Search Results - "VIONNET, N"

Weight Loss Directly Influences Intermediate-Term Remission of Diabetes Mellitus After Bariatric Surgery: A Retrospective Case-Control Study by de La Harpe, R., Rüeger, S., Kutalik, Z., Ballabeni, P., Suter, M., Vionnet, N., Laferrère, B., Pralong, F.

“…Purpose Roux en Y gastric bypass surgery (RYGB) is an effective therapy for patients with severe obesity. It induces both significant weight loss and rapid…”
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V16A polymorphism in SOD2 is associated with increased risk of diabetic nephropathy and cardiovascular disease in type 1 diabetes by Möllsten, A, Jorsal, A, Lajer, M, Vionnet, N, Tarnow, L

“…Aims/hypothesis Hyperglycaemia increases oxidative stress and may thereby increase the risk of diabetic complications, including diabetic nephropathy. Cells…”
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polymorphism in the gene encoding carnosinase (CNDP1) as a predictor of mortality and progression from nephropathy to end-stage renal disease in type 1 diabetes mellitus by Alkhalaf, A, Bakker, S. J. L, Bilo, H. J. G, Gans, R. O. B, Navis, G. J, Postmus, D, Forsblom, C, Groop, P. H, Vionnet, N, Hadjadj, S, Marre, M, Parving, H. H, Rossing, P, Tarnow, L

“…Aims/hypothesis Homozygosity for a five leucine repeat (5L-5L) in the carnosinase gene (CNDP1) has been found to be cross-sectionally associated with a low…”
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Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus by Vionnet, N, Stoffel, M, Takeda, J, Yasuda, K, Bell, G. I, Zouali, H, Lesage, S, Velho, G, Iris, F, Passa, Ph, Froguel, Ph, Cohen, D

“…Maturity-onset diabetes of the young (MODY) is a form of non-insulin-dependent (type 2) diabetes mellitus (NIDDM) which is characterized by an early age at…”
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Cloning, functional expression, and chromosomal localization of the human pancreatic islet glucose-dependent insulinotropic polypeptide receptor by Gremlich, S., Porret, A., Hani, E. H., Cherif, D., Vionnet, N., Froguel, P., Thorens, B.

“…Cloning, functional expression, and chromosomal localization of the human pancreatic islet glucose-dependent insulinotropic polypeptide receptor. S Gremlich ,…”
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Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus by Froguel, Ph, Vaxillaire, M, Sun, F, Velho, G, Zouali, H, Butel, M. O, Lesage, S, Vionnet, N, Clément, K, Fougerousse, F, Tanizawa, Y, Weissenbach, J, Beckmann, J. S, Lathrop, G. M, Passa, Ph, Permutt, M. A, Cohen, D

“…Non-insulin-dependent diabetes mellitus (NIDDM) is a major health problem, affecting 5% of the world population. Genetic factors are important in NIDDM, but…”
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Genetic studies of the sulfonylurea receptor gene locus in NIDDM and in morbid obesity among French Caucasians by Hani, E. H., Clement, K., Velho, G., Vionnet, N., Hager, J., Philippi, A., Dina, C., Inoue, H., Permutt, M. A., Basdevant, A., North, M., Demenais, F., Guy-Grand, B., Froguel, P.

“…Genetic studies of the sulfonylurea receptor gene locus in NIDDM and in morbid obesity among French Caucasians. E H Hani , K Clément , G Velho , N Vionnet , J…”
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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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Human Glucokinase Gene: Isolation, Characterization, and Identification of Two Missense Mutations Linked to Early-Onset Non-Insulin-Dependent (type 2) Diabetes Mellitus by Stoffel, M., Ph. Froguel, Takeda, J., Zouali, H., Vionnet, N., Nishi, S., Weber, I. T., Harrison, R. W., Pilkis, S. J., Lesage, S., Vaxillaire, M., Velho, G., Sun, F., Iris, F., Ph. Passa, Cohen, D., Bell, G. I.

“…DNA polymorphisms in the glucokinase gene have recently been shown to be tightly linked to early-onset non-insulin-dependent diabetes mellitus in ≈80% of…”
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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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Glucokinase Mutations Associated with Non-Insulin-Dependent (Type 2) Diabetes Mellitus have Decreased Enzymatic Activity: Implications for Structure/Function Relationships by Gidh-Jain, M., Takeda, J., Xu, L. Z., Lange, A. J., Vionnet, N., Stoffel, M, Froguel, P., Velho, G., Sun, F., Cohen, D., Patel, P., Y.-M. D. Lo, Hattersley, A. T., Luthman, H., Wedell, A., St. Charles, R., Harrison, R. W., Weber, I. T., Bell, G. I., Pilkis, S. J.

“…The glycolytic enzyme glucokinase plays an important role in the regulation of insulin secretion and recent studies have shown that mutations in the human…”
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A missense mutation in the glucagon receptor gene is associated with non-insulin-dependent diabetes mellitus by Hager, J, Hansen, L, Vaisse, C, Vionnet, N, Philippi, A, Poller, W, Velho, G, Carcassi, C, Contu, L, Julier, C, Cambien, F, Passa, P, Lathrop, M, Kindsvogel, W, Demenais, F, Nishimura, E, Froguel, P

“…Non-insulin-dependent diabetes mellitus (NIDDM) affects about 5% of the world population. The disease presents a polygenic mode of inheritance, but mechanisms…”
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Prevalence of mitochondrial gene mutations in families with diabetes mellitus by Vionnet, N, Passa, P, Froguel, P

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Genetics of NIDDM in France: studies with 19 candidate genes in affected sib pairs by Vionnet, N., Hani, E. H., Lesage, S., Philippi, A., Hager, J., Varret, M., Stoffel, M., Tanizawa, Y., Chiu, K. C., Glaser, B., Permutt, M. A., Passa, P., Demenais, F., Froguel, P.

“…Genetics of NIDDM in France: studies with 19 candidate genes in affected sib pairs. N Vionnet , E H Hani , S Lesage , A Philippi , J Hager , M Varret , M…”
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Identification of glucokinase mutations in subjects with gestational diabetes mellitus by M Stoffel, K L Bell, C L Blackburn, K L Powell, T S Seo, J Takeda, N Vionnet, K S Xiang, M Gidh-Jain, S J Pilkis

“…Identification of glucokinase mutations in subjects with gestational diabetes mellitus. M Stoffel , K L Bell , C L Blackburn , K L Powell , T S Seo , J Takeda…”
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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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Linkage analysis and molecular scanning of glucokinase gene in NIDDM families by Zouali, H., Vaxillaire, M., Lesage, S., Sun, F., Velho, G., Vionnet, N., Chiu, K., Passa, P., Permutt, A., Demenais, F., et, al

“…Linkage analysis and molecular scanning of glucokinase gene in NIDDM families. H Zouali , M Vaxillaire , S Lesage , F Sun , G Velho , N Vionnet , K Chiu , P…”
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Is prealbumine a good biomarker of lean mass loss after gastric bypass? by Santini, S., Vionnet, N., Barigou, M., Pasquier, J., Favre, L.

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Weight-loss on liraglutide in a real-life swiss obese cohort by Santini, S., Vionnet, N., Pitteloud, N., Favre, L.

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Linkage analyses of the MODY3 locus on chromosome 12q with late-onset NIDDM by Lesage, S., Hani, E. H., Philippi, A., Vaxillaire, M., Hager, J., Passa, P., Demenais, F., Froguel, P., Vionnet, N.

“…Linkage analyses of the MODY3 locus on chromosome 12q with late-onset NIDDM. S Lesage , E H Hani , A Philippi , M Vaxillaire , J Hager , P Passa , F Demenais ,…”
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