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

J Lake

Showing results (281-290 of 288) with videos related to

Pageof 29
Sort By:
You have reached the last page of results.This site can display upto 288 results.
Medrxiv : the Preprint Server for Health Sciences|December 16, 2024
Epigenome-wide Association Analysis of Mitochondrial Heteroplasmy Provides Insight into Molecular Mechanisms of DiseaseMeng Lai, Kyeezu Kim, Yinan Zheng, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|September 11, 2012
Solid-organ transplantation in older adults: current status and future researchM Abecassis, N D Bridges, C J Clancy, et al.
Nature Communications|December 2, 2025
Epigenome-wide association study of nuclear DNA methylation in relation to mitochondrial heteroplasmyMeng Lai, Kyeezu Kim, Yinan Zheng, et al.
Med (New York, N.Y.)|February 12, 2021
Fatal perinatal mitochondrial cardiac failure caused by recurrent <i>de novo</i> duplications in the <i>ATAD3</i> locusAnn E Frazier, Alison G Compton, Yoshihito Kishita, et al.
The Journal of Trauma|March 10, 2001
Penetrating esophageal injuries: multicenter study of the American Association for the Surgery of TraumaJ A Asensio, S Chahwan, W Forno, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 14, 2024
Upregulation versus loss of function of NTRK2 in 44 affected individuals leads to 2 distinct neurodevelopmental disordersEva Berger, Robin-Tobias Jauss, Judith D Ranells, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 21, 2024
The Australian Genomics Mitochondrial Flagship: A national program delivering mitochondrial diagnosesRocio Rius, Alison G Compton, Naomi L Baker, et al.
Nature Genetics|October 22, 2025
Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic functionReza Asadollahi, Aisha Ahmad, Paranchai Boonsawat, et al.
Pageof 29

Showing results (281-290 of 288) with videos related to

Sort By:
Pageof 29
You have reached the last page of results.This site can display upto 288 results.
Medrxiv : the Preprint Server for Health Sciences|December 16, 2024
Epigenome-wide Association Analysis of Mitochondrial Heteroplasmy Provides Insight into Molecular Mechanisms of DiseaseMeng Lai, Kyeezu Kim, Yinan Zheng, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|September 11, 2012
Solid-organ transplantation in older adults: current status and future researchM Abecassis, N D Bridges, C J Clancy, et al.
Nature Communications|December 2, 2025
Epigenome-wide association study of nuclear DNA methylation in relation to mitochondrial heteroplasmyMeng Lai, Kyeezu Kim, Yinan Zheng, et al.
Med (New York, N.Y.)|February 12, 2021
Fatal perinatal mitochondrial cardiac failure caused by recurrent <i>de novo</i> duplications in the <i>ATAD3</i> locusAnn E Frazier, Alison G Compton, Yoshihito Kishita, et al.
The Journal of Trauma|March 10, 2001
Penetrating esophageal injuries: multicenter study of the American Association for the Surgery of TraumaJ A Asensio, S Chahwan, W Forno, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 14, 2024
Upregulation versus loss of function of NTRK2 in 44 affected individuals leads to 2 distinct neurodevelopmental disordersEva Berger, Robin-Tobias Jauss, Judith D Ranells, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 21, 2024
The Australian Genomics Mitochondrial Flagship: A national program delivering mitochondrial diagnosesRocio Rius, Alison G Compton, Naomi L Baker, et al.
Nature Genetics|October 22, 2025
Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic functionReza Asadollahi, Aisha Ahmad, Paranchai Boonsawat, et al.
Pageof 29