HNF1B-associated renal and extra-renal disease—an expanding clinical spectrum | Nature Reviews Nephrology
ADTKD-HNF1B (renal cyst and diabetes syndrome) in a 35 year-old female.... | Download Scientific Diagram
Frontiers | Case Report: A case of HNF1B mutation patient with first presentation of diabetic ketosis
Phenotypes seen in diabetes with extra-pancreatic features. (A) Renal... | Download Scientific Diagram
Diabetes Typ 3 und die verschiedenen Unterkategorien
A novel splice-site mutation of the HNF1B gene in a family with maturity onset diabetes of the young type 5 (MODY5) in: Endocrinology, Diabetes & Metabolism Case Reports Volume 2020 Issue 1 (2020)
The epidemiology, molecular pathogenesis, diagnosis, and treatment of maturity-onset diabetes of the young (MODY) | Clinical Diabetes and Endocrinology | Full Text
Cells | Free Full-Text | The Landscape of HNF1B Deficiency: A Syndrome Not Yet Fully Explored
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Genomics & Informatics
Maturity-Onset Diabetes of the Young (MODY) - ppt video online download
Early Developmental Perturbations in a Human Stem Cell Model of MODY5/HNF1B Pancreatic Hypoplasia - ScienceDirect
Analysis of expression, epigenetic, and genetic changes of HNF1B in 130 kidney tumours | Scientific Reports
Screening for HNF1B Gene Mutations, in Four People with Typical Diabetes MODY5 Clinical Characteristics
Featured Articles
The role of hepatocyte nuclear factor 1β in disease and development - El‐Khairi - 2016 - Diabetes, Obesity and Metabolism - Wiley Online Library
Common Genetic Variants in the HNF1B Gene Contribute to Diabetes and Multiple Cancers
Polymorphism in microRNA-binding site in HNF1B influences the susceptibility of type 2 diabetes mellitus: a population based case–control study – topic of research paper in Biological sciences. Download scholarly article PDF and
Inhibition of hepatocyte nuclear factor 1b induces hepatic steatosis through DPP4/NOX1-mediated regulation of superoxide - ScienceDirect
Pedigrees of families with alterations in the HNF1B gene. The two index... | Download Scientific Diagram
HNF1B-associated renal and extra-renal disease—an expanding clinical spectrum | Nature Reviews Nephrology
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De novo HNF1 homeobox B mutation as a cause for chronic, treatment-resistant hypomagnesaemia in: Endocrinology, Diabetes & Metabolism Case Reports Volume 2018 Issue 1 (2018)
Prenatal diagnosis of HNF1B‐associated renal cysts: Is there a need to differentiate intragenic variants from 17q12 microdeletion syndrome? - Vasileiou - 2019 - Prenatal Diagnosis - Wiley Online Library
Genetische Defekte der Betazellfunktion - MODY-Diabetes
Renal Cysts and Diabetes: Int'l Textbook of Diabetes Mellitus, Ex.156
