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Michael Wolf

Showing results (461-470 of 466) with videos related to

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JACC. Clinical Electrophysiology|December 21, 2019
Ultra-High-Density Activation Mapping to Aid Isthmus Identification of Atrial Tachycardias in Congenital Heart DiseaseClaire A Martin, Arthur Yue, Ruairidh Martin, et al.
Hemasphere|February 23, 2026
Wnt-dependent spatiotemporal reprogramming of bone marrow niches drives fibrosisBella Banjanin, James Nagai, YeVin Mun, et al.
Molecular Cancer|October 15, 2025
Thyroid hormone receptor beta signaling is a targetable driver of prostate cancer growthAleksandra Fesiuk, Daniel Pölöske, Elvin D de Araujo, et al.
Clinical Genetics|October 28, 2020
Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1Zippora Brownstein, Suleyman Gulsuner, Tom Walsh, et al.
Brain : a Journal of Neurology|May 2, 2017
Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxiaMartina Minnerop, Delia Kurzwelly, Holger Wagner, et al.
JAMA Pediatrics|February 28, 2017
Families as Partners in Hospital Error and Adverse Event SurveillanceAlisa Khan, Maitreya Coffey, Katherine P Litterer, et al.
Pageof 47

Showing results (461-470 of 466) with videos related to

Sort By:
Pageof 47
You have reached the last page of results.This site can display upto 466 results.
JACC. Clinical Electrophysiology|December 21, 2019
Ultra-High-Density Activation Mapping to Aid Isthmus Identification of Atrial Tachycardias in Congenital Heart DiseaseClaire A Martin, Arthur Yue, Ruairidh Martin, et al.
Hemasphere|February 23, 2026
Wnt-dependent spatiotemporal reprogramming of bone marrow niches drives fibrosisBella Banjanin, James Nagai, YeVin Mun, et al.
Molecular Cancer|October 15, 2025
Thyroid hormone receptor beta signaling is a targetable driver of prostate cancer growthAleksandra Fesiuk, Daniel Pölöske, Elvin D de Araujo, et al.
Clinical Genetics|October 28, 2020
Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1Zippora Brownstein, Suleyman Gulsuner, Tom Walsh, et al.
Brain : a Journal of Neurology|May 2, 2017
Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxiaMartina Minnerop, Delia Kurzwelly, Holger Wagner, et al.
JAMA Pediatrics|February 28, 2017
Families as Partners in Hospital Error and Adverse Event SurveillanceAlisa Khan, Maitreya Coffey, Katherine P Litterer, et al.
Pageof 47