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HNF1B
Publication
Class
Person
Publication
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publication
Liver, kidneys and diabetes: three faces of HNF1B gene deficit
2014 |
Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
publication
HNF1B nephropathy has a slow-progressive phenotype in childhood-with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood Registry
2019 |
Second Faculty of Medicine
publication
The Role of HNF1B in Tumorigenesis of Solid Tumours: a Review of Current Knowledge
2018 |
First Faculty of Medicine
publication
Next-Generation Sequencing Approach in Methylation Analysis of HNF1B and GATA4 Genes: Searching for Biomarkers in Ovarian Cancer
2017 |
Faculty of Medicine in Hradec Králové
publication
Comprehensive quantitative analysis of alternative splicing variants reveals the HNF1B mRNA splicing pattern in various tumour and non-tumour tissues
2022 |
First Faculty of Medicine
publication
First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B
2022 |
Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
publication
Analysis of expression, epigenetic, and genetic changes of HNF1B in 130 kidney tumours
2020 |
First Faculty of Medicine
publication
Expression, Epigenetic, and Genetic Changes of HNF1B in Colorectal Lesions: an Analysis of 145 Cases
2020 |
First Faculty of Medicine, Faculty of Physical Education and Sport
publication
HNF1B, EZH2 and ECI2 in prostate carcinoma. Molecular, immunohistochemical and clinico-pathological study
2020 |
First Faculty of Medicine
publication
Hepatic phenotypes of HNF1B gene mutations: A case of neonatal cholestasis requiring portoenterostomy and literature review
2015 |
Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
publication
Identification of novel HNF1B mRNA splicing variants and their qualitative and semi-quantitative profile in selected healthy and tumour tissues
2020 |
First Faculty of Medicine
publication
Expression, Epigenetic and Genetic Changes of HNF1B in Endometrial Lesions
2016 |
First Faculty of Medicine, Faculty of Physical Education and Sport
publication
A comprehensive analysis of the expression, epigenetic and genetic changes of HNF1B and ECI2 in 122 cases of high-grade serous ovarian carcinoma
2021 |
First Faculty of Medicine
publication
Choledochal Cyst with 17q12 Chromosomal Duplication
2018 |
Second Faculty of Medicine
publication
Lessons from whole-exome sequencing in MODYX families
2014 |
Second Faculty of Medicine
publication
Blood pressure in children with renal cysts and diabetes syndrome
2021 |
Second Faculty of Medicine
publication
Renal cysts and diabetes syndrome
2015 |
Second Faculty of Medicine
publication
Autosomal dominant tubulointerstitial kidney disease
2019 |
First Faculty of Medicine
publication
MODY diabetes: what should we know for proper diagnostics and treatment?
2012 |
Second Faculty of Medicine
publication
Hepatocyte nuclear factors and diabetes mellitus
2017 |
Third Faculty of Medicine
publication
Lack of PAX4 mutations in 53 Czech MODYX families
2010 |
Second Faculty of Medicine
publication
A case of digenic maturity onset diabetes of the young with heterozygous variants in both HNF1Α and HNF1Β genes
2021 |
Second Faculty of Medicine
publication
Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer
2018 |
Second Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management-A KDIGO consensus report
2015 |
First Faculty of Medicine
publication
MODY in Ukraine: genes, clinical phenotypes and treatment
2017 |
Second Faculty of Medicine
publication
Autosomal dominant tubulointerstitial kidney disease (ADTKD) in Ireland
2019 |
First Faculty of Medicine
publication
Identification of a four-gene methylation biomarker panel in high-grade serous ovarian carcinoma
2020 |
Faculty of Medicine in Hradec Králové
publication
Results of targeted next-generation sequencing in children with cystic kidney diseases often change the clinical diagnosis
2020 |
Second Faculty of Medicine, First Faculty of Medicine
publication
A comprehensive immunohistochemical analysis of 26 markers in 250 cases of serous ovarian tumors
2023 |
Second Faculty of Medicine, First Faculty of Medicine, Faculty of Medicine in Hradec Králové, Third Faculty of Medicine