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

Paul Liu

Showing results (141-150 of 144) with videos related to

Pageof 15
Sort By:
You have reached the last page of results.This site can display upto 144 results.
Proceedings of the National Academy of Sciences of the United States of America|September 5, 2020
CHD7 and Runx1 interaction provides a braking mechanism for hematopoietic differentiationJingmei Hsu, Hsuan-Ting Huang, Chung-Tsai Lee, et al.
Haematologica|July 8, 2021
The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancyClaire C Homan, Sarah L King-Smith, David M Lawrence, et al.
Blood|December 21, 2022
Differential diagnosis of bone marrow failure syndromes guided by machine learningFernanda Gutierrez-Rodrigues, Eric Munger, Xiaoyang Ma, et al.
Blood Advances|July 5, 2023
Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41Claire C Homan, Michael W Drazer, Kai Yu, et al.
Pageof 15

Showing results (141-150 of 144) with videos related to

Sort By:
Pageof 15
You have reached the last page of results.This site can display upto 144 results.
Proceedings of the National Academy of Sciences of the United States of America|September 5, 2020
CHD7 and Runx1 interaction provides a braking mechanism for hematopoietic differentiationJingmei Hsu, Hsuan-Ting Huang, Chung-Tsai Lee, et al.
Haematologica|July 8, 2021
The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancyClaire C Homan, Sarah L King-Smith, David M Lawrence, et al.
Blood|December 21, 2022
Differential diagnosis of bone marrow failure syndromes guided by machine learningFernanda Gutierrez-Rodrigues, Eric Munger, Xiaoyang Ma, et al.
Blood Advances|July 5, 2023
Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41Claire C Homan, Michael W Drazer, Kai Yu, et al.
Pageof 15