Wessman M - Search Results

1

Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effect.

Bachinski LL, Udd B, Meola G, Sansone V, Bassez G, Eymard B, Thornton CA, Moxley RT, Harper PS, Rogers MT, Jurkat-Rott K, Lehmann-Horn F, Wieser T, Gamez J, Navarro C, Bottani A, Kohler A, Shriver MD, Sallinen R, Wessman M, Zhang S, Wright FA, Krahe R. Bachinski LL, et al. Among authors: wessman m. Am J Hum Genet. 2003 Oct;73(4):835-48. doi: 10.1086/378566. Epub 2003 Sep 10. Am J Hum Genet. 2003. PMID: 12970845 Free PMC article.

2

Assignment of laminin alpha 2-chain gene (Lama2) to mouse chromosome 10A4-B1 by fluorescence in situ hybridization.

Sallinen R, Kuang W, Engvall E, Palotie A, Wessman M, Horelli-Kuitunen N. Sallinen R, et al. Among authors: wessman m. Cytogenet Cell Genet. 1999;87(3-4):195-6. doi: 10.1159/000015464. Cytogenet Cell Genet. 1999. PMID: 10702665 No abstract available.

3

Assignment of a novel locus for autosomal recessive congenital ichthyosis to chromosome 19p13.1-p13.2.

Virolainen E, Wessman M, Hovatta I, Niemi KM, Ignatius J, Kere J, Peltonen L, Palotie A. Virolainen E, et al. Among authors: wessman m. Am J Hum Genet. 2000 Mar;66(3):1132-7. doi: 10.1086/302813. Am J Hum Genet. 2000. PMID: 10712223 Free PMC article.

4

Fine mapping of Hyplip1 and the human homolog, a potential locus for FCHL.

Pajukanta P, Bodnar JS, Sallinen R, Chu M, Airaksinen T, Xiao Q, Castellani LW, Sheth SS, Wessman M, Palotie A, Sinsheimer JS, Demant P, Lusis AJ, Peltonen L. Pajukanta P, et al. Among authors: wessman m. Mamm Genome. 2001 Mar;12(3):238-45. doi: 10.1007/s003350010265. Mamm Genome. 2001. PMID: 11252174

5

Physical mapping of mouse collagen genes on chromosome 10 by high-resolution FISH.

Sallinen R, Latvanlehto A, Kvist AP, Rehn M, Eerola I, Chu ML, Bonaldo P, Saitta B, Bressan GM, Pihlajaniemi T, Vuorio E, Palotie A, Wessman M, Horelli-Kuitunen N. Sallinen R, et al. Among authors: wessman m. Mamm Genome. 2001 May;12(5):340-6. doi: 10.1007/s003350010271. Mamm Genome. 2001. PMID: 11331940

6

Quantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groups.

Perola M, Ohman M, Hiekkalinna T, Leppävuori J, Pajukanta P, Wessman M, Koskenvuo M, Palotie A, Lange K, Kaprio J, Peltonen L. Perola M, et al. Among authors: wessman m. Am J Hum Genet. 2001 Jul;69(1):117-23. doi: 10.1086/321286. Epub 2001 Jun 15. Am J Hum Genet. 2001. PMID: 11410840 Free PMC article.

7

Chromosomal localization of SLC12A5/Slc12a5, the human and mouse genes for the neuron-specific K(+)-Cl(-) cotransporter (KCC2) defines a new region of conserved homology.

Sallinen R, Tornberg J, Putkiranta M, Horelli-Kuitunen N, Airaksinen MS, Wessman M. Sallinen R, et al. Among authors: wessman m. Cytogenet Cell Genet. 2001;94(1-2):67-70. doi: 10.1159/000048785. Cytogenet Cell Genet. 2001. PMID: 11701957

8

Novel splice site CACNA1A mutation causing episodic ataxia type 2.

Kaunisto MA, Harno H, Kallela M, Somer H, Sallinen R, Hämäläinen E, Miettinen PJ, Vesa J, Orpana A, Palotie A, Färkkilä M, Wessman M. Kaunisto MA, et al. Among authors: wessman m. Neurogenetics. 2004 Feb;5(1):69-73. doi: 10.1007/s10048-003-0161-0. Epub 2003 Oct 7. Neurogenetics. 2004. PMID: 14530926

9

New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2).

Sallinen R, Vihola A, Bachinski LL, Huoponen K, Haapasalo H, Hackman P, Zhang S, Sirito M, Kalimo H, Meola G, Horelli-Kuitunen N, Wessman M, Krahe R, Udd B. Sallinen R, et al. Among authors: wessman m. Neuromuscul Disord. 2004 Apr;14(4):274-83. doi: 10.1016/j.nmd.2004.01.002. Neuromuscul Disord. 2004. PMID: 15019706

10

DDOST, PRKCSH and LGALS3, which encode AGE-receptors 1, 2 and 3, respectively, are not associated with diabetic nephropathy in type 1 diabetes.

Hoverfelt A, Sallinen R, Söderlund JM, Forsblom C, Pettersson-Fernholm K, Parkkonen M, Groop PH, Wessman M; FinnDiane Study Group. Hoverfelt A, et al. Among authors: wessman m. Diabetologia. 2010 Sep;53(9):1903-7. doi: 10.1007/s00125-010-1771-3. Epub 2010 May 21. Diabetologia. 2010. PMID: 20490454

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