Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Dana Shuey

Showing results (1-10 of 9) with videos related to

Pageof 1
Sort By:
Birth Defects Research. Part B, Developmental and Reproductive Toxicology|July 20, 2011
Overview: developmental toxicology: new directionsDana Shuey, James H Kim
Birth Defects Research. Part B, Developmental and Reproductive Toxicology|October 19, 2011
Developmental toxicology: new directions workshop: refining testing strategies and study designsKimberly C Brannen, Suzanne E Fenton, Deborah K Hansen, et al.
Toxicology and Applied Pharmacology|September 7, 2024
Do longer duration nonclinical toxicology studies provide predictive clinical safety value? The IQ consortium longer duration nonclinical to clinical translational databaseThomas M Monticello, David M Potter, Qihong Huang, et al.
Regulatory Toxicology and Pharmacology : RTP|December 31, 2022
FDA and industry collaboration: Identifying opportunities to further reduce reliance on nonhuman primates for nonclinical safety evaluationsDavid Ackley, Joanne Birkebak, Jorg Blumel, et al.
Regulatory Toxicology and Pharmacology : RTP|February 27, 2025
Nonclinical teratogenicity safety assessment of CRBN-engaging targeted protein degraders: Points to considerLise I Loberg, William R Proctor, Andrew D Burdick, et al.
Regulatory Toxicology and Pharmacology : RTP|September 10, 2020
Nonclinical safety assessment of epigenetic modulatory drugs: Current status and industry perspectiveVincent L Reynolds, Paul Butler, Matthew M Abernathy, et al.
The Journal of Pharmacology and Experimental Therapeutics|November 12, 2017
INCB040093 Is a Novel PI3K<i>δ</i> Inhibitor for the Treatment of B Cell Lymphoid MalignanciesNiu Shin, Yun-Long Li, Song Mei, et al.
Regulatory Toxicology and Pharmacology : RTP|February 17, 2016
Extending (Q)SARs to incorporate proprietary knowledge for regulatory purposes: A case study using aromatic amine mutagenicityErnst Ahlberg, Alexander Amberg, Lisa D Beilke, et al.
The Journal of Pharmacology and Experimental Therapeutics|April 30, 2020
Parsaclisib Is a Next-Generation Phosphoinositide 3-Kinase <i>δ</i> Inhibitor with Reduced Hepatotoxicity and Potent Antitumor and Immunomodulatory Activities in Models of B-Cell MalignancyNiu Shin, Matthew Stubbs, Holly Koblish, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Birth Defects Research. Part B, Developmental and Reproductive Toxicology|July 20, 2011
Overview: developmental toxicology: new directionsDana Shuey, James H Kim
Birth Defects Research. Part B, Developmental and Reproductive Toxicology|October 19, 2011
Developmental toxicology: new directions workshop: refining testing strategies and study designsKimberly C Brannen, Suzanne E Fenton, Deborah K Hansen, et al.
Toxicology and Applied Pharmacology|September 7, 2024
Do longer duration nonclinical toxicology studies provide predictive clinical safety value? The IQ consortium longer duration nonclinical to clinical translational databaseThomas M Monticello, David M Potter, Qihong Huang, et al.
Regulatory Toxicology and Pharmacology : RTP|December 31, 2022
FDA and industry collaboration: Identifying opportunities to further reduce reliance on nonhuman primates for nonclinical safety evaluationsDavid Ackley, Joanne Birkebak, Jorg Blumel, et al.
Regulatory Toxicology and Pharmacology : RTP|February 27, 2025
Nonclinical teratogenicity safety assessment of CRBN-engaging targeted protein degraders: Points to considerLise I Loberg, William R Proctor, Andrew D Burdick, et al.
Regulatory Toxicology and Pharmacology : RTP|September 10, 2020
Nonclinical safety assessment of epigenetic modulatory drugs: Current status and industry perspectiveVincent L Reynolds, Paul Butler, Matthew M Abernathy, et al.
The Journal of Pharmacology and Experimental Therapeutics|November 12, 2017
INCB040093 Is a Novel PI3K<i>δ</i> Inhibitor for the Treatment of B Cell Lymphoid MalignanciesNiu Shin, Yun-Long Li, Song Mei, et al.
Regulatory Toxicology and Pharmacology : RTP|February 17, 2016
Extending (Q)SARs to incorporate proprietary knowledge for regulatory purposes: A case study using aromatic amine mutagenicityErnst Ahlberg, Alexander Amberg, Lisa D Beilke, et al.
The Journal of Pharmacology and Experimental Therapeutics|April 30, 2020
Parsaclisib Is a Next-Generation Phosphoinositide 3-Kinase <i>δ</i> Inhibitor with Reduced Hepatotoxicity and Potent Antitumor and Immunomodulatory Activities in Models of B-Cell MalignancyNiu Shin, Matthew Stubbs, Holly Koblish, et al.
Pageof 1