The α2-HeremansSchmid glycoprotein (AHSG) promotes growth in head and neck squamous cell carcinoma (HNSCC)

por Thompson, Pamela D, Sakwe, Amos, Ochieng, Josiah, Pratap, Siddharth, Marshall, Dana R
Publicado 2013

Genetic Variation in the Extended Major Histocompatibility Complex and Susceptibility to Childhood Acute Lymphoblastic Leukemia: A Review of the Evidence

por Urayama, Kevin Y., Thompson, Pamela D., Taylor, Malcolm, Trachtenberg, Elizabeth A., Chokkalingam, Anand P.
Publicado 2013

Claudin 13, a Member of the Claudin Family Regulated in Mouse Stress Induced Erythropoiesis

por Thompson, Pamela D., Tipney, Hannah, Brass, Andy, Noyes, Harry, Kemp, Steve, Naessens, Jan, Tassabehji, May
Publicado 2010

Reduced annexin A6 expression promotes the degradation of activated epidermal growth factor receptor and sensitizes invasive breast cancer cells to EGFR-targeted tyrosine kinase in...

por Koumangoye, Rainelli B, Nangami, Gladys N, Thompson, Pamela D, Agboto, Vincent K, Ochieng, Josiah, Sakwe, Amos M
Publicado 2013

The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A

por Vijayakrishnan, Jayaram, Henrion, Marc, Moorman, Anthony V., Fiege, Bettina, Kumar, Rajiv, Inacio da Silva Filho, Miguel, Holroyd, Amy, Koehler, Rolf, Thomsen, Hauke, Irving, Julie A., Allan, James M., Lightfoot, Tracy, Roman, Eve, Kinsey, Sally E., Sheridan, Eamonn, Thompson, Pamela D., Hoffmann, Per, Nöthen, Markus M., Mühleisen, Thomas W., Eisele, Lewin, Bartram, Claus R., Schrappe, Martin, Greaves, Mel, Hemminki, Kari, Harrison, Christine J., Stanulla, Martin, Houlston, Richard S.
Publicado 2015

Heritable variation at the chromosome 21 gene ERG is associated with acute lymphoblastic leukemia risk in children with and without Down syndrome

por de Smith, Adam J., Walsh, Kyle M., Morimoto, Libby M., Francis, Stephen S., Hansen, Helen M., Jeon, Soyoung, Gonseth, Semira, Chen, Minhui, Sun, Hanxiao, Luna-Fineman, Sandra, Antillón, Federico, Girón, Verónica, Kang, Alice Y., Smirnov, Ivan, Shao, Xiaorong, Whitehead, Todd P., Barcellos, Lisa F., Jolly, Kent W., Healy, Jasmine, Laverdière, Caroline, Sinnett, Daniel, Taub, Jeffrey W., Birch, Jillian M., Thompson, Pamela D., Pombo-de-Oliveira, Maria S., Spector, Logan G., DeWan, Andrew T., Mueller, Beth A., Chiang, Charleston, Metayer, Catherine, Ma, Xiaomei, Wiemels, Joseph L.
Publicado 2019

Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia

por Vijayakrishnan, Jayaram, Studd, James, Broderick, Peter, Kinnersley, Ben, Holroyd, Amy, Law, Philip J., Kumar, Rajiv, Allan, James M., Harrison, Christine J., Moorman, Anthony V., Vora, Ajay, Roman, Eve, Rachakonda, Sivaramakrishna, Kinsey, Sally E., Sheridan, Eamonn, Thompson, Pamela D., Irving, Julie A., Koehler, Rolf, Hoffmann, Per, Nöthen, Markus M., Heilmann-Heimbach, Stefanie, Jöckel, Karl-Heinz, Easton, Douglas F., Pharaoh, Paul D. P., Dunning, Alison M., Peto, Julian, Canzian, Frederico, Swerdlow, Anthony, Eeles, Rosalind A., Kote-Jarai, ZSofia, Muir, Kenneth, Pashayan, Nora, Greaves, Mel, Zimmerman, Martin, Bartram, Claus R., Schrappe, Martin, Stanulla, Martin, Hemminki, Kari, Houlston, Richard S.
Publicado 2018

Author Correction: Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia

por Vijayakrishnan, Jayaram, Studd, James, Broderick, Peter, Kinnersley, Ben, Holroyd, Amy, Law, Philip J., Kumar, Rajiv, Allan, James M., Harrison, Christine J., Moorman, Anthony V., Vora, Ajay, Roman, Eve, Rachakonda, Sivaramakrishna, Kinsey, Sally E., Sheridan, Eamonn, Thompson, Pamela D., Irving, Julie A., Koehler, Rolf, Hoffmann, Per, Nöthen, Markus M., Heilmann-Heimbach, Stefanie, Jöckel, Karl-Heinz, Easton, Douglas F., Pharaoh, Paul D. P., Dunning, Alison M., Peto, Julian, Canzian, Frederico, Swerdlow, Anthony, Eeles, Rosalind A., Kote-Jarai, Zsofia, Muir, Kenneth, Pashayan, Nora, Greaves, Mel, Zimmerman, Martin, Bartram, Claus R., Schrappe, Martin, Stanulla, Martin, Hemminki, Kari, Houlston, Richard S.
Publicado 2019