Search research articles
Contact Us
Filters
Showing results (201-210 of 204) with videos related to
Page
of 21
Sort By:
You have reached the last page of results.
This site can display upto 204 results.
Current Research in Pharmacology and Drug Discovery
|
December 3, 2025
MAO-B inhibition by selegiline blunts cardiac functions improved by high-fat diet: Role of inflammation, apoptosis, and calcium-handling
Szabolcs Hambalkó, Csilla Pelyhe, Csenger Kovácsházi, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 12, 2021
The feasibility of home monitoring of young people with cystic fibrosis: Results from CLIMB-CF
C Edmondson, N Westrupp, P Seddon, et al.
American Journal of Human Genetics
|
March 3, 2018
Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2
Petra Lassuthova, Adriana P Rebelo, Gianina Ravenscroft, 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.
Page
of 21
Search research articles
Search
Showing results (201-210 of 204) with videos related to
Sort By:
Page
of 21
You have reached the last page of results.
This site can display upto 204 results.
Current Research in Pharmacology and Drug Discovery
|
December 3, 2025
MAO-B inhibition by selegiline blunts cardiac functions improved by high-fat diet: Role of inflammation, apoptosis, and calcium-handling
Szabolcs Hambalkó, Csilla Pelyhe, Csenger Kovácsházi, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 12, 2021
The feasibility of home monitoring of young people with cystic fibrosis: Results from CLIMB-CF
C Edmondson, N Westrupp, P Seddon, et al.
American Journal of Human Genetics
|
March 3, 2018
Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2
Petra Lassuthova, Adriana P Rebelo, Gianina Ravenscroft, 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.
Page
of 21