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Bienvenut W.V.Submitted (JUN-2005)
to UniProtKB
Lubec G., Afjehi-Sadat L., Chen W.-Q., Sun Y.Submitted (DEC-2008)
to UniProtKB
Complementary DNA sequence of a human cytoplasmic actin. Interspecies divergence of 3' non-coding regions.Hanukoglu I., Tanese N., Fuchs E.J. Mol. Biol. 163:673-678(1983)
Exportin 6
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Emerin caps the pointed end of actin filaments
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HGAL, a lymphoma prognostic biomarker, interacts with the cytoskeleton and mediates the effects of IL-6 on cell migration.Lu X., Chen J., Malumbres R., Cubedo Gil E., Helfman D.M., Lossos I.S.Blood 110:4268-4277(2007)
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A mutation of beta -actin that alters depolymerization dynamics is associated with autosomal dominant developmental malformations, deafness, and dystonia.Procaccio V., Salazar G., Ono S., Styers M.L., Gearing M., Davila A., Jimenez R., Juncos J., Gutekunst C.-A., Meroni G., Fontanella B., Sontag E., Sontag J.-M., Faundez V., Wainer B.H.Am. J. Hum. Genet. 78:947-960(2006)
GlcNAcylation of a histone methyltransferase in retinoic-acid-induced granulopoiesis.Fujiki R., Chikanishi T., Hashiba W., Ito H., Takada I., Roeder R.G., Kitagawa H., Kato S.Nature 459:455-459(2009)
ALKBH4-dependent demethylation of actin regulates actomyosin dynamics.Li M.M., Nilsen A., Shi Y., Fusser M., Ding Y.H., Fu Y., Liu B., Niu Y., Wu Y.S., Huang C.M., Olofsson M., Jin K.X., Lv Y., Xu X.Z., He C., Dong M.Q., Rendtlew Danielsen J.M., Klungland A., Yang Y.G.Nat. Commun. 4:1832-1832(2013)
De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome.Riviere J.B., van Bon B.W., Hoischen A., Kholmanskikh S.S., O'Roak B.J., Gilissen C., Gijsen S., Sullivan C.T., Christian S.L., Abdul-Rahman O.A., Atkin J.F., Chassaing N., Drouin-Garraud V., Fry A.E., Fryns J.P., Gripp K.W., Kempers M., Kleefstra T., Mancini G.M., Nowaczyk M.J., van Ravenswaaij-Arts C.M., Roscioli T., Marble M., Rosenfeld J.A., Siu V.M., de Vries B.B., Shendure J., Verloes A., Veltman J.A., Brunner H.G., Ross M.E., Pilz D.T., Dobyns W.B.Nat. Genet. 44:440-444(2012)