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1A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY
المؤلفون: Kettunen, Jarno L.T., Rantala, Elina, Dwivedi, Om P., Isomaa, Bo, Sarelin, Leena, Kokko, Paula, Hakaste, Liisa, Miettinen, Päivi J., Groop, Leif C., Tuomi, Tiinamaija
المصدر: Diabetologia EXODIAB: Excellence of Diabetes Research in Sweden. 65(4):632-643
مصطلحات موضوعية: Age at onset, Glucagon, HNF1A-MODY, Insulin deficiency, Lipolysis, Maturity-onset diabetes of the young (MODY), MODY3, Monogenic diabetes, NEFA, Polygenic risk score for type 2 diabetes, Medicin och hälsovetenskap, Klinisk medicin, Endokrinologi och diabetes, Medical and Health Sciences, Clinical Medicine, Endocrinology and Diabetes
الوصول الحر: https://lup.lub.lu.se/record/90d7e8d1-66fa-4bd6-80ec-08f40a56d076Test
http://dx.doi.org/10.1007/s00125-021-05631-zTest -
2دورية أكاديميةA multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY
المؤلفون: Kettunen, Jarno L. T., Rantala, Elina, Dwivedi, Om P., Isomaa, Bo, Sarelin, Leena, Kokko, Paula, Hakaste, Liisa, Miettinen, Päivi J., Groop, Leif C., Tuomi, Tiinamaija
المساهمون: Institute for Molecular Medicine Finland, HUS Abdominal Center, Endokrinologian yksikkö, CAMM - Research Program for Clinical and Molecular Metabolism, HUS Children and Adolescents, Clinicum, Research Programs Unit, Children's Hospital, STEMM - Stem Cells and Metabolism Research Program, Department of Medicine
مصطلحات موضوعية: Age at onset, Glucagon, HNF1A-MODY, Insulin deficiency, Lipolysis, Maturity-onset diabetes of the young (MODY), MODY3, Monogenic diabetes, NEFA, Polygenic risk score for type 2 diabetes, HEPATIC NUCLEAR FACTOR-1-ALPHA, HOMEOSTASIS MODEL ASSESSMENT, INSULIN SENSITIVITY, CELL DYSFUNCTION, ALPHA-GENE, YOUNG MODY, C-PEPTIDE, ONSET, GLUCOSE, MUTATION, Biomedicine
وصف الملف: application/pdf
العلاقة: Open Access funding provided by University of Helsinki including Helsinki University Central Hospital. The Botnia, FINNMODY and PPP-Botnia studies have been financially supported by grants from Folkhalsan Research Foundation, the Sigrid Juselius Foundation, the Academy of Finland (grants no. 263401, 267882, 312063, 336822 to LCG; 312072 and 336826 to TT), the University of Helsinki, the Nordic Center of Excellence in Disease Genetics, the EU (EXGENESIS, MOSAIC FP7-600914), the Ollqvist Foundation, the Swedish Cultural Foundation in Finland, the Finnish Diabetes Research Foundation, the Foundation for Life and Health in Finland, the Signe and Ane Gyllenberg Foundation, the Finnish Medical Society, the Paavo Nurmi Foundation, State Research Funding via the Helsinki University Hospital, the Perklen Foundation, Narpes Health Care Foundation and the Ahokas Foundation. These studies have also been supported by the Ministry of Education in Finland, the Municipal Health Care Center and Hospital in Jakobstad, and Health Care Centers in Vasa, Narpes and Korsholm.; Kettunen , J L T , Rantala , E , Dwivedi , O P , Isomaa , B , Sarelin , L , Kokko , P , Hakaste , L , Miettinen , P J , Groop , L C & Tuomi , T 2022 , ' A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY ' , Diabetologia , vol. 65 , no. 4 , pp. 632–643 . https://doi.org/10.1007/s00125-021-05631-zTest; ORCID: /0000-0002-8306-6202/work/111173625; ORCID: /0000-0002-5184-9616/work/111175276; ORCID: /0000-0002-9995-698X/work/111175325; http://hdl.handle.net/10138/342495Test; 8c98c354-c157-42e1-b5a3-4d2086a40533; 000734005000001