Fast SOP variation measurement on WDM systems are the OPMDC fast enough? von Salaun, S., Neddam, F., Poirrier, J., Raguenes, B., Moignard, M.

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Mutations of the pancreatic secretory trypsin inhibitor (PSTI) gene in idiopathic chronic pancreatitis von Chen, Jian–Min, Mercier, Bernard, Audrezet, Marie–Pierre, Raguenes, Odile, Quere, Isabelle, Ferec, Claude

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novel mcl PHA-producing bacterium, Pseudomonas guezennei sp. nov., isolated from a 'kopara' mat located in Rangiroa, an atoll of French Polynesia von Simon-Colin, C, Alain, K, Colin, S, Cozien, J, Costa, B, Guezennec, J.G, Raguénès, G.H.C

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Biosynthesis of medium chain length poly(3-hydroxyalkanoates) (mcl PHAs) from cosmetic co-products by Pseudomonas raguenesii sp. nov., isolated from Tetiaroa, French Polynesia von Simon-Colin, C., Alain, K., Raguénès, G., Schmitt, S., Kervarec, N., Gouin, C., Crassous, P., Costa, B., Guezennec, J.G.

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Hereditary Hemochromatosis: Effect of Excessive Alcohol Consumption on Disease Expression in Patients Homozygous for the C282Y Mutation von Scotet, Virginie, Mérour, Marie-Christine, Mercier, Anne-Yvonne, Chanu, Brigitte, Le Faou, Thérèse, Raguénes, Odile, Le Gac, Gérald, Mura, Catherine, Nousbaum, Jean-Baptiste, Férec, Claude

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Mutations in the cationic trypsinogen gene and evidence for genetic heterogeneity in hereditary pancreatitis von Férec, C, Raguénès, O, Salomon, R, Roche, C, Bernard, J P, Guillot, M, Quéré, I, Faure, C, Mercier, B, Audrézet, M P, Guillausseau, P J, Dupont, C, Munnich, A, Bignon, J D, Le Bodic, L

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2 Identification of two Alu insertions in the CFTR gene von Audrezet, M.P, Masson, E, Macek, M, Raguenes, O, Fercot, B, Chen, J.M, Férec, C

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Phenotype-genotype correlation in haemochromatosis subjects von MURA, C, NOUSBAUM, J.-B, VERGER, P, MOALIC, M.-T, RAGUENES, O, MERCIER, A.-Y, FEREC, C

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The Hereditary Pancreatitis Gene Maps to Long Arm of Chromosome 7 von Le Bodic, Louis, Bignon, Jean-Denis, Raguénès, Odile, Mercier, Bernard, Georgelin, Thierry, Schnee, Mathieu, Soulard, François, Gagne, Katia, Bonneville, Françoise, Muller, Jean-Yves, Bachner, Lucien, Férec, Claude

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The Annexin A3−Membrane Interaction Is Modulated by an N-Terminal Tryptophan von Hofmann, Andreas, Raguénès-Nicol, Céline, Favier-Perron, Béatrice, Mesonero, Jose, Huber, Robert, Russo-Marie, Françoise, Lewit-Bentley, Anita

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A novel exopolymer-producing bacterium, Paracoccus zeaxanthinifaciens subsp. payriae, isolated from a "kopara" mat located in Rangiroa, an atoll of French Polynesia von Raguénès, Gérard, Moppert, Xavier, Richert, Laurent, Ratiskol, Jacqueline, Payri, Claude, Costa, Bernard, Guezennec, Jean

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Hereditary chronic pancreatitis (HPC): Heterogeneity of mutations of the gene of cationic trysinogen von Férec, C, Raguenes, O, Mercier, B, Bignon, JD, Georgelin, T, Soulard, F, Le Bodic, L

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Complete detection of mutations in cystic fibrosis patients of Native American origin von Mercier, B, Raguénès, O, Estivill, X, Morral, N, Kaplan, G C, McClure, M, Grebe, T A, Kessler, D, Pignatti, P F, Marigo, C

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The hemochromatosis gene (HFE). Molecular analysis--diagnostic applications von Ferec, C, Raguenes, O, Mercier, A Y, Le Faou, T, Chanu, B, Le Poupon, A M, Mercier, B, Mura, C

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Rapid diagnostic test for detection of Cys282Tyr mutation in hereditary hemochromatosis von Andre, M T, Jacquemont, S, Renault, S, Airaud, F, Herbert, O, Moisan, J P, Benichou, B, Raguenes, O

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Genotype analysis of adult cystic fibrosis patients von Férec, Claude, Verlingue, Claudine, Gulllermit, Hervé, Quéré, Isabelle, Raguénès, Odile, Feigelson, Jean, Audrézet, Marie-Plerre, Moullier, Philippe, Mercier, Bernard

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Linkage disequilibrium between the four most common cystic fibrosis mutations and microsatellite haplotypes in the Celtic population of Brittany von DE BRAEKELEER, M, CHAVENTRE, A, BERTORELLE, G, VERLINGUE, C, RAGUENES, O, MERCIER, B, FEREC, C

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HLA-DRB AND -DBQ TYPING BY PCR AMPLIFICATION USING SEQUENCE-SPECIFIC PRIMERS (PCR-SSP): ASSESSMENT AFTER 1 YEAR OF ROUTINE USE BY THREE LABORATORIES von Mercier, B., Daccak, R. Al, Samaan, A., David, F., Carta, A., Cracco, P., Raguenes, O., Dufosse, F., Ferec, C., Charron, D., Loiseau, P.

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Association of 1078 del T cystic fibrosis mutation with severe disease von Moullier, P, Jéhanne, M, Audrézet, M P, Mercier, B, Verlingue, C, Quéré, I, Guillermit, H, Raguénès, O, Storni, V, Rault, G

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A cluster of cystic fibrosis mutations in exon 17b of the CFTR gene: a site for rare mutations von Mercier, B, Lissens, W, Novelli, G, Kalaydjieva, L, de Arce, M, Kapranov, N, Canki Klain, N, Estivill, X, Palacio, A, Cashman, S

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