Search Results - Toro, Tumi

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  1. 1
    Predicting Clinical Outcome through Molecular Profiling in Stage III Melanoma

    Predicting Clinical Outcome through Molecular Profiling in Stage III Melanoma by JOHN, Thomas, BLACK, Michael A, TORO, Tumi T, LEADER, Debbie, GEDYE, Craig A, DAVIS, Ian D, GUILFORD, Parry J, CEBON, Jonathan S

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  2. 2
    Multiple Gene Expression Classifiers from Different Array Platforms Predict Poor Prognosis of Colorectal Cancer

    Multiple Gene Expression Classifiers from Different Array Platforms Predict Poor Prognosis of Colorectal Cancer by LIN, Yu-Hsin, FRIEDERICHS, Jan, MERRIE, Arend E, VAN RIJ, Andre, YOON, Han-Seung, MCCALL, John L, SIEWERT, Jörg Rudiger, HOLZMANN, Bernhard, REEVE, Anthony E, BLACK, Michael A, MAGES, Jörg, ROSENBERG, Robert, GUILFORD, Parry J, PHILLIPS, Vicky, THOMPSON -FAWCETT, Mark, KASABOV, Nikola, TORO, Tumi

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  3. 3
    Development of a Multiplex RNA Urine Test for the Detection and Stratification of Transitional Cell Carcinoma of the Bladder

    Development of a Multiplex RNA Urine Test for the Detection and Stratification of Transitional Cell Carcinoma of the Bladder by HOLYOAKE, Andrew, O'SULLIVAN, Paul, DA SILVA TATLEY, Fernanda, CAMBRIDGE, Lisa, TORO, Tumi, OGAWA, Osamu, GUILFORD, Parry, POLLOCK, Rob, BEST, Terry, WATANABE, Jun, KAJITA, Yoichiro, MATSUI, Yoshiyuki, ITO, Masaaki, NISHIYAMA, Hiroyuki, KERR, Natalie

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  4. 4
    E-cadherin germline mutations define an inherited cancer syndrome dominated by diffuse gastric cancer

    E-cadherin germline mutations define an inherited cancer syndrome dominated by diffuse gastric cancer by Guilford, Parry J., Hopkins, Justin B.W., Grady, William M., Markowitz, Sanford D., Willis, Joseph, Lynch, Henry, Rajput, Ashwani, Wiesner, Georgia L., Lindor, Noralane M., Burgart, Lawrence J., Toro, Tumi T., Lee, Don, Limacher, Jean-Marc, Shaw, David W., Findlay, Michael P.N., Reeve, Anthony E.

    Published in Human mutation
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  5. 5
    A serine/threonine kinase gene defective in Peutz-Jeghers syndrome

    A serine/threonine kinase gene defective in Peutz-Jeghers syndrome by Aaltonen, Lauri A, Hemminki, Akseli, Markie, David, Tomlinson, Ian, Avizienyte, Egle, Roth, Stina, Loukola, Anu, Bignell, Graham, Warren, William, Aminoff, Maria, Höglund, Pia, Järvinen, Heikki, Kristo, Paula, Pelin, Katarina, Ridanpää, Maaret, Salovaara, Reijo, Toro, Tumi, Bodmer, Walter, Olschwang, Sylviane, Olsen, Anne S, Stratton, Michael R, de la Chapelle, Albert

    Published in Nature (London)
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  6. 6
    Novel germline CDH1 mutations in hereditary diffuse gastric cancer families

    Novel germline CDH1 mutations in hereditary diffuse gastric cancer families by Humar, Bostjan, Toro, Tumi, Graziano, Francesco, Müller, Hansjakob, Dobbie, Zuzana, Kwang-Yang, Han, Eng, Charis, Hampel, Heather, Gilbert, Dale, Winship, Ingrid, Parry, Susan, Ward, Robyn, Findlay, Mike, Christian, Alice, Tucker, Monica, Tucker, Kathy, Merriman, Tony, Guilford, Parry

    Published in Human mutation
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  7. 7
    A serine/threonine kinase gene defective in Peutz–Jeghers syndrome

    A serine/threonine kinase gene defective in Peutz–Jeghers syndrome by Hemminki, Akseli, Markie, David, Tomlinson, Ian, Avizienyte, Egle, Roth, Stina, Loukola, Anu, Bignell, Graham, Warren, William, Aminoff, Maria, Höglund, Pia, Järvinen, Heikki, Kristo, Paula, Pelin, Katarina, Ridanpää, Maaret, Salovaara, Reijo, Toro, Tumi, Bodmer, Walter, Olschwang, Sylviane, Olsen, Anne S., Stratton, Michael R., de la Chapelle, Albert, Aaltonen, Lauri A.

    Published in Nature (London)
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  8. 8
    Novel germline CDH1 mutations in hereditary diffuse gastric cancer families: CDH1 Mutations in Hereditary Gastric Cancer

    Novel germline CDH1 mutations in hereditary diffuse gastric cancer families: CDH1 Mutations in Hereditary Gastric Cancer by Humar, Bostjan, Toro, Tumi, Graziano, Francesco, Müller, Hansjakob, Dobbie, Zuzana, Kwang-Yang, Han, Eng, Charis, Hampel, Heather, Gilbert, Dale, Winship, Ingrid, Parry, Susan, Ward, Robyn, Findlay, Mike, Christian, Alice, Tucker, Monica, Tucker, Kathy, Merriman, Tony, Guilford, Parry

    Published in Human mutation
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