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Iscience
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January 6, 2026
TET3 protects the <i>Dlk1-Dio3</i> imprinted locus from DNA hypomethylation during adult NSC reprogramming
Laura 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 programming
Elizabeth 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 disorders
Olivia 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 metabolism
Elizabeth 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 Everest
Denny 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 Metabolism
Goran 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 cognition
Kerry R McGreevy, Patricia Tezanos, Iria Ferreiro-Villar, et al.
Nature
|
September 28, 2018
Common genetic variants contribute to risk of rare severe neurodevelopmental disorders
Mari 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 variation
Elizabeth J Radford, Hong-Kee Tan, Malin H L Andersson, et al.
Nature
|
November 20, 2024
Examining the role of common variants in rare neurodevelopmental conditions
Qin Qin Huang, Emilie M Wigdor, Daniel S Malawsky, et al.
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Search research articles
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Showing results (11-20 of 22) with videos related to
Sort By:
Page
of 3
Iscience
|
January 6, 2026
TET3 protects the <i>Dlk1-Dio3</i> imprinted locus from DNA hypomethylation during adult NSC reprogramming
Laura 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 programming
Elizabeth 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 disorders
Olivia 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 metabolism
Elizabeth 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 Everest
Denny 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 Metabolism
Goran 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 cognition
Kerry R McGreevy, Patricia Tezanos, Iria Ferreiro-Villar, et al.
Nature
|
September 28, 2018
Common genetic variants contribute to risk of rare severe neurodevelopmental disorders
Mari 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 variation
Elizabeth J Radford, Hong-Kee Tan, Malin H L Andersson, et al.
Nature
|
November 20, 2024
Examining the role of common variants in rare neurodevelopmental conditions
Qin Qin Huang, Emilie M Wigdor, Daniel S Malawsky, et al.
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of 3