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

M DeAngelis

Showing results (501-510 of 512) with videos related to

Pageof 52
Sort By:
Acta Neuropathologica|September 12, 2025
Prospective characterization of germline variants in patients with gliomas and glioneuronal tumorsSubhiksha Nandakumar, Miika Mehine, Yelena Kemel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 11, 2019
ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorderLloyd B Williams, Asif Javed, Amin Sabri, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 3, 2019
Genomic Correlates of Disease Progression and Treatment Response in Prospectively Characterized GliomasPhilip Jonsson, Andrew L Lin, Robert J Young, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|February 5, 2019
Buparlisib in Patients With Recurrent Glioblastoma Harboring Phosphatidylinositol 3-Kinase Pathway Activation: An Open-Label, Multicenter, Multi-Arm, Phase II TrialPatrick Y Wen, Mehdi Touat, Brian M Alexander, et al.
Science (New York, N.Y.)|December 22, 1995
An STS-based map of the human genomeT J Hudson, L D Stein, S S Gerety, et al.
Nature Genetics|January 16, 2019
Tumor mutational load predicts survival after immunotherapy across multiple cancer typesRobert M Samstein, Chung-Han Lee, Alexander N Shoushtari, et al.
Nature Genetics|September 17, 2013
Identification of a rare coding variant in complement 3 associated with age-related macular degenerationXiaowei Zhan, David E Larson, Chaolong Wang, et al.
Human Molecular Genetics|June 6, 2014
Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degenerationRinki Ratnapriya, Xiaowei Zhan, Robert N Fariss, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 14, 2010
Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degenerationWei Chen, Dwight Stambolian, Albert O Edwards, et al.
Nature Microbiology|June 10, 2020
Roadmap for naming uncultivated Archaea and BacteriaAlison E Murray, John Freudenstein, Simonetta Gribaldo, et al.
Pageof 52

Showing results (501-510 of 512) with videos related to

Sort By:
Pageof 52
Acta Neuropathologica|September 12, 2025
Prospective characterization of germline variants in patients with gliomas and glioneuronal tumorsSubhiksha Nandakumar, Miika Mehine, Yelena Kemel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 11, 2019
ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorderLloyd B Williams, Asif Javed, Amin Sabri, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 3, 2019
Genomic Correlates of Disease Progression and Treatment Response in Prospectively Characterized GliomasPhilip Jonsson, Andrew L Lin, Robert J Young, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|February 5, 2019
Buparlisib in Patients With Recurrent Glioblastoma Harboring Phosphatidylinositol 3-Kinase Pathway Activation: An Open-Label, Multicenter, Multi-Arm, Phase II TrialPatrick Y Wen, Mehdi Touat, Brian M Alexander, et al.
Science (New York, N.Y.)|December 22, 1995
An STS-based map of the human genomeT J Hudson, L D Stein, S S Gerety, et al.
Nature Genetics|January 16, 2019
Tumor mutational load predicts survival after immunotherapy across multiple cancer typesRobert M Samstein, Chung-Han Lee, Alexander N Shoushtari, et al.
Nature Genetics|September 17, 2013
Identification of a rare coding variant in complement 3 associated with age-related macular degenerationXiaowei Zhan, David E Larson, Chaolong Wang, et al.
Human Molecular Genetics|June 6, 2014
Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degenerationRinki Ratnapriya, Xiaowei Zhan, Robert N Fariss, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 14, 2010
Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degenerationWei Chen, Dwight Stambolian, Albert O Edwards, et al.
Nature Microbiology|June 10, 2020
Roadmap for naming uncultivated Archaea and BacteriaAlison E Murray, John Freudenstein, Simonetta Gribaldo, et al.
Pageof 52