نتایج جستجو برای: tndm

تعداد نتایج: 37  

2015
Huseyin Demirbilek Ved Bhushan Arya Mehmet Nuri Ozbek Jayne A L Houghton Riza Taner Baran Melek Akar Selahattin Tekes Heybet Tuzun Deborah J Mackay Sarah E Flanagan Andrew T Hattersley Sian Ellard Khalid Hussain

BACKGROUND Neonatal diabetes mellitus (NDM) is a rare form of monogenic diabetes and usually presents in the first 6 months of life. We aimed to describe the clinical characteristics and molecular genetics of a large Turkish cohort of NDM patients from a single centre and estimate an annual incidence rate of NDM in South-Eastern Anatolian region of Turkey. DESIGN AND METHODS NDM patients pres...

Journal: :Clinical genetics 2011
M Begemann S Spengler D Kanber A Haake M Baudis I Leisten G Binder S Markus T Rupprecht H Segerer S Fricke-Otto R Mühlenberg R Siebert K Buiting T Eggermann

In all known congenital imprinting disorders an association with aberrant methylation or mutations at specific loci was well established. However, several patients with transient neonatal diabetes mellitus (TNDM), Silver-Russell syndrome (SRS) and Beckwith-Wiedemann syndrome (BWS) exhibiting multilocus hypomethylation (MLH) have meanwhile been described. Whereas TNDM patients with MLH show clin...

2012
Emmanuelle S Topiol Laurie A Minarich Charles A Williams Roberto T Zori David W Kays Michael J Haller

Neonatal diabetes mellitus (NDM) is a rare metabolic disorder, affecting approximately 1 in 500,000 live births. The management of NDM is challenging, as the benefits of controlling hyperglycemia must be balanced with the risks of iatrogenic hypoglycemia. NDM occurs in both permanent and transient forms, which have been genetically and phenotypically well characterized. Herein, we present the p...

Journal: :EMBO reports 2008
Heidi de Wet Peter Proks Mathilde Lafond Jussi Aittoniemi Mark S P Sansom Sarah E Flanagan Ewan R Pearson Andrew T Hattersley Frances M Ashcroft

Activating mutations in the pore-forming Kir6.2 (KCNJ11) and regulatory sulphonylurea receptor SUR1 (ABCC8) subunits of the K(ATP) channel are a common cause of transient neonatal diabetes mellitus (TNDM). We identified a new TNDM mutation (R826W) in the first nucleotide-binding domain (NBD1) of SUR1. The mutation was found in a region that heterodimerizes with NBD2 to form catalytic site 2. Fu...

2015
Kapil Kumar Soni Rohit Vyas Vivek Sharma

Bit parallelism is an inherent property of computer to perform bitwise a parallel operation on computer word, but it is performed only on data available in single computer word. Bit parallelism inherently favors parallelism of bit operations within computer word. Parallel computing comprises bit parallelism and analyzed that it can be carried out “in parallel” which ensures utilizing the word s...

2017
Claire E L Smith Alexia Alexandraki Sarah F Cordery Rekha Parmar David T Bonthron Elizabeth M A Valleley

The imprinted gene PLAGL1 is an important regulator of apoptosis and cell cycle arrest. Loss of its expression has been implicated in tumorigenesis in a range of different cancers, and overexpression during fetal development causes transient neonatal diabetes mellitus (TNDM). PLAGL1 lies within an imprinted region of chromosome 6q24, and monoallelic expression from the major, differentially met...

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