Search Results - "Meier, Muriel"

Prevalence of Mutations in AGPAT2 Among Human Lipodystrophies by 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

“…Prevalence of Mutations in AGPAT2 Among Human Lipodystrophies Jocelyne Magré 1 , Marc Delépine 2 , Lionel Van Maldergem 3 , Jean-Jacques Robert 4 , J. Antonie…”
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Association of a Homozygous Nonsense Caveolin-1 Mutation with Berardinelli-Seip Congenital Lipodystrophy by 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

“…Context: Berardinelli-Seip congenital lipodystrophy (BSCL) is a rare recessive disease characterized by near absence of adipose tissue, resulting in severe…”
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The role of skin self-examination at the Swiss skin cancer day by Badertscher, Nina, Meier, Muriel, Rosemann, Thomas, Braun, Ralph, Cozzio, Antonio, Tag, Brigitte, Wensing, Michel, Tandjung, Ryan

“…The rising incidence of melanoma - Switzerland has the highest incidence in Europe - is a major public health challenge. Swiss dermatologist introduced the…”
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Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13 by Gedde-Dahl, Tobias, Mégarbané, André, Sobel, Eric, Meier, Muriel, Lathrop, Mark, Capeau, Jacqueline, Papp, Jeanette, Khallouf, Eliane, Van Maldergem, Lionel, Magré, Jocelyne, Delépine, Marc

“…Congenital generalized lipodystrophy, or Berardinelli-Seip syndrome (BSCL), is a rare autosomal recessive disease characterized by a near-absence of adipose…”
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Leptin therapy for partial lipodystrophy linked to a PPAR-γ mutation by Guettier, Jean-Marc, Park, Jean Y., Cochran, Elaine K., Poitou, Christine, Basdevant, Arnaud, Meier, Muriel, Clément, Karine, Magré, Jocelyne, Gorden, Phillip

“…Summary Aims/hypothesis  Partial lipodystrophy (PL) is most commonly characterized by loss of subcutaneous fat in the extremities with preservation of truncal…”
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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 by VIGOUROUX, C, FAJAS, L, KHALLOUF, E, MEIER, M, GYAPAY, G, LASCOLS, O, AUWERX, J, WEISSENBACH, J, CAPEAU, J, MAGRE, J

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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 by MAGRE, J, KARAYANNI, C, HADJIATHANASIOU, C. G, DESBOIS-MOUTHON, C, MEIER, M, VIGOUROUX, C, STAVRINADIS, C, SINANIOTIS, C, CARON, M, CAPEAU, J

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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 by Vigouroux, C, Fajas, L, Khallouf, E, Meier, M, Gyapay, G, Lascols, O, Auwerx, J, Weissenbach, J, Capeau, J, Magré, J

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Human placental microvilli as a source of antigen for the preparation of a polyclonal antibody directed against the LDL receptor by Goldstein, S, Moreau, M, Barbu, V, Meier, M, Alsat, E, Mazière, C, Mazière, J C, Polonovski, J

“…Polyclonal antibodies were prepared by immunization of rabbits with partially purified LDL receptor obtained from human placental microvilli. The antiserum…”
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