Functional overlap between ABCD1 (ALD) and ABCD2 (ALDR) transporters: a therapeutic target for X-adrenoleukodystrophy
Pujol, Aurora, Ferrer, Isidre, Camps, Carme, Metzger, Elisabeth, Hindelang, Colette, Callizot, Noëlle, Ruiz, Montse, Pàmpols, Teresa, Giròs, Marisa, Mandel, Jean Louis
Published in Human molecular genetics (01.12.2004)
Published in Human molecular genetics (01.12.2004)
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Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage
Ferrer, Isidre, Kapfhammer, Josef P., Hindelang, Colette, Kemp, Stephan, Troffer-Charlier, Nathalie, Broccoli, Vania, Callyzot, Noëlle, Mooyer, Petra, Selhorst, Jacqueline, Vreken, Peter, Wanders, Ronald J.A., Mandel, Jean Louis, Pujol, Aurora
Published in Human molecular genetics (01.12.2005)
Published in Human molecular genetics (01.12.2005)
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Journal Article
Orphan Receptor DAX-1 Is a Shuttling RNA Binding Protein Associated with Polyribosomes via mRNA
Lalli, Enzo, Ohe, Kenji, Hindelang, Colette, Sassone-Corsi, Paolo
Published in Molecular and Cellular Biology (01.07.2000)
Published in Molecular and Cellular Biology (01.07.2000)
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Preferential nuclear localization of the human papillomavirus type 16 E6 oncoprotein in cervical carcinoma cells
Masson, Murielle, Hindelang, Colette, Sibler, Annie-Paule, Schwalbach, Georges, Trave, Gilles, Weiss, Etienne
Published in Journal of general virology (01.08.2003)
Published in Journal of general virology (01.08.2003)
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Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits
Simon, Delphine, Hindelang, Colette, Koenig, Michel, Criqui-Filipe, Paola, Tiziano, Francesco, Melki, Judith, Puccio, Hélène, Rustin, Pierre, Cossée, Mireille, Matyas, Robert
Published in Nature genetics (01.02.2001)
Published in Nature genetics (01.02.2001)
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Late onset neurological phenotype of the X-ALD gene inactivation in mice: a mouse model for adrenomyeloneuropathy
PUJOL, Aurora, HINDELANG, Colette, CALLIZOT, Noëlle, BARTSCH, Udo, SCHACHNER, Melitta, MANDEL, Jean Louis
Published in Human molecular genetics (01.03.2002)
Published in Human molecular genetics (01.03.2002)
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Defects of the Chorioallantoic Placenta in Mouse RXRα Null Fetuses
Sapin, Vincent, Dollé, Pascal, Hindelang, Colette, Kastner, Philippe, Chambon, Pierre
Published in Developmental biology (01.11.1997)
Published in Developmental biology (01.11.1997)
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Frataxin is Reduced in Friedreich Ataxia Patients and is Associated with Mitochondrial Membranes
Campuzano, Victoria, Montermini, Laura, Lutz, Yves, Cova, Lidia, Hindelang, Colette, Jiralerspong, Sarn, Trottier, Yvon, Kish, Stephen J., Faucheux, Baptiste, Trouillas, Paul, Authier, François J., Dürr, Alexandra, Mandel, Jean-Louis, Vescovi, Angelo, Pandolfo, Massimo, Koenig, Michel
Published in Human molecular genetics (01.10.1997)
Published in Human molecular genetics (01.10.1997)
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Cellular retinol-binding protein I is essential for vitamin A homeostasis
Ghyselinck, Norbert B., Båvik, Claes, Sapin, Vincent, Mark, Manuel, Bonnier, Dominique, Hindelang, Colette, Dierich, Andrée, Nilsson, Charlotte B., Håkansson, Helen, Sauvant, Patrick, Azaïs-Braesco, Véronique, Frasson, Maria, Picaud, Serge, Chambon, Pierre
Published in The EMBO journal (15.09.1999)
Published in The EMBO journal (15.09.1999)
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NUFIP1 (nuclear FMRP interacting protein 1) is a nucleocytoplasmic shuttling protein associated with active synaptoneurosomes
Bardoni, Barbara, Willemsen, Rob, Weiler, Ivan Jeanne, Schenck, Annette, Severijnen, Lies-Anne, Hindelang, Colette, Lalli, Enzo, Mandel, Jean-Louis
Published in Experimental cell research (10.09.2003)
Published in Experimental cell research (10.09.2003)
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Retinal Dystrophy Resulting from Ablation of RXRα in the Mouse Retinal Pigment Epithelium
Mori, Mikiro, Metzger, Daniel, Picaud, Serge, Hindelang, Colette, Simonutti, Manuel, Sahel, José, Chambon, Pierre, Mark, Manuel
Published in The American journal of pathology (01.02.2004)
Published in The American journal of pathology (01.02.2004)
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A Transgenic Mouse Model for Inducible and Reversible Dysmyelination
Mathis, Carole, Hindelang, Colette, LeMeur, Marianne, Borrelli, Emiliana
Published in The Journal of neuroscience (15.10.2000)
Published in The Journal of neuroscience (15.10.2000)
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Normal innervation and differentiation of X-linked myotubular myopathy muscle cells in a nerve-muscle coculture system
Dorchies, Olivier M, Laporte, Jocelyn, Wagner, Stéphanie, Hindelang, Colette, Warter, Jean-Marie, Mandel, Jean-Louis, Poindron, Philippe
Published in Neuromuscular disorders : NMD (01.11.2001)
Published in Neuromuscular disorders : NMD (01.11.2001)
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Retinal Dystrophy Resulting from Ablation of RXR{alpha} in the Mouse Retinal Pigment Epithelium
Mori, Mikiro, Metzger, Daniel, Picaud, Serge, Hindelang, Colette, Simonutti, Manuel, Sahel, Jose, Chambon, Pierre, Mark, Manuel
Published in The American journal of pathology (01.02.2004)
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Published in The American journal of pathology (01.02.2004)
Journal Article
Induction of D2 dopamine receptor mRNA synthesis in a 6-hydroxydopamine parkinsonian rat model
Lisovoski, F, Haby, C, Borrelli, E, Schleef, C, Revel, M O, Hindelang, C, Zwiller, J
Published in Brain research bulletin (01.05.1992)
Published in Brain research bulletin (01.05.1992)
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