Found: 6

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  • Comparison of Eight Technologies to Determine Genotype at the UGT1A1 (TA)n Repeat Polymorphism: Potential Clinical Consequences of Genotyping Errors?

    Published in:
    International Journal of Molecular Sciences, 2020, v. 21, n. 3, p. 896, doi. 10.3390/ijms21030896
    By:
    • Sissung, Tristan M.;
    • Barbier, Roberto H.;
    • Price, Douglas K.;
    • Plona, Teri M.;
    • Pike, Kristen M.;
    • Mellott, Stephanie D.;
    • Baugher, Ryan N.;
    • Whiteley, Gordon R.;
    • Soppet, Daniel R.;
    • Venzon, David;
    • Berman, Arlene;
    • Rajan, Arun;
    • Giaccone, Giuseppe;
    • Meltzer, Paul;
    • Figg, William D.
    Publication type:
    Article

  • Organoids and metastatic orthotopic mouse model for mismatch repair-deficient colorectal cancer.

    Published in:
    Frontiers in Oncology, 2023, p. 1, doi. 10.3389/fonc.2023.1223915
    By:
    • Yurong Song;
    • Kerr, Travis D.;
    • Sanders, Chelsea;
    • Lisheng Dai;
    • Baxter, Shaneen S.;
    • Somerville, Brandon;
    • Baugher, Ryan N.;
    • Mellott, Stephanie D.;
    • Young, Todd B.;
    • Lawhorn, Heidi E.;
    • Plona, Teri M.;
    • Bingfang Xu;
    • Lei Wei;
    • Qiang Hu;
    • Song Liu;
    • Hutson, Alan;
    • Karim, Baktiar;
    • Burkett, Sandra;
    • Difilippantonio, Simone;
    • Pinto, Ligia
    Publication type:
    Article

  • Mesothelioma Mouse Models with Mixed Genomic States of Chromosome and Microsatellite Instability.

    Published in:
    Cancers, 2022, v. 14, n. 13, p. N.PAG, doi. 10.3390/cancers14133108
    By:
    • Song, Yurong;
    • Baxter, Shaneen S.;
    • Dai, Lisheng;
    • Sanders, Chelsea;
    • Burkett, Sandra;
    • Baugher, Ryan N.;
    • Mellott, Stephanie D.;
    • Young, Todd B.;
    • Lawhorn, Heidi E.;
    • Difilippantonio, Simone;
    • Karim, Baktiar;
    • Kadariya, Yuwaraj;
    • Pinto, Ligia A.;
    • Testa, Joseph R.;
    • Shoemaker, Robert H.
    Publication type:
    Article

  • A novel mouse model of PMS2 founder mutation that causes mismatch repair defect due to aberrant splicing.

    Published in:
    Cell Death & Disease, 2021, v. 12, n. 9, p. 1, doi. 10.1038/s41419-021-04130-8
    By:
    • Biswas, Kajal;
    • Couillard, Martin;
    • Cavallone, Luca;
    • Burkett, Sandra;
    • Stauffer, Stacey;
    • Martin, Betty K.;
    • Southon, Eileen;
    • Reid, Susan;
    • Plona, Teri M.;
    • Baugher, Ryan N.;
    • Mellott, Stephanie D.;
    • Pike, Kristen M.;
    • Albaugh, Mary E.;
    • Maedler-Kron, Chelsea;
    • Hamel, Nancy;
    • Tessarollo, Lino;
    • Marcus, Victoria;
    • Foulkes, William D.;
    • Sharan, Shyam K.
    Publication type:
    Article

  • Pharmacogenomics Implementation at the National Institutes of Health Clinical Center.

    Published in:
    Journal of Clinical Pharmacology, 2017, v. 57, p. S67, doi. 10.1002/jcph.993
    By:
    • Sissung, Tristan M.;
    • McKeeby, Jon W.;
    • Patel, Jharana;
    • Lertora, Juan J.;
    • Kumar, Parag;
    • Flegel, Willy A.;
    • Adams, Sharon D.;
    • Eckes, Ellen J.;
    • Mickey, Frank;
    • Plona, Teri M.;
    • Mellott, Stephanie D.;
    • Baugher, Ryan N.;
    • Wu, Xiaolin;
    • Soppet, Daniel R.;
    • Barcus, Mary E.;
    • Datta, Vivekananda;
    • Pike, Kristen M.;
    • DiPatrizio, Gary;
    • Figg, William D.;
    • Goldspiel, Barry R.
    Publication type:
    Article

  • Frameshift mutations in peripheral blood as a biomarker for surveillance of Lynch syndrome.

    Published in:
    JNCI: Journal of the National Cancer Institute, 2024, v. 116, n. 6, p. 957, doi. 10.1093/jnci/djae060
    By:
    • Song, Yurong;
    • Loomans-Kropp, Holli;
    • Baugher, Ryan N;
    • Somerville, Brandon;
    • Baxter, Shaneen S;
    • Kerr, Travis D;
    • Plona, Teri M;
    • Mellott, Stephanie D;
    • Young, Todd B;
    • Lawhorn, Heidi E;
    • Wei, Lei;
    • Hu, Qiang;
    • Liu, Song;
    • Hutson, Alan;
    • Pinto, Ligia;
    • Potter, John D;
    • Sei, Shizuko;
    • Gelincik, Ozkan;
    • Lipkin, Steven M;
    • Gebert, Johannes
    Publication type:
    Article