Found: 118
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Tooth mortality and endodontic status of a selected population group. Observations before and after treatment.
- Published in:
- 1976
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- Publication type:
- journal article
The apical level of root fillings.
- Published in:
- 1976
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- Publication type:
- journal article
MC1R, ASIP, TYR, and TYRP1 gene variants in a population-based series of multiple primary melanomas.
- Published in:
- Genes, Chromosomes & Cancer, 2012, v. 51, n. 7, p. 654, doi. 10.1002/gcc.21952
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- Publication type:
- Article
Population-based prevalence of CDKN2A and CDK4 mutations in patients with multiple primary melanomas.
- Published in:
- Genes, Chromosomes & Cancer, 2008, v. 47, n. 2, p. 175, doi. 10.1002/gcc.20518
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- Publication type:
- Article
Characterisation of HNF1A variants in paediatric diabetes in Norway using functional and clinical investigations to unmask phenotype and monogenic diabetes.
- Published in:
- Diabetologia, 2023, v. 66, n. 12, p. 2226, doi. 10.1007/s00125-023-06012-4
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- Publication type:
- Article
Targeted next-generation sequencing reveals MODY in up to 6.5% of antibody-negative diabetes cases listed in the Norwegian Childhood Diabetes Registry.
- Published in:
- Diabetologia, 2017, v. 60, n. 4, p. 625, doi. 10.1007/s00125-016-4167-1
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- Publication type:
- Article
Heterogeneity of proliferative markers in pancreatic β-cells of patients with severe hypoglycemia following Roux-en-Y gastric bypass.
- Published in:
- Acta Diabetologica, 2017, v. 54, n. 8, p. 737, doi. 10.1007/s00592-017-1001-2
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- Publication type:
- Article
Mutations in the VNTR of the carboxyl-ester lipase gene ( CEL) are a rare cause of monogenic diabetes.
- Published in:
- Human Genetics, 2010, v. 127, n. 1, p. 55, doi. 10.1007/s00439-009-0740-8
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- Publication type:
- Article
Pathogenic Carboxyl Ester Lipase (CEL) Variants Interact with the Normal CEL Protein in Pancreatic Cells.
- Published in:
- Cells (2073-4409), 2020, v. 9, n. 1, p. 1, doi. 10.3390/cells9010244
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- Publication type:
- Article
Exocrine pancreatic function in hepatocyte nuclear factor 1β-maturity-onset diabetes of the young ( HNF1B- MODY) is only moderately reduced: compensatory hypersecretion from a hypoplastic pancreas.
- Published in:
- 2013
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- Publication type:
- Journal Article
Exocrine pancreatic function in hepatocyte nuclear factor 1β-maturity-onset diabetes of the young ( HNF1B- MODY) is only moderately reduced: compensatory hypersecretion from a hypoplastic pancreas.
- Published in:
- Diabetic Medicine, 2013, v. 30, n. 8, p. 946, doi. 10.1111/dme.12190
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- Publication type:
- Article
Prevalence of HNF1A (MODY3) mutations in a Norwegian population (the HUNT2 Study)
- Published in:
- 2008
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- Publication type:
- Journal Article
Prevalence of HNF1A (MODY3) mutations in a Norwegian population (the HUNT2 Study).
- Published in:
- Diabetic Medicine, 2008, v. 25, n. 7, p. 775, doi. 10.1111/j.1464-5491.2008.02459.x
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- Publication type:
- Article
Lack of pancreatic body and tail in HNF1B mutation carriers.
- Published in:
- Diabetic Medicine, 2008, v. 25, n. 7, p. 782, doi. 10.1111/j.1464-5491.2008.02460.x
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- Publication type:
- Article
Diagnostic screening of NEUROD1 (MODY6) in subjects with MODY or gestational diabetes mellitus.
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- Diabetic Medicine, 2005, v. 22, n. 8, p. 1012, doi. 10.1111/j.1464-5491.2005.01565.x
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- Publication type:
- Article
Molecular analysis of the PI3K-AKT pathway in uterine cervical neoplasia: Frequent PIK3CA amplification and AKT phosphorylation.
- Published in:
- International Journal of Cancer, 2006, v. 118, n. 8, p. 1877, doi. 10.1002/ijc.21461
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- Publication type:
- Article
A comparison of the dentin-removing ability of five root canal instruments.
- Published in:
- European Journal of Oral Sciences, 1970, v. 78, n. 1-4, p. 500, doi. 10.1111/j.1600-0722.1970.tb02103.x
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- Publication type:
- Article
Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy.
- Published in:
- 2004
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- Publication type:
- journal article
Permanent Neonatal Diabetes due to Mutations in KCNJ11Encoding Kir6.2.
- Published in:
- Diabetes, 2004, v. 53, n. 10, p. 2713, doi. 10.2337/diabetes.53.10.2713
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- Publication type:
- Article
Familial hyperinsulinemic hypoglycemia caused by a defect in the SCHAD enzyme of mitochondrial fatty acid oxidation.
- Published in:
- 2004
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- Publication type:
- journal article
Permanent Neonatal Diabetes Caused by Glucokinase Deficiency.
- Published in:
- Diabetes, 2003, v. 52, n. 11, p. 2854, doi. 10.2337/diabetes.52.11.2854
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- Publication type:
- Article
Permanent neonatal diabetes caused by glucokinase deficiency: inborn error of the glucose-insulin signaling pathway.
- Published in:
- 2003
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- Publication type:
- journal article
Disease progression and search for monogenic diabetes among children with new onset type 1 diabetes negative for ICA, GAD- and IA-2Antibodies.
- Published in:
- BMC Endocrine Disorders, 2010, v. 10, p. 16, doi. 10.1186/1472-6823-10-16
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- Publication type:
- Article
Assessment of exocrine pancreatic function by secretin-stimulated magnetic resonance cholangiopancreaticography and diffusion-weighted imaging in healthy controls.
- Published in:
- Journal of Magnetic Resonance Imaging, 2014, v. 39, n. 2, p. 448, doi. 10.1002/jmri.24167
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- Publication type:
- Article
Author Correction: Telomere length and survival in primary cutaneous melanoma patients.
- Published in:
- 2018
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- Publication type:
- Correction Notice
83-OR: Pancreatic Exocrine to Endocrine Cell Cross Talk Mediates Endoplasmic Reticulum Stress and Beta-Cell Dysfunction in MODY8.
- Published in:
- Diabetes, 2020, v. 69, p. N.PAG, doi. 10.2337/db20-83-OR
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- Publication type:
- Article
Mice Carrying a Dominant-Negative Human PI3K Mutation Are Protected From Obesity and Hepatic Steatosis but Not Diabetes.
- Published in:
- 2018
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- Publication type:
- journal article
Functional Investigations of HNF1A Identify Rare Variants as Risk Factors for Type 2 Diabetes in the General Population.
- Published in:
- 2017
- By:
- Publication type:
- journal article
The Hypoglycemic Phenotype Is Islet Cell-Autonomous in Short-Chain Hydroxyacyl-CoA Dehydrogenase-Deficient Mice.
- Published in:
- 2016
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- Publication type:
- journal article
Carboxyl-Ester Lipase Maturity-Onset Diabetes of the Young Is Associated With Development of Pancreatic Cysts and Upregulated MAPK Signaling in Secretin-Stimulated Duodenal Fluid.
- Published in:
- Diabetes, 2014, v. 63, n. 1, p. 259, doi. 10.2337/db13-1012
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- Publication type:
- Article
FTO, Type 2 Diabetes, and Weight Gain Throughout Adult Life.
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- Diabetes, 2011, v. 60, n. 5, p. 1637, doi. 10.2337/db10-1340
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- Publication type:
- Article
FTO, type 2 diabetes, and weight gain throughout adult life: a meta-analysis of 41,504 subjects from the Scandinavian HUNT, MDC, and MPP studies.
- Published in:
- 2011
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- Publication type:
- journal article
Polygenic Risk Variants for Type 2 Diabetes Susceptibility Modify Age at Diagnosis in Monogenic HNF1A Diabetes.
- Published in:
- Diabetes, 2010, v. 59, n. 1, p. 266, doi. 10.2337/db09-0555
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- Publication type:
- Article
Mutations in the Insulin Gene Can Cause MODY and Autoantibody-Negative Type 1 Diabetes.
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- Diabetes, 2008, v. 57, n. 4, p. 1131, doi. 10.2337/db07-1467
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- Publication type:
- Article
Studies in 3,523 Norwegians and meta-analysis in 11,571 subjects indicate that variants in the hepatocyte nuclear factor 4 alpha (HNF4A) P2 region are associated with type 2 diabetes in Scandinavians.
- Published in:
- 2007
- By:
- Publication type:
- Journal Article
Studies in 3,523 Norwegians and Meta-Analysis in 11,571 Subjects Indicate That Variants in the Hepatocyte Nuclear Factor 4α (HNF4A) P2 Region Are Associated With Type 2 Diabetes in Scandinavians.
- Published in:
- Diabetes, 2007, v. 56, n. 12, p. 3112, doi. 10.2337/db07-0513
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- Publication type:
- Article
Pancreatic Lipomatosis Is a Structural Marker in Nondiabetic Children With Mutations in Carboxyl-Ester Lipase.
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- Diabetes, 2007, v. 56, n. 2, p. 444, doi. 10.2337/db06-0859
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- Publication type:
- Article
A hepatocyte nuclear factor-4alpha gene (HNF4A) P2 promoter haplotype linked with late-onset diabetes: studies of HNF4A variants in the Norwegian MODY Registry.
- Published in:
- 2006
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- Publication type:
- Journal Article
A Hepatocyte Nuclear Factor-4α Gene (HNF4A) P2 Promoter Haplotype Linked With Late-Onset Diabetes.
- Published in:
- Diabetes, 2006, v. 55, n. 6, p. 1899, doi. 10.2337/db05-1677
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- Publication type:
- Article
From Clinicogenetic Studies of Maturity-Onset Diabetes of the Young to Unraveling Complex Mechanisms of Glucokinase Regulation.
- Published in:
- Diabetes, 2006, v. 55, n. 6, p. 1713, doi. 10.2337/db05-1513
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- Publication type:
- Article
A large Norwegian family with inherited malignant melanoma, multiple atypical nevi, and CDK4 mutation.
- Published in:
- Genes, Chromosomes & Cancer, 2005, v. 44, n. 1, p. 10, doi. 10.1002/gcc.20202
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- Publication type:
- Article
BUILDING A PATIENT OMBUDSMAN SCHEME: THE NORWEGIAN EXPERIENCE.
- Published in:
- Medicine & Law (World Association for Medical Law), 2012, v. 31, n. 1, p. 57
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- Publication type:
- Article
Root resorption and apical breakdown during orthodontic treatment of a maxillary lateral incisor with dens invaginatus.
- Published in:
- Dental Traumatology, 1998, v. 14, n. 5, p. 241, doi. 10.1111/j.1600-9657.1998.tb00847.x
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- Publication type:
- Article
Follow-up after periapical surgery: the value of the one-year control.
- Published in:
- Dental Traumatology, 1991, v. 7, n. 6, p. 246, doi. 10.1111/j.1600-9657.1991.tb00211.x
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- Publication type:
- Article
Scanning electron microscopy of bacteria in the apical part of root canals in permanent teeth with periapical lesions.
- Published in:
- Dental Traumatology, 1991, v. 7, n. 5, p. 226, doi. 10.1111/j.1600-9657.1991.tb00441.x
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- Publication type:
- Article
BRAF and NRAS Mutations Are Frequent in Nodular Melanoma but Are not Associated with Tumor Cell Proliferation or Patient Survival.
- Published in:
- Journal of Investigative Dermatology, 2005, v. 125, n. 2, p. 312, doi. 10.1111/j.0022-202X.2005.23788.x
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- Publication type:
- Article
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma.
- Published in:
- Nature Genetics, 2015, v. 47, n. 9, p. 987, doi. 10.1038/ng.3373
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- Publication type:
- Article
A recombined allele of the lipase gene CEL and its pseudogene CELP confers susceptibility to chronic pancreatitis.
- Published in:
- Nature Genetics, 2015, v. 47, n. 5, p. 518, doi. 10.1038/ng.3249
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- Publication type:
- Article
Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes.
- Published in:
- Nature Genetics, 2013, v. 45, n. 11, p. 1380, doi. 10.1038/ng.2794
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- Publication type:
- Article
Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction.
- Published in:
- Nature Genetics, 2006, v. 38, n. 1, p. 54, doi. 10.1038/ng1708
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- Publication type:
- Article