Lehto M - Search Results

1

Genetic factors affect the susceptibility to bacterial infections in diabetes.

Simonsen JR, Käräjämäki A, Antikainen AA, Toppila I, Ahlqvist E, Prasad R, Mansour-Aly D, Harjutsalo V, Järvinen A, Tuomi T, Groop L, Forsblom C, Groop PH, Sandholm N, Lehto M. Simonsen JR, et al. Among authors: lehto m. Sci Rep. 2021 May 4;11(1):9464. doi: 10.1038/s41598-021-88273-w. Sci Rep. 2021. PMID: 33947878 Free PMC article.

2

Association of a polymorphism in the beta 3-adrenergic-receptor gene with features of the insulin resistance syndrome in Finns.

Widén E, Lehto M, Kanninen T, Walston J, Shuldiner AR, Groop LC. Widén E, et al. Among authors: lehto m. N Engl J Med. 1995 Aug 10;333(6):348-51. doi: 10.1056/NEJM199508103330604. N Engl J Med. 1995. PMID: 7609751 Free article.

3

Polymorphism of the glycogen synthase gene in hypertensive and normotensive subjects.

Schalin-Jäntti C, Nikula-Ijäs P, Huang X, Lehto M, Knudsen P, Syvänne M, Lehtovirta MT, Tikkanen T, Tikkanen I, Groop LC. Schalin-Jäntti C, et al. Among authors: lehto m. Hypertension. 1996 Jan;27(1):67-71. doi: 10.1161/01.hyp.27.1.67. Hypertension. 1996. PMID: 8591890

4

Lack of association between the Gly40Ser polymorphism in the glucagon receptor gene and NIDDM in Finland.

Huang X, Orho M, Lehto M, Groop L. Huang X, et al. Among authors: lehto m. Diabetologia. 1995 Oct;38(10):1246-8. doi: 10.1007/BF00422376. Diabetologia. 1995. PMID: 8690179

5

Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families.

Mahtani MM, Widén E, Lehto M, Thomas J, McCarthy M, Brayer J, Bryant B, Chan G, Daly M, Forsblom C, Kanninen T, Kirby A, Kruglyak L, Munnelly K, Parkkonen M, Reeve-Daly MP, Weaver A, Brettin T, Duyk G, Lander ES, Groop LC. Mahtani MM, et al. Among authors: lehto m. Nat Genet. 1996 Sep;14(1):90-4. doi: 10.1038/ng0996-90. Nat Genet. 1996. PMID: 8782826

6

Human hexokinase II gene: exon-intron organization, mutation screening in NIDDM, and its relationship to muscle hexokinase activity.

Lehto M, Huang X, Davis EM, Le Beau MM, Laurila E, Eriksson KF, Bell GI, Groop L. Lehto M, et al. Diabetologia. 1995 Dec;38(12):1466-74. doi: 10.1007/BF00400608. Diabetologia. 1995. PMID: 8786021

7

Characterization of the MODY3 phenotype. Early-onset diabetes caused by an insulin secretion defect.

Lehto M, Tuomi T, Mahtani MM, Widén E, Forsblom C, Sarelin L, Gullström M, Isomaa B, Lehtovirta M, Hyrkkö A, Kanninen T, Orho M, Manley S, Turner RC, Brettin T, Kirby A, Thomas J, Duyk G, Lander E, Taskinen MR, Groop L. Lehto M, et al. J Clin Invest. 1997 Feb 15;99(4):582-91. doi: 10.1172/JCI119199. J Clin Invest. 1997. PMID: 9045858 Free PMC article.

8

Chronic diabetic complications in patients with MODY3 diabetes.

Isomaa B, Henricsson M, Lehto M, Forsblom C, Karanko S, Sarelin L, Häggblom M, Groop L. Isomaa B, et al. Among authors: lehto m. Diabetologia. 1998 Apr;41(4):467-73. doi: 10.1007/s001250050931. Diabetologia. 1998. PMID: 9562352

9

Mutation in the HNF-4alpha gene affects insulin secretion and triglyceride metabolism.

Lehto M, Bitzén PO, Isomaa B, Wipemo C, Wessman Y, Forsblom C, Tuomi T, Taskinen MR, Groop L. Lehto M, et al. Diabetes. 1999 Feb;48(2):423-5. doi: 10.2337/diabetes.48.2.423. Diabetes. 1999. PMID: 10334325 No abstract available.

10

High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes.

Lehto M, Wipemo C, Ivarsson SA, Lindgren C, Lipsanen-Nyman M, Weng J, Wibell L, Widén E, Tuomi T, Groop L. Lehto M, et al. Diabetologia. 1999 Sep;42(9):1131-7. doi: 10.1007/s001250051281. Diabetologia. 1999. PMID: 10447526

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