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Page 1
Regulation of the actin cytoskeleton by PI(4,5)P2 and PI(3,4,5)P3.
Curr Top Microbiol Immunol. 2004;282:117-63. doi: 10.1007/978-3-642-18805-3_5.
Curr Top Microbiol Immunol. 2004.
PMID: 14594216
Review.
Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy.
Wallgren-Pettersson C, Pelin K, Hilpelä P, Donner K, Porfirio B, Graziano C, Swoboda KJ, Fardeau M, Urtizberea JA, Muntoni F, Sewry C, Dubowitz V, Iannaccone S, Minetti C, Pedemonte M, Seri M, Cusano R, Lammens M, Castagna-Sloane A, Beggs AH, Laing NG, de la Chapelle A.
Wallgren-Pettersson C, et al. Among authors: hilpela p.
Neuromuscul Disord. 1999 Dec;9(8):564-72. doi: 10.1016/s0960-8966(99)00061-9.
Neuromuscul Disord. 1999.
PMID: 10619714
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SWAP-70 identifies a transitional subset of actin filaments in motile cells.
Hilpelä P, Oberbanscheidt P, Hahne P, Hund M, Kalhammer G, Small JV, Bähler M.
Hilpelä P, et al.
Mol Biol Cell. 2003 Aug;14(8):3242-53. doi: 10.1091/mbc.e03-01-0043. Epub 2003 Apr 17.
Mol Biol Cell. 2003.
PMID: 12925760
Free PMC article.
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Functional role for the class IX myosin myr5 in epithelial cell infection by Shigella flexneri.
Graf B, Bähler M, Hilpelä P, Böwe C, Adam T.
Graf B, et al. Among authors: hilpela p.
Cell Microbiol. 2000 Dec;2(6):601-16. doi: 10.1046/j.1462-5822.2000.00084.x.
Cell Microbiol. 2000.
PMID: 11207612
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Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy.
Pelin K, Hilpelä P, Donner K, Sewry C, Akkari PA, Wilton SD, Wattanasirichaigoon D, Bang ML, Centner T, Hanefeld F, Odent S, Fardeau M, Urtizberea JA, Muntoni F, Dubowitz V, Beggs AH, Laing NG, Labeit S, de la Chapelle A, Wallgren-Pettersson C.
Pelin K, et al. Among authors: hilpela p.
Proc Natl Acad Sci U S A. 1999 Mar 2;96(5):2305-10. doi: 10.1073/pnas.96.5.2305.
Proc Natl Acad Sci U S A. 1999.
PMID: 10051637
Free PMC article.
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