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James Cranley

Showing results (11-20 of 20) with videos related to

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Nature Cardiovascular Research|March 20, 2023
A single-cell comparison of adult and fetal human epicardium defines the age-associated changes in epicardial activityVincent R Knight-Schrijver, Hongorzul Davaapil, Semih Bayraktar, et al.
Nature Cardiovascular Research|April 26, 2024
Erratum: Author Correction: A single-cell comparison of adult and fetal human epicardium defines the age-associated changes in epicardial activityVincent R Knight-Schrijver, Hongorzul Davaapil, Semih Bayraktar, et al.
Radiology|July 16, 2024
Multidimensional Analysis of the Adult Human Heart in Health and Disease Using Hierarchical Phase-Contrast TomographyJoseph Brunet, Andrew C Cook, Claire L Walsh, et al.
Nature|November 20, 2024
A multi-omic atlas of human embryonic skeletal developmentKen To, Lijiang Fei, J Patrick Pett, et al.
Nature|March 21, 2025
Author Correction: Spatially resolved multiomics of human cardiac nichesKazumasa Kanemaru, James Cranley, Daniele Muraro, et al.
Nature|July 12, 2023
Spatially resolved multiomics of human cardiac nichesKazumasa Kanemaru, James Cranley, Daniele Muraro, et al.
Nature Medicine|November 20, 2024
An organotypic atlas of human vascular cellsSam N Barnett, Ana-Maria Cujba, Lu Yang, et al.
Science (New York, N.Y.)|August 4, 2022
Pathogenic variants damage cell composition and single cell transcription in cardiomyopathiesDaniel Reichart, Eric L Lindberg, Henrike Maatz, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2024
Biallelic variants in <i>POPDC2</i> cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
American Journal of Human Genetics|May 23, 2025
Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Nature Cardiovascular Research|March 20, 2023
A single-cell comparison of adult and fetal human epicardium defines the age-associated changes in epicardial activityVincent R Knight-Schrijver, Hongorzul Davaapil, Semih Bayraktar, et al.
Nature Cardiovascular Research|April 26, 2024
Erratum: Author Correction: A single-cell comparison of adult and fetal human epicardium defines the age-associated changes in epicardial activityVincent R Knight-Schrijver, Hongorzul Davaapil, Semih Bayraktar, et al.
Radiology|July 16, 2024
Multidimensional Analysis of the Adult Human Heart in Health and Disease Using Hierarchical Phase-Contrast TomographyJoseph Brunet, Andrew C Cook, Claire L Walsh, et al.
Nature|November 20, 2024
A multi-omic atlas of human embryonic skeletal developmentKen To, Lijiang Fei, J Patrick Pett, et al.
Nature|March 21, 2025
Author Correction: Spatially resolved multiomics of human cardiac nichesKazumasa Kanemaru, James Cranley, Daniele Muraro, et al.
Nature|July 12, 2023
Spatially resolved multiomics of human cardiac nichesKazumasa Kanemaru, James Cranley, Daniele Muraro, et al.
Nature Medicine|November 20, 2024
An organotypic atlas of human vascular cellsSam N Barnett, Ana-Maria Cujba, Lu Yang, et al.
Science (New York, N.Y.)|August 4, 2022
Pathogenic variants damage cell composition and single cell transcription in cardiomyopathiesDaniel Reichart, Eric L Lindberg, Henrike Maatz, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2024
Biallelic variants in <i>POPDC2</i> cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
American Journal of Human Genetics|May 23, 2025
Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
Pageof 2