Results 1 to 10 of about 1,599 (104)

Localized increases in CEPT1 and ATGL elevate plasmalogen phosphatidylcholines in HDLs contributing to atheroprotective lipid profiles in hyperglycemic GCK-MODY [PDF]

open access: yesRedox Biology, 2021
Glucokinase-maturity onset diabetes of the young (GCK-MODY) represents a rare genetic disorder due to mutation in the glucokinase (GCK) gene. The low incidence of vascular complications in GCK-MODY makes it a natural paradigm for interrogating molecular ...
Xinhua Xiao, Huabing Zhang, Miao Yu
exaly   +4 more sources

GCK‐MODY in pregnancy: A pregnant woman with diabetes and a small‐for‐gestational‐age fetus [PDF]

open access: yesClinical Case Reports (discontinued), 2022
Glucokinase‐maturity‐onset diabetes of the young (GCK‐MODY) is often misdiagnosed as other forms of diabetes. A 42‐year‐old pregnant lady with pre‐existing diabetes was treated with insulin during first trimester. Fetal growth restriction was noted since
Ma Rcw, Stephanie C Y Yu
exaly   +3 more sources

GCK exonic mutations induce abnormal biochemical activities and result in GCK-MODY [PDF]

open access: yesFrontiers in Genetics, 2023
Objective: Glucokinase-maturity-onset diabetes of the young (GCK-MODY; MODY2) is a rare genetic disorder caused by mutations in the glucokinase (GCK) gene.
Tongtong Dai   +14 more
exaly   +4 more sources

Distinguishing the lipid profile of GCK-MODY patients and its correlation with hsCRP levels [PDF]

open access: yesFrontiers in Endocrinology, 2022
AimsGlucokinase–maturity-onset diabetes of the young (GCK-MODY) is the most common monogenic diabetes in China. We have previously reported on the low levels of high-sensitivity C-reactive protein (hsCRP) in patients with GCK-MODY.
Fan Ping, Junling Fu, Xinhua Xiao
doaj   +2 more sources

GCK‐MODY、HNF1A‐MODY和2型糖尿病的基础辅助检查的见解:一项系统回顾和meta分析 [PDF]

open access: yesJournal of Diabetes, 2023
Background Glucokinase maturity‐onset diabetes of the young (GCK‐MODY) is difficult to distinguish from other diabetic forms. This article aims to characterize the differences in results from routine examinations between GCK‐MODY and hepatocyte nuclear ...
Jing Liu   +3 more
doaj   +2 more sources

Course of pregnancy and 10-year observation of twins diagnosed with GCK-MODY in the neonatal period: a case report [PDF]

open access: yesFrontiers in Endocrinology
Monogenic diabetes accounts for 5% of all incidence of hyperglycemia and Maturity Onset Diabetes of the Young (MODY) is the most common form. In GCK-MODY, one of the most common forms of MODY, hyperglycemia is caused by a mutation of a gene responsible ...
Barbara Katra   +3 more
doaj   +2 more sources

Genetic and clinical characteristics of Chinese children with Glucokinase-maturity-onset diabetes of the young (GCK-MODY) [PDF]

open access: yesBMC Pediatrics, 2018
Background There is scarcity of information on the clinical features and genetics of glucokinase-maturity-onset diabetes of the young (GCK-MODY) in China.
Xiuzhen Li   +8 more
doaj   +2 more sources

Personalized management of glucokinase-related monogenic diabetes (GCK-MODY) during pregnancy: a case report [PDF]

open access: yesFrontiers in Endocrinology
BackgroundManagement of glucokinase-related monogenic diabetes (GCK-MODY) during pregnancy can be challenging.Case presentationWe present the case report of a 33-year-old woman, diagnosed with diabetes since the age of 9.
Ana Filipa Bolas   +12 more
doaj   +2 more sources

“Pesto” Mutation: Phenotypic and Genotypic Characteristics of Eight GCK/MODY Ligurian Patients [PDF]

open access: yesInternational Journal of Molecular Sciences, 2023
Renata Bocciardi   +2 more
exaly   +2 more sources

Case Report: A novel likely pathogenic GCK variant in a young Chinese girl with severe insulin resistance [PDF]

open access: yesFrontiers in Endocrinology
ObjectiveTo report a novel GCK variant (c.263T>C) identified in a patient with glucokinase-maturity-onset diabetes of the young (GCK-MODY) and to evaluate its pathogenicity and potential structural impact using in silico analyses.
Haoyu Bai   +6 more
doaj   +2 more sources

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