10 results for author:"McEwen D.P." in Literature citations
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| Gene therapy rescues cilia defects and restores olfactory function in a mammalian ciliopathy model. McIntyre J.C., Davis E.E., Joiner A., Williams C.L., Tsai I.C., Jenkins P.M., McEwen D.P., Zhang L., Escobado J., Thomas S. et al. Nat. Med. 18:1423-1428(2012) · Mapped (10) |
| Single molecule imaging reveals differences in microtubule track selection between Kinesin motors. Cai D., McEwen D.P., Martens J.R., Meyhofer E., Verhey K.J. PLoS Biol. 7:e1000216-e1000216(2009) · Mapped (19) |
| The voltage-gated Na+ channel beta3 subunit does not mediate trans homophilic cell adhesion or associate with the cell adhesion molecule contactin. McEwen D.P., Chen C., Meadows L.S., Lopez-Santiago L., Isom L.L. Neurosci. Lett. 462:272-275(2009) · Mapped (1) |
| Antiarrhythmic drug-induced internalization of the atrial-specific k+ channel kv1.5. Schumacher S.M., McEwen D.P., Zhang L., Arendt K.L., Van Genderen K.M., Martens J.R. Circ. Res. 104:1390-1398(2009) · Mapped (2) |
| Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome. Layman W.S., McEwen D.P., Beyer L.A., Lalani S.R., Fernbach S.D., Oh E., Swaroop A., Hegg C.C., Raphael Y., Martens J.R. et al. Hum. Mol. Genet. 18:1909-1923(2009) · Mapped (36) |
| Hypomorphic CEP290/NPHP6 mutations result in anosmia caused by the selective loss of G proteins in cilia of olfactory sensory neurons. McEwen D.P., Koenekoop R.K., Khanna H., Jenkins P.M., Lopez I., Swaroop A., Martens J.R. Proc. Natl. Acad. Sci. U.S.A. 104:15917-15922(2007) · Mapped (7) |
| Sodium channel Scn1b null mice exhibit prolonged QT and RR intervals. Lopez-Santiago L.F., Meadows L.S., Ernst S.J., Chen C., Malhotra J.D., McEwen D.P., Speelman A., Noebels J.L., Maier S.K., Lopatin A.N. et al. J. Mol. Cell. Cardiol. 43:636-647(2007) · Mapped (41) |
| Rab-GTPase-dependent endocytic recycling of Kv1.5 in atrial myocytes. McEwen D.P., Schumacher S.M., Li Q., Benson M.D., Iniguez-Lluhi J.A., Van Genderen K.M., Martens J.R. J. Biol. Chem. 282:29612-29620(2007) · Mapped (1) |
| A novel epilepsy mutation in the sodium channel SCN1A identifies a cytoplasmic domain for beta subunit interaction. Spampanato J., Kearney J.A., de Haan G., McEwen D.P., Escayg A., Aradi I., MacDonald B.T., Levin S.I., Soltesz I., Benna P. et al. J. Neurosci. 24:10022-10034(2004) · UniProtKB (1) · Mapped (6) |
| Mice lacking sodium channel beta1 subunits display defects in neuronal excitability, sodium channel expression, and nodal architecture. Chen C., Westenbroek R.E., Xu X., Edwards C.A., Sorenson D.R., Chen Y., McEwen D.P., O'Malley H.A., Bharucha V., Meadows L.S. et al. J. Neurosci. 24:4030-4042(2004) · Mapped (6) |