Acute Ethanol Administration Oxidatively Damages and Depletes Mitochondrial DNA in Mouse Liver, Brain, Heart, and Skeletal Muscles: Protective Effects of Antioxidants
Mansouri, A, Demeilliers, C, Amsellem, S, Pessayre, D, Fromenty, B
Published in The Journal of pharmacology and experimental therapeutics (01.08.2001)
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Published in The Journal of pharmacology and experimental therapeutics (01.08.2001)
Journal Article
Foxg1-Cre Mediated Lrp2 Inactivation in the Developing Mouse Neural Retina, Ciliary and Retinal Pigment Epithelia Models Congenital High Myopia
Cases, Olivier, Joseph, Antoine, Obry, Antoine, Santin, Mathieu D, Ben-Yacoub, Sirine, Pâques, Michel, Amsellem-Levera, Sabine, Bribian, Ana, Simonutti, Manuel, Augustin, Sébastien, Debeir, Thomas, Sahel, José Alain, Christ, Annabel, de Castro, Fernando, Lehéricy, Stéphane, Cosette, Pascal, Kozyraki, Renata
Published in PloS one (24.06.2015)
Published in PloS one (24.06.2015)
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Journal Article
Intronic mutations outside of Alu-repeat-rich domains of the LDL receptor gene are a cause of familial hypercholesterolemia
AMSELLEM, Sabine, BRIFFAUT, Dorothée, DE GENNES, Jean Luc, BRUKERT, Eric, BENLIAN, Pascale, CARRIE, Alain, RABES, Jean Pierre, GIRARDET, Jean Philippe, FREDENRICH, Alexandre, MOULIN, Philippe, KREMPF, Michel, REZNIK, Yves, VIALETTES, Bernard
Published in Human genetics (01.12.2002)
Published in Human genetics (01.12.2002)
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Journal Article
Cubilin Is Essential for Albumin Reabsorption in the Renal Proximal Tubule
AMSELLEM, Sabine, GBUREK, Jakub, HAMARD, Ghislaine, NIELSEN, Rikke, WILLNOW, Thomas E, DEVUYST, Olivier, NEXO, Ebba, VERROUST, Pierre J, CHRISTENSEN, Erik I, KOZYRAKI, Renata
Published in Journal of the American Society of Nephrology (01.11.2010)
Published in Journal of the American Society of Nephrology (01.11.2010)
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Journal Article
Novel mutations of thePCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia
Allard, Delphine, Amsellem, Sabine, Abifadel, Marianne, Trillard, Mélanie, Devillers, Martine, Luc, Gérald, Krempf, Michel, Reznik, Yves, Girardet, Jean-Philippe, Fredenrich, Alexandre, Junien, Claudine, Varret, Mathilde, Boileau, Catherine, Benlian, Pascale, Rabès, Jean-Pierre
Published in Human mutation (01.11.2005)
Published in Human mutation (01.11.2005)
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Journal Article
Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia
Allard, Delphine, Amsellem, Sabine, Abifadel, Marianne, Trillard, Mélanie, Devillers, Martine, Luc, Gérald, Krempf, Michel, Reznik, Yves, Girardet, Jean-Philippe, Fredenrich, Alexandre, Junien, Claudine, Varret, Mathilde, Boileau, Catherine, Benlian, Pascale, Rabès, Jean-Pierre
Published in Human mutation (01.11.2005)
Published in Human mutation (01.11.2005)
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Journal Article
Cubilin, a High Affinity Receptor for Fibroblast Growth Factor 8, Is Required for Cell Survival in the Developing Vertebrate Head
Cases, Olivier, Perea-Gomez, Aitana, Aguiar, Diego P., Nykjaer, Anders, Amsellem, Sabine, Chandellier, Jacqueline, Umbhauer, Muriel, Cereghini, Silvia, Madsen, Mette, Collignon, Jérôme, Verroust, Pierre, Riou, Jean-François, Creuzet, Sophie E., Kozyraki, Renata
Published in The Journal of biological chemistry (07.06.2013)
Published in The Journal of biological chemistry (07.06.2013)
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Journal Article
Detailed investigations of proximal tubular function in Imerslund-Gräsbeck syndrome
Storm, Tina, Zeitz, Christina, Cases, Olivier, Amsellem, Sabine, Verroust, Pierre J, Madsen, Mette, Benoist, Jean-François, Passemard, Sandrine, Lebon, Sophie, Jønsson, Iben Møller, Emma, Francesco, Koldsø, Heidi, Hertz, Jens Michael, Nielsen, Rikke, Christensen, Erik I, Kozyraki, Renata
Published in BMC medical genetics (24.10.2013)
Published in BMC medical genetics (24.10.2013)
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Journal Article
Diagnosis Scoring for Clinical Identification of Children With Heterozygous Familial Hypercholesterolemia
Benlian, Pascale, Turquet, Anne, Carrat, Fabrice, Amsellem, Sabine, Sanchez, Lydie, Briffaut, Dorothée, Girardet, Jean Philippe
Published in Journal of pediatric gastroenterology and nutrition (01.04.2009)
Published in Journal of pediatric gastroenterology and nutrition (01.04.2009)
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Journal Article
An alcoholic binge causes massive degradation of hepatic mitochondrial DNA in mice
Mansouri, A, Gaou, I, De Kerguenec, C, Amsellem, S, Haouzi, D, Berson, A, Moreau, A, Feldmann, G, Lettéron, P, Pessayre, D, Fromenty, B
Published in Gastroenterology (New York, N.Y. 1943) (01.07.1999)
Published in Gastroenterology (New York, N.Y. 1943) (01.07.1999)
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Journal Article
Erratum: Novel mutations of thePCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia
Allard, Delphine, Amsellem, Sabine, Abifadel, Marianne, Trillard, Mélanie, Devillers, Martine, Luc, Gérald, Krempf, Michel, Reznik, Yves, Girardet, Jean-Philippe, Fredenrich, Alexandre, Junien, Claudine, Varret, Mathilde, Boileau, Catherine, Benlian, Pascale, Rabès, Jean-Pierre
Published in Human mutation (01.12.2005)
Published in Human mutation (01.12.2005)
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Journal Article
Erratum: Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia
Allard, Delphine, Amsellem, Sabine, Abifadel, Marianne, Trillard, Mélanie, Devillers, Martine, Luc, Gérald, Krempf, Michel, Reznik, Yves, Girardet, Jean-Philippe, Fredenrich, Alexandre, Junien, Claudine, Varret, Mathilde, Boileau, Catherine, Benlian, Pascale, Rabès, Jean-Pierre
Published in Human mutation (01.12.2005)
Published in Human mutation (01.12.2005)
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Journal Article
Magnitude of HDL Cholesterol Variation After High-Dose Atorvastatin Is Genetically Determined at the LDL Receptor Locus in Patients With Homozygous Familial Hypercholesterolemia
Sposito, Andrei C, Gonbert, Sophie, Bruckert, Eric, Atassi, Marielle, Beucler, Isabel, Amsellem, Sabine, Khallouf, Oumayma, Benlian, Pascale, Turpin, Gerard
Published in Arteriosclerosis, thrombosis, and vascular biology (01.11.2003)
Published in Arteriosclerosis, thrombosis, and vascular biology (01.11.2003)
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Journal Article
Detailed investigations of proximal tubular function in Imerslund-Graesbeck syndrome
Storm, Tina, Zeitz, Christina, Cases, Olivier, Amsellem, Sabine, Verroust, Pierre J, Madsen, Mette, Benoist, Jean-Francois, Passemard, Sandrine, Lebon, Sophie, Joensson, Iben Moeller, Emma, Francesco, Koldsoe, Heidi, Hertz, Jens Michael, Nielsen, Rikke, Christensen, Erik I, Kozyraki, Renata
Published in BMC genetics (01.01.2013)
Published in BMC genetics (01.01.2013)
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Journal Article
Foxg1-Cre Mediated Lrp2 Inactivation in the Developing Mouse Neural Retina, Ciliary and Retinal Pigment Epithelia Models Congenital High Myopia: e0129518
Cases, Olivier, Joseph, Antoine, Obry, Antoine, Santin, Mathieu D, Ben-Yacoub, Sirine, Paques, Michel, Amsellem-Levera, Sabine, Bribian, Ana, Simonutti, Manuel, Augustin, Sebastien
Published in PloS one (01.06.2015)
Published in PloS one (01.06.2015)
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