Pages that link to "Q37821513"

The following pages link to Systematic review of TCF2 anomalies in renal cysts and diabetes syndrome/maturity onset diabetes of the young type 5. (Q37821513):

Displaying 27 items.

• Maturity-Onset Diabetes of the Young: What Do Clinicians Need to Know? (Q26771916) (← links)
• HNF1β is essential for nephron segmentation during nephrogenesis (Q30415639) (← links)
• Exploring the genetic basis of early-onset chronic kidney disease (Q34508359) (← links)
• Identification and Functional Characterization of P159L Mutation in HNF1B in a Family with Maturity-Onset Diabetes of the Young 5 (MODY5) (Q35088721) (← links)
• Hepatic phenotypes of HNF1B gene mutations: a case of neonatal cholestasis requiring portoenterostomy and literature review (Q35128278) (← links)
• Hnf1b controls pancreas morphogenesis and the generation of Ngn3+ endocrine progenitors (Q35157481) (← links)
• A novel mutation of the HNF1B gene associated with hypoplastic glomerulocystic kidney disease and neonatal renal failure: a case report and mutation update (Q36009572) (← links)
• Hepatocyte Nuclear Factor 1β-Associated Kidney Disease: More than Renal Cysts and Diabetes. (Q36514988) (← links)
• When to consider a diagnosis of MODY at the presentation of diabetes: aetiology matters for correct management (Q36912662) (← links)
• Monogenic Diabetes: What It Teaches Us on the Common Forms of Type 1 and Type 2 Diabetes (Q36960085) (← links)
• Chromosome 17q12 microdeletions but not intragenic HNF1B mutations link developmental kidney disease and psychiatric disorder (Q37026249) (← links)
• Pancreatic developmental defect evaluated by celiac artery angiography in a patient with MODY5. (Q37092762) (← links)
• HNF1B-associated renal and extra-renal disease-an expanding clinical spectrum. (Q38299096) (← links)
• HNF1B-associated clinical phenotypes: the kidney and beyond (Q38544627) (← links)
• Liver involvement in kidney disease and vice versa. (Q39395392) (← links)
• A Single Nucleotide Variant in HNF-1β is Associated with Maturity-Onset Diabetes of the Young in a Large Chinese Family (Q40525737) (← links)
• Long-lasting response to oral therapy in a young male with monogenic diabetes as part of HNF1B-related disease (Q41018980) (← links)
• A novel mutation in the hepatocyte nuclear factor-1β gene in maturity onset diabetes of the young 5 with multiple renal cysts and pancreas hypogenesis: A case report (Q41623705) (← links)
• Maturity-onset diabetes of the young (MODY) as a model for elucidating the multifactorial origin of type 2 diabetes mellitus (Q50182672) (← links)
• Assessment of the HNF1B Score as a Tool to Select Patients for HNF1B Genetic Testing. (Q54916334) (← links)
• Primary male factor infertility due to asthenospermia in maturity-onset diabetes of the young type 5 (MODY 5): uncommon presentation of an uncommon disease (Q88159901) (← links)
• Genome-wide methylomic analysis in individuals with HNF1B intragenic mutation and 17q12 microdeletion (Q90319801) (← links)
• Identifying gene mutations of Chinese patients with polycystic kidney disease through targeted next-generation sequencing technology (Q91773359) (← links)
• Pancreatic Ductal Deletion of Hnf1b Disrupts Exocrine Homeostasis, Leads to Pancreatitis, and Facilitates Tumorigenesis (Q92959992) (← links)
• Variable phenotype in HNF1B mutations: extrarenal manifestations distinguish affected individuals from the population with congenital anomalies of the kidney and urinary tract (Q95728545) (← links)
• Genetics and Pathophysiology of Maturity-onset Diabetes of the Young (MODY): A Review of Current Trends (Q96136733) (← links)
• A novel HNF1B mutation p.R177Q in autosomal dominant tubulointerstitial kidney disease and maturity-onset diabetes of the young type 5: A pedigree-based case report (Q98210361) (← links)