نتایج جستجو برای: ژن kcnj11

تعداد نتایج: 16247  

Journal: :Diabetic Medicine 2007
E. Zeggini

The field of complex disease genetics has witnessed rapid progress over the past few months. The advent of genome-wide association scans (GWAS) has mediated a change in gear and the Type 2 diabetes (T2D) research community has set an unprecedented record with five genome-wide association studies published since February 2007 [1–6], increasing the number of confirmed Type 2 diabetes susceptibili...

2011
Rochelle N Naylor Siri Atma W Greeley Graeme I Bell Louis H Philipson

Neonatal diabetes mellitus (NDM) is the term commonly used to describe diabetes with onset before 6 months-of-age. It occurs in approximately one out of every 100,000-300,000 live births. Although this term encompasses diabetes of any etiology, it is recognized that NDM diagnosed before 6 months-of-age is most often monogenic in nature. Clinically, NDM subgroups include transient (TNDM) and per...

2013
Yu-Wen Lin Anlong Li Valeria Grasso Domenica Battaglia Antonino Crinò Carlo Colombo Fabrizio Barbetti Colin G. Nichols

ATP-sensitive potassium (K(ATP)) channels are widely distributed in various tissues and cell types where they couple cell metabolism to cell excitability. Gain of channel function (GOF) mutations in the genes encoding Kir6.2 (KCNJ11) or the associated regulatory ssulfonylurea receptor 1 subunit (ABCC8), cause developmental delay, epilepsy and neonatal diabetes (DEND) due to suppressed cell exci...

Journal: :The Journal of clinical investigation 2011
Jean-Claude Henquin Myriam Nenquin Christine Sempoux Yves Guiot Christine Bellanné-Chantelot Timo Otonkoski Pascale de Lonlay Claire Nihoul-Fékété Jacques Rahier

Congenital hyperinsulinism (CHI) is the major cause of persistent neonatal hypoglycemia. CHI most often occurs due to mutations in the ABCC8 (which encodes sulfonylurea receptor 1) or KCNJ11 (which encodes the potassium channel Kir6.2) gene, which result in a lack of functional KATP channels in pancreatic β cells. Diffuse forms of CHI (DiCHI), in which all β cells are abnormal, often require su...

2010
Sven Pörksen Lene Bjerke Laborie Lotte Nielsen Marie Louise Max Andersen Tone Sandal Heidi de Wet Erik Schwarcz Jan Åman Peter Swift Mirjana Kocova Eugen J Schönle Carine de Beaufort Philip Hougaard Frances Ashcroft Anders Molven Mikael Knip Henrik B Mortensen Lars Hansen Pål R Njølstad

BACKGROUND To investigate disease progression the first 12 months after diagnosis in children with type 1 diabetes negative (AAB negative) for pancreatic autoantibodies [islet cell autoantibodies(ICA), glutamic acid decarboxylase antibodies (GADA) and insulinoma-associated antigen-2 antibodies (IA-2A)]. Furthermore the study aimed at determining whether mutations in KCNJ11, ABCC8, HNF1A, HNF4A ...

2009
Cheng Hu Rong Zhang Congrong Wang Jie Wang Xiaojing Ma Jingyi Lu Wen Qin Xuhong Hou Chen Wang Yuqian Bao Kunsan Xiang Weiping Jia

BACKGROUND Recent advance in genetic studies added the confirmed susceptible loci for type 2 diabetes to eighteen. In this study, we attempt to analyze the independent and joint effect of variants from these loci on type 2 diabetes and clinical phenotypes related to glucose metabolism. METHODS/PRINCIPAL FINDINGS Twenty-one single nucleotide polymorphisms (SNPs) from fourteen loci were success...

2011
Jean-Baptiste Arnoux Virginie Verkarre Cécile Saint-Martin Françoise Montravers Anaïs Brassier Vassili Valayannopoulos Francis Brunelle Jean-Christophe Fournet Jean-Jacques Robert Yves Aigrain Christine Bellanné-Chantelot Pascale de Lonlay

Congenital hyperinsulinism (HI) is an inappropriate insulin secretion by the pancreatic β-cells secondary to various genetic disorders. The incidence is estimated at 1/50, 000 live births, but it may be as high as 1/2, 500 in countries with substantial consanguinity. Recurrent episodes of hyperinsulinemic hypoglycemia may expose to high risk of brain damage. Hypoglycemias are diagnosed because ...

2013
Wojciech Fendler Iwona Pietrzak Melissa F. Brereton Carolina Lahmann Mariusz Gadzicki Malgorzata Bienkiewicz Izabela Drozdz Maciej Borowiec Maciej T. Malecki Frances M. Ashcroft Wojciech M. Mlynarski

OBJECTIVE Activating mutations in the KCNJ11 gene, encoding the Kir6.2 subunit of the KATP channel, result in permanent neonatal diabetes mellitus. They also may cause neurologic symptoms such as mental retardation and motor problems (iDEND syndrome) and epilepsy (DEND syndrome). Sulphonylurea (SU) treatment is reported to alleviate both the neurologic symptoms and diabetes in such cases. The s...

Journal: :Journal of medical genetics 2009
C James R R Kapoor D Ismail K Hussain

Congenital hyperinsulinism (CHI) is biochemically characterised by the dysregulated secretion of insulin from pancreatic beta-cells. It is a major cause of persistent hyperinsulinaemic hypoglycaemia (HH) in the newborn and infancy period. Genetically CHI is a heterogeneous condition with mutations in seven different genes described. The genetic basis of CHI involves defects in key genes which r...

Journal: :American journal of medical genetics. Part A 2016
Asma Deeb Abdelhadi Habeb Walid Kaplan Salima Attia Suha Hadi Amani Osman Jamal Al-Jubeh Sarah Flanagan Elisa DeFranco Sian Ellard

Neonatal diabetes mellitus (NDM) can be transient (TNDM) or permanent (PNDM). Data on NDM from the Gulf region are limited to few studies on PNDM.The objective of this study was to describe the genetic and clinical spectrum of NDM and estimate its incidence in AbuDhabi, capital of the United Arab Emirate (UAE). Patients were identified from the pediatric diabetes clinics and sequencing of known...

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