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Elizabeth J Radford

Showing results (11-20 of 22) with videos related to

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Iscience|January 6, 2026
TET3 protects the <i>Dlk1-Dio3</i> imprinted locus from DNA hypomethylation during adult NSC reprogrammingLaura Lázaro-Carot, Esteban Jiménez-Villalba, Jordi Planells, et al.
Plos Genetics|April 19, 2012
An unbiased assessment of the role of imprinted genes in an intergenerational model of developmental programmingElizabeth J Radford, Elvira Isganaitis, Josep Jimenez-Chillaron, et al.
Genome Medicine|October 31, 2025
Investigating the interplay between prematurity and genetic variation in the context of rare developmental disordersOlivia Wootton, Patrick Campbell, Sarah Richardson, et al.
Science (New York, N.Y.)|July 12, 2014
In utero effects. In utero undernourishment perturbs the adult sperm methylome and intergenerational metabolismElizabeth J Radford, Mitsuteru Ito, Hui Shi, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 22, 2011
Acclimatization of skeletal muscle mitochondria to high-altitude hypoxia during an ascent of EverestDenny Z Levett, Elizabeth J Radford, David A Menassa, et al.
Plos Genetics|March 4, 2016
Role of the BAHD1 Chromatin-Repressive Complex in Placental Development and Regulation of Steroid MetabolismGoran Lakisic, Alice Lebreton, Renaud Pourpre, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 24, 2019
Intergenerational transmission of the positive effects of physical exercise on brain and cognitionKerry R McGreevy, Patricia Tezanos, Iria Ferreiro-Villar, et al.
Nature|September 28, 2018
Common genetic variants contribute to risk of rare severe neurodevelopmental disordersMari E K Niemi, Hilary C Martin, Daniel L Rice, et al.
Nature Communications|December 6, 2023
Saturation genome editing of DDX3X clarifies pathogenicity of germline and somatic variationElizabeth J Radford, Hong-Kee Tan, Malin H L Andersson, et al.
Nature|November 20, 2024
Examining the role of common variants in rare neurodevelopmental conditionsQin Qin Huang, Emilie M Wigdor, Daniel S Malawsky, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Iscience|January 6, 2026
TET3 protects the <i>Dlk1-Dio3</i> imprinted locus from DNA hypomethylation during adult NSC reprogrammingLaura Lázaro-Carot, Esteban Jiménez-Villalba, Jordi Planells, et al.
Plos Genetics|April 19, 2012
An unbiased assessment of the role of imprinted genes in an intergenerational model of developmental programmingElizabeth J Radford, Elvira Isganaitis, Josep Jimenez-Chillaron, et al.
Genome Medicine|October 31, 2025
Investigating the interplay between prematurity and genetic variation in the context of rare developmental disordersOlivia Wootton, Patrick Campbell, Sarah Richardson, et al.
Science (New York, N.Y.)|July 12, 2014
In utero effects. In utero undernourishment perturbs the adult sperm methylome and intergenerational metabolismElizabeth J Radford, Mitsuteru Ito, Hui Shi, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 22, 2011
Acclimatization of skeletal muscle mitochondria to high-altitude hypoxia during an ascent of EverestDenny Z Levett, Elizabeth J Radford, David A Menassa, et al.
Plos Genetics|March 4, 2016
Role of the BAHD1 Chromatin-Repressive Complex in Placental Development and Regulation of Steroid MetabolismGoran Lakisic, Alice Lebreton, Renaud Pourpre, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 24, 2019
Intergenerational transmission of the positive effects of physical exercise on brain and cognitionKerry R McGreevy, Patricia Tezanos, Iria Ferreiro-Villar, et al.
Nature|September 28, 2018
Common genetic variants contribute to risk of rare severe neurodevelopmental disordersMari E K Niemi, Hilary C Martin, Daniel L Rice, et al.
Nature Communications|December 6, 2023
Saturation genome editing of DDX3X clarifies pathogenicity of germline and somatic variationElizabeth J Radford, Hong-Kee Tan, Malin H L Andersson, et al.
Nature|November 20, 2024
Examining the role of common variants in rare neurodevelopmental conditionsQin Qin Huang, Emilie M Wigdor, Daniel S Malawsky, et al.
Pageof 3