IJMS | Free Full-Text | HNF1A Mutations and Beta Cell Dysfunction in Diabetes
SLC19A2 mutation in a family with autosomal dominant diabetes. A:... | Download Scientific Diagram
Neu entdeckter Gendefekt löst Diabetes aus | Management-Krankenhaus
ZYG11A mutation in a family with autosomal dominant diabetes. (A)... | Download Scientific Diagram
Mutations and variants of ONECUT1 in diabetes | Nature Medicine
Monogenic Diabetes – UMR1283
Non classic presentations of a genetic mutation typically associated with transient neonatal diabetes in: Endocrinology, Diabetes & Metabolism Case Reports Volume 2020 Issue 1 (2020)
Frontiers | Modeling Maturity Onset Diabetes of the Young in Pluripotent Stem Cells: Challenges and Achievements
Modeling Monogenic Diabetes using Human ESCs Reveals Developmental and Metabolic Deficiencies Caused by Mutations in HNF1A - ScienceDirect
IJMS | Free Full-Text | HNF1A Mutations and Beta Cell Dysfunction in Diabetes
Pedigreeshowingaffectedfamilymemberswith diabetes mellitus and/or... | Download Scientific Diagram
A dominant negative ADIPOQ mutation in a diabetic family with renal disease, hypoadiponectinemia, and hyperceramidemia | npj Genomic Medicine
Clinical and molecular genetics of neonatal diabetes due to mutations in the insulin gene | SpringerLink
Infancy‐onset diabetes caused by de‐regulated AMPylation of the human endoplasmic reticulum chaperone BiP | EMBO Molecular Medicine
Neonatal diabetes mutations disrupt a chromatin pioneering function that activates the human insulin gene - ScienceDirect
Diabetes mellitus Vorlesung
Insulin mutations impair beta-cell development in a patient-derived iPSC model of neonatal diabetes | eLife
JCI Insight - A KCNK16 mutation causing TALK-1 gain of function is associated with maturity-onset diabetes of the young
Neonatal diabetes caused by mutations in KCNJ11 or ABCC8 // Diabetes Genes
Insulin gene mutations as a cause of permanent neonatal diabetes | PNAS
Mitochondrialer Diabetes | SpringerLink
Genetic Mutation Could Explain Why Some Families Are More Susceptible to Diabetes | Technology Networks
KCNJ11 activating mutations are associated with developmental delay, epilepsy and neonatal diabetes syndrome and other neurological features | European Journal of Human Genetics
Type 2 diabetes: MedlinePlus Genetics
IJMS | Free Full-Text | The Role of Mitochondrial Mutations and Chronic Inflammation in Diabetes
Developmental classification of permanent neonatal diabetes.... | Download Scientific Diagram
