ADTKD-HNF1B (renal cyst and diabetes syndrome) in a 35 year-old female.... | Download Scientific Diagram
Analysis of expression, epigenetic, and genetic changes of HNF1B in 130 kidney tumours | Scientific Reports
Common Genetic Variants in the Hnf1b Gene Contribute to Diabetes and Multiple Cancers
HNF1B sequencing and genetic analysis of the patient's family. (A)... | Download Scientific Diagram
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)
Screening for HNF1B Gene Mutations, in Four People with Typical Diabetes MODY5 Clinical Characteristics
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
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Renal Cysts and Diabetes: Int'l Textbook of Diabetes Mellitus, Ex.156
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Modeling HNF1B-associated monogenic diabetes using human iPSCs reveals an early stage impairment of the pancreatic developmental program - ScienceDirect
Phenotypes seen in diabetes with extra-pancreatic features. (A) Renal... | Download Scientific Diagram
Variable Expressivity of HNF1B Nephropathy, From Renal Cysts and Diabetes to Medullary Sponge Kidney Through Tubulo-interstitial Kidney Disease - ScienceDirect
Genomics & Informatics
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
HNF1B-associated renal and extra-renal disease—an expanding clinical spectrum | Nature Reviews Nephrology
Cells | Free Full-Text | The Landscape of HNF1B Deficiency: A Syndrome Not Yet Fully Explored
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
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)
Variable Expressivity of HNF1B Nephropathy, From Renal Cysts and Diabetes to Medullary Sponge Kidney Through Tubulo-interstitial
Maturity-Onset Diabetes of the Young (MODY) - ppt video online download
Endocrines | Free Full-Text | Maturity-Onset Diabetes of the Young (MODY): Genetic Causes, Clinical Characteristics, Considerations for Testing, and Treatment Options
HNF1B - Wikipedia
