroscience.

Neurotoxic Calcium Transfer from Endoplasmic Reticulum to Mitochondria Is Regulated by Cyclin-Dependent Kinase 5-Dependent Phosphorylation of Tau

M. Ruberg, A. Brice, M. Muriel, 2005, The Journal of Neuroscience.

Ultrastructural localization of parkin in the rat brainstem, thalamus and basal ganglia

E. Hirsch, A. Brice, M. Muriel, 2004, Journal of Neural Transmission.

The autophagy/lysosome pathway is impaired in SCA7 patients and SCA7 knock-in mice

M. Priault, M. Ruberg, A. Durr, 2014, Acta Neuropathologica.

Glial cell participation in the degeneration of dopaminergic neurons in Parkinson's disease.

E. Hirsch, Y. Agid, M. Ruberg, 1999, Advances in neurology.

Mitochondrial free calcium levels (Rhod‐2 fluorescence) and ultrastructural alterations in neuronally differentiated PC12 cells during ceramide‐dependent cell death

E. Hirsch, Y. Agid, M. Ruberg, 2000, The Journal of comparative neurology.

Nuclear translocation of NF-kappaB is increased in dopaminergic neurons of patients with parkinson disease.

Y Agid, E. Hirsch, Y. Agid, 1997, Proceedings of the National Academy of Sciences of the United States of America.

Nuclear translocation of NFk B is increased in dopaminergic neurons of patients with Parkinson disease

E. Hirsch, Y. Agid, M. Ruberg, 1997 .

Mutations in the SPG3A gene encoding the GTPase atlastin interfere with vesicle trafficking in the ER/Golgi interface and Golgi morphogenesis

M. Ruberg, C. Duyckaerts, C. Depienne, 2007, Molecular and Cellular Neuroscience.

Loss of spatacsin function alters lysosomal lipid clearance leading to upper and lower motor neuron degeneration

A. Brice, G. Stevanin, F. Santorelli, 2017, Neurobiology of Disease.

Atlastin‐1, the dynamin‐like GTPase responsible for spastic paraplegia SPG3A, remodels lipid membranes and may form tubules and vesicles in the endoplasmic reticulum

M. Ruberg, A. Brice, M. Muriel, 2009, Journal of neurochemistry.

The gene responsible for hereditary spastic paraplegia SPG3A encodes atlastin-1 (ATL), a dynamin-like GTPase

M. Ruberg, A. Brice, M. Muriel, 2009 .

Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families.

M. Ruberg, N. Birouk, O. Dubourg, 2006, Brain : a journal of neurology.

Phenotypical features of a Moroccan family with autosomal recessive Charcot-Marie-Tooth disease associated with the S194X mutation in the GDAP1 gene.

A. Brice, N. Birouk, E. Le Guern, 2003, Archives of neurology.

Caspase-3: A vulnerability factor and final effector in apoptotic death of dopaminergic neurons in Parkinson's disease.

E. Hirsch, Y. Agid, M. Ruberg, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Persistent Increase in Olfactory Type G-Protein α Subunit Levels May Underlie D1 Receptor Functional Hypersensitivity in Parkinson Disease

J. Girault, E. Hirsch, J. Féger, 2004, The Journal of Neuroscience.

Dopamine depletion impairs precursor cell proliferation in Parkinson disease

Charles Duyckaerts, E. Hirsch, C. Duyckaerts, 2004, Nature Neuroscience.

VEGF-C is a trophic factor for neural progenitors in the vertebrate embryonic brain

P. Carmeliet, M. Karkkainen, K. Alitalo, 2006, Nature Neuroscience.

A Conditional Pan-Neuronal Drosophila Model of Spinocerebellar Ataxia 7 with a Reversible Adult Phenotype Suitable for Identifying Modifier Genes

M. Ruberg, A. Brice, G. Stevanin, 2007, The Journal of Neuroscience.

Parkin prevents mitochondrial swelling and cytochrome c release in mitochondria-dependent cell death.

E. Hirsch, M. Ruberg, A. Brice, 2003, Human molecular genetics.

Parkin maintains mitochondrial levels of the protective Parkinson’s disease-related enzyme 17-β hydroxysteroid dehydrogenase type 10

A. Lees, A. Brice, D. Guédin, 2015, Cell Death and Differentiation.

Parkin immunoreactivity in the brain of human and non‐human primates: An immunohistochemical analysis in normal conditions and in Parkinsonian syndromes

A. Parent, E. Hirsch, Y. Agid, 2001, The Journal of comparative neurology.

Parkin depletion delays motor decline dose-dependently without overtly affecting neuropathology in α-synuclein transgenic mice

A. Brice, R. Barbour, H. Lashuel, 2013, BMC Neuroscience.

Plasticity of afferent fibers to striatal neurons bearing D1 dopamine receptors in Parkinson's disease

E. Hirsch, Y. Agid, M. Muriel, 2001, Movement disorders : official journal of the Movement Disorder Society.

Structural Requirement of TAG-1 for Retinal Ganglion Cell Axons and Myelin in the Mouse Optic Nerve

Patricia Gaspar, Elli Chatzopoulou, Bernard Zalc, 2008, The Journal of Neuroscience.

Neurobiology of Disease Persistent Increase in Olfactory Type G-Protein Subunit Levels May Underlie D 1 Receptor Functional Hypersensitivity in Parkinson Disease

J. Girault, E. Hirsch, J. Féger, 2004 .

Localization of D1a dopamine receptors on cell bodies and axonal endings in the substantia nigra pars reticulata of the rat

E. Hirsch, C. François, C. Jan, 2007, Journal of Neural Transmission.

Levodopa induces a cytoplasmic localization of D1 dopamine receptors in striatal neurons in Parkinson's disease

Yves Agid, Bertrand Bloch, D. Abrous, 1999, Annals of neurology.

Internal pallidum and substantia nigra control different parts of the mesopontine reticular formation in primate

E. Hirsch, C. François, C. Karachi, 2011, Movement disorders : official journal of the Movement Disorder Society.

Levodopa but not ropinirole induces an internalization of D1 dopamine receptors in parkinsonian rats

E. Hirsch, G. Orieux, M. Muriel, 2002, Movement disorders : official journal of the Movement Disorder Society.

Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia.

A. Durr, C. Depienne, A. Brice, 2014, American journal of human genetics.

Cellular distribution and subcellular localization of spatacsin and spastizin, two proteins involved in hereditary spastic paraplegia

C. Duyckaerts, A. Brice, G. Stevanin, 2011, Molecular and Cellular Neuroscience.