Diabetes Genetics & Epidemiology (posters)

MON-796

LONG QT INTERVAL IN TURNER SYNDROME – A HIGH PREVALENCE OF LQTS GENE MUTATIONS
Christian Trolle, Kristian Havmand Mortensen, Lisbeth Nørum Pedersen, Agnethe Berglund, Henrik Kjærulf Jensen, Niels Holmark Andersen and Claus H. Gravholt

MON-797

Treatment with Exenatide improves Beta cell function in patients with type 2 diabetes carriers of rs7903146 polymorphism of TCF7L2 gene
Mari Cassol Ferreira, Maria Do Carmo Arruda Marques, Rosa Tsenushiro Fukui, Maysa V De Souza, Maria Elizabeth Rossi Silva and Rosa F Santos

MON-798

Plasma PTX3 increases during exercise: An exercise-factor from the heart
Anders Rinnov, Jakob Hansen, Bente Klarlund Pedersen, Claus Brandt and Peter Plomgaard

MON-799

The A allele of the -866G/A polymorphism in the UCP2 gene is associated with increased UCP2 protein concentrations in human retina from cadaveric cornea donors
Bianca Marmontel de Souza, Letícia de Almeida Brondani, Lúcia M. Klienman, Luis Henrique Canani and Daisy Crispim

MON-800

Effect of PPARγ2 gene polymorphism (Pro12Ala) on HbA1C and its association with BMI in Type 2 diabetes subjects from Western India
Avisek Majumder, Jayesh J Sheth, Frenny Sheth, Manan Patel, Bhavik Doshi, Navneet N Shah, Premal Thakor and Rama Vaidya

MON-801

Replication of Genome Wide Association-Validated Loci for Type 2 Diabetes Mellitus in the Saudi Arabian Population
Nasser Mohmmed Al-Daghri, Khalid Alkharfy, Majed S Alokail, Amal Alenad, Omar Al-Attas, Abdul Khader Mohammed, Shaun Sabico and Omar Albagha

MON-802

The presence of the 299Gly/399Ile haplotype in the toll-like receptor 4 (TLR4) gene is associated with protection to type 2 diabetes mellitus (T2DM) in Brazilian population
Tais Silveira Assmann, Natalia Emerim Lemos, Letícia de Almeida Brondani, Luis Henrique Canani and Daisy Crispim

MON-803

Metabolic Syndrome: evaluation of PPARG, KCNJ11, HHEX, HNF4A, ECA, FTO and ABCA1 gene polymorphisms in Maya children
Barbara Itzel Peña-Espinoza, MA Granados-Silvestre, Julio Lara-Riegos, Isela Montúfar-Robles, Carlos Juarez-Lopez, Maria Guadalupe Ortiz-Lopez and Marta Menjivar

MON-804

Metabolism of oral antidiabetic: evaluation of CYP2C9 polymorphisms in Maya population
Marta Menjivar, Luz Camacho, Julio Lara-Riegos, Isela Montúfar-Robles, María de los Angeles Granados-Silvestre, Adrian Llerena and María Guadalupe Ortiz-López

MON-805

rs9282541 POLYMORPHISM OF ABCA1 IS ASSOCIATED WITH TYPE 2 DIABETES IN MAYA POPULATION
Julio Lara-Riegos, Maria Guadalupe Ortiz-Lopez, Barbara Itzel Peña-Espinoza, Isela Montúfar-Robles, Jesus Castro-Ramirez, Miguel Peña-Rico, Luz Camacho, MA de los Ángeles Granados-Silvestre and Marta Menjivar

MON-806

MON-807

TYPE 2 DIABETES RISK ALLELES FREQUENCIES IN THE PORTUGUESE POPULATION
Duarte Pignatelli, Aida Palmeiro, Alexandra Lopes, Luis Dias, Purificação Tavares and Paula Rendeiro

MON-808

THE EFFECT OF CALPAIN-10 GENE POLYMORPHISM ON THE DEVELOPMENT OF TYPE 2 DIABETES MELLITUS IN TURKISH POPULATION
Emre Arslan, Leyla Acik, Gulsah Gunaltili, Goksun Ayvaz, Alev E. Altinova and Metin Arslan

MON-809

The rs1746661 and rs3480 polymorphisms in the FNDC5 (Irisin) gene are associated with increased systolic blood pressure in white patients with type 2 diabetes mellitus
Letícia de Almeida Brondani, Tais Silveira Assmann, Gabriela Boelter, Luis Henrique Canani and Daisy Crispim

MON-810

HEPATIC 11BETA-HYDROXYSTEROID DEHYDROGENASE TYPE I and ATHEROSCLEROSIS RISK
Kajal Manwani, Tak Yung Man, Christopher J Kenyon, Ruth Andrew, Karen Elizabeth Chapman and Jonathan Robert Seckl

MON-811

MON-813

Association between BDNF polymorphism and psychiatric symptoms
Min Kyung Kim, Jiyoon Ha, Haeri Baek, Sohee Kim, Chanhee Kyung, Youngmi Lee, Tae Woong Noh, Shinae Kang, Kyung Rae Kim, Jong Suk Park and Chul Woo Ahn

MON-814

25-hydroxyvitamin D level and vitamin D gene polymorphisms in Korean youth with type 1 diabetes mellitus
Hyo-Kyoung Nam, Joon Woo Baek, Yeon Joung Oh, Young Jun Rhie and Kee-Hyoung Lee

MON-817

Dominant Protein Interactions Influencing the Pathogenesis of Protein Misfolding Diseases of the Endocrine System
Peter Arvan, Jordan Wright, Leena Haataja, Xiaofan Wang, Jaemin Lee, Ming Liu and Aaron Kellogg