Search research articles
Contact Us
Filters
Showing results (241-250 of 244) with videos related to
Page
of 25
Sort By:
You have reached the last page of results.
This site can display upto 244 results.
Plos One
|
June 14, 2018
Traditional and systems biology based drug discovery for the rare tumor syndrome neurofibromatosis type 2
, Robert Allaway, Steve P Angus, et al.
Plos One
|
July 15, 2021
Brigatinib causes tumor shrinkage in both NF2-deficient meningioma and schwannoma through inhibition of multiple tyrosine kinases but not ALK
Long-Sheng Chang, Janet L Oblinger, Abbi E Smith, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 11, 2026
Clinical, <i>in vitro,</i> and <i>in vivo</i> evidence of <i>WAPL</i> as a novel cohesinopathy gene and phenotypic driver of 10q22.3q23.2 genomic disorder
Philip M Boone, Serkan Erdin, Abucar Mohamed, et al.
American Journal of Human Genetics
|
July 10, 2026
Clinical, in vitro, and in vivo evidence of WAPL as a cohesinopathy-associated gene and phenotypic driver of 10q22.3q23.2 genomic disorder
Philip M Boone, Serkan Erdin, Abucar Mohamed, et al.
Page
of 25
Search research articles
Search
Showing results (241-250 of 244) with videos related to
Sort By:
Page
of 25
You have reached the last page of results.
This site can display upto 244 results.
Plos One
|
June 14, 2018
Traditional and systems biology based drug discovery for the rare tumor syndrome neurofibromatosis type 2
, Robert Allaway, Steve P Angus, et al.
Plos One
|
July 15, 2021
Brigatinib causes tumor shrinkage in both NF2-deficient meningioma and schwannoma through inhibition of multiple tyrosine kinases but not ALK
Long-Sheng Chang, Janet L Oblinger, Abbi E Smith, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 11, 2026
Clinical, <i>in vitro,</i> and <i>in vivo</i> evidence of <i>WAPL</i> as a novel cohesinopathy gene and phenotypic driver of 10q22.3q23.2 genomic disorder
Philip M Boone, Serkan Erdin, Abucar Mohamed, et al.
American Journal of Human Genetics
|
July 10, 2026
Clinical, in vitro, and in vivo evidence of WAPL as a cohesinopathy-associated gene and phenotypic driver of 10q22.3q23.2 genomic disorder
Philip M Boone, Serkan Erdin, Abucar Mohamed, et al.
Page
of 25