OpenURL Connection Search

Select item for more details and to access through your institution.

Diagnostic heterogeneity of diabetes in lean young adults: classification based on immunological and genetic parameters.
Published in:
1997
By:
- Dussoix P;
- Vaxillaire M;
- Iynedjian PB;
- Tiercy J;
- Ruiz J;
- Spinas GA;
- Berger W;
- Zahnd G;
- Froguel P;
- Philippe J;
- Dussoix, P;
- Vaxillaire, M;
- Iynedjian, P B;
- Tiercy, J M;
- Ruiz, J;
- Spinas, G A;
- Berger, W;
- Zahnd, G;
- Froguel, P;
- Philippe, J
Publication type:
journal article
Search for a third susceptibility gene for maturity-onset diabetes of the young. Studies with eleven candidate genes.
Published in:
1994
By:
- Vaxillaire, Martine;
- Vionnet, Nathalie;
- Vigouroux, Corinne;
- Fang Sun;
- Espinosa III, Rafael;
- Lebeau, Michelle M.;
- Stoffel, Markus;
- Lehto, Markku;
- Beckmann, Jacques S.;
- Detheux, Michel;
- Passa, Philippe;
- Cohen, Daniel;
- Van Schaftingen, Emile;
- Velho, Gilberto;
- Bell, Graeme I.;
- Froguel, Philippe;
- Vaxillaire, M;
- Vionnet, N;
- Vigouroux, C;
- Sun, F
Publication type:
journal article
Linkage analysis and molecular scanning of glucokinase gene in NIDDM families.
Published in:
1993
By:
- Zouali, Habib;
- Vaxillaire, Martine;
- Lesage, Suzanne;
- Fang Sun;
- Velho, Gilberto;
- Vionnet, Nathallie;
- Ken Chiu;
- Passa, Philippe;
- Permutt, Alan;
- Demenias, Florence;
- Cohen, Daniel;
- Beckmann, Jacques S.;
- Froguel, Philippe;
- Zouali, H;
- Vaxillaire, M;
- Lesage, S;
- Sun, F;
- Velho, G;
- Vionnet, N;
- Chiu, K
Publication type:
journal article
Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin dependent diabetes...
Published in:
Nature, 1992, v. 356, n. 6365, p. 162, doi. 10.1038/356162a0
By:
- Froguel, P.;
- Vaxillaire, M.
Publication type:
Article
The EIF2AK3 gene region and type I diabetes in subjects from South India.
Published in:
Genes & Immunity, 2004, v. 5, n. 8, p. 648, doi. 10.1038/sj.gene.6364139
By:
- Allotey, R A;
- Mohan, V;
- McDermott, M F;
- Deepa, R;
- Premalatha, G;
- Hassan, Z;
- Cassell, P G;
- North, B V;
- Vaxillaire, M;
- Mein, C A;
- Swan, D C;
- O'Grady, E;
- Ramachandran, A;
- Snehalatha, C;
- Sinnot, P J;
- Hemmatpour, S K;
- Froguel, P;
- Hitman, G A
Publication type:
Article
The genetic abnormality in the beta cell determines the response to an oral glucose load.
Published in:
Diabetologia, 2002, v. 45, n. 3, p. 427, doi. 10.1007/s00125-001-0770-9
By:
- Stride, A.;
- Vaxillaire, M.;
- Tuomi, T.;
- Barbetti, F.;
- Njølstad, P. R.;
- Hansen, T.;
- Costa, A.;
- Conget, I.;
- Pedersen, O.;
- Søvik, O.;
- Lorini, R.;
- Groop, L.;
- Froguel, P.;
- Hattersley, A. T.
Publication type:
Article
Glucokinase gene mutations are not a common cause of permanent neonatal diabetes in France.
Published in:
Diabetologia, 2002, v. 45, n. 3, p. 454, doi. 10.1007/s00125-001-0741-1
By:
- Vaxillaire, M.;
- Samson, C.;
- Cave, H.;
- Metz, C.;
- Froguel, P.;
- Polak, M.
Publication type:
Article
No evidence for diabetes-associated mutations of PEK/EIF2AK3 gene in French patients with early-onset Type II diabetes.
Published in:
Diabetologia, 2001, v. 44, n. 6, p. 786
By:
- Vaxillaire, M.;
- Benmezroua, Y.;
- Durand, E.;
- Vasseur, F.;
- Froguel, P.
Publication type:
Article
G-allele of intronic rs10830963 in MTNR1B confers increased risk of impaired fasting glycemia and type 2 diabetes through an impaired glucose-stimulated insulin release: studies involving 19,605 Europeans.
Published in:
2009
By:
- Sparsø T;
- Bonnefond A;
- Andersson E;
- Bouatia-Naji N;
- Holmkvist J;
- Wegner L;
- Grarup N;
- Gjesing AP;
- Banasik K;
- Cavalcanti-Proença C;
- Marchand M;
- Vaxillaire M;
- Charpentier G;
- Jarvelin MR;
- Tichet J;
- Balkau B;
- Marre M;
- Lévy-Marchal C;
- Faerch K;
- Borch-Johnsen K
Publication type:
journal article
A rare mutation in ABCC8/SUR1 leading to altered ATP-sensitive K+ channel activity and beta-cell glucose sensing is associated with type 2 diabetes in adults.
Published in:
2008
By:
- Tarasov AI;
- Nicolson TJ;
- Riveline JP;
- Taneja TK;
- Baldwin SA;
- Baldwin JM;
- Charpentier G;
- Gautier JF;
- Froguel P;
- Vaxillaire M;
- Rutter GA;
- Tarasov, Andrei I;
- Nicolson, Tamara J;
- Riveline, Jean-Pierre;
- Taneja, Tarvinder K;
- Baldwin, Stephen A;
- Baldwin, Jocelyn M;
- Charpentier, Guillaume;
- Gautier, Jean-François;
- Froguel, Philippe
Publication type:
journal article
The PPARG Pro12Ala polymorphism is associated with a decreased risk of developing hyperglycemia over 6 years and combines with the effect of the APM1 G-11391A single nucleotide polymorphism: the Data From an Epidemiological Study on the Insulin Resistance Syndrome (DESIR) study.
Published in:
2006
By:
- Jaziri R;
- Lobbens S;
- Aubert R;
- Péan F;
- Lahmidi S;
- Vaxillaire M;
- Porchay I;
- Bellili N;
- Tichet J;
- Balkau B;
- Froguel P;
- Marre M;
- Fumeron F;
- DESIR Study Group;
- Jaziri, Riphed;
- Lobbens, Stephane;
- Aubert, Roberte;
- Péan, Franck;
- Lahmidi, Saida;
- Vaxillaire, Martine
Publication type:
journal article
Genetic variation in the hepatocyte nuclear factor-3beta gene (HNF3B) does not contribute to maturity-onset diabetes of the young in French Caucasians.
Published in:
2000
By:
- Abderrahmani, A;
- Chèvre, J C;
- Otabe, S;
- Chikri, M;
- Hani, E H;
- Vaxillaire, M;
- Hinokio, Y;
- Horikawa, Y;
- Bell, G I;
- Froguel, P
Publication type:
journal article
Glucose utilization and production in patients with maturity-onset diabetes of the young caused by a mutation of the hepatocyte nuclear factor-1alpha gene.
Published in:
1998
By:
- Surmely, Jean-Francois;
- Guenat, Eliane;
- Philippe, Jacques;
- Dussoix, Philippe;
- Schneiter, Philippe;
- Temler, Evelyne;
- Vaxillaire, Martine;
- Froguel, Philippe;
- Jequier, Eric;
- Tappy, Luc;
- Surmely, J F;
- Guenat, E;
- Philippe, J;
- Dussoix, P;
- Schneiter, P;
- Temler, E;
- Vaxillaire, M;
- Froguel, P;
- Jéquier, E;
- Tappy, L
Publication type:
journal article
An automated fluorescent single-strand conformation polymorphism technique for screening mutations in the hepatocyte nuclear factor-1alpha gene (maturity-onset diabetes of the young).
Published in:
1997
By:
- Boutin, Philippe;
- Chèvre, Jean Claude;
- Haiti, El Habib;
- Gomis, Ramon;
- Pardini, Victor C.;
- Guillausseau, Pierre-Jean;
- Vaxillaire, Martine;
- Velho, Gilberto;
- Froguel, Philippe;
- Boutin, P;
- Chèvre, J C;
- Hani, E H;
- Gomis, R;
- Pardini, V C;
- Guillausseau, P J;
- Vaxillaire, M;
- Velho, G;
- Froguel, P
Publication type:
journal article
Novel MODY3 mutations in the hepatocyte nuclear factor-1alpha gene: evidence for a hyperexcitability of pancreatic beta-cells to intravenous secretagogues in a glucose-tolerant carrier of a P447L mutation.
Published in:
1997
By:
- Hansen, Torben;
- Eiberg, Hans;
- Rouard, Mathias;
- Vaxillaire, Martine;
- Møller, Ann M.;
- Rasmussen, Søren K.;
- Fridberg, Marianne;
- Urhammer, Søren A.;
- Hoist, Jens J.;
- Almind, Katrine;
- Echwald, Søren M.;
- Hansen, Lars;
- Bell, Graeme I.;
- Pedersen, Oluf;
- Hansen, T;
- Eiberg, H;
- Rouard, M;
- Vaxillaire, M;
- Møller, A M;
- Rasmussen, S K
Publication type:
journal article
Identification of trinucleotide repeat-containing genes in human pancreatic islets.
Published in:
1996
By:
- Aoki, Minoru;
- Koranyi, Laszlo;
- Riggs, Andre C.;
- Wasson, Jon;
- Chiu, Ken C.;
- Vaxillaire, Martine;
- Froguel, Philippe;
- Gough, Stephen;
- Li Liu;
- Donis-Keller, Helen;
- Permutt, M. Alan;
- Aoki, M;
- Koranyi, L;
- Riggs, A C;
- Wasson, J;
- Chiu, K C;
- Vaxillaire, M;
- Froguel, P;
- Gough, S;
- Liu, L
Publication type:
journal article
Linkage analyses of the MODY3 locus on chromosome 12q with late-onset NIDDM.
Published in:
1995
By:
- Lesage, Suzanne;
- Hani, El Habib;
- Philippi, Anne;
- Vaxillaire, Martine;
- Hager, Jörg;
- Passa, Philippe;
- Demenais, Florence;
- Froguel, Philippe;
- Vionnet, Nathalie;
- Lesage, S;
- Hani, E H;
- Philippi, A;
- Vaxillaire, M;
- Hager, J;
- Passa, P;
- Demenais, F;
- Froguel, P;
- Vionnet, N
Publication type:
journal article
Characterization of the LIM/homeodomain gene islet-1 and single nucleotide screening in NIDDM.
Published in:
1995
By:
- Riggs, Andrew C.;
- Tanizawa, Yukio;
- Aoki, Minoru;
- Wasson, Jon;
- Ferrer, Jorge;
- Rabin, Daniel U.;
- Vaxillaire, Martine;
- Froguel, Philippe;
- Permutt, M. Alan;
- Riggs, A C;
- Tanizawa, Y;
- Aoki, M;
- Wasson, J;
- Ferrer, J;
- Rabin, D U;
- Vaxillaire, M;
- Froguel, P;
- Permutt, M A
Publication type:
journal article
Isolation of the human LIM/homeodomain gene islet-1 and identification of a simple sequence repeat polymorphism [corrected].
Published in:
1994
By:
- Tanizawa, Yukio;
- Riggs, Andrew C.;
- Dagogo-Jack, Samuel;
- Vaxillaire, Martine;
- Froguel, Philippe;
- Li Liu;
- Donis-Keller, Helen;
- Permutt, M. Alan;
- Tanizawa, Y;
- Riggs, A C;
- Dagogo-Jack, S;
- Vaxillaire, M;
- Froguel, P;
- Liu, L;
- Donis-Keller, H;
- Permutt, M A
Publication type:
journal article
Predicting diabetes: clinical, biological, and genetic approaches: data from the Epidemiological Study on the Insulin Resistance Syndrome (DESIR).
Published in:
2008
By:
- Balkau B;
- Lange C;
- Fezeu L;
- Tichet J;
- Lauzon-Guillain B;
- Czernichow S;
- Fumeron F;
- Froguel P;
- Vaxillaire M;
- Cauchi S;
- Ducimetière P;
- Eschwège E;
- Balkau, Beverley;
- Lange, Céline;
- Fezeu, Leopold;
- Tichet, Jean;
- de Lauzon-Guillain, Blandine;
- Czernichow, Sebastien;
- Fumeron, Frederic;
- Froguel, Philippe
Publication type:
journal article
Diabetes complications in NIDDM kindreds linked to the MODY3 locus on chromosome 12q.
Published in:
1996
By:
- Velho, Gilberto;
- Vaxillaire, Martine;
- Boccio, Valérie;
- Charpentier, Guillaume;
- Froguel, Philippe;
- Velho, G;
- Vaxillaire, M;
- Boccio, V;
- Charpentier, G;
- Froguel, P
Publication type:
journal article
Arginine-induced insulin release in glucokinase-deficient subjects.
Published in:
1994
By:
- Pueyo, Maria E.;
- Clement, Karine;
- Vaxillaire, Martine;
- Passa, Philippe;
- Froguel, Philippe;
- Robert, Jean-Jacques;
- Velho, Gilberto;
- Pueyo, M E;
- Clement, K;
- Vaxillaire, M;
- Passa, P;
- Froguel, P;
- Robert, J J;
- Velho, G
Publication type:
journal article
Reassessment of the putative role of BLK-p.A71T loss-of-function mutation in MODY and type 2 diabetes.
Published in:
Diabetologia, 2013, v. 56, n. 3, p. 492, doi. 10.1007/s00125-012-2794-8
By:
- Bonnefond, A.;
- Yengo, L.;
- Philippe, J.;
- Dechaume, A.;
- Ezzidi, I.;
- Vaillant, E.;
- Gjesing, A.;
- Andersson, E.;
- Czernichow, S.;
- Hercberg, S.;
- Hadjadj, S.;
- Charpentier, G.;
- Lantieri, O.;
- Balkau, B.;
- Marre, M.;
- Pedersen, O.;
- Hansen, T.;
- Froguel, P.;
- Vaxillaire, M.
Publication type:
Article
GATA6 inactivating mutations are associated with heart defects and, inconsistently, with pancreatic agenesis and diabetes.
Published in:
2012
By:
- Bonnefond, A.;
- Sand, O.;
- Guerin, B.;
- Durand, E.;
- Graeve, F.;
- Huyvaert, M.;
- Rachdi, L.;
- Kerr-Conte, J.;
- Pattou, F.;
- Vaxillaire, M.;
- Polak, M.;
- Scharfmann, R.;
- Czernichow, P.;
- Froguel, P.
Publication type:
Letter
A large multi-centre European study validates high-sensitivity C-reactive protein (hsCRP) as a clinical biomarker for the diagnosis of diabetes subtypes.
Published in:
Diabetologia, 2011, v. 54, n. 11, p. 2801, doi. 10.1007/s00125-011-2261-y
By:
- Thanabalasingham, G.;
- Shah, N.;
- Vaxillaire, M.;
- Hansen, T.;
- Tuomi, T.;
- Gašperíková, D.;
- Szopa, M.;
- Tjora, E.;
- James, T.;
- Kokko, P.;
- Loiseleur, F.;
- Andersson, E.;
- Gaget, S.;
- Isomaa, B.;
- Nowak, N.;
- Raeder, H.;
- Stanik, J.;
- Njolstad, P.;
- Malecki, M.;
- Klimes, I.
Publication type:
Article
Mutations in G6PC2 do not contribute to monogenic forms of early infancy diabetes and beta cell dysfunction.
Published in:
2009
By:
- Bonnefond, A.;
- Bouatia-Naji, N.;
- Simon, A.;
- Saint-Martin, C.;
- Dechaume, A.;
- Lonlay, P.;
- Polak, M.;
- Bellanné-Chantelot, C.;
- Froguel, P.;
- Vaxillaire, M.
Publication type:
Letter
No major contribution of TCF7L2 sequence variants to maturity onset of diabetes of the young (MODY) or neonatal diabetes mellitus in French white subjects.
Published in:
2007
By:
- Cauchi, S.;
- Vaxillaire, M.;
- Choquet, H.;
- Durand, E.;
- Duval, A.;
- Polak, M.;
- Froguel, P.
Publication type:
Letter
Effect of common polymorphisms in theHNF4apromoter on susceptibility to type 2 diabetes in the French Caucasian population.
Published in:
Diabetologia, 2005, v. 48, n. 3, p. 440, doi. 10.1007/s00125-004-1665-3
By:
- Vaxillaire, M.;
- Dina, C.;
- Lobbens, S.;
- Dechaume, A.;
- Vasseur-Delannoy, V.;
- Helbecque, N.;
- Charpentier, G.;
- Froguel, P.
Publication type:
Article
Does the -11377 promoter variant of APM1 gene contribute to the genetic risk for Type 2 diabetes mellitus in Japanese families?
Published in:
Diabetologia, 2003, v. 46, n. 3, p. 443, doi. 10.1007/s00125-003-1050-7
By:
- Populaire, C.;
- Mori, Y.;
- Dina, C.;
- Vasseur, F.;
- Vaxillaire, M.;
- Kadowaki, T.;
- Froguel, P.
Publication type:
Article
Rare variants identified in the HNF-4α β-cell-specific promoter and alternative exon 1 lack biological significance in maturity onset diabetes of the young and young onset Type II diabetes S.M.S. Mitchell et al.: HNF-4α P2 variation and diabetes susceptibility
Published in:
Diabetologia, 2002, v. 45, n. 9, p. 1344, doi. 10.1007/s00125-002-0913-7
By:
- Mitchell, S.;
- Vaxillaire, M.;
- Thomas, H.;
- Parrizas, M.;
- Benmezroua, Y.;
- Costa, A.;
- Hansen, T.;
- Owen, K.;
- Tuomi, T.;
- Pirie, F.;
- Ryffel, G.;
- Ferrer, J.;
- Froguel, P.;
- Hattersley, A.;
- Frayling, T.
Publication type:
Article
Epistasis Between Type 2 Diabetes Susceptibility Loci on Chromosomes 1q21-25 and 10q23-26 in Northern Europeans.
Published in:
Annals of Human Genetics, 2006, v. 70, n. 6, p. 726, doi. 10.1111/j.1469-1809.2006.00289.x
By:
- Wiltshire, S.;
- Bell, J. T.;
- Groves, C. J.;
- Dina, C.;
- Hattersley, A. T.;
- Frayling, T. M.;
- Walker, M.;
- Hitman, G. A.;
- Vaxillaire, M.;
- Farrall, M.;
- Froguel, P.;
- McCarthy, M. I.
Publication type:
Article

Found: 31