Publicaciones en las que colabora con Antonio Felipe Campo (12)

2015

  1. An unconventional calmodulin-anchoring site within the AB module of Kv7.2 channels

    Journal of Cell Science, Vol. 128, Núm. 16, pp. 3155-3163

2014

  1. Functional assembly of Kv7.1/Kv7.5 channels with emerging properties on vascular muscle physiology

    Arteriosclerosis, Thrombosis, and Vascular Biology, Vol. 34, Núm. 7, pp. 1522-1530

2012

  1. Targeting of Kv7.5 (KCNQ5)/KCNE channels to surface microdomains of cell membranes

    Muscle and Nerve, Vol. 45, Núm. 1, pp. 48-54

2010

  1. Impact of KCNE subunits on KCNQ1 (Kv7.1) channel membrane surface targeting

    Journal of Cellular Physiology, Vol. 225, Núm. 3, pp. 692-700

2009

  1. Functional implications of KCNE subunit expression for the Kv7.5 (KCNQ5) channel

    Cellular Physiology and Biochemistry, Vol. 24, Núm. 5-6, pp. 325-334

2008

  1. Kv1.5 association modifies Kv1.3 traffic and membrane localization

    Journal of Biological Chemistry, Vol. 283, Núm. 13, pp. 8756-8764

2007

  1. Kv1.3/Kv1.5 heteromeric channels compromise pharmacological responses in macrophages

    Biochemical and Biophysical Research Communications, Vol. 352, Núm. 4, pp. 913-918

2006

  1. Association of Kv1.5 and Kv1.3 contributes to the major voltage-dependent K+ channel in macrophages

    Journal of Biological Chemistry, Vol. 281, Núm. 49, pp. 37675-37685

2005

  1. Erratum: Differential voltage-dependent K+ channel responses during proliferation and activation in macrophages (The Journal of Biological Chemistry (2003) 278 (46307-46320))

    Journal of Biological Chemistry

  2. Pattern of Kvβ subunit expression in macrophages depends upon proliferation and the mode of activation

    Journal of Immunology, Vol. 174, Núm. 8, pp. 4736-4744

2003

  1. Differential Voltage-dependent K+ Channel Responses during Proliferation and Activation in Macrophages

    Journal of Biological Chemistry, Vol. 278, Núm. 47, pp. 46307-46320

2001

  1. ATP release from the electric organ of Torpedo and from Xenopus oocytes

    Drug Development Research