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Search Results - Moumné, Lara
Search Results - Moumné, Lara
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Oligonucleotide Therapeutics: From Discovery and Development to Patentability
by
Moumné, Lara
,
Marie, Anne-Céline
,
Crouvezier, Nicolas
Published in
Pharmaceutics
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Genetic knock-down of HDAC3 does not modify disease-related phenotypes in a mouse model of Huntington's disease
by
Moumné, Lara
,
Campbell, Ken
,
Howland, David
,
Ouyang, Yingbin
,
Bates, Gillian P
Published in
PloS one
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Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivation
by
Beysen, Diane
,
Moumné, Lara
,
Veitia, Reiner
,
Peters, Hartmut
,
Leroy, Bart P.
,
De Paepe, Anne
,
De Baere, Elfride
Published in
Human molecular genetics
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CYP46A1, the rate-limiting enzyme for cholesterol degradation, is neuroprotective in Huntington's disease
by
Boussicault, Lydie
,
Alves, Sandro
,
Lamazière, Antonin
,
Planques, Anabelle
,
Heck, Nicolas
,
Moumné, Lara
,
Despres, Gaëtan
,
Bolte, Susanne
,
Hu, Amélie
,
Pagès, Christiane
,
Galvan, Laurie
,
Piguet, Francoise
,
Aubourg, Patrick
,
Cartier, Nathalie
,
Caboche, Jocelyne
,
Betuing, Sandrine
Published in
Brain (London, England : 1878)
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Deletions in the polyAlanine-containing transcription factor FOXL2 lead to intranuclear aggregation
by
Moumné, Lara
,
Fellous, Marc
,
Veitia, Reiner A.
Published in
Human molecular genetics
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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 Alteration...
by
Salery, Marine
,
Dos Santos, Marc
,
Saint-Jour, Estefani
,
Moumné, Lara
,
Pagès, Christiane
,
Kappès, Vincent
,
Parnaudeau, Sébastien
,
Caboche, Jocelyne
,
Vanhoutte, Peter
Published in
Biological psychiatry (1969)
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Multiple Aspects of Gene Dysregulation in Huntington's Disease
by
Moumné, Lara
,
Betuing, Sandrine
,
Caboche, Jocelyne
Published in
Frontiers in neurology
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Oral administration of the pimelic diphenylamide HDAC inhibitor HDACi 4b is unsuitable for chronic inhibition of HDAC activity in the CNS in vivo
by
Beconi, Maria
,
Aziz, Omar
,
Matthews, Kim
,
Moumné, Lara
,
O'Connell, Catherine
,
Yates, Dawn
,
Clifton, Steven
,
Pett, Hannah
,
Vann, Julie
,
Crowley, Lynsey
,
Haughan, Alan F
,
Smith, Donna L
,
Woodman, Ben
,
Bates, Gillian P
,
Brookfield, Fred
,
Bürli, Roland W
,
McAllister, George
,
Dominguez, Celia
,
Munoz-Sanjuan, Ignacio
,
Beaumont, Vahri
Published in
PloS one
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Differential aggregation and functional impairment induced by polyalanine expansions in FOXL2, a transcription factor involved in cranio-facial and ovarian development
by
Moumné, Lara
,
Dipietromaria, Aurélie
,
Batista, Frank
,
Kocer, Ayhan
,
Fellous, Marc
,
Pailhoux, Eric
,
Veitia, Reiner A.
Published in
Human molecular genetics
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A novel polyalanine expansion in FOXL2 : the first evidence for a recessive form of the blepharophimosis syndrome (BPES) associated with ovarian dysfunction
by
NALLATHAMBI, Jeyabalan
,
MOUMNE, Lara
,
DE BAERE, Elfride
,
BEYSEN, Diane
,
USHA, Kim
,
SUNDARESAN, Periasamy
,
VEITIA, Reiner A
Published in
Human genetics
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Differential functional effects of novel mutations of the transcription factor FOXL2 in BPES patients
by
Nallathambi, Jeyabalan
,
Laissue, Paul
,
Batista, Frank
,
Benayoun, Bérénice A
,
Lesaffre, Corinne
,
Moumné, Lara
,
Pandaranayaka, PJ Eswari
,
Usha, Kim
,
Krishnaswamy, Sankaran
,
Sundaresan, Periasamy
,
Veitia, Reiner A
Published in
Human mutation
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A novel polyalanine expansion in FOXL2: the first evidence for a recessive form of the blepharophimosis syndrome
by
Nallathambi, Jeyabalan
,
Moumné, Lara
,
De Baere, Elfride
,
Beysen, Diane
,
Usha, Kim
,
Sundaresan, Periasamy
,
Veitia, Reiner A
Published in
Human genetics
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