Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1995 | 1 |
1998 | 2 |
1999 | 1 |
2012 | 1 |
2013 | 1 |
2024 | 0 |
Search Results
5 results
Results by year
Filters applied: . Clear all
Page 1
A de novo mutation in alpha-tropomyosin that causes hypertrophic cardiomyopathy.
Circulation. 1995 May 1;91(9):2302-5. doi: 10.1161/01.cir.91.9.2302.
Circulation. 1995.
PMID: 7729014
A mutant tropomyosin that causes hypertrophic cardiomyopathy is expressed in vivo and associated with an increased calcium sensitivity.
Bottinelli R, Coviello DA, Redwood CS, Pellegrino MA, Maron BJ, Spirito P, Watkins H, Reggiani C.
Bottinelli R, et al.
Circ Res. 1998 Jan 9-23;82(1):106-15. doi: 10.1161/01.res.82.1.106.
Circ Res. 1998.
PMID: 9440709
Item in Clipboard
The cardiac beta-myosin heavy chain gene is not the predominant gene for hypertrophic cardiomyopathy in the Finnish population.
Jääskeläinen P, Soranta M, Miettinen R, Saarinen L, Pihlajamäki J, Silvennoinen K, Tikanoja T, Laakso M, Kuusisto J.
Jääskeläinen P, et al.
J Am Coll Cardiol. 1998 Nov 15;32(6):1709-16. doi: 10.1016/s0735-1097(98)00448-3.
J Am Coll Cardiol. 1998.
PMID: 9822100
Free article.
Item in Clipboard
Mouse model of a familial hypertrophic cardiomyopathy mutation in alpha-tropomyosin manifests cardiac dysfunction.
Muthuchamy M, Pieples K, Rethinasamy P, Hoit B, Grupp IL, Boivin GP, Wolska B, Evans C, Solaro RJ, Wieczorek DF.
Muthuchamy M, et al.
Circ Res. 1999 Jul 9;85(1):47-56. doi: 10.1161/01.res.85.1.47.
Circ Res. 1999.
PMID: 10400910
Item in Clipboard
Two founder mutations in the alpha-tropomyosin and the cardiac myosin-binding protein C genes are common causes of hypertrophic cardiomyopathy in the Finnish population.
Jääskeläinen P, Heliö T, Aalto-Setälä K, Kaartinen M, Ilveskoski E, Hämäläinen L, Melin J, Nieminen MS, Laakso M, Kuusisto J; FinHCM study group; Kervinen H, Mustonen J, Juvonen J, Niemi M, Uusimaa P, Huttunen M, Kotila M, Pietilä M.
Jääskeläinen P, et al.
Ann Med. 2013 Feb;45(1):85-90. doi: 10.3109/07853890.2012.671534. Epub 2012 Apr 2.
Ann Med. 2013.
PMID: 22462493
Item in Clipboard
Cite
Cite