1 - 25 of 31 results for author:"Boutin P." in Literature citations
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| Tumor endothelial marker 7 (TEM-7): a novel target for antiangiogenic therapy. Bagley R.G., Rouleau C., Weber W., Mehraein K., Smale R., Curiel M., Callahan M., Roy A., Boutin P., St Martin T. et al. Microvasc. Res. 82:253-262(2011) · Mapped (4) |
| Evaluating the association of FAAH common gene variation with childhood, adult severe obesity and type 2 diabetes in the French population. Durand E., Lecoeur C., Delplanque J., Benzinou M., Degraeve F., Boutin P., Marre M., Balkau B., Charpentier G., Froguel P. et al. Obes Facts 1:305-309(2008) · Mapped (2) |
| Endosialin/TEM 1/CD248 is a pericyte marker of embryonic and tumor neovascularization. Bagley R.G., Honma N., Weber W., Boutin P., Rouleau C., Shankara S., Kataoka S., Ishida I., Roberts B.L., Teicher B.A. Microvasc. Res. 76:180-188(2008) · Mapped (1) |
| Human endothelial precursor cells express tumor endothelial marker 1/endosialin/CD248. Bagley R.G., Rouleau C., St Martin T., Boutin P., Weber W., Ruzek M., Honma N., Nacht M., Shankara S., Kataoka S. et al. Mol. Cancer Ther. 7:2536-2546(2008) · Mapped (1) |
| Common nonsynonymous variants in PCSK1 confer risk of obesity. Benzinou M., Creemers J.W.M., Choquet H., Lobbens S., Dina C., Durand E., Guerardel A., Boutin P., Jouret B., Heude B. et al. |
| A genome-wide association study identifies novel risk loci for type 2 diabetes. Sladek R., Rocheleau G., Rung J., Dina C., Shen L., Serre D., Boutin P., Vincent D., Belisle A., Hadjadj S. et al. |
| Genotype-by-nutrient interactions assessed in European obese women. A case-only study. Santos J.L., Boutin P., Verdich C., Holst C., Larsen L.H., Toubro S., Dina C., Saris W.H., Blaak E.E., Hoffstedt J. et al. Eur J Nutr 45:454-462(2006) · Mapped (16) |
| Distinct impaired regulation of SOCS3 and long and short isoforms of the leptin receptor in visceral and subcutaneous fat of lean and obese women. Seron K., Corset L., Vasseur F., Boutin P., Gomez-Ambrosi J., Salvador J., Fruhbeck G., Froguel P. Biochem. Biophys. Res. Commun. 348:1232-1238(2006) · Mapped (5) |
| Genetic analysis of ADIPOR1 and ADIPOR2 candidate polymorphisms for type 2 diabetes in the Caucasian population. Vaxillaire M., Dechaume A., Vasseur-Delannoy V., Lahmidi S., Vatin V., Lepretre F., Boutin P., Hercberg S., Charpentier G., Dina C. et al. Diabetes 55:856-861(2006) · Mapped (2) |
| Protein tyrosine phosphatase PRL-3 in malignant cells and endothelial cells: expression and function. Rouleau C., Roy A., St Martin T., Dufault M.R., Boutin P., Liu D., Zhang M., Puorro-Radzwill K., Rulli L., Reczek D. et al. Mol. Cancer Ther. 5:219-229(2006) · Mapped (1) |
| Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes. Meyre D., Bouatia-Naji N., Tounian A., Samson C., Lecoeur C., Vatin V., Ghoussaini M., Wachter C., Hercberg S., Charpentier G. et al. Nat. Genet. 37:863-867(2005) · Mapped (7) |
| Hypoadiponectinaemia and high risk of type 2 diabetes are associated with adiponectin-encoding (ACDC) gene promoter variants in morbid obesity: evidence for a role of ACDC in diabesity. Vasseur F., Helbecque N., Lobbens S., Vasseur-Delannoy V., Dina C., Clement K., Boutin P., Kadowaki T., Scherer P.E., Froguel P. Diabetologia 48:892-899(2005) · Mapped (3) |
| Analysis of sequence variability in the CART gene in relation to obesity in a Caucasian population. Guerardel A., Barat-Houari M., Vasseur F., Dina C., Vatin V., Clement K., Eberle D., Vasseur-Delannoy V., Bell C.G., Galan P. et al. BMC Genet. 6:19-19(2005) · Mapped (1) |
| Is glutamate decarboxylase 2 (GAD2) a genetic link between low birth weight and subsequent development of obesity in children? Meyre D., Boutin P., Tounian A., Deweirder M., Aout M., Jouret B., Heude B., Weill J., Tauber M., Tounian P. et al. J. Clin. Endocrinol. Metab. 90:2384-2390(2005) · Mapped (5) |
| Identification of a binding partner for the endothelial cell surface proteins TEM7 and TEM7R. Nanda A., Buckhaults P., Seaman S., Agrawal N., Boutin P., Shankara S., Nacht M., Teicher B., Stampfl J., Singh S. et al. |
| Polymorphisms in the amino acid transporter solute carrier family 6 (neurotransmitter transporter) member 14 gene contribute to polygenic obesity in French Caucasians. Durand E., Boutin P., Meyre D., Charles M.A., Clement K., Dina C., Froguel P. Diabetes 53:2483-2486(2004) · Mapped (4) |
| GAD2 on chromosome 10p12 is a candidate gene for human obesity. Boutin P., Dina C., Vasseur F., Dubois S., Corset L., Seron K., Bekris L., Cabellon J., Neve B., Vasseur-Delannoy V. et al. PLoS Biol. 1:E68-E68(2003) · Mapped (5) |
| Islet-brain1/C-Jun N-terminal kinase interacting protein-1 (IB1/JIP-1) promoter variant is associated with Alzheimer's disease. Helbecque N., Abderrahamani A., Meylan L., Riederer B., Mooser V., Miklossy J., Delplanque J., Boutin P., Nicod P., Haefliger J.A. et al. Mol. Psychiatry 8:413-22, 2003:363-363(2003) · Mapped (5) |
| Mutations in the glucokinase regulatory protein gene in 2p23 in obese French caucasians. Veiga-da-Cunha M., Delplanque J., Gillain A., Bonthron D.T., Boutin P., Van Schaftingen E., Froguel P. Diabetologia 46:704-711(2003) · Mapped (5) |
| Single-nucleotide polymorphism haplotypes in the both proximal promoter and exon 3 of the APM1 gene modulate adipocyte-secreted adiponectin hormone levels and contribute to the genetic risk for type 2 diabetes in French Caucasians. Vasseur F., Helbecque N., Dina C., Lobbens S., Delannoy V., Gaget S., Boutin P., Vaxillaire M., Lepretre F., Dupont S. et al. Hum. Mol. Genet. 11:2607-2614(2002) · UniProtKB (1) · Mapped (2) |
| No association between the G482S polymorphism of the proliferator-activated receptor-gamma coactivator-1 (PGC-1) gene and Type II diabetes in French Caucasians. Lacquemant C., Chikri M., Boutin P., Samson C., Froguel P. Diabetologia 45:602-3; author reply 2002:604-604(2002) · Mapped (10) |
| Prevalence of the missense mutation Gly574Ser in the hepatocyte nuclear factor-1alpha in Africans with diabetes. Collet C., Ducorps M., Mayaudon H., Dupuy O., Ceppa F., Boutin P., Froguel P., Bauduceau B. Diabetes Metab. 28:39-44(2002) · Mapped (17) |
| Mutation screening of the urocortin gene: identification of new single nucleotide polymorphisms and association studies with obesity in French Caucasians. Delplanque J., Vasseur F., Durand E., Abderrahmani A., Dina C., Waeber G., Guy-Grand B., Clement K., Weill J., Boutin P. et al. J. Clin. Endocrinol. Metab. 87:867-869(2002) · Mapped (1) |
| Genetic variation in the gene encoding adiponectin is associated with an increased risk of type 2 diabetes in the Japanese population. Hara K., Boutin P., Mori Y., Tobe K., Dina C., Yasuda K., Yamauchi T., Otabe S., Okada T., Eto K. et al. |
| Routine mutation screening of HNF-1alpha and GCK genes in MODY diagnosis: how effective are the techniques of DHPLC and direct sequencing used in combination? Boutin P., Vasseur F., Samson C., Wahl C., Froguel P. Diabetologia 44:775-778(2001) · Mapped (20) |