Prevalence of Mutations in AGPAT2 Among Human Lipodystrophies
MAGRE, Jocelyne, DELEPINE, Marc, SEEMANOVA, Eva, BUCHANAN, Charles R, LACOMBE, Didier, VIGOUROUX, Corinne, LASCOLS, Olivier, KAHN, C. Ronald, CAPEAU, Jacqueline, LATHROP, Mark, VAN MALDERGEM, Lionel, ROBERT, Jean-Jacques, MAASSEN, J. Antonie, MEIER, Muriel, PANZ, Vanessa R, CHONG AE KIM, TUBIANA-RUFI, Nadia, CZERNICHOW, Paul
Published in Diabetes (New York, N.Y.) (01.06.2003)
Published in Diabetes (New York, N.Y.) (01.06.2003)
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Association of a Homozygous Nonsense Caveolin-1 Mutation with Berardinelli-Seip Congenital Lipodystrophy
Kim, C. A, Delépine, Marc, Boutet, Emilie, El Mourabit, Haquima, Le Lay, Soazig, Meier, Muriel, Nemani, Mona, Bridel, Etienne, Leite, Claudia C, Bertola, Debora R, Semple, Robert K, O’Rahilly, Stephen, Dugail, Isabelle, Capeau, Jacqueline, Lathrop, Mark, Magré, Jocelyne
Published in The journal of clinical endocrinology and metabolism (01.04.2008)
Published in The journal of clinical endocrinology and metabolism (01.04.2008)
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The role of skin self-examination at the Swiss skin cancer day
Badertscher, Nina, Meier, Muriel, Rosemann, Thomas, Braun, Ralph, Cozzio, Antonio, Tag, Brigitte, Wensing, Michel, Tandjung, Ryan
Published in BMC health services research (19.11.2014)
Published in BMC health services research (19.11.2014)
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Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13
Gedde-Dahl, Tobias, Mégarbané, André, Sobel, Eric, Meier, Muriel, Lathrop, Mark, Capeau, Jacqueline, Papp, Jeanette, Khallouf, Eliane, Van Maldergem, Lionel, Magré, Jocelyne, Delépine, Marc
Published in Nature genetics (01.08.2001)
Published in Nature genetics (01.08.2001)
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Leptin therapy for partial lipodystrophy linked to a PPAR-γ mutation
Guettier, Jean-Marc, Park, Jean Y., Cochran, Elaine K., Poitou, Christine, Basdevant, Arnaud, Meier, Muriel, Clément, Karine, Magré, Jocelyne, Gorden, Phillip
Published in Clinical endocrinology (Oxford) (01.04.2008)
Published in Clinical endocrinology (Oxford) (01.04.2008)
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Human peroxisome proliferator-activated receptor-γ2 : Genetic mapping, identification of a variant in the coding sequence, and exclusion as the gene responsible for lipoatrophic diabetes
VIGOUROUX, C, FAJAS, L, KHALLOUF, E, MEIER, M, GYAPAY, G, LASCOLS, O, AUWERX, J, WEISSENBACH, J, CAPEAU, J, MAGRE, J
Published in Diabetes (New York, N.Y.) (1998)
Published in Diabetes (New York, N.Y.) (1998)
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Dominant transmission of insulin resistance in a type A family resulting from a heterozygous nonsense mutation in the insulin receptor gene and associated with decreased mRNA level and insulin binding sites
MAGRE, J, KARAYANNI, C, HADJIATHANASIOU, C. G, DESBOIS-MOUTHON, C, MEIER, M, VIGOUROUX, C, STAVRINADIS, C, SINANIOTIS, C, CARON, M, CAPEAU, J
Published in Diabetes (New York, N.Y.) (01.11.1997)
Published in Diabetes (New York, N.Y.) (01.11.1997)
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Human peroxisome proliferator-activated receptor-gamma2: genetic mapping, identification of a variant in the coding sequence, and exclusion as the gene responsible for lipoatrophic diabetes
Vigouroux, C, Fajas, L, Khallouf, E, Meier, M, Gyapay, G, Lascols, O, Auwerx, J, Weissenbach, J, Capeau, J, Magré, J
Published in Diabetes (New York, N.Y.) (01.03.1998)
Published in Diabetes (New York, N.Y.) (01.03.1998)
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Human placental microvilli as a source of antigen for the preparation of a polyclonal antibody directed against the LDL receptor
Goldstein, Sopia, Moreau, Martine, Barbu, Véronique, Meier, Muriel, Alsat, Eliane, Mazière, Cécile, Mazière, Jean-Claude, Polonovski, Jacques
Published in Biochimie (01.03.1989)
Published in Biochimie (01.03.1989)
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