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T Tuomi

Showing results (131-140 of 137) with videos related to

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Nature Genetics|September 6, 2000
The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetesD Altshuler, J N Hirschhorn, M Klannemark, et al.
American Journal of Human Genetics|January 16, 2002
Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia studyC M Lindgren, M M Mahtani, E Widén, et al.
The Journal of Clinical Investigation|February 15, 1997
Characterization of the MODY3 phenotype. Early-onset diabetes caused by an insulin secretion defectM Lehto, T Tuomi, M M Mahtani, et al.
Diabetes|June 1, 1997
Novel mutations and a mutational hotspot in the MODY3 geneM A Glucksmann, M Lehto, O Tayber, et al.
Diabetologia|August 5, 2011
A large multi-centre European study validates high-sensitivity C-reactive protein (hsCRP) as a clinical biomarker for the diagnosis of diabetes subtypesG Thanabalasingham, N Shah, M Vaxillaire, et al.
Nature Metabolism|October 17, 2024
Genetic architecture of oral glucose-stimulated insulin release provides biological insights into type 2 diabetes aetiologyA L Madsen, S Bonàs-Guarch, S Gheibi, et al.
Diabetologia|November 20, 2012
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypesA Albrechtsen, N Grarup, Y Li, et al.
Pageof 14

Showing results (131-140 of 137) with videos related to

Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 137 results.
Nature Genetics|September 6, 2000
The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetesD Altshuler, J N Hirschhorn, M Klannemark, et al.
American Journal of Human Genetics|January 16, 2002
Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia studyC M Lindgren, M M Mahtani, E Widén, et al.
The Journal of Clinical Investigation|February 15, 1997
Characterization of the MODY3 phenotype. Early-onset diabetes caused by an insulin secretion defectM Lehto, T Tuomi, M M Mahtani, et al.
Diabetes|June 1, 1997
Novel mutations and a mutational hotspot in the MODY3 geneM A Glucksmann, M Lehto, O Tayber, et al.
Diabetologia|August 5, 2011
A large multi-centre European study validates high-sensitivity C-reactive protein (hsCRP) as a clinical biomarker for the diagnosis of diabetes subtypesG Thanabalasingham, N Shah, M Vaxillaire, et al.
Nature Metabolism|October 17, 2024
Genetic architecture of oral glucose-stimulated insulin release provides biological insights into type 2 diabetes aetiologyA L Madsen, S Bonàs-Guarch, S Gheibi, et al.
Diabetologia|November 20, 2012
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypesA Albrechtsen, N Grarup, Y Li, et al.
Pageof 14