نتایج جستجو برای: mody

تعداد نتایج: 686  

2012
Siobhan Bacon Ma Peyh Kyithar Jasmin Schmid Syed R Rizvi Caroline Bonner Rolf Graf Jochen HM Prehn Maria M Byrne

BACKGROUND Mutations in the transcription factor hepatocyte nuclear factor-1-alpha (HNF1A) result in the commonest type of maturity onset diabetes of the young (MODY). HNF1A-MODY carriers have reduced pancreatic beta cell mass, partially due to an increased rate of apoptosis. To date, it has not been possible to determine when apoptosis is occurring in HNF1A-MODY.We have recently demonstrated t...

2017
Inés Urrutia Rosa Martínez Tamara López-Euba Teresa Velayos Idoia Martínez de LaPiscina José Ramón Bilbao Itxaso Rica Luis Castaño

OBJECTIVE The aim of this study was to determine the frequency of susceptible HLA-DRB1 alleles for type 1 diabetes in a cohort of pediatric patients with a confirmed genetic diagnosis of MODY. MATERIALS AND METHODS 160 families with a proband diagnosed with type 1 diabetes and 74 families with a molecular diagnosis of MODY (61 GCK-MODY and 13 HNF1A-MODY) were categorized at high definition fo...

2015
Sung-Hoon Kim

Maturity-onset diabetes of the young (MODY) is a monogenic form of diabetes that is characterized by an early onset, autosomal dominant mode of inheritance and a primary defect in pancreatic β-cell function. MODY represents less than 2% of all diabetes cases and is commonly misdiagnosed as type 1 or type 2 diabetes mellitus. At least 13 MODY subtypes with distinct genetic etiologies have been i...

2014
Rochelle N. Naylor Priya M. John Aaron N. Winn David Carmody Siri Atma W. Greeley Louis H. Philipson Graeme I. Bell Elbert S. Huang

OBJECTIVE To evaluate the cost-effectiveness of a genetic testing policy for HNF1A-, HNF4A-, and GCK-MODY in a hypothetical cohort of type 2 diabetic patients 25-40 years old with a MODY prevalence of 2%. RESEARCH DESIGN AND METHODS We used a simulation model of type 2 diabetes complications based on UK Prospective Diabetes Study data, modified to account for the natural history of disease by g...

Journal: :Diabetes 2004
Sung-Hoon Kim Xiaowei Ma Stanislawa Weremowicz Tonino Ercolino Christine Powers Wojciech Mlynarski K Aviva Bashan James H Warram Josyf Mychaleckyj Stephen S Rich Andrzej S Krolewski Alessandro Doria

Maturity-onset diabetes of the young (MODY) is a subtype of diabetes defined by an autosomal dominant inheritance and a young onset. Six MODY genes have been discovered to date. To identify additional MODY loci, we conducted a genome scan in 21 extended U.S. families (15 white and 6 from minorities, for a total of 237 individuals) in which MODY was not caused by known MODY genes. Seven chromoso...

Journal: :Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 1999
V C Pardini G Velho R Reis S Purisch H Blanché J G Vieira R C Moisés

Glucokinase (GCK) is an enzyme that regulates insulin secretion, keeping glucose levels within a narrow range. Mutations in the glucokinase gene cause a rare form of diabetes called maturity-onset diabetes of the young (MODY). An early onset (less than 25 years), autosomal dominant inheritance and low insulin secretion stimulated by glucose characterize MODY patients. Specific insulin and proin...

Journal: :Diabetes Care 2011

Journal: :Diabetes 2003
Timothy M Frayling Cecilia M Lindgren Jean Claude Chevre Stephan Menzel Marie Wishart Yamina Benmezroua Alison Brown Julie C Evans Pamidghantam Subba Rao Christian Dina Cécile Lecoeur Timo Kanninen Peter Almgren Michael P Bulman Youxiang Wang James Mills Rosemarie Wright-Pascoe Melanie M Mahtani Francesco Prisco Angels Costa Ignacio Cognet Torben Hansen Oluf Pedersen Sian Ellard Tiinamaija Tuomi Leif C Groop Philippe Froguel Andrew T Hattersley Martine Vaxillaire

Maturity-onset diabetes of the young (MODY) is a heterogeneous single gene disorder characterized by non-insulin-dependent diabetes, an early onset and autosomal dominant inheritance. Mutations in six genes have been shown to cause MODY. Approximately 15-20% of families fitting MODY criteria do not have mutations in any of the known genes. These families provide a rich resource for the identifi...

Journal: :Journal of Personalized Medicine 2023

Background: Mutation of the gene encoding Hepatocyte Nuclear transcription Factor-1 Beta (HNF1B) causes a rare monogenetic subtype Maturity-Onset Diabetes Young (MODY). HNF1B-related MODY results in dysfunction multiple organ systems. However, genetic analysis enables personalized medicine for patients and families. Aims: To understand clinical characteristics explore mutations Croatian patient...

2015
Magdalena Szopa Maria Kapusta Bartlomiej Matejko Tomasz Klupa Teresa Koblik Beata Kiec-Wilk Maciej Borowiec Maciej T. Malecki

INTRODUCTION We previously showed that in HNF1A-MODY the cystatin C-based glomerular filtration rate (GFR) estimate is higher than the creatinine-based estimate. Currently, we aimed to replicate this finding and verify its clinical significance. METHODS The study included 72 patients with HNF1A-MODY, 72 with GCK-MODY, 53 with type 1 diabetes (T1DM), 70 with type 2 diabetes (T2DM), and 65 cont...

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