Search research articles
Contact Us
Filters
Showing results (111-120 of 142) with videos related to
Page
of 15
Sort By:
Journal of Child and Adolescent Psychopharmacology
|
February 19, 2025
Predictors of Placebo Response in the Study of Oxytocin in Autism to Improve Reciprocal Social Behaviors
Alyssa Verdes, Suvekcha Bhattachan, Alexander Kolevzon, et al.
Scientific Reports
|
April 12, 2020
Circulating MicroRNA Profiling in Non-ST Elevated Coronary Artery Syndrome Highlights Genomic Associations with Serial Platelet Reactivity Measurements
Kristian C Becker, Lydia Coulter Kwee, Megan L Neely, et al.
BMC Medicine
|
October 23, 2009
Genomic and epigenetic evidence for oxytocin receptor deficiency in autism
Simon G Gregory, Jessica J Connelly, Aaron J Towers, et al.
Human Genetics
|
February 8, 2011
Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease
Mollie A Minear, David R Crosslin, Beth S Sutton, et al.
Plos One
|
May 29, 2019
Pharmacodynamic study of radium-223 in men with bone metastatic castration resistant prostate cancer
Andrew J Armstrong, Santosh Gupta, Patrick Healy, et al.
Blood Advances
|
January 24, 2025
Cutaneous dysbiosis characterizes the post-allogeneic hematopoietic stem cell transplantation period
Adela R Cardones, Akintunde Emiola, Russell P Hall, et al.
Human Molecular Genetics
|
August 6, 2013
Epigenetic regulation of COL15A1 in smooth muscle cell replicative aging and atherosclerosis
Jessica J Connelly, Olga A Cherepanova, Jennifer F Doss, et al.
BMC Medical Genetics
|
April 24, 2008
Genetic and functional association of FAM5C with myocardial infarction
Jessica J Connelly, Svati H Shah, Jennifer F Doss, et al.
Cell Genomics
|
December 5, 2022
Single-cell genome-wide association reveals that a nonsynonymous variant in <i>ERAP1</i> confers increased susceptibility to influenza virus
Benjamin H Schott, Liuyang Wang, Xinyu Zhu, et al.
American Journal of Human Genetics
|
March 16, 2007
Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease
Liyong Wang, Elizabeth R Hauser, Svati H Shah, et al.
Page
of 15
Search research articles
Search
Showing results (111-120 of 142) with videos related to
Sort By:
Page
of 15
Journal of Child and Adolescent Psychopharmacology
|
February 19, 2025
Predictors of Placebo Response in the Study of Oxytocin in Autism to Improve Reciprocal Social Behaviors
Alyssa Verdes, Suvekcha Bhattachan, Alexander Kolevzon, et al.
Scientific Reports
|
April 12, 2020
Circulating MicroRNA Profiling in Non-ST Elevated Coronary Artery Syndrome Highlights Genomic Associations with Serial Platelet Reactivity Measurements
Kristian C Becker, Lydia Coulter Kwee, Megan L Neely, et al.
BMC Medicine
|
October 23, 2009
Genomic and epigenetic evidence for oxytocin receptor deficiency in autism
Simon G Gregory, Jessica J Connelly, Aaron J Towers, et al.
Human Genetics
|
February 8, 2011
Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease
Mollie A Minear, David R Crosslin, Beth S Sutton, et al.
Plos One
|
May 29, 2019
Pharmacodynamic study of radium-223 in men with bone metastatic castration resistant prostate cancer
Andrew J Armstrong, Santosh Gupta, Patrick Healy, et al.
Blood Advances
|
January 24, 2025
Cutaneous dysbiosis characterizes the post-allogeneic hematopoietic stem cell transplantation period
Adela R Cardones, Akintunde Emiola, Russell P Hall, et al.
Human Molecular Genetics
|
August 6, 2013
Epigenetic regulation of COL15A1 in smooth muscle cell replicative aging and atherosclerosis
Jessica J Connelly, Olga A Cherepanova, Jennifer F Doss, et al.
BMC Medical Genetics
|
April 24, 2008
Genetic and functional association of FAM5C with myocardial infarction
Jessica J Connelly, Svati H Shah, Jennifer F Doss, et al.
Cell Genomics
|
December 5, 2022
Single-cell genome-wide association reveals that a nonsynonymous variant in <i>ERAP1</i> confers increased susceptibility to influenza virus
Benjamin H Schott, Liuyang Wang, Xinyu Zhu, et al.
American Journal of Human Genetics
|
March 16, 2007
Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease
Liyong Wang, Elizabeth R Hauser, Svati H Shah, et al.
Page
of 15