Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

A Glass

Showing results (621-630 of 684) with videos related to

Pageof 69
Sort By:
Journal of Medical Genetics|February 5, 2016
Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestaltNataliya Di Donato, Teresa Neuhann, Anne-Karin Kahlert, et al.
The American Journal of Sports Medicine|July 10, 2018
The Incidence of Glenohumeral Bone and Cartilage Lesions at the Time of Anterior Shoulder Stabilization Surgery: A Comparison of Patients Undergoing Primary and Revision SurgeryKyle R Duchman, Carolyn M Hettrich, Natalie A Glass, et al.
Journal of Shoulder and Elbow Surgery|December 5, 2024
The effect of reverse shoulder arthroplasty design and surgical indications on deltoid and rotator cuff muscle lengthMichael J Maxwell, Evan A Glass, Adam R Bowler, et al.
Brain : a Journal of Neurology|September 6, 2023
MerTK is a mediator of alpha-synuclein fibril uptake by human microgliaMarie-France Dorion, Moein Yaqubi, Konstantin Senkevich, et al.
The Journal of Biological Chemistry|June 24, 2022
Impaired mitophagy in Sanfilippo a mice causes hypertriglyceridemia and brown adipose tissue activationMiguel Tillo, William C Lamanna, Chrissa A Dwyer, et al.
Science (New York, N.Y.)|October 19, 2019
Spatiotemporal expansion of primary progenitor zones in the developing human cerebellumParthiv Haldipur, Kimberly A Aldinger, Silvia Bernardo, et al.
Nature Neuroscience|June 18, 2021
Spatial and cell type transcriptional landscape of human cerebellar developmentKimberly A Aldinger, Zachary Thomson, Ian G Phelps, et al.
Medrxiv : the Preprint Server for Health Sciences|January 23, 2024
<i>De novo</i> variants in <i>PLCG1</i> are associated with hearing impairment, ocular pathology, and cardiac defectsMengqi Ma, Yiming Zheng, Shenzhao Lu, et al.
Annals of Neurology|March 9, 2018
Recessive mutations in VPS13D cause childhood onset movement disordersJulie Gauthier, Inge A Meijer, Davor Lessel, et al.
Medrxiv : the Preprint Server for Health Sciences|May 7, 2026
Genome-wide detection and clinical prioritization of tandem repeat outliers using long-read sequencingSophia B Gibson, Nikhita Damaraju, J Gus Gustafson, et al.
Pageof 69

Showing results (621-630 of 684) with videos related to

Sort By:
Pageof 69
Journal of Medical Genetics|February 5, 2016
Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestaltNataliya Di Donato, Teresa Neuhann, Anne-Karin Kahlert, et al.
The American Journal of Sports Medicine|July 10, 2018
The Incidence of Glenohumeral Bone and Cartilage Lesions at the Time of Anterior Shoulder Stabilization Surgery: A Comparison of Patients Undergoing Primary and Revision SurgeryKyle R Duchman, Carolyn M Hettrich, Natalie A Glass, et al.
Journal of Shoulder and Elbow Surgery|December 5, 2024
The effect of reverse shoulder arthroplasty design and surgical indications on deltoid and rotator cuff muscle lengthMichael J Maxwell, Evan A Glass, Adam R Bowler, et al.
Brain : a Journal of Neurology|September 6, 2023
MerTK is a mediator of alpha-synuclein fibril uptake by human microgliaMarie-France Dorion, Moein Yaqubi, Konstantin Senkevich, et al.
The Journal of Biological Chemistry|June 24, 2022
Impaired mitophagy in Sanfilippo a mice causes hypertriglyceridemia and brown adipose tissue activationMiguel Tillo, William C Lamanna, Chrissa A Dwyer, et al.
Science (New York, N.Y.)|October 19, 2019
Spatiotemporal expansion of primary progenitor zones in the developing human cerebellumParthiv Haldipur, Kimberly A Aldinger, Silvia Bernardo, et al.
Nature Neuroscience|June 18, 2021
Spatial and cell type transcriptional landscape of human cerebellar developmentKimberly A Aldinger, Zachary Thomson, Ian G Phelps, et al.
Medrxiv : the Preprint Server for Health Sciences|January 23, 2024
<i>De novo</i> variants in <i>PLCG1</i> are associated with hearing impairment, ocular pathology, and cardiac defectsMengqi Ma, Yiming Zheng, Shenzhao Lu, et al.
Annals of Neurology|March 9, 2018
Recessive mutations in VPS13D cause childhood onset movement disordersJulie Gauthier, Inge A Meijer, Davor Lessel, et al.
Medrxiv : the Preprint Server for Health Sciences|May 7, 2026
Genome-wide detection and clinical prioritization of tandem repeat outliers using long-read sequencingSophia B Gibson, Nikhita Damaraju, J Gus Gustafson, et al.
Pageof 69