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1960P Differential induction of gene expression may explain differences in reported adverse event profiles between the FGFR-inhibitors derazantinib and erdafitinib: An analysis in safety relevant normal tissues from urothelial cancer (UC) patient-derived mouse xenograft (PDX) models

Publication ,  Conference
McSheehy, P; Guo, J; Beebe, K; Eisner, JR; Anderson, S; Braun, S; Engelhardt, M; Kellenberger, L; Lane, H; Milburn, M
Published in: Annals of Oncology
September 2020

Duke Scholars

Published In

Annals of Oncology

DOI

ISSN

0923-7534

Publication Date

September 2020

Volume

31

Start / End Page

S1103 / S1104

Publisher

Elsevier BV

Related Subject Headings

  • Oncology & Carcinogenesis
  • 3211 Oncology and carcinogenesis
  • 3202 Clinical sciences
  • 1112 Oncology and Carcinogenesis
 

Citation

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McSheehy, P., Guo, J., Beebe, K., Eisner, J. R., Anderson, S., Braun, S., … Milburn, M. (2020). 1960P Differential induction of gene expression may explain differences in reported adverse event profiles between the FGFR-inhibitors derazantinib and erdafitinib: An analysis in safety relevant normal tissues from urothelial cancer (UC) patient-derived mouse xenograft (PDX) models. In Annals of Oncology (Vol. 31, pp. S1103–S1104). Elsevier BV. https://doi.org/10.1016/j.annonc.2020.08.1352
McSheehy, P., J. Guo, K. Beebe, J. R. Eisner, S. Anderson, S. Braun, M. Engelhardt, L. Kellenberger, H. Lane, and M. Milburn. “1960P Differential induction of gene expression may explain differences in reported adverse event profiles between the FGFR-inhibitors derazantinib and erdafitinib: An analysis in safety relevant normal tissues from urothelial cancer (UC) patient-derived mouse xenograft (PDX) models.” In Annals of Oncology, 31:S1103–4. Elsevier BV, 2020. https://doi.org/10.1016/j.annonc.2020.08.1352.
Journal cover image

Published In

Annals of Oncology

DOI

ISSN

0923-7534

Publication Date

September 2020

Volume

31

Start / End Page

S1103 / S1104

Publisher

Elsevier BV

Related Subject Headings

  • Oncology & Carcinogenesis
  • 3211 Oncology and carcinogenesis
  • 3202 Clinical sciences
  • 1112 Oncology and Carcinogenesis