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Neil C Chi

Showing results (71-80 of 83) with videos related to

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Journal of Molecular and Cellular Cardiology|May 21, 2017
Impaired mitophagy facilitates mitochondrial damage in Danon diseaseSherin I Hashem, Anne N Murphy, Ajit S Divakaruni, et al.
Stem Cell Reports|August 21, 2018
Cell-Surface Marker Signature for Enrichment of Ventricular Cardiomyocytes Derived from Human Embryonic Stem CellsJennifer Veevers, Elie N Farah, Mirko Corselli, et al.
Nature Genetics|May 26, 2015
Inactivating mutations in MFSD2A, required for omega-3 fatty acid transport in brain, cause a lethal microcephaly syndromeAlicia Guemez-Gamboa, Long N Nguyen, Hongbo Yang, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 10, 2011
Iroquois homeobox gene 3 establishes fast conduction in the cardiac His-Purkinje networkShan-Shan Zhang, Kyoung-Han Kim, Anna Rosen, et al.
Medrxiv : the Preprint Server for Health Sciences|November 14, 2023
<i>CXCL12</i> drives natural variation in coronary artery anatomy across diverse populationsPamela E Rios Coronado, Daniela Zanetti, Jiayan Zhou, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2025
Single cell multiomics and 3D genome architecture reveal novel pathways of human heart failureYang Xie, Luca Tucciarone, Elie N Farah, et al.
Cell|March 6, 2025
CXCL12 drives natural variation in coronary artery anatomy across diverse populationsPamela E Rios Coronado, Jiayan Zhou, Xiaochen Fan, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2025
Single cell multiomics reveals drivers of metabolic dysfunction-associated steatohepatitisWeston Elison, Lei Chang, Yang Xie, et al.
Neuron|April 15, 2018
Mutations in KATNB1 Cause Complex Cerebral Malformations by Disrupting Asymmetrically Dividing Neural ProgenitorsKetu Mishra-Gorur, Ahmet Okay Çağlayan, Ashleigh E Schaffer, et al.
Cell|May 14, 2013
Epigenomic analysis of multilineage differentiation of human embryonic stem cellsWei Xie, Matthew D Schultz, Ryan Lister, et al.
Pageof 9

Showing results (71-80 of 83) with videos related to

Sort By:
Pageof 9
Journal of Molecular and Cellular Cardiology|May 21, 2017
Impaired mitophagy facilitates mitochondrial damage in Danon diseaseSherin I Hashem, Anne N Murphy, Ajit S Divakaruni, et al.
Stem Cell Reports|August 21, 2018
Cell-Surface Marker Signature for Enrichment of Ventricular Cardiomyocytes Derived from Human Embryonic Stem CellsJennifer Veevers, Elie N Farah, Mirko Corselli, et al.
Nature Genetics|May 26, 2015
Inactivating mutations in MFSD2A, required for omega-3 fatty acid transport in brain, cause a lethal microcephaly syndromeAlicia Guemez-Gamboa, Long N Nguyen, Hongbo Yang, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 10, 2011
Iroquois homeobox gene 3 establishes fast conduction in the cardiac His-Purkinje networkShan-Shan Zhang, Kyoung-Han Kim, Anna Rosen, et al.
Medrxiv : the Preprint Server for Health Sciences|November 14, 2023
<i>CXCL12</i> drives natural variation in coronary artery anatomy across diverse populationsPamela E Rios Coronado, Daniela Zanetti, Jiayan Zhou, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2025
Single cell multiomics and 3D genome architecture reveal novel pathways of human heart failureYang Xie, Luca Tucciarone, Elie N Farah, et al.
Cell|March 6, 2025
CXCL12 drives natural variation in coronary artery anatomy across diverse populationsPamela E Rios Coronado, Jiayan Zhou, Xiaochen Fan, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2025
Single cell multiomics reveals drivers of metabolic dysfunction-associated steatohepatitisWeston Elison, Lei Chang, Yang Xie, et al.
Neuron|April 15, 2018
Mutations in KATNB1 Cause Complex Cerebral Malformations by Disrupting Asymmetrically Dividing Neural ProgenitorsKetu Mishra-Gorur, Ahmet Okay Çağlayan, Ashleigh E Schaffer, et al.
Cell|May 14, 2013
Epigenomic analysis of multilineage differentiation of human embryonic stem cellsWei Xie, Matthew D Schultz, Ryan Lister, et al.
Pageof 9