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Lijiang Ma

Showing results (51-60 of 62) with videos related to

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Nature Cardiovascular Research|April 10, 2025
Single-cell RNA sequencing reveals sex differences in the subcellular composition and associated gene-regulatory network activity of human carotid plaquesKatyayani Sukhavasi, Giuseppe Mocci, Lijiang Ma, et al.
Human Genetics|September 30, 2016
De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart diseaseLijiang Ma, Yavuz Bayram, Heather M McLaughlin, et al.
Circulation Research|October 12, 2020
Genetic Regulation of Atherosclerosis-Relevant Phenotypes in Human Vascular Smooth Muscle CellsRedouane Aherrahrou, Liang Guo, V Peter Nagraj, et al.
Nature Cardiovascular Research|September 13, 2024
Integrative gene regulatory network analysis discloses key driver genes of fibromuscular dysplasiaValentina d'Escamard, Daniella Kadian-Dodov, Lijiang Ma, et al.
Circulation Research|April 19, 2024
Single-Cell Gene-Regulatory Networks of Advanced Symptomatic AtherosclerosisGiuseppe Mocci, Katyayani Sukhavasi, Tiit Örd, et al.
Science (New York, N.Y.)|January 20, 2016
De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomaliesJason Homsy, Samir Zaidi, Yufeng Shen, et al.
Nature|May 14, 2013
De novo mutations in histone-modifying genes in congenital heart diseaseSamir Zaidi, Murim Choi, Hiroko Wakimoto, et al.
Circulation. Genomic and Precision Medicine|October 26, 2018
Loss-of-Function ABCC8 Mutations in Pulmonary Arterial HypertensionMichael S Bohnen, Lijiang Ma, Na Zhu, et al.
Nature Genetics|May 29, 2023
Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulationDavid Adlam, Takiy-Eddine Berrandou, Adrien Georges, et al.
Nature Communications|October 16, 2021
Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseasesAdrien Georges, Min-Lee Yang, Takiy-Eddine Berrandou, et al.
Pageof 7

Showing results (51-60 of 62) with videos related to

Sort By:
Pageof 7
Nature Cardiovascular Research|April 10, 2025
Single-cell RNA sequencing reveals sex differences in the subcellular composition and associated gene-regulatory network activity of human carotid plaquesKatyayani Sukhavasi, Giuseppe Mocci, Lijiang Ma, et al.
Human Genetics|September 30, 2016
De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart diseaseLijiang Ma, Yavuz Bayram, Heather M McLaughlin, et al.
Circulation Research|October 12, 2020
Genetic Regulation of Atherosclerosis-Relevant Phenotypes in Human Vascular Smooth Muscle CellsRedouane Aherrahrou, Liang Guo, V Peter Nagraj, et al.
Nature Cardiovascular Research|September 13, 2024
Integrative gene regulatory network analysis discloses key driver genes of fibromuscular dysplasiaValentina d'Escamard, Daniella Kadian-Dodov, Lijiang Ma, et al.
Circulation Research|April 19, 2024
Single-Cell Gene-Regulatory Networks of Advanced Symptomatic AtherosclerosisGiuseppe Mocci, Katyayani Sukhavasi, Tiit Örd, et al.
Science (New York, N.Y.)|January 20, 2016
De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomaliesJason Homsy, Samir Zaidi, Yufeng Shen, et al.
Nature|May 14, 2013
De novo mutations in histone-modifying genes in congenital heart diseaseSamir Zaidi, Murim Choi, Hiroko Wakimoto, et al.
Circulation. Genomic and Precision Medicine|October 26, 2018
Loss-of-Function ABCC8 Mutations in Pulmonary Arterial HypertensionMichael S Bohnen, Lijiang Ma, Na Zhu, et al.
Nature Genetics|May 29, 2023
Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulationDavid Adlam, Takiy-Eddine Berrandou, Adrien Georges, et al.
Nature Communications|October 16, 2021
Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseasesAdrien Georges, Min-Lee Yang, Takiy-Eddine Berrandou, et al.
Pageof 7