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Non classic presentations of a genetic mutation typically associated with  transient neonatal diabetes in: Endocrinology, Diabetes & Metabolism Case  Reports Volume 2020 Issue 1 (2020)
Non classic presentations of a genetic mutation typically associated with transient neonatal diabetes in: Endocrinology, Diabetes & Metabolism Case Reports Volume 2020 Issue 1 (2020)

An HNF1α truncation associated with maturity-onset diabetes of the young  impairs pancreatic progenitor differentiation by antagonizing HNF1β  function - ScienceDirect
An HNF1α truncation associated with maturity-onset diabetes of the young impairs pancreatic progenitor differentiation by antagonizing HNF1β function - ScienceDirect

JCI Insight - A KCNK16 mutation causing TALK-1 gain of function is  associated with maturity-onset diabetes of the young
JCI Insight - A KCNK16 mutation causing TALK-1 gain of function is associated with maturity-onset diabetes of the young

Neonatal diabetes due to potassium channel mutation: Response to  sulfonylurea according to the genotype - Garcin - 2020 - Pediatric Diabetes  - Wiley Online Library
Neonatal diabetes due to potassium channel mutation: Response to sulfonylurea according to the genotype - Garcin - 2020 - Pediatric Diabetes - Wiley Online Library

Mitochondrialer Diabetes | SpringerLink
Mitochondrialer Diabetes | SpringerLink

Neonatal diabetes caused by mutations in KCNJ11 or ABCC8 // Diabetes Genes
Neonatal diabetes caused by mutations in KCNJ11 or ABCC8 // Diabetes Genes

Genetics and Pathophysiology of Maturity-onset Diabetes of the Young  (MODY): A Review of Current Trends | Middle East Medical Portal
Genetics and Pathophysiology of Maturity-onset Diabetes of the Young (MODY): A Review of Current Trends | Middle East Medical Portal

Type 2 diabetes: MedlinePlus Genetics
Type 2 diabetes: MedlinePlus Genetics

A dominant negative ADIPOQ mutation in a diabetic family with renal  disease, hypoadiponectinemia, and hyperceramidemia | npj Genomic Medicine
A dominant negative ADIPOQ mutation in a diabetic family with renal disease, hypoadiponectinemia, and hyperceramidemia | npj Genomic Medicine

Neu entdeckter Gendefekt löst Diabetes aus | Management-Krankenhaus
Neu entdeckter Gendefekt löst Diabetes aus | Management-Krankenhaus

New Type of Diabetes Caused by Gene Mutation Discovered – Diabetes Daily
New Type of Diabetes Caused by Gene Mutation Discovered – Diabetes Daily

Monogenic Diabetes (Neonatal Diabetes Mellitus & MODY) | NIDDK
Monogenic Diabetes (Neonatal Diabetes Mellitus & MODY) | NIDDK

Pedigreeshowingaffectedfamilymemberswith diabetes mellitus and/or... |  Download Scientific Diagram
Pedigreeshowingaffectedfamilymemberswith diabetes mellitus and/or... | Download Scientific Diagram

Monogenic Diabetes – UMR1283
Monogenic Diabetes – UMR1283

Modeling Monogenic Diabetes using Human ESCs Reveals Developmental and  Metabolic Deficiencies Caused by Mutations in HNF1A - ScienceDirect
Modeling Monogenic Diabetes using Human ESCs Reveals Developmental and Metabolic Deficiencies Caused by Mutations in HNF1A - ScienceDirect

Identification of Maturity-Onset-Diabetes of the Young (MODY) mutations in  a country where diabetes is endemic | Scientific Reports
Identification of Maturity-Onset-Diabetes of the Young (MODY) mutations in a country where diabetes is endemic | Scientific Reports

SLC19A2 mutation in a family with autosomal dominant diabetes. A:... |  Download Scientific Diagram
SLC19A2 mutation in a family with autosomal dominant diabetes. A:... | Download Scientific Diagram

Case of a novel PAX6 mutation with aniridia and insulin‐dependent diabetes  mellitus - Motoda - 2019 - Journal of Diabetes Investigation - Wiley Online  Library
Case of a novel PAX6 mutation with aniridia and insulin‐dependent diabetes mellitus - Motoda - 2019 - Journal of Diabetes Investigation - Wiley Online Library

Infancy‐onset diabetes caused by de‐regulated AMPylation of the human  endoplasmic reticulum chaperone BiP | EMBO Molecular Medicine
Infancy‐onset diabetes caused by de‐regulated AMPylation of the human endoplasmic reticulum chaperone BiP | EMBO Molecular Medicine

IJMS | Free Full-Text | HNF1A Mutations and Beta Cell Dysfunction in  Diabetes
IJMS | Free Full-Text | HNF1A Mutations and Beta Cell Dysfunction in Diabetes

IJMS | Free Full-Text | The Role of Mitochondrial Mutations and Chronic  Inflammation in Diabetes
IJMS | Free Full-Text | The Role of Mitochondrial Mutations and Chronic Inflammation in Diabetes

Mutations and variants of ONECUT1 in diabetes | Nature Medicine
Mutations and variants of ONECUT1 in diabetes | Nature Medicine

KCNJ11 activating mutations are associated with developmental delay,  epilepsy and neonatal diabetes syndrome and other neurological features |  European Journal of Human Genetics
KCNJ11 activating mutations are associated with developmental delay, epilepsy and neonatal diabetes syndrome and other neurological features | European Journal of Human Genetics

Maturity-onset diabetes of the young: MedlinePlus Genetics
Maturity-onset diabetes of the young: MedlinePlus Genetics

Insulin mutations impair beta-cell development in a patient-derived iPSC  model of neonatal diabetes | eLife
Insulin mutations impair beta-cell development in a patient-derived iPSC model of neonatal diabetes | eLife

Activating Mutations in the ABCC8 Gene in Neonatal Diabetes Mellitus | NEJM
Activating Mutations in the ABCC8 Gene in Neonatal Diabetes Mellitus | NEJM