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Pharmaceutics|February 26, 2022
Oligonucleotide Therapeutics: From Discovery and Development to PatentabilityLara Moumné, Anne-Céline Marie, Nicolas Crouvezier
Frontiers in Neurology|October 30, 2013
Multiple Aspects of Gene Dysregulation in Huntington's DiseaseLara Moumné, Sandrine Betuing, Jocelyne Caboche
Medecine Sciences : M/S|February 17, 2023
[Mechanisms of action and patentability of therapeutic oligonucleotides]Nicolas Crouvezier, Anne-Céline Marie, Lara Moumné
Human Molecular Genetics|October 13, 2005
Deletions in the polyAlanine-containing transcription factor FOXL2 lead to intranuclear aggregationLara Moumné, Marc Fellous, Reiner A Veitia
Plos One|February 21, 2012
Genetic knock-down of HDAC3 does not modify disease-related phenotypes in a mouse model of Huntington's diseaseLara Moumné, Ken Campbell, David Howland, et al.
Human Molecular Genetics|December 26, 2007
Differential aggregation and functional impairment induced by polyalanine expansions in FOXL2, a transcription factor involved in cranio-facial and ovarian developmentLara Moumné, Aurélie Dipietromaria, Frank Batista, et al.
Human Genetics|November 8, 2006
A novel polyalanine expansion in FOXL2: the first evidence for a recessive form of the blepharophimosis syndrome (BPES) associated with ovarian dysfunctionJeyabalan Nallathambi, Lara Moumné, Elfride De Baere, et al.
Human Molecular Genetics|March 29, 2008
Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivationDiane Beysen, Lara Moumné, Reiner Veitia, et al.
Biological Psychiatry|August 28, 2016
Activity-Regulated Cytoskeleton-Associated Protein Accumulates in the Nucleus in Response to Cocaine and Acts as a Brake on Chromatin Remodeling and Long-Term Behavioral AlterationsMarine Salery, Marc Dos Santos, Estefani Saint-Jour, et al.
Human Mutation|May 20, 2008
Differential functional effects of novel mutations of the transcription factor FOXL2 in BPES patientsJeyabalan Nallathambi, Paul Laissue, Frank Batista, et al.
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