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American Journal of Human Genetics
|
August 10, 2010
Microdeletions of 3q29 confer high risk for schizophrenia
Jennifer Gladys Mulle, Anne F Dodd, John A McGrath, et al.
Medical Care
|
August 4, 2018
Building Meaningful Patient Engagement in Research: Case Study From ADVANCE Clinical Data Research Network
Nathaniel T Warren, James A Gaudino, Sonja Likumahuwa-Ackman, et al.
Molecular Autism
|
July 11, 2018
Case-control meta-analysis of blood DNA methylation and autism spectrum disorder
Shan V Andrews, Brooke Sheppard, Gayle C Windham, et al.
Blood
|
June 11, 2021
Heterozygous variants of CLPB are a cause of severe congenital neutropenia
Julia T Warren, Ryan R Cupo, Peeradol Wattanasirakul, et al.
Molecular Psychiatry
|
April 13, 2019
Behavioral changes and growth deficits in a CRISPR engineered mouse model of the schizophrenia-associated 3q29 deletion
Timothy P Rutkowski, Ryan H Purcell, Rebecca M Pollak, et al.
Human Molecular Genetics
|
April 12, 2017
Novel nesprin-1 mutations associated with dilated cardiomyopathy cause nuclear envelope disruption and defects in myogenesis
Can Zhou, Chen Li, Bin Zhou, et al.
Plos Genetics
|
November 22, 2011
Relative burden of large CNVs on a range of neurodevelopmental phenotypes
Santhosh Girirajan, Zoran Brkanac, Bradley P Coe, et al.
The EMBO Journal
|
August 29, 2009
Structural basis for the preferential recognition of immature flaviviruses by a fusion-loop antibody
Mickaël V Cherrier, Bärbel Kaufmann, Grant E Nybakken, et al.
Science Translational Medicine
|
September 21, 2012
Reversal of disease-related pathologies in the fragile X mouse model by selective activation of GABAB receptors with arbaclofen
Christina Henderson, Lasani Wijetunge, Mika Nakamoto Kinoshita, et al.
Biorxiv : the Preprint Server for Biology
|
July 16, 2025
Aiolos restricts the generation of antigen-inexperienced, virtual memory CD8<sup>+</sup> T cells
Srijana Pokhrel, Devin M Jones, Melissa R Leonard, et al.
Page
of 48
Search research articles
Search
Showing results (421-430 of 471) with videos related to
Sort By:
Page
of 48
American Journal of Human Genetics
|
August 10, 2010
Microdeletions of 3q29 confer high risk for schizophrenia
Jennifer Gladys Mulle, Anne F Dodd, John A McGrath, et al.
Medical Care
|
August 4, 2018
Building Meaningful Patient Engagement in Research: Case Study From ADVANCE Clinical Data Research Network
Nathaniel T Warren, James A Gaudino, Sonja Likumahuwa-Ackman, et al.
Molecular Autism
|
July 11, 2018
Case-control meta-analysis of blood DNA methylation and autism spectrum disorder
Shan V Andrews, Brooke Sheppard, Gayle C Windham, et al.
Blood
|
June 11, 2021
Heterozygous variants of CLPB are a cause of severe congenital neutropenia
Julia T Warren, Ryan R Cupo, Peeradol Wattanasirakul, et al.
Molecular Psychiatry
|
April 13, 2019
Behavioral changes and growth deficits in a CRISPR engineered mouse model of the schizophrenia-associated 3q29 deletion
Timothy P Rutkowski, Ryan H Purcell, Rebecca M Pollak, et al.
Human Molecular Genetics
|
April 12, 2017
Novel nesprin-1 mutations associated with dilated cardiomyopathy cause nuclear envelope disruption and defects in myogenesis
Can Zhou, Chen Li, Bin Zhou, et al.
Plos Genetics
|
November 22, 2011
Relative burden of large CNVs on a range of neurodevelopmental phenotypes
Santhosh Girirajan, Zoran Brkanac, Bradley P Coe, et al.
The EMBO Journal
|
August 29, 2009
Structural basis for the preferential recognition of immature flaviviruses by a fusion-loop antibody
Mickaël V Cherrier, Bärbel Kaufmann, Grant E Nybakken, et al.
Science Translational Medicine
|
September 21, 2012
Reversal of disease-related pathologies in the fragile X mouse model by selective activation of GABAB receptors with arbaclofen
Christina Henderson, Lasani Wijetunge, Mika Nakamoto Kinoshita, et al.
Biorxiv : the Preprint Server for Biology
|
July 16, 2025
Aiolos restricts the generation of antigen-inexperienced, virtual memory CD8<sup>+</sup> T cells
Srijana Pokhrel, Devin M Jones, Melissa R Leonard, et al.
Page
of 48