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Search Results - Dhaenens, C.M.
Search Results - Dhaenens, C.M.
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Overexpression of MBNL1 fetal isoforms and modified splicing of Tau in the DM1 brain: Two individual consequences of CUG trinucleotide repeats
by
Dhaenens, C.M.
,
Schraen-Maschke, S.
,
Tran, H.
,
Vingtdeux, V.
,
Ghanem, D.
,
Leroy, O.
,
Delplanque, J.
,
Vanbrussel, E.
,
Delacourte, A.
,
Vermersch, P.
,
Maurage, C.A.
,
Gruffat, H.
,
Sergeant, A.
,
Mahadevan, M.S.
,
Ishiura, S.
,
Buée, L.
,
Cooper, T.A.
,
Caillet-Boudin, M.L.
,
Charlet-Berguerand, N.
,
Sablonnière, B.
,
Sergeant, N.
Published in
Experimental neurology
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Study of the diagnostic yield of gene panels in long QT syndrome in pediatrics
by
Daire, E.
,
Dirani, S.
,
Klug, D.
,
Dhaenens, C.M.
,
Kyndt, F.
,
Fressart, V.
,
Jedraszak, G.
Published in
Archives of cardiovascular diseases supplements
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Tau exon 2 responsive elements deregulated in myotonic dystrophy type I are proximal to exon 2 and synergistically regulated by MBNL1 and MBNL2
by
Carpentier, C.
,
Ghanem, D.
,
Fernandez-Gomez, F.J.
,
Jumeau, F.
,
Philippe, J.V.
,
Freyermuth, F.
,
Labudeck, A.
,
Eddarkaoui, S.
,
Dhaenens, C.M.
,
Holt, I.
,
Behm-Ansmant, I.
,
Marmier-Gourrier, N.
,
Branlant, C.
,
Charlet-Berguerand, N.
,
Marie, J.
,
Schraen-Maschke, S.
,
Buée, L.
,
Sergeant, N.
,
Caillet-Boudin, M.L.
Published in
Biochimica et biophysica acta. Molecular basis of disease
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Mis-splicing of Tau exon 10 in myotonic dystrophy type 1 is reproduced by overexpression of CELF2 but not by MBNL1 silencing
by
Dhaenens, C.M.
,
Tran, H.
,
Frandemiche, M.-L.
,
Carpentier, C.
,
Schraen-Maschke, S.
,
Sistiaga, A.
,
Goicoechea, M.
,
Eddarkaoui, S.
,
Van Brussels, E.
,
Obriot, H.
,
Labudeck, A.
,
Gevaert, M.H.
,
Fernandez-Gomez, F.
,
Charlet-Berguerand, N.
,
Deramecourt, V.
,
Maurage, C.A.
,
Buée, L.
,
de Munain, A. Lopez
,
Sablonnière, B.
,
Caillet-Boudin, M.L.
,
Sergeant, N.
Published in
Biochimica et biophysica acta. Molecular basis of disease
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Association of corticobasal degeneration and Huntington's disease: Can Tau aggregates protect Huntingtin toxicity?
by
Caparros-Lefebvre, Dominique
,
Kerdraon, Olivier
,
Devos, David
,
Dhaenens, C.M.
,
Blum, David
,
Maurage, C.A
,
Delacourte, André
,
Sablonnière, Bernard
Published in
Movement disorders
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Cancer papillaire thyroïdien et dystrophie myotonique de Steinert
by
Ben Hamou, A.
,
Vantyghem, M.C.
,
Caiazzo, R.
,
Dhaenens, C.M.
Published in
Annales d'endocrinologie
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Mis-splicing of Tau exon 10 in myotonic dystrophy type I is reproduced by overexpression of CELF2 but not by MBNL1 silencing
by
Dhaenens, C.M.
,
Tran, H.
,
Frandemiche, M.-L.
,
Carpentier, C.
,
Schraen-Maschke, S.
,
Sistiaga, A.
,
Goicoechea, M.
,
Eddarkaoui, S.
,
van Brussels, E.
,
Obriot, H.
,
Labudeck, A.
,
Gevaert, M.H.
,
Fernandez-Gomez, F.
,
Charlet-Berguerand, N.
,
Deramecourt, V.
,
Maurage, C.A.
,
Buée, Luc
,
de Munain, A. Lopez
,
Sablonnière, B.
,
Caillet-Boudin, M.L.
,
Sergeant, Nicolas
Published in
Biochimica et biophysica acta. Molecular basis of disease
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P1-5 Régulation de l’épissage alternatif des exons 2/3 et 6 des ARNm de Tau, deux processus d’épissage modifiés dans les cerveaux de patients atteints de Dystrophie myotonique de t...
by
Leroy, O.
,
Dhaenens, C.M.
,
Schraen-Maschke, S.
,
Maurage, C.A.
,
Buée, L.
,
Sablonnière, B.
,
Sergeant, N.
,
Caillet-Boudin, M.L.
Published in
Revue neurologique
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Cardiac Outcomes in Adults With Mitochondrial Diseases
by
Savvatis, Konstantinos
,
Vissing, Christoffer Rasmus
,
Klouvi, Lori
,
Florian, Anca
,
Rahman, Mehjabin
,
Béhin, Anthony
,
Fayssoil, Abdallah
,
Masingue, Marion
,
Stojkovic, Tanya
,
Bécane, Henri Marc
,
Berber, Nawal
,
Mochel, Fanny
,
Duboc, Denis
,
Fontaine, Bertrand
,
Krett, Bjørg
,
Stalens, Caroline
,
Lejeune, Julie
,
Pitceathly, Robert D S
,
Lopes, Luis
,
Saadi, Malika
,
Gossios, Thomas
,
Procaccio, Vincent
,
Spinazzi, Marco
,
Tard, Céline
,
De Groote, Pascal
,
Dhaenens, Claire-Marie
,
Douillard, Claire
,
Echaniz-Laguna, Andoni
,
Quinlivan, Ros
,
Hanna, Michael G
,
Yilmaz, Ali
,
Vissing, John
,
Laforêt, Pascal
,
Elliott, Perry
,
Wahbi, Karim
Published in
Journal of the American College of Cardiology
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Biochimica Et Biophysica Acta. Molecular Basis Of Disease
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