Publikationen in Zusammenarbeit mit Forschern von Universitat de Barcelona (12)

2010

  1. Putative one-pot prebiotic polypeptides with ribonucleolytic activity

    Chemistry - A European Journal, Vol. 16, Núm. 18, pp. 5314-5323

2008

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

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

  2. N-terminal CFTR missense variants severely affect the behavior of the CFTR chloride channel

    Human Mutation, Vol. 29, Núm. 5, pp. 738-749

  3. Preparation of ribonuclease S domain-swapped dimers conjugated with DNA and PNA: Modulating the activity of ribonucleases

    Bioconjugate Chemistry, Vol. 19, Núm. 1, pp. 263-270

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. Direct, two-step synthetic pathway to novel dibenzo[a,c]phenanthridines

    Journal of Organic Chemistry, Vol. 70, Núm. 8, pp. 3178-3187

  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

2004

  1. Gadolinium inhibition of ecto-nucleoside triphosphate diphosphohydrolase activity in Torpedo electric organ

    Neurochemical Research, Vol. 29, Núm. 9, pp. 1711-1714

  2. Modulation of aqueous humor outflow by ionic mechanisms involved in trabecular meshwork cell volume regulation

    Investigative Ophthalmology and Visual Science, Vol. 45, Núm. 10, pp. 3650-3661

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