Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Norris-Kirby A"'
Autor:
Kamiyama, Hirohiko, Kamiyama, Mihoko, Hong, Seung-Mo, Karikari, Collins A, Lin, Ming-Tseh, Borges, Michael W, Griffith, Margaret, Young, Angela, Norris-Kirby, Alexis, Lubek, Conrad, Mizuma, Masamichi, Feldmann, Georg, Shi, Chanjuan, Liang, Hong, Goggins, Michael G, Maitra, Anirban, Hruban, Ralph H, Eshleman, James R
Publikováno v:
In Laboratory Investigation May 2010 90(5):665-673
Autor:
Norris-Kirby, Alexis, Hagenkord, Jill M., Kshirsagar, Malti P., Ronnett, Brigitte M., Murphy, Kathleen M.
Publikováno v:
In The Journal of Molecular Diagnostics 2010 12(4):525-529
Autor:
Tsiatis, Athanasios C., Norris-Kirby, Alexis, Rich, Roy G., Hafez, Michael J., Gocke, Christopher D., Eshleman, James R., Murphy, Kathleen M.
Publikováno v:
In The Journal of Molecular Diagnostics 2010 12(4):425-432
Autor:
Jinawath, Natini, Norris-Kirby, Alexis, Smith, B. Douglas, Gocke, Christopher D., Batista, Denise A., Griffin, Constance A., Murphy, Kathleen M.
Publikováno v:
In The Journal of Molecular Diagnostics 2009 11(4):359-363
Autor:
Kathleen M. Murphy, Lisa M. Williams, Laura Morsberger, Natini Jinawath, Pedram Argani, Alexis Norris-Kirby, Constance A. Griffin, Raluca Yonescu
Publikováno v:
Cancer Genetics and Cytogenetics. 201:42-47
The Ewing sarcoma (ES) family of tumors is characterized by nonrandom chromosomal translocations involving the EWSR1 gene on chromosome 22 with one of the members of the ETS family of transcription factors. The majority of ES tumors are characterized
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94e28b471585137b4504dd4cbcf4d36c
https://doi.org/10.1016/j.cancergencyto.2010.04.021
https://doi.org/10.1016/j.cancergencyto.2010.04.021
Autor:
Avinoam Nevler, Alexis Norris-Kirby, Fernando F. Blanco, Jordan M. Winter, Samantha Z. Brown, Henry T. Thomsett, Jonathan R. Brody, Joseph A. Cozzitorto, Charles J. Yeo, Shruti Lal, James R. Eshleman, Mahsa Zarei
Publikováno v:
Cancer Research. 78:4441-4441
The RNA-binding protein Human Antigen R (HuR) is upregulated in pancreatic ductal adenocarcinoma (PDA), where it promotes tumorigenesis via its mRNA pro-survival targets. PDA cells exposed to DNA damage upregulate the mitotic inhibitor kinase, WEE1,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9d13ce4fc7b30d60b2e939cfe0440ad
https://doi.org/10.1158/1538-7445.am2018-4441
https://doi.org/10.1158/1538-7445.am2018-4441
Autor:
James R. Eshleman, Christopher D. Gocke, Athanasios C. Tsiatis, Alexis Norris-Kirby, Michael J. Hafez, Kathleen M. Murphy, Roy G. Rich
Publikováno v:
The Journal of Molecular Diagnostics. 12:425-432
Mutations in codons 12 and 13 of the KRAS oncogene are relatively common in colorectal and lung adenocarcinomas. Recent data indicate that these mutations result in resistance to anti-epidermal growth factor receptor therapy. Therefore, we assessed S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c22118f30aa5e147ff0fb517e0de41c
https://doi.org/10.2353/jmoldx.2010.090188
https://doi.org/10.2353/jmoldx.2010.090188
Autor:
Angela Young, Margaret Griffith, Anirban Maitra, Mihoko Kamiyama, Seung-Mo Hong, Hong Liang, Georg Feldmann, Chanjuan Shi, Collins Karikari, Masamichi Mizuma, Ralph H. Hruban, Alexis Norris-Kirby, Michael Goggins, James R. Eshleman, Michael Borges, Conrad Lubek, Hirohiko Kamiyama, Ming Tseh Lin
Publikováno v:
Laboratory investigation; a journal of technical methods and pathology
Background Intraductal papillary mucinous neoplasms (IPMNs) are one of the 3 known curable precursor lesions of invasive pancreatic ductal adenocarcinoma, an almost uniformly fatal disease. Cell lines from IPMNs and their invasive counterparts should
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0eee198a45f988934bd6ea5584f4e10
https://doi.org/10.1038/labinvest.2010.51
https://doi.org/10.1038/labinvest.2010.51
Autor:
Kathleen M. Murphy, Constance A. Griffin, Alexis Norris-Kirby, B. Douglas Smith, Denise A.S. Batista, Natini Jinawath, Christopher D. Gocke
Publikováno v:
The Journal of Molecular Diagnostics. 11:359-363
Patients with chronic myelogenous leukemia have a t(9;22)(q34;q11.2) or variant translocation that results in a BCR-ABL fusion gene. BCR-ABL detection by quantitative reverse transcriptase-polymerase chain reaction (RT-PCR) is the standard practice f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3de3ddd9aed15401e96dca2b7602f197
https://doi.org/10.2353/jmoldx.2009.090008
https://doi.org/10.2353/jmoldx.2009.090008
Autor:
Alexis Norris-Kirby, Kathleen M. Murphy, Malti Kshirsagar, Brigitte M. Ronnett, Jill M. Hagenkord
Publikováno v:
The Journal of molecular diagnostics : JMD. 12(4)
The vast majority of trisomies in spontaneous abortions (SAB) are single and of maternal origin, most frequently due to meiosis I errors. Triple trisomies are exceedingly rare (approximately 0.05% of spontaneous abortions), most often of maternal ori
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cc53d8f43f5c1172f30b859bc196228
https://pubmed.ncbi.nlm.nih.gov/20413680
https://pubmed.ncbi.nlm.nih.gov/20413680