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Otey, C.A., Kalnoski, M.H., Bulinski, J.C., 1987. Identification and quantification of actin
isoforms in vertebrate cells and tissues. J. Cell Biochem. 34, 113-124.
Otey, C.A., Kalnoski, M.H., Lessard, J.L., Bulinski, J.C., 1986. Immunolocalization of the
gamma isoform of nonmuscle actin in cultured cells. J. Cell Biol. 102, 1726-1737.
Pagliardini, S., Giavazzi, A., Setola, V., Lizier, C., Di Luca, M., DeBiasi, S., Battaglia, G., 2000.
Subcellular localization and axonal transport of the survival motor neuron (SMN)
protein in the developing rat spinal cord. Hum. Mol. Genet. 9, 47-56.
Pak, C.W., Flynn, K.C., Bamburg, J.R., 2008. Actin-binding proteins take the reins in growth
cones. Nat. Rev. Neurosci. 9, 136-147.
Pappenberger, G., McCormack, E.A., Willison, K.R., 2006. Quantitative actin folding
reactions using yeast CCT purified via an internal tag in the CCT3/gamma subunit. J.
Mol. Biol. 360, 484-496.
Parkitna, J.R., Bilbao, A., Rieker, C., Engblom, D., Piechota, M., Nordheim, A., Spanagel,
R., Schutz, G., 2010. Loss of the serum response factor in the dopamine system leads to
hyperactivity. FASEB J. 24, 2427-2435.
Penzes, P., Cahill, M.E., Jones, K.A.,VanLeeuwen, J.E., Woolfrey, K.M., 2011. Dendritic spine
pathology in neuropsychiatric disorders. Nat. Neurosci. 14, 285-293.
Perrin, B.J., Sonnemann, K.J., Ervasti, J.M., 2010. beta-actin and gamma-actin are each
dispensable for auditory hair cell development but required for Stereocilia maintenance.
PLoS Genet. 6, e1001158.
Perycz, M., Urbanska, A.S., Krawczyk, P.S., Parobczak, K., Jaworski, J., 2011. Zipcode bind-
ing protein 1 regulates the development of dendritic arbors in hippocampal neurons.
J. Neurosci. 31, 5271-5285.
Plantier, M., Der Terrossian, E., Represa, A., 1998. Beta-actin immunoreactivity in rat
microglial cells: developmental pattern and participation in microglial reaction after
kainate injury. Neurosci. Lett. 247, 49-52.
Pollard, T.D., Blanchoin, L., Mullins, R.D., 2000. Molecular mechanisms controlling actin
filament dynamics in nonmuscle cells. Annu. Rev. Biophys. Biomol. Struct. 29, 545-576.
Pollard, T.D., Borisy, G.G., 2003. Cellular motility driven by assembly and disassembly of
actin filaments. Cell 112, 453-465.
Popko, J., Fernandes, A., Brites, D., Lanier, L.M., 2009. Automated analysis of NeuronJ tracing
data. Cytometry A 75, 371-376.
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., 2006. A mutation of beta -actin that alters depolymerization dynamics is associated
with autosomal dominant developmental malformations, deafness, and dystonia. Am. J.
Hum. Genet. 78, 947-960.
Rash, B.G., Richards, L.J., 2001. A role for cingulate pioneering axons in the development
of the corpus callosum. J. Comp. Neurol. 434, 147-157.
Rendtorff, N.D., Zhu, M., Fagerheim, T., Antal, T.L., Jones, M., Teslovich, T.M., Gillanders,
E.M., Barmada, M., Teig, E., Trent, J.M., Friderici, K.H., Stephan, D.A., Tranebjaerg, L.,
2006. A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian
DFNA20/26 family, but ACTG1 mutations are not frequent among families with
hereditary hearing impairment. Eur. J. Hum. Genet. EJHG 14, 1097-1105.
Richards, L.J., Plachez, C., Ren, T., 2004. Mechanisms regulating the development of the
corpus callosum and its agenesis in mouse and human. Clin. Genet. 66, 276-289.
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., 2012. De novo mutations in the actin genes
ACTB and ACTG1 cause Baraitser-Winter syndrome. Nat. Genet. 44 (440-4), S1-S2.
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