Search Results - Trevor Lucas

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  1. 1
    A Rac1/Cdc42 GTPase-Specific Small Molecule Inhibitor Suppresses Growth of Primary Human Prostate Cancer Xenografts and Prolongs Survival in Mice

    A Rac1/Cdc42 GTPase-Specific Small Molecule Inhibitor Suppresses Growth of Primary Human Prostate Cancer Xenografts and Prolongs Survival in Mice by Karin Zins, Trevor Lucas, Patrick Reichl, Dietmar Abraham, Seyedhossein Aharinejad

    Published 2013
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  2. 2
    Targeting Cdc42 with the small molecule drug AZA197 suppresses primary colon cancer growth and prolongs survival in a preclinical mouse xenograft model by downregulation of PAK1 activity

    Targeting Cdc42 with the small molecule drug AZA197 suppresses primary colon cancer growth and prolongs survival in a preclinical mouse xenograft model by downregulation of PAK1 ac... by Karin Zins, Sandun Gunawardhana, Trevor Lucas, Dietmar Abraham, Seyedhossein Aharinejad

    Published 2013
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  3. 3
    Stromal cell‐derived CSF‐1 blockade prolongs xenograft survival of CSF‐1‐negative neuroblastoma

    Stromal cell‐derived CSF‐1 blockade prolongs xenograft survival of CSF‐1‐negative neuroblastoma by Dietmar Abraham, Karin Zins, Mouldy Sioud, Trevor Lucas, Romana Schäfer, E. Richard Stanley, Seyedhossein Aharinejad

    Published 2009
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  4. 4
    The ETV6-NTRK3 gene fusion encodes a chimeric protein tyrosine kinase that transforms NIH3T3 cells

    The ETV6-NTRK3 gene fusion encodes a chimeric protein tyrosine kinase that transforms NIH3T3 cells by Daniel Wai, Stevan R. Knezevich, Trevor Lucas, Burkhard Jansen, Robert J. Kay, Poul H. Sorensen

    Published 2000
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  5. 5
    Adenocarcinoma de Cólon em Paciente de 19 Anos: Diagnóstico de Síndrome de Lynch com Mutação no Gene PMS2

    Adenocarcinoma de Cólon em Paciente de 19 Anos: Diagnóstico de Síndrome de Lynch com Mutação no Gene PMS2 by D. Neves, Renato de Souza Melo, Trevor Lucas, L. V.P. Dias, P. H.B. Silva, André Antônio Abissamra

    Published 2021
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  6. 6
    A homozygous deletion of a normal variation locus in a patient with hearing loss from non-consanguineous parents

    A homozygous deletion of a normal variation locus in a patient with hearing loss from non-consanguineous parents by Jeroen Knijnenburg, Saskia A.J. Lesnik Oberstein, Klemens Frei, Trevor Lucas, A.C.J. Gijsbers, Claudia Ruivenkamp, Hans J. Tanke, Károly Szuhai

    Published 2009
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