| scholarly article | Q13442814 |
| P356 | DOI | 10.1111/J.1464-5491.2008.02460.X |
| P698 | PubMed publication ID | 18644064 |
| P50 | author | Ingfrid S Haldorsen | Q30512739 |
| Anders Molven | Q41520946 | ||
| Pål R Njølstad | Q43236392 | ||
| Oddmund Søvik | Q99672682 | ||
| P2093 | author name string | M Vesterhus | |
| D K Jensen | |||
| H Raeder | |||
| P433 | issue | 7 | |
| P304 | page(s) | 782-787 | |
| P577 | publication date | 2008-07-01 | |
| P1433 | published in | Diabetic Medicine | Q15758639 |
| P1476 | title | Lack of pancreatic body and tail in HNF1B mutation carriers | |
| P478 | volume | 25 |
| Q33734037 | Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes |
| Q54916334 | Assessment of the HNF1B Score as a Tool to Select Patients for HNF1B Genetic Testing. |
| Q36746976 | Assignment of Functional Relevance to Genes at Type 2 Diabetes-Associated Loci Through Investigation of β-Cell Mass Deficits |
| Q37026249 | Chromosome 17q12 microdeletions but not intragenic HNF1B mutations link developmental kidney disease and psychiatric disorder |
| Q38808702 | Common and rare forms of diabetes mellitus: towards a continuum of diabetes subtypes |
| Q36678758 | Early Developmental Perturbations in a Human Stem Cell Model of MODY5/HNF1B Pancreatic Hypoplasia |
| Q57646454 | Exocrine pancreatic dysfunction is common in hepatocyte nuclear factor 1β-associated renal disease and can be symptomatic |
| Q37793985 | From Genetic Association to Molecular Mechanism |
| Q90319801 | Genome-wide methylomic analysis in individuals with HNF1B intragenic mutation and 17q12 microdeletion |
| Q38544627 | HNF1B-associated clinical phenotypes: the kidney and beyond |
| Q38299096 | HNF1B-associated renal and extra-renal disease-an expanding clinical spectrum. |
| Q47823023 | Hepatocyte Nuclear Factor-1β Controls Mitochondrial Respiration in Renal Tubular Cells. |
| Q35157481 | Hnf1b controls pancreas morphogenesis and the generation of Ngn3+ endocrine progenitors |
| Q37242220 | Investigating maturity onset diabetes of the young. |
| Q90676502 | Investigation of HNF-1B as a diagnostic biomarker for pancreatic ductal adenocarcinoma |
| Q38701408 | Loss of transcriptional activation of the potassium channel Kir5.1 by HNF1β drives autosomal dominant tubulointerstitial kidney disease. |
| Q33622236 | Many faces of monogenic diabetes |
| Q36960085 | Monogenic Diabetes: What It Teaches Us on the Common Forms of Type 1 and Type 2 Diabetes |
| Q27013756 | Neonatal diabetes: an expanding list of genes allows for improved diagnosis and treatment |
| Q42402538 | Neurological features and enzyme therapy in patients with endocrine and exocrine pancreas dysfunction due to CEL mutations |
| Q26995562 | New opportunities: harnessing induced pluripotency for discovery in diabetes and metabolism |
| Q42637088 | Sonographic features of agenesis of dorsal pancreas |
| Q34158320 | TCF2 attenuates FFA-induced damage in islet β-cells by regulating production of insulin and ROS. |
| Q38217616 | The HNF1B score is a simple tool to select patients for HNF1B gene analysis |
| Q37962349 | The role of pancreatic imaging in monogenic diabetes mellitus |
| Q91605783 | Two cases of agenesis of the dorsal pancreas and a review of the literature |
| Q63682146 | Urinary proteome signature of Renal Cysts and Diabetes syndrome in children |
| Q37413302 | Variation in HNF1B and Obesity May Influence Prostate Cancer Risk in African American Men: A Pilot Study. |
Search more.