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Natacha Roblot

Research Profile

Chemicals & Drugs

Disorders

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Anatomy

Physiology

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Publications

TOP 3
Coralie Fassier; Jamilé Hazan; Didier Job; Julien Lefèvre; Philippe Mailly; Sabrina Courageot; Patrick A Curmi; Cécile Dalard; Stéphanie Delga; Leticia Peris; Natacha Roblot; Anne Tarrade; Judith Melki
Microtubule-targeting drugs rescue axonal swellings in cortical neurons from spastin knockout mice.
Jeremie Vitte; Coralie Fassier; Francesco D Tiziano; Cécile Dalard; Sabrina Soave; Natacha Roblot; Christina Brahe; Pascale Saugier-Veber; Jean Paul Bonnefont; Judith Melki
Refined characterization of the expression and stability of the SMN gene products.
Anne Tarrade; Coralie Fassier; Sabrina Courageot; Delphine Charvin; Jeremie Vitte; Leticia Peris; Alain Thorel; Etienne Mouisel; Nuria Fonknechten; Natacha Roblot; Danielle Seilhean; Andrée Diérich; JEAN-JACQUES HAUW; Judith Melki
A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition.

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All Publications

2013: Coralie Fassier; Jamilé Hazan; Didier Job; Julien Lefèvre; Philippe Mailly; Sabrina Courageot; Patrick A Curmi; Cécile Dalard; Stéphanie Delga; Leticia Peris; Natacha Roblot; Anne Tarrade; Judith Melki
Microtubule-targeting drugs rescue axonal swellings in cortical neurons from spastin knockout mice.
Disease models & mechanisms 2013;6(1):72-83.
2007: Jeremie Vitte; Coralie Fassier; Francesco D Tiziano; Cécile Dalard; Sabrina Soave; Natacha Roblot; Christina Brahe; Pascale Saugier-Veber; Jean Paul Bonnefont; Judith Melki
Refined characterization of the expression and stability of the SMN gene products.
The American journal of pathology 2007;171(4):1269-80.
2006: Anne Tarrade; Coralie Fassier; Sabrina Courageot; Delphine Charvin; Jeremie Vitte; Leticia Peris; Alain Thorel; Etienne Mouisel; Nuria Fonknechten; Natacha Roblot; Danielle Seilhean; Andrée Diérich; JEAN-JACQUES HAUW; Judith Melki
A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition.
Human molecular genetics 2006;15(24):3544-58.
2006: Nouzha Salah-Mohellibi; Gaelle Millet; Isabelle André-Schmutz; Bénédicte Desforges; Robert Olaso; Natacha Roblot; Sabrina Courageot; Gilbert Bensimon; Marina Cavazzana-Calvo; Judith Melki
Bone marrow transplantation attenuates the myopathic phenotype of a muscular mouse model of spinal muscular atrophy.
Stem cells (Dayton, Ohio) 2006;24(12):2723-32.
2006: Robert Olaso; Vandana Joshi; Julien Fernandez; Natacha Roblot; Sabrina Courageot; Jean Paul Bonnefont; Judith Melki
Activation of RNA metabolism-related genes in mouse but not human tissues deficient in SMN.
Physiological genomics 2006;24(2):97-104.
2005: Veronique L Billat; Etienne Mouisel; Natacha Roblot; Judith Melki
Inter- and intrastrain variation in mouse critical running speed.
Journal of applied physiology (Bethesda, Md. : 1985) 2005;98(4):1258-63.
2004: Jeremie Vitte; Bénédicte Davoult; Natacha Roblot; Michèle Mayer; Vandana Joshi; Sabrina Courageot; François Tronche; Jacqueline Vadrot; Marie Helene Moreau; François Kemeny; Judith Melki
Deletion of murine Smn exon 7 directed to liver leads to severe defect of liver development associated with iron overload.
The American journal of pathology 2004;165(5):1731-41.
2003: Hafedh Haddad; Carmen Cifuentes-Diaz; Audrey Miroglio; Natacha Roblot; Vandana Joshi; Judith Melki
Riluzole attenuates spinal muscular atrophy disease progression in a mouse model.
Muscle & nerve 2003;28(4):432-7.
2003: Sophie Nicole; Benedicte Desforges; Gaelle Millet; Jeanne-Claire Lesbordes; Carmen Cifuentes-Diaz; Dora Vertes; My Linh Cao; Fabienne De Backer; Laetitia Languille; Natacha Roblot; Vandana Joshi; Jean-Marie Gillis; Judith Melki
Intact satellite cells lead to remarkable protection against Smn gene defect in differentiated skeletal muscle.
The Journal of cell biology 2003;161(3):571-82.
2002: Carmen Cifuentes-Diaz; Sophie Nicole; Maria E Velasco; Christophe Borra-Cebrian; Cristina Panozzo; Tony Frugier; Gaelle Millet; Natacha Roblot; Vandana Joshi; Judith Melki
Neurofilament accumulation at the motor endplate and lack of axonal sprouting in a spinal muscular atrophy mouse model.
Human molecular genetics 2002;11(12):1439-47.
2001: Carmen Cifuentes-Diaz; Tony Frugier; Francesco D Tiziano; E Lacène; Natacha Roblot; Vandana Joshi; M H Moreau; Judith Melki
Deletion of murine SMN exon 7 directed to skeletal muscle leads to severe muscular dystrophy.
The Journal of cell biology 2001;152(5):1107-14.
2000: Tony Frugier; Francesco D Tiziano; Carmen Cifuentes-Diaz; P Miniou; Natacha Roblot; Andrée Dierich; Marianne Le Meur; Judith Melki
Nuclear targeting defect of SMN lacking the C-terminus in a mouse model of spinal muscular atrophy.
Human molecular genetics 2000;9(5):849-58.
1999: P Miniou; D Tiziano; Tony Frugier; Natacha Roblot; Marianne Le Meur; Judith Melki
Gene targeting restricted to mouse striated muscle lineage.
Nucleic acids research 1999;27(19):e27.