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Chunyu Liu

Showing results (631-640 of 749) with videos related to

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Clinical Epigenetics|October 27, 2023
Multi-tissue epigenetic analysis identifies distinct associations underlying insulin resistance and Alzheimer's disease at CPT1A locusChloé Sarnowski, Tianxiao Huan, Yiyi Ma, et al.
Medrxiv : the Preprint Server for Health Sciences|February 9, 2026
ASSOCIATION ANALYSIS OF MITOCHONDRIAL HETEROPLASMIC VARIANTS AND CARDIOMETABOLIC TRAITSXianbang Sun, Xue Liu, Katia Bulekova, et al.
Nature Communications|August 9, 2018
Evaluation of chromatin accessibility in prefrontal cortex of individuals with schizophreniaJulien Bryois, Melanie E Garrett, Lingyun Song, et al.
Reproductive Biology and Endocrinology : RB&E|January 4, 2022
Homozygous mutation in SLO3 leads to severe asthenoteratozoospermia due to acrosome hypoplasia and mitochondrial sheath malformationsMingrong Lv, Chunyu Liu, Chunjie Ma, et al.
Science China. Life Sciences|December 20, 2024
Homozygous deleterious variants in MYCBPAP induce asthenoteratozoospermia involving abnormal acrosome biogenesis, manchette structure and sperm tail assembly in humans and miceYiling Zhou, Chaofeng Tu, Charles Coutton, et al.
Epigenomics|January 26, 2023
Opioid medication use and blood DNA methylation: epigenome-wide association meta-analysisMikyeong Lee, Roby Joehanes, Daniel L McCartney, et al.
American Journal of Human Genetics|July 8, 2021
Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and miceChaofeng Tu, Jiangshan Cong, Qianjun Zhang, et al.
European Heart Journal|April 17, 2012
Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) ConsortiumArtur Fedorowski, Nora Franceschini, Jennifer Brody, et al.
American Journal of Human Genetics|April 2, 2019
Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and MiceWangjie Liu, Xiaojin He, Shenmin Yang, et al.
Nature Communications|August 17, 2018
Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular diseaseChen Yao, George Chen, Ci Song, et al.
Pageof 75

Showing results (631-640 of 749) with videos related to

Sort By:
Pageof 75
Clinical Epigenetics|October 27, 2023
Multi-tissue epigenetic analysis identifies distinct associations underlying insulin resistance and Alzheimer's disease at CPT1A locusChloé Sarnowski, Tianxiao Huan, Yiyi Ma, et al.
Medrxiv : the Preprint Server for Health Sciences|February 9, 2026
ASSOCIATION ANALYSIS OF MITOCHONDRIAL HETEROPLASMIC VARIANTS AND CARDIOMETABOLIC TRAITSXianbang Sun, Xue Liu, Katia Bulekova, et al.
Nature Communications|August 9, 2018
Evaluation of chromatin accessibility in prefrontal cortex of individuals with schizophreniaJulien Bryois, Melanie E Garrett, Lingyun Song, et al.
Reproductive Biology and Endocrinology : RB&E|January 4, 2022
Homozygous mutation in SLO3 leads to severe asthenoteratozoospermia due to acrosome hypoplasia and mitochondrial sheath malformationsMingrong Lv, Chunyu Liu, Chunjie Ma, et al.
Science China. Life Sciences|December 20, 2024
Homozygous deleterious variants in MYCBPAP induce asthenoteratozoospermia involving abnormal acrosome biogenesis, manchette structure and sperm tail assembly in humans and miceYiling Zhou, Chaofeng Tu, Charles Coutton, et al.
Epigenomics|January 26, 2023
Opioid medication use and blood DNA methylation: epigenome-wide association meta-analysisMikyeong Lee, Roby Joehanes, Daniel L McCartney, et al.
American Journal of Human Genetics|July 8, 2021
Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and miceChaofeng Tu, Jiangshan Cong, Qianjun Zhang, et al.
European Heart Journal|April 17, 2012
Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) ConsortiumArtur Fedorowski, Nora Franceschini, Jennifer Brody, et al.
American Journal of Human Genetics|April 2, 2019
Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and MiceWangjie Liu, Xiaojin He, Shenmin Yang, et al.
Nature Communications|August 17, 2018
Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular diseaseChen Yao, George Chen, Ci Song, et al.
Pageof 75