Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Robert Scharpf"'
Autor:
Farhad Vesuna, Ivan Akhrymuk, Amy Smith, Paul T. Winnard, Shih-Chao Lin, Lauren Panny, Robert Scharpf, Kylene Kehn-Hall, Venu Raman
Publikováno v:
Frontiers in Microbiology, Vol 13 (2022)
SARS-CoV-2, the virus behind the deadly COVID-19 pandemic, continues to spread globally even as vaccine strategies are proving effective in preventing hospitalizations and deaths. However, evolving variants of the virus appear to be more transmissive
Externí odkaz:
https://doaj.org/article/8955e83bf9ba4aa1a0372b40e904b979
Publikováno v:
BioTechniques, Vol 34, Iss 3S, Pp S22-S29 (2003)
Current cancer classifications using morphological criteria produce heterogeneous classes with variable prognosis and clinical course. By measuring gene expression for thousands of genes in a single hybridization experiment, microarrays have the pote
Externí odkaz:
https://doaj.org/article/528d8af33e12417dadc402cc8fb75d05
Autor:
Nilanjan Chatterjee, Elle Kim, Robert Scharpf, Montserrat García-Closas, Kala Visvanathan, Victor Velculescu
Our proof-of-concept study reveals the potential of risk stratification by the combined effects of age, polygenic risk scores (PRS), and non-genetic risk factors in increasing the risk-benefit balance of rapidly emerging non-invasive multicancer liqu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5918aff72066a8d03eef69bf046eaecc
https://doi.org/10.21203/rs.3.rs-2382811/v1
https://doi.org/10.21203/rs.3.rs-2382811/v1
Autor:
Alessandro Leal, Iris van 't Erve, Keith Lumbard, Laurel Keefer, Jacob Carey, Tony Wu, Debbie Jakubowski, Denise Butler, Michael Rongione, Bryan Chesnick, Cornelis J. A. Punt, Gerrit A. Meijer, Nicholas C Dracopoli, Tara Maddala, Robert Scharpf, Peter Brian Bach, Victor E. Velculescu, Remond Fijneman
Publikováno v:
Journal of Clinical Oncology. 40:3541-3541
3541 Background: Measurement of plasma mutant allele fraction (MAF) in patients with cancer provides prognostic information, but this approach typically relies on prior tumor tissue analyses or knowledge of specific mutations. There is a clinical nee
Complementary DNA (cDNA) microarrays are a powerful tool for genomic analysis, but have noise components that make inferences regarding gene expression inefficient and potentially misleading. Background fluorescence, whether attributable to non-speci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______645::52af9fe1f51ab85a2328aed06a3c98b1
http://www.bepress.com/cgi/viewcontent.cgi?article=1050&context=jhubiostat
http://www.bepress.com/cgi/viewcontent.cgi?article=1050&context=jhubiostat