Search Results - "Chèvre, J C"

Defective mutations in the insulin promoter factor-1 (IPF-1) gene in late-onset type 2 diabetes mellitus by Hani, E H, Stoffers, D A, Chèvre, J C, Durand, E, Stanojevic, V, Dina, C, Habener, J F, Froguel, P

“…Type 2 diabetes mellitus is a common disabling disease with onset in middle-aged individuals, caused by an imbalance between insulin production and action…”
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Insulin promoter factor 1 gene is not a major cause of maturity-onset diabetes of the young in French Caucasians by CHEVRE, J.-C, EL HABIB HANI, STOFFERS, D. A, HABENER, J. F, FROGUEL, P

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Mutation screening in 18 Caucasian families suggest the existence of other MODY genes by CHEVRE, J.-C, HANI, E. H, BECKERS, D, MAES, M, BELLANNE-CHANTELOT, C, VELHO, G, FROGUEL, P, BOUTIN, P, VAXILLAIRE, M, BLANCHE, H, VIONNET, N, PARDINI, V. C, TIMSIT, J, LARGER, E, CHARPENTIER, G

“…Maturity-onset diabetes of the young (MODY) is a heterogeneous subtype of non-insulin-dependent diabetes mellitus characterised by early onset, autosomal…”
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A missense mutation in hepatocyte nuclear factor-4 alpha, resulting in a reduced transactivation activity, in human late-onset non-insulin-dependent diabetes mellitus by Hani, E H, Suaud, L, Boutin, P, Chèvre, J C, Durand, E, Philippi, A, Demenais, F, Vionnet, N, Furuta, H, Velho, G, Bell, G I, Laine, B, Froguel, P

“…Non-insulin-dependent diabetes mellitus (NIDDM) is a heterogeneous disorder characterized by hyperglycemia resulting from defects in insulin secretion and…”
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Identification of nine novel mutations in the hepatocyte nuclear factor 1 alpha gene associated with maturity-onset diabetes of the young (MODY3) by VAXILLAIRE, M, ROUARD, M, DUSSOIX, P, PHILIPPE, J, TIMSIT, J, CHARPENTIER, G, VELHO, G, BELL, G. I, FROGUEL, P, YAMAGATA, K, ODA, N, KAISAKI, P. J, BORIRAJ, V. V, CHEVRE, J.-C, BOCCIO, V, COX, R. D, LATHROP, G. M

“…Maturity-onset diabetes of the young (MODY) is a genetically heterogeneous subtype of non-insulin-dependent diabetes mellitus (NIDDM) characterised by early…”
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No evidence of linkage or diabetes-associated mutations in the transcription factors BETA2/NEUROD1 and PAX4 in Type II diabetes in France by DUPONT, S, VIONNET, N, CHEVRE, J. C, GALLINA, S, DINA, C, SEINO, Y, YAMADA, Y, FROGUEL, P

“…The identification of mutations in hepatocyte nuclear factors-1alpha, -4alpha, -1beta and insulin promoter factor-1 in maturity onset diabetes of the young…”
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Genetic and clinical characterisation of maturity-onset diabetes of the young in Spanish families by Costa, A, Bescos, M, Velho, G, Chevre, J, Vidal, J, Sesmilo, G, Bellanne-Chantelot, C, Froguel, P, Casamitjana, R, Rivera-Fillat, F, Gomis, R, Conget, I

“…OBJECTIVE: To investigate the frequencies of the major maturity-onset diabetes of the young (MODY) subtypes in a panel of Spanish families and to assess…”
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Genetic variation in the hepatocyte nuclear factor-3beta gene (HNF3B) does not contribute to maturity-onset diabetes of the young in French Caucasians by Abderrahmani, A, Chèvre, J C, Otabe, S, Chikri, M, Hani, E H, Vaxillaire, M, Hinokio, Y, Horikawa, Y, Bell, G I, Froguel, P

“…Genetic variation in the hepatocyte nuclear factor-3beta gene (HNF3B) does not contribute to maturity-onset diabetes of the young in French Caucasians. A…”
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Mutations in the hepatocyte nuclear factor-1α gene in maturity-onset diabetes of the young (MODY3) by Yamagata, Kazuya, Oda, Naohisa, Kaisaki, Pamela J, Menzel, Stephan, Furuta, Hiroto, Vaxillaire, Martine, Southam, Lorraine, Cox, Roger D, Lathrop, G. Mark, Boriraj, V. Vicky, Chen, Xiangna, Cox, Nancy J, Oda, Yukie, Yano, Hideki, Le Beau, Michelle M, Yamada, Shirou, Nishigori, Hidekazu, Takeda, Jun, Fajans, Stefan S, Hattersley, Andrew T, Iwasaki, Naoko, Hansen, Torben, Pedersen, Oluf, Polonsky, Kenneth S, Turner, Robert C, Velho, Gilberto, Chèvre, Jean-Claude, Froguel, Philippe, Bell, Graeme I

“…The disease non-insulin-dependent (type 2) diabetes mellitus (NIDDM) is characterized by abnormally high blood glucose resulting from a relative deficiency of…”
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Transmission of serologically silent hepatitis B virus along with hepatitis C virus in two cases of posttransfusion hepatitis by Baginski, I, Chemin, I, Hantz, O, Pichoud, C, Jullien, A M, Chevre, J C, Li, J S, Vitvitski, L, Sninsky, J J, Trepo, C

“…The polymerase chain reaction (PCR) was used to investigate the presence of hepatitis B virus (HBV)-related DNA sequences in blood from three blood donors and…”
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A novel highly-penetrant form of obesity due to microdeletions on chromosome 16p11.2 by Walters, R. G., Jacquemont, S., Valsesia, A., de Smith, A. J., Martinet, D., Andersson, J., Falchi, M., Chen, F., Andrieux, J., Lobbens, S., Delobel, B., Stutzmann, F., Moustafa, J. S. El-Sayed, Chèvre, J.-C., Lecoeur, C., Vatin, V., Bouquillon, S., Buxton, J. L., Boute, O., Holder-Espinasse, M., Cuisset, J.-M., Lemaitre, M.-P., Ambresin, A.-E., Brioshi, A., Gaillard, M., Giusti, V., Fellmann, F., Ferrarini, A., Hadjikhani, N., Campion, D., Guilmatre, A., Goldenberg, A., Calmels, N., Mandel, J.-L., Le Caignec, C., David, A., Isidor, B., Cordier, M.-P., Dupuis-Girod, S., Labalme, A., Sanlaville, D., Béri-Deixheimer, M., Jonveaux, P., Leheup, B., Õunap, K., Bochukova, E. G., Henning, E., Keogh, J., Ellis, R. J., MacDermot, K. D., Vincent-Delorme, C., Plessis, G., Touraine, R., Philippe, A., Malan, V., Mathieu-Dramard, M., Chiesa, J., Blaumeiser, B., Kooy, R. F., Caiazzo, R., Pigeyre, M., Balkau, B., Sladek, R., Bergmann, S., Mooser, V., Waterworth, D., Reymond, A., Vollenweider, P., Waeber, G., Kurg, A., Palta, P., Esko, T., Metspalu, A., Nelis, M., Elliott, P., Hartikainen, A.-L., McCarthy, M. I., Peltonen, L., Carlsson, L., Jacobson, P., Sjöström, L., Huang, N., Hurles, M. E., O’Rahilly, S., Farooqi, I. S., Männik, K., Jarvelin, M.-R., Pattou, F., Meyre, D., Walley, A. J., Coin, L. J. M., Blakemore, A. I. F., Froguel, P., Beckmann, J. S.

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Genetic variation in the hepatocyte nuclear factor-3β gene (HNF3B) does not contribute to maturity-onset diabetes of the young in French caucasians by ABDERRAHMANI, A, CHEVRE, J.-C, OTABE, S, CHIKRI, M, EL HABIB HANI, VAXILLAIRE, M, HINOKIO, Y, HORIKAWA, Y, BELL, G. I, FROGUEL, P

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An automated fluorescent single-strand conformation polymorphism technique for screening mutations in the hepatocyte nuclear factor-1α gene (maturity-onset diabetes of the young) by BOUTIN, P, CHEVRE, J. C, EL HABIB HANI, GOMIS, R, PARDINI, V. C, GUILLAUSSEAU, P.-J, VAXILLAIRE, M, VELHO, G, FROGUEL, P

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Identification of seven novel nucleotide variants in the hepatocyte nuclear factor-1alpha (TCF1) promoter region in MODY patients by Godart, F, Bellanné-Chantelot, C, Clauin, S, Gragnoli, C, Abderrahmani, A, Blanché, H, Boutin, P, Chèvre, J C, Froguel, P, Bailleul, B

“…Maturity onset diabetes of the young (MODY) is a heterogeneous subtype of type II diabetes mellitus. To date, five MODY genes have been identified. Mutations…”
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An automated fluorescent single-strand conformation polymorphism technique for screening mutations in the hepatocyte nuclear factor-1alpha gene (maturity-onset diabetes of the young) by Boutin, P, Chèvre, J C, Hani, E H, Gomis, R, Pardini, V C, Guillausseau, P J, Vaxillaire, M, Velho, G, Froguel, P

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A genome-wide scan in families with maturity-onset diabetes of the young: Evidence for further genetic heterogeneity by FRAYLING, Timothy M, LINDGREN, Cecilia M, LECOEUR, Cécile, KANNINEN, Timo, ALMGREN, Peter, BULMAN, Michael P, YOUXIANG WANG, MILLS, James, WRIGHT-PASCOE, Rosemarie, MAHTANI, Melanie M, PRISCO, Francesco, COSTA, Angels, CHEVRE, Jean Claude, COGNET, Ignacio, HANSEN, Torben, PEDERSEN, Oluf, ELLARD, Sian, TUOMI, Tiinamaija, GROOP, Leif C, FROGUEL, Philippe, HATTERSLEY, Andrew T, VAXILLAIRE, Martine, MENZEL, Stephan, WISHART, Marie, BENMEZROUA, Yamina, BROWN, Alison, EVANS, Julie C, PAMIDGHANTAM SUBBA RAO, DINA, Christian

“…Maturity-onset diabetes of the young (MODY) is a heterogeneous single gene disorder characterized by non-insulin-dependent diabetes, an early onset and…”
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Identification of Seven Novel Nucleotide Variants in the Hepatocyte Nuclear Factor-1 alpha (TCF1) Promoter Region in MODY Patients by Godart, F, Bellanne-Chantelot, C, Clauin, S, Gragnoli, C, Abderrahmani, A, Blanche, H, Boutin, P, Chevre, J C, Froguel, P, Bailleul, B

“…Maturity onset diabetes of the young (MODY) is a heterogeneous subtype of type II diabetes mellitus. To date, five MODY genes have been identified. Mutations…”
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Identification of seven novel nucleotide variants in the hepatocyte nuclear factor-1α (TCF1) promoter region in MODY patients by Godart, François, Bellanné-Chantelot, Christine, Clauin, Séverine, Gragnoli, Claudia, Abderrahmani, Amar, Blanché, Hélène, Boutin, Philippe, Chèvre, Jean Claude, Froguel, Philippe, Bailleul, Bernard

“…Maturity onset diabetes of the young (MODY) is a heterogeneous subtype of type II diabetes mellitus. To date, five MODY genes have been identified. Mutations…”
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Neoplastic metastases and invasions of the heart and of the great vessels of its base by Guillaud-Bourgeois, M, Dargent, M, Chevre, J C

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