Zobrazeno 1 - 10
of 160
pro vyhledávání: '"CECILE ROSE"'
Autor:
Ryan D. Gentzler, John Guittar, Akash Mitra, Wade T. Iams, Terri Driessen, Regina Schwind, Michelle M. Stein, Kristiyana Kaneva, Seung Won Hyun, Yan Liu, Adam J. Dugan, Cecile Rose T. Vibat, Chithra Sangli, Jonathan Freaney, Zachary Rivers, Josephine L. Feliciano, Christine Lo, Kate Sasser, Rotem Ben-Shachar, Halla Nimeiri, Jyoti D. Patel, Aadel A. Chaudhuri
Publikováno v:
Oncology and Therapy, Vol 12, Iss 3, Pp 509-524 (2024)
Abstract Introduction A dynamic molecular biomarker that can identify early efficacy of immune checkpoint inhibitor (ICI) therapy remains an unmet clinical need. Here we evaluate if a novel circulating tumor DNA (ctDNA) assay, xM, used for treatment
Externí odkaz:
https://doaj.org/article/e9866030c92c41cc8282109a54d5780e
Autor:
Robert Cohen, Cecile Rose, Leonard Go, Lauren Zell-Baran, Kirsten Almberg, Emily Sarver, Heather Lowers, Cayla Iwaniuk, Sidney Clingerman, Diane Richardson, Jerrold Abraham, Carlyne Cool, Angela Franko, Ann Hubbs, Jill Murray, Marlene Orandle, Soma Sanyal, Naseema Vorajee, Edward Petsonk, Rafia Zulfikar, Francis Green
Publikováno v:
Safety and Health at Work, Vol 13, Iss , Pp S54- (2022)
Externí odkaz:
https://doaj.org/article/3be7046ad30b43bb954110a66a561236
Autor:
Megan R. Reed, A. Geoffrey Lyle, Annick De Loose, Katrina Learned, Cecile Rose T. Vibat, Christopher P. Wardell, Robert L. Eoff, Olena M. Vaske, Analiz Rodriguez
Publikováno v:
Journal of Clinical and Translational Science, Vol 6, Pp 58-58 (2022)
OBJECTIVES/GOALS: A functional precision medicine platform to identify therapeutic targets for a glioblastoma patient with Li Fraumeni syndrome was performed. Comparative transcriptomics identified druggable targets and patient derived organoids and
Externí odkaz:
https://doaj.org/article/c2c3317ab6de45a186e45d9014a1a342
Autor:
Megan R. Reed, A. Geoffrey Lyle, Annick De Loose, Leena Maddukuri, Katrina Learned, Holly C. Beale, Ellen T. Kephart, Allison Cheney, Anouk van den Bout, Madison P. Lee, Kelsey N. Hundley, Ashley M. Smith, Teresa M. DesRochers, Cecile Rose T. Vibat, Murat Gokden, Sofie Salama, Christopher P. Wardell, Robert L. Eoff, Olena M. Vaske, Analiz Rodriguez
Publikováno v:
Cells, Vol 10, Iss 12, p 3400 (2021)
Li Fraumeni syndrome (LFS) is a hereditary cancer predisposition syndrome caused by germline mutations in TP53. TP53 is the most common mutated gene in human cancer, occurring in 30–50% of glioblastomas (GBM). Here, we highlight a precision medicin
Externí odkaz:
https://doaj.org/article/9dc85f09d7834fddbaa84d2a1a8e9843
Autor:
Jason C Poole, Shan-Fu Wu, Timothy T Lu, Cecile Rose T Vibat, Anh Pham, Errin Samuelsz, Manisha Patel, Jeffrey Chen, Tony Daher, Veena M Singh, Lyle J Arnold
Publikováno v:
PLoS ONE, Vol 14, Iss 10, p e0223112 (2019)
BackgroundPersonalized medicine requires accurate molecular profiling for targeted therapy decisions. Insufficient tissue yield or tumor heterogeneity frequently limits the correct tissue biomarker determination. As a noninvasive complement to tradit
Externí odkaz:
https://doaj.org/article/ddb7907e25c84418a98c0e082043cc61
Autor:
Gentzler, Ryan D., Guittar, John, Mitra, Akash, Iams, Wade T., Driessen, Terri, Schwind, Regina, Stein, Michelle M., Kaneva, Kristiyana, Hyun, Seung Won, Liu, Yan, Dugan, Adam J., Vibat, Cecile Rose T., Sangli, Chithra, Freaney, Jonathan, Rivers, Zachary, Feliciano, Josephine L., Lo, Christine, Sasser, Kate, Ben-Shachar, Rotem, Nimeiri, Halla
Publikováno v:
Oncology & Therapy; Sep2024, Vol. 12 Issue 3, p509-524, 16p
Autor:
Reckamp, Karen L., Melnikova, Vladislava O., Karlovich, Chris, Sequist, Lecia V., Camidge, D. Ross, Wakelee, Heather, Perol, Maurice, Oxnard, Geoffrey R., Kosco, Karena, Croucher, Peter, Samuelsz, Errin, Vibat, Cecile Rose, Guerrero, Shiloh, Geis, Jennifer, Berz, David, Mann, Elaina, Matheny, Shannon, Rolfe, Lindsey, Raponi, Mitch, Erlander, Mark G., Gadgeel, Shirish
Publikováno v:
In Journal of Thoracic Oncology October 2016 11(10):1690-1700
Autor:
Omar Abdel-Wahab, Filip Janku, Mark G. Erlander, Razelle Kurzrock, José Baselga, Funda Meric-Bernstam, Neal Rosen, Mario E. Lacouture, Raajit Rampal, Young Rock Chung, Maria E. Arcila, Timothy T. Lu, Goran Cabrilo, Veronica R. Holley, Minal Patel, Jason C. Poole, Latifa Hassaine, Cecile Rose T. Vibat, Eli L. Diamond, David M. Hyman
Supplemental Figure 1: BRAFV600E mutant allele burden in cell-free DNA (cfDNA) of urine and plasma from treatment naïve patients based on BRAFV600E tissue genotype result.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a277f843ce038a80eacf835c55f496a
https://doi.org/10.1158/2159-8290.22529876.v1
https://doi.org/10.1158/2159-8290.22529876.v1
Autor:
Omar Abdel-Wahab, Filip Janku, Mark G. Erlander, Razelle Kurzrock, José Baselga, Funda Meric-Bernstam, Neal Rosen, Mario E. Lacouture, Raajit Rampal, Young Rock Chung, Maria E. Arcila, Timothy T. Lu, Goran Cabrilo, Veronica R. Holley, Minal Patel, Jason C. Poole, Latifa Hassaine, Cecile Rose T. Vibat, Eli L. Diamond, David M. Hyman
Supplemental Figure 2: Radiographic, histologic, and molecular evaluation of KRASG12S mutant patient with Erdheim-Chester Disease (ECD).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e762a21c526c3d7637ce66bf1ece2c9
https://doi.org/10.1158/2159-8290.22529873.v1
https://doi.org/10.1158/2159-8290.22529873.v1
Autor:
Omar Abdel-Wahab, Filip Janku, Mark G. Erlander, Razelle Kurzrock, José Baselga, Funda Meric-Bernstam, Neal Rosen, Mario E. Lacouture, Raajit Rampal, Young Rock Chung, Maria E. Arcila, Timothy T. Lu, Goran Cabrilo, Veronica R. Holley, Minal Patel, Jason C. Poole, Latifa Hassaine, Cecile Rose T. Vibat, Eli L. Diamond, David M. Hyman
Supplemental Table 3: Plasma and urine cfDNA mutation detection zscores for KRAS (G12A, G12C, G12D, G12R, G12S, G12V, G13D) with tissue biopsy KRASG12 genotyping from patient with Erdheim-Chester Disease (ECD).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4dd72dc0328866fed3c6fd44cf7b7e83
https://doi.org/10.1158/2159-8290.22529864
https://doi.org/10.1158/2159-8290.22529864