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Chunyu Liu

Showing results (561-570 of 749) with videos related to

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Clinical Epigenetics|October 27, 2022
Marijuana use and DNA methylation-based biological age in young adultsDrew R Nannini, Yinan Zheng, Brian T Joyce, et al.
Science (New York, N.Y.)|May 23, 2024
Developmental isoform diversity in the human neocortex informs neuropsychiatric risk mechanismsAshok Patowary, Pan Zhang, Connor Jops, et al.
JCI Insight|July 22, 2022
The epigenetic reader PHF21B modulates murine social memory and synaptic plasticity-related genesEunice Wm Chin, Qi Ma, Hongyu Ruan, et al.
Journal of Assisted Reproduction and Genetics|April 22, 2020
A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferensHuan Wu, Yang Gao, Cong Ma, et al.
Neurobiology of Aging|August 16, 2021
Absence of coding somatic single nucleotide variants within well-known candidate genes in late-onset sporadic Alzheimer's Disease based on the analysis of multi-omics dataShishi Min, Zongchang Li, Annie Shieh, et al.
Obesity (Silver Spring, Md.)|July 21, 2006
PAI-1 Gene 4G/5G polymorphism and risk of type 2 diabetes in a population-based sampleJames B Meigs, Josée Dupuis, Chunyu Liu, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 6, 2009
Common and rare variants of DAOA in bipolar disorderManjula Maheshwari, Jiajun Shi, Judith A Badner, et al.
Journal of the American Heart Association|June 10, 2023
Metabolomic Profiles, Ideal Cardiovascular Health, and Risk of Heart Failure and Atrial Fibrillation: Insights From the Framingham Heart StudyYi Li, Ayana Gray, Liying Xue, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|June 23, 2024
Deficiency of MFSD6L, an acrosome membrane protein, causes oligoasthenoteratozoospermia in humans and miceDapeng Zhou, Huan Wu, Lingbo Wang, et al.
Molecular Medicine (Cambridge, Mass.)|July 11, 2008
Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritisChunyu Liu, Franak Batliwalla, Wentian Li, et al.
Pageof 75

Showing results (561-570 of 749) with videos related to

Sort By:
Pageof 75
Clinical Epigenetics|October 27, 2022
Marijuana use and DNA methylation-based biological age in young adultsDrew R Nannini, Yinan Zheng, Brian T Joyce, et al.
Science (New York, N.Y.)|May 23, 2024
Developmental isoform diversity in the human neocortex informs neuropsychiatric risk mechanismsAshok Patowary, Pan Zhang, Connor Jops, et al.
JCI Insight|July 22, 2022
The epigenetic reader PHF21B modulates murine social memory and synaptic plasticity-related genesEunice Wm Chin, Qi Ma, Hongyu Ruan, et al.
Journal of Assisted Reproduction and Genetics|April 22, 2020
A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferensHuan Wu, Yang Gao, Cong Ma, et al.
Neurobiology of Aging|August 16, 2021
Absence of coding somatic single nucleotide variants within well-known candidate genes in late-onset sporadic Alzheimer's Disease based on the analysis of multi-omics dataShishi Min, Zongchang Li, Annie Shieh, et al.
Obesity (Silver Spring, Md.)|July 21, 2006
PAI-1 Gene 4G/5G polymorphism and risk of type 2 diabetes in a population-based sampleJames B Meigs, Josée Dupuis, Chunyu Liu, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 6, 2009
Common and rare variants of DAOA in bipolar disorderManjula Maheshwari, Jiajun Shi, Judith A Badner, et al.
Journal of the American Heart Association|June 10, 2023
Metabolomic Profiles, Ideal Cardiovascular Health, and Risk of Heart Failure and Atrial Fibrillation: Insights From the Framingham Heart StudyYi Li, Ayana Gray, Liying Xue, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|June 23, 2024
Deficiency of MFSD6L, an acrosome membrane protein, causes oligoasthenoteratozoospermia in humans and miceDapeng Zhou, Huan Wu, Lingbo Wang, et al.
Molecular Medicine (Cambridge, Mass.)|July 11, 2008
Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritisChunyu Liu, Franak Batliwalla, Wentian Li, et al.
Pageof 75