Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Christopher E. Freeman"'
Autor:
Susan J. Hsiao, Anthony N. Sireci, Richard D. Carvajal, Brian S. Henick, Mahesh Mansukhani, Helen Fernandes, Danielle Pendrick, Christopher E. Freeman, Jennifer A. Oberg, Gary K. Schwartz, Kevin A. Roth
Publikováno v:
JCO Precision Oncology. :1038-1048
PURPOSE The routine use of large next-generation sequencing (NGS) pan-cancer panels is required to identify the increasing number of, but often uncommon, actionable alterations to guide therapy. Inconsistent coverage and variable payment is hindering
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8370de52761fb12f960ad85dc50f90e
https://doi.org/10.1200/po.20.00048
https://doi.org/10.1200/po.20.00048
Autor:
Michael J Lipsky, James M. McKiernan, Christopher B. Anderson, Thomas Matthews, Mahesh Mansukhani, Christopher E. Freeman, Matthias Szabolcs, Gen Li, Caitlin E. Walsh, Subhadra V. Nandula, Vundavalli V. Murty
Publikováno v:
Genes, chromosomescancer.
The cytogenetic alterations in renal oncocytoma (RO) are poorly understood. We analyzed 130 consecutive RO for karyotypic alterations. Clonal chromosome abnormalities were identified in 63 (49%) cases, which could be categorized into three classes of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbf8f4fe7c5a120b0eb426c8af6053e4
https://pubmed.ncbi.nlm.nih.gov/31112346
https://pubmed.ncbi.nlm.nih.gov/31112346
Autor:
Sharon E. Oberfield, Brynn Levy, Tamar G. Baer, Claudia Cujar, Rosanna G. Abellar, Bahadur Singh, Xiaowei Chen, Mahesh M. Mansukhani, Christopher E Freeman
Although monosomy X is the most common karyotype in patients with Turner syndrome, the presence of Y chromosome material has been observed in about 10% of patients. Y chromosome material in patients with Turner syndrome poses an increased risk of gon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33040d6a48755a4483515dab869b9ba7
https://europepmc.org/articles/PMC5832898/
https://europepmc.org/articles/PMC5832898/
Autor:
Christopher E Freeman, Danielle Pendrick, Gary K. Schwartz, Jennifer A. Oberg, Anthony N. Sireci, Susan Jean Hsiao, Richard D. Carvajal, Mahesh M. Mansukhani, Jessica Yang
Publikováno v:
Journal of Clinical Oncology. 37:6593-6593
6593 Background: The routine use of large next generation sequencing (NGS) cancer panels is required to identify the increasing number of, but often uncommon actionable alterations present across multiple tumor histologies to guide therapy. Inconsist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::307f183aed796cf5f43ee8d38b7119ea
https://doi.org/10.1200/jco.2019.37.15_suppl.6593
https://doi.org/10.1200/jco.2019.37.15_suppl.6593
Publikováno v:
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences. 41(4)
The most frequent chromosomal rearrangement reported in acute promyelocytic leukemia (APL) is t(15; 17) (q22; q21). The t(15; 17) generates the PML/RARA fusion gene that blocks the transcription of genes involved in myeloid cell differentiation. A sm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a258834dd93244b03acbb2bd095a319f
https://pubmed.ncbi.nlm.nih.gov/19727242
https://pubmed.ncbi.nlm.nih.gov/19727242
Publikováno v:
Cancer Research. 71:314-314
The application of chromosomal microarray analysis (CMA) in cancer research has produced a wealth of useful information about copy number alterations (CNAs) and their implications in cancer classification, disease progression, therapy response, and p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5802d65462a0384d2d1da96a3cb797cf
https://doi.org/10.1158/1538-7445.am2011-314
https://doi.org/10.1158/1538-7445.am2011-314