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Diabetes, ISSN 0012-1797, 05/2013, Volume 62, Issue 5, pp. 1689 - 1696
Congenital hyperinsulinism causes persistent hypoglycemia in neonates and infants. Most often, uncontrolled insulin secretion (IS) results from a lack of... 
Glucose metabolism | Glucokinase | Physiological aspects | Metabolic diseases | Development and progression | Genetic aspects | Research | Risk factors
Journal Article
Diabetes Care, ISSN 0149-5992, 09/2012, Volume 35, Issue 9, pp. 1832 - 1834
OBJECTIVE-In women with hyperglycemia due to heterozygous glucokinase (GCK mutations, the fetal genotype determines its growth. If the fetus inherits the... 
BIRTH | GENE | GLUCOSE | SIZE | ENDOCRINOLOGY & METABOLISM | PREGNANCY | Pregnancy | Diabetes, Gestational - genetics | Humans | Adult | Female | Genotype | Glucokinase - genetics | Mutation | Prenatal Diagnosis - methods | Hyperglycemia - genetics | Hyperglycemia | Growth | Pregnant women | Isoenzymes | Fetus | Genetic aspects | Diabetes | Fetuses | Birth weight | Insulin | Index Medicus | Original Research
Journal Article
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 556 - 6
We have utilized a high-diversity phage display library to engineer antibody fragments (Fabs) that can modulate the activity of the enzyme isocitrate... 
EFFECTOR | GLUCOKINASE | PROTEINS | ENZYMES | MULTIDISCIPLINARY SCIENCES | SMALL-MOLECULE ACTIVATORS | Phage display | Isocitrate dehydrogenase | Brain tumors | Cancer | Index Medicus
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 04/2004, Volume 350, Issue 18, pp. 1838 - 1849
Journal Article
Journal of Clinical Research in Pediatric Endocrinology, ISSN 1308-5727, 06/2017, Volume 9, Issue 2, p. 22
Journal Article
Journal Article
Clinical Endocrinology, ISSN 0300-0664, 12/2014, Volume 81, Issue 6, pp. 855 - 861
ContextGlucokinase (GCK) phosphorylates and thereby traps glucose in cells, thus serving as a gatekeeper for cellular glucose metabolism, particularly in... 
TRIGLYCERIDE | OVEREXPRESSION | GLUCOSE | LIVER | ENDOCRINOLOGY & METABOLISM | HYPOGLYCEMIA | VARIANT | Humans | Middle Aged | Glucokinase - genetics | Male | Sequence Analysis, DNA | Pedigree | Hyperinsulinism - genetics | Adult | Family | Female | Heterozygote | Aged | Mutation | Pancreatic beta cells | Isoenzymes | Blood sugar | Genetic aspects | Triglycerides | Adults | Glucose tolerance tests | Index Medicus
Journal Article
Diabetes Research and Clinical Practice, ISSN 0168-8227, 2017, Volume 130, pp. 86 - 89
Highlights • We describe a novel GCK-MODY mutation in a Macedonian family. • To our knowledge,it is a first GCK mutation detected in a child in the Balkan... 
Endocrinology & Metabolism | GCK mutation | Mild hyperglycemia | GCK-MODY | POPULATION | YOUNG | ENDOCRINOLOGY & METABOLISM | LINKAGE | Greece | Glucose Tolerance Test | Diabetes Mellitus, Type 2 - genetics | Humans | Diabetes Mellitus, Type 2 - therapy | Child, Preschool | Female | Glucokinase - genetics | Male | Mutation | Hyperglycemia - genetics | Hyperglycemia | Gene mutations | Isoenzymes | Genes | Index Medicus
Journal Article