Results 121 to 130 of about 12,946 (215)

Retrospective examination of pediatric patients followed with the diagnosis of monogenic diabetes type 2 (mody type 2-GCK)

open access: yes, 2022
Gençlikte ortaya çıkan erişkin tip diyabet (MODY), tek gende meydana gelen otozomal dominant mutasyonlar nedeniyle pankreas β hücrelerinde fonksiyon bozukluğuna yol açan diyabet formudur. Günümüzde MODY’ye yol açan 14 farklı gen mutasyonu tanımlanmıştır.
Tula, Burak
core  

GCK gene-body hypomethylation is associated with the risk of coronary heart disease. Biomed Res Int

open access: yes, 2020
Objectives. Glucokinase encoded by GCK is a key enzyme that facilitates phosphorylation of glucose to glucose-6-phosphate. Variants of GCK gene were shown to be associated with type 2 diabetes (T2D) and coronary heart disease (CHD).
Lina Zhang   +18 more
core  

Co-occurrence of Loss-of-Function GCK and ABCC8 Variants in a Pedigree With a Spectrum of Dysglycemia. [PDF]

open access: yesDiabetes
Saint-Martin C   +6 more
europepmc   +1 more source

Cost Effectiveness of GCK-MODY Genetic Screening for Selected Individuals Referred to the Diabetes Prevention Programme

open access: yes
MODY accounts for 1 5% of diabetes cases, of these GCK-MODY comprises approximately 30%.GCKMODY is associated with minimal risk of complications. Efficiently diagnosing GCK-MODY leads to more appropriate management and resource allocation.
Noble, Jane   +3 more
core  

Treatment Options for Patients with Maturity-Onset Diabetes of the Young (MODY): A Systematic Review of Literature: 2026 Update. [PDF]

open access: yesDiabetes Ther
Zagaroli L   +7 more
europepmc   +1 more source

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