Search research articles
Contact Us
Filters
Showing results (371-380 of 374) with videos related to
Page
of 38
Sort By:
You have reached the last page of results.
This site can display upto 374 results.
Cell Reports
|
October 24, 2019
The Lineage Determining Factor GRHL2 Collaborates with FOXA1 to Establish a Targetable Pathway in Endocrine Therapy-Resistant Breast Cancer
Kimberly J Cocce, Jeff S Jasper, Taylor K Desautels, et al.
Journal of Medicinal Chemistry
|
July 10, 2026
Discovery of Potential First-in-Class Dual Ligand-Directed Degrader and Antagonist of the Androgen Receptor: BMS-986365
Deborah S Mortensen, Surendra Nayak, Veronique Plantevin-Krenitsky, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 10, 2023
Rare variants in <i>PPFIA3</i> cause delayed development, intellectual disability, autism, and epilepsy
Maimuna S Paul, Sydney L Michener, Hongling Pan, et al.
American Journal of Human Genetics
|
January 5, 2024
A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3
Maimuna S Paul, Sydney L Michener, Hongling Pan, et al.
Page
of 38
Search research articles
Search
Showing results (371-380 of 374) with videos related to
Sort By:
Page
of 38
You have reached the last page of results.
This site can display upto 374 results.
Cell Reports
|
October 24, 2019
The Lineage Determining Factor GRHL2 Collaborates with FOXA1 to Establish a Targetable Pathway in Endocrine Therapy-Resistant Breast Cancer
Kimberly J Cocce, Jeff S Jasper, Taylor K Desautels, et al.
Journal of Medicinal Chemistry
|
July 10, 2026
Discovery of Potential First-in-Class Dual Ligand-Directed Degrader and Antagonist of the Androgen Receptor: BMS-986365
Deborah S Mortensen, Surendra Nayak, Veronique Plantevin-Krenitsky, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 10, 2023
Rare variants in <i>PPFIA3</i> cause delayed development, intellectual disability, autism, and epilepsy
Maimuna S Paul, Sydney L Michener, Hongling Pan, et al.
American Journal of Human Genetics
|
January 5, 2024
A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3
Maimuna S Paul, Sydney L Michener, Hongling Pan, et al.
Page
of 38