نتایج جستجو برای: kcnj11

تعداد نتایج: 484  

Journal: :Diabetes Care 2008
Juraj Staník Mark Lethby Sarah E. Flanagan Daniela Gašperíková Beata Milošovičová Margaret Lever Hilary Bullman Lejla Zubcevic Andrew T. Hattersley Sian Ellard Frances M. Ashcroft Iwar Klimeš

OBJECTIVE Neonatal diabetes is a heterogeneous group of disorders with diabetes manifestation in the first 6 months of life. The most common etiology in permanent neonatal diabetes is mutations of the ATP-sensitive K(+) channel subunits; in transient neonatal diabetes, chromosome 6q24 abnormalities are the most common cause. RESEARCH DESIGN AND METHODS We report a sporadic case of diabetes wi...

2010
Maria Al-Mahdi Angham Al Mutair Mohammed Al Balwi Khalid Hussain

Neonatal diabetes mellitus is considered a rare disease that is diagnosed in the first six months of life, and can be either transient or permanent. Recent advances in molecular genetics have shown that activating mutations in KCNJ11 (the gene that encodes for the Kir6.2 subunit of the K ATP potassium channel of the pancreatic beta-cell) is a common cause of permanent neonatal diabetes mellitus...

Journal: :Diabetes 2004
Christina Eftychi Joanna M M Howson Bryan J Barratt Adrian Vella Felicity Payne Deborah J Smyth Rebecca C J Twells Neil M Walker Helen E Rance Eva Tuomilehto-Wolf Jaakko Tuomilehto Dag E Undlien Kjersti S Rønningen Cristian Guja Constantin Ionescu-Tîirgovişte David A Savage John A Todd

It has been proposed that type 1 and 2 diabetes might share common pathophysiological pathways and, to some extent, genetic background. However, to date there has been no convincing data to establish a molecular genetic link between them. We have genotyped three single nucleotide polymorphisms associated with type 2 diabetes in a large type 1 diabetic family collection of European descent: Gly9...

Journal: :The Lancet Diabetes & Endocrinology 2018

Journal: :Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia 2013
Maria Pietrzak-Nowacka Krzysztof Safranow Agnieszka Binczak-Kuleta Leszek Domanski Andrzej Ciechanowicz Kazimierz Ciechanowski

The aim of our study was to investigate an association between E23K KCNJ11 gene polymorphism with anthropometric, biochemical, beta-cell secretion and insulin sensitivity parameters among adult ADPKD patients with normal kidney function and no diagnosis of diabetes. The comparison of genotype-phenotype associations between ADPKD and non-ADPKD subjects could reveal a hypothetical mechanism of ge...

2013
Suresh Chandran Fabian Yap Kok Peng Victor Samuel Rajadurai Yap Te Lu Kenneth T E Chang S E Flanagan S Ellard Khalid Hussain

BACKGROUND Congenital hyperinsulinism (CHI) is a rare genetic disorder characterised by inappropriate insulin secretion in the face of severe hypoglycaemia. There are two histological subtypes of CHI namely diffuse and focal. Diffuse CHI is most common due to recessive mutations in ABCC8/KCNJ11 (which encode the SUR/KIR6.2 components of the pancreatic β-cell KATP channel) whereas focal CHI is d...

2009
Alena Stančáková Teemu Kuulasmaa Jussi Paananen Anne U. Jackson Lori L. Bonnycastle Francis S. Collins Michael Boehnke Johanna Kuusisto Markku Laakso

OBJECTIVE We investigated the effects of 18 confirmed type 2 diabetes risk single nucleotide polymorphisms (SNPs) on insulin sensitivity, insulin secretion, and conversion of proinsulin to insulin. RESEARCH DESIGN AND METHODS A total of 5,327 nondiabetic men (age 58 +/- 7 years, BMI 27.0 +/- 3.8 kg/m(2)) from a large population-based cohort were included. Oral glucose tolerance tests and geno...

2010
Rosalind J. Neuman Jon Wasson Gil Atzmon Julio Wainstein Yair Yerushalmi Joseph Cohen Nir Barzilai Ilana Blech Benjamin Glaser M. Alan Permutt

BACKGROUND Evidence has accumulated that multiple genetic and environmental factors play important roles in determining susceptibility to type 2 diabetes (T2D). Although variants from candidate genes have become prime targets for genetic analysis, few studies have considered their interplay. Our goal was to evaluate interactions among SNPs within genes frequently identified as associated with T...

2015
Luísa Martins Rita Lourenço Ana Lúcia Maia Paula Maciel Maria Isabel Monteiro Lucinda Pacheco João Anselmo Rui César Maria Fernanda Gomes

Neonatal diabetes is a monogenic form of diabetes. Herein, we report on a newborn presenting diabetic ketoacidosis at 17 days of life. A KCNJ11 mutation was identified. In such cases, insulin can be replaced by sulfonylurea with a successful metabolic control, as an example of how molecular diagnosis may influence the clinical management of the disorder.

2011
SIRI ATMA W. GREELEY JOSEPH ORNELAS REBECCA B. LIPTON ELBERT S. HUANG

OBJECTIVE—Neonatal diabetes mellitus is a rare form of diabetes diagnosed in infancy. Nearly half of patients with permanent neonatal diabetes have mutations in the genes for the ATP-sensitive potassium channel (KCNJ11 and ABCC8) that allow switching from insulin to sulfonylurea therapy. Although treatment conversion has dramatic benefits, the cost-effectiveness of routine genetic testing is un...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید