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 |
---|---|
2009 | 3 |
2010 | 4 |
2024 | 0 |
Search Results
6 results
Results by year
Filters applied: . Clear all
Page 1
Functional muscle analysis of the Tcap knockout mouse.
Hum Mol Genet. 2010 Jun 1;19(11):2268-83. doi: 10.1093/hmg/ddq105. Epub 2010 Mar 16.
Hum Mol Genet. 2010.
PMID: 20233748
Free PMC article.
Mutations and polymorphisms of the skeletal muscle alpha-actin gene (ACTA1).
Laing NG, Dye DE, Wallgren-Pettersson C, Richard G, Monnier N, Lillis S, Winder TL, Lochmüller H, Graziano C, Mitrani-Rosenbaum S, Twomey D, Sparrow JC, Beggs AH, Nowak KJ.
Laing NG, et al.
Hum Mutat. 2009 Sep;30(9):1267-77. doi: 10.1002/humu.21059.
Hum Mutat. 2009.
PMID: 19562689
Free PMC article.
Item in Clipboard
Cell membrane expression of cardiac sodium channel Na(v)1.5 is modulated by alpha-actinin-2 interaction.
Ziane R, Huang H, Moghadaszadeh B, Beggs AH, Levesque G, Chahine M.
Ziane R, et al.
Biochemistry. 2010 Jan 12;49(1):166-78. doi: 10.1021/bi901086v.
Biochemistry. 2010.
PMID: 19943616
Free PMC article.
Item in Clipboard
Mutations of tropomyosin 3 (TPM3) are common and associated with type 1 myofiber hypotrophy in congenital fiber type disproportion.
Lawlor MW, Dechene ET, Roumm E, Geggel AS, Moghadaszadeh B, Beggs AH.
Lawlor MW, et al.
Hum Mutat. 2010 Feb;31(2):176-83. doi: 10.1002/humu.21157.
Hum Mutat. 2010.
PMID: 19953533
Free PMC article.
Item in Clipboard
Altered myofilament function depresses force generation in patients with nebulin-based nemaline myopathy (NEM2).
Ottenheijm CA, Hooijman P, DeChene ET, Stienen GJ, Beggs AH, Granzier H.
Ottenheijm CA, et al.
J Struct Biol. 2010 May;170(2):334-43. doi: 10.1016/j.jsb.2009.11.013. Epub 2009 Nov 26.
J Struct Biol. 2010.
PMID: 19944167
Free PMC article.
Item in Clipboard
Serotonin-related FEV gene variant in the sudden infant death syndrome is a common polymorphism in the African-American population.
Broadbelt KG, Barger MA, Paterson DS, Holm IA, Haas EA, Krous HF, Kinney HC, Markianos K, Beggs AH.
Broadbelt KG, et al.
Pediatr Res. 2009 Dec;66(6):631-5. doi: 10.1203/PDR.0b013e3181bd5a31.
Pediatr Res. 2009.
PMID: 19707175
Free PMC article.
Item in Clipboard
Cite
Cite